ANNIE PARDO CEMO



DATOS GENERALES
Nombre completo   ANNIE PARDO CEMO
Máximo nivel de estudios   DOCTORADO
Antigüedad académica en la UNAM   59 años
NOMBRAMIENTOS
Vigente   PROFESOR ASIGNATURA B Definitivo
Facultad de Ciencias
Desde 16-01-2011
PROFESOR DE CARRERA EMERITO Definitivo
Facultad de Ciencias
Desde 16-03-2014
PROFESOR DE CARRERA TITULAR C TC Definitivo
Facultad de Ciencias
Desde 01-01-2008 (fecha inicial de registros en el SIIA) hasta 15-03-2014
ESTIMULOS, PROGRAMAS, PREMIOS Y RECONOCIMIENTOS
* SNI Emérito2019 - VIGENTE
* SNI III - 2018
* PUN Investigación en ciencias naturales2018

INFORMACIÓN DE PUBLICACIONES
Firmas  
Pardo A. Pardo Cemo, A. Pardo Semo, Annie Pardo, A Pardo, A. Pardo, Anne
Pardo, Annie
ID's SCOPUS  
56013744200 58976811700 7102208701
ORCID's  
0000-0003-2168-9073
Áreas de conocimiento  
Allergy Biochemistry & molecular biology Biochemistry and molecular biology Biology Cardiac & cardiovascular systems
Cell biology Endocrinology and metabolism Genetics & heredity Genetics and heredity Geriatrics and gerontology
Gerontology Hematology Immunology Infectious diseases Instruments and instrumentation
Mathematical and computational biology Medical laboratory technology Medicine, general & internal Medicine, general and internal Multidisciplinary sciences
Oncology Pathology Pharmacology & pharmacy Pharmacology and pharmacy Physiology
Respiratory system Rheumatology Toxicology Aging Agricultural and biological sciences (miscellaneous)
Anatomy Biochemistry Biochemistry (medical) Biochemistry, genetics and molecular biology (miscellaneous) Cell biology
Clinical Biochemistry Critical care and intensive care medicine Dermatology Genetics Genetics (clinical)
Geriatrics and gerontology Immunology and Allergy Information systems Medicine (miscellaneous) Molecular Biology
Multidisciplinary Neurology Oncology Pathology and Forensic Medicine Pharmacology
Pharmacology (medical) Physiology Pulmonary and respiratory medicine Spectroscopy
Coautorías con entidades de la UNAM  
  • Centro de Ciencias Genómicas
  • Instituto de Química
  • Instituto de Fisiología Celular
  • Facultad de Ciencias
  • Facultad de Medicina
  • Facultad de Química
  • Facultad de Medicina Veterinaria y Zootecnia
  • Facultad de Estudios Superiores "Iztacala"
  • Escuela Nacional Colegio de Ciencias y Humanidades "Vallejo"
Revistas en las que ha publicado  (78):
  1. AGEING RESEARCH REVIEWS, Irlanda (2021)
  2. Aging Cell, Estados Unidos America (2016)
  3. Aging-Us, Estados Unidos America (2018, 2021)
  4. Allergy, Estados Unidos America (2011)
  5. AMERICAN JOURNAL OF PATHOLOGY, Estados Unidos America (1998, 2005)
  6. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, Estados Unidos America (1995, 1996, 1997, 1998, 1999, 2000, 2003, 2006, 2010, 2012, 2013, 2014, 2015, 2019, 2020, 2021)
  7. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, Estados Unidos America (1996, 1999, 2000, 2001, 2003, 2006, 2007, 2008, 2009, 2010, 2012, 2013, 2014, 2015, 2017, 2018, 2019, 2020, 2021, 2022, 2023, 2024, 2025, 2026)
  8. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, Estados Unidos America (1999, 2001, 2003, 2008, 2013, 2015, 2016, 2017, 2018, 2021)
  9. ANNALS OF INTERNAL MEDICINE, Estados Unidos America (2001)
  10. ANNALS OF THE AMERICAN THORACIC SOCIETY, Estados Unidos America (2006, 2010, 2016)
  11. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, Estados Unidos America (1991, 1999)
  12. ARCHIVOS DE BRONCONEUMOLOGIA, España (2004)
  13. ARTHRITIS AND RHEUMATISM, Estados Unidos America (1999)
  14. Autoimmunity, Reino Unido (2011)
  15. Autophagy, Estados Unidos America (2015)
  16. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, Países Bajos (1975)
  17. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, Países Bajos (1994)
  18. Biomolecules, Suiza (2021)
  19. BIOSENSORS-BASEL, Suiza (2021)
  20. BMC GENETICS, Reino Unido (2016)
  21. Brazilian Journal Of Medical And Biological Research, Brasil (1996)
  22. CANCER RESEARCH, Estados Unidos America (2007)
  23. Cells, Suiza (2022)
  24. CELLULAR SIGNALLING, Estados Unidos America (2020)
  25. CLINICAL BIOCHEMISTRY, Canada (2010)
  26. Clinical Pulmonary Medicine, Estados Unidos America (1995)
  27. Collagen And Related Research, (1986, 1987)
  28. CONNECTIVE TISSUE RESEARCH, Reino Unido (1974, 1980, 1991, 1992)
  29. Chest, Países Bajos (1989, 1991, 1992, 1995, 1998, 2000, 2001, 2002, 2003, 2004, 2015)
  30. DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION, Reino Unido (2017)
  31. Drugs, Nueva Zelanda (2004)
  32. ERJ Open Research, Suiza (2020, 2024)
  33. EUROPEAN RESPIRATORY JOURNAL, Reino Unido (2001, 2012, 2013, 2015, 2016, 2018, 2019, 2021, 2024, 2025, 2026)
  34. EXPERIMENTAL AND MOLECULAR PATHOLOGY, Estados Unidos America (1994, 2008, 2010, 2011)
  35. EXPERIMENTAL LUNG RESEARCH, Estados Unidos America (2006)
  36. EXPERT OPINION ON EMERGING DRUGS, Reino Unido (2011)
  37. FASEB JOURNAL, Estados Unidos America (2008, 2009, 2010, 2011, 2012, 2014, 2016, 2017, 2020)
  38. FEBS JOURNAL, Estados Unidos America (2014)
  39. Fibrogenesis and Tissue Repair, Reino Unido (2012)
  40. FREE RADICAL BIOLOGY AND MEDICINE, Estados Unidos America (2017)
  41. Frontiers in Bioscience-Landmark, Estados Unidos America (2002)
  42. FRONTIERS IN IMMUNOLOGY, Suiza (2022)
  43. Frontiers In Medicine, Suiza (2021)
  44. HISTOLOGY AND HISTOPATHOLOGY, España (1999)
  45. HUMAN GENETICS, Estados Unidos America (2003, 2005, 2008, 2009)
  46. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, Reino Unido (1997, 2002, 2005, 2007, 2008)
  47. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, Suiza (2021)
  48. JOURNAL OF BIOLOGICAL CHEMISTRY, Estados Unidos America (2013)
  49. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, Estados Unidos America (1983, 2020, 2024)
  50. JOURNAL OF INFECTIOUS DISEASES, Estados Unidos America (2000)
  51. JOURNAL OF LEUKOCYTE BIOLOGY, Estados Unidos America (2001)
  52. JOURNAL OF PATHOLOGY, Estados Unidos America (2016)
  53. JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, Estados Unidos America (2017)
  54. LABORATORY INVESTIGATION, Estados Unidos America (2011)
  55. Lancet, Estados Unidos America (2011)
  56. LANCET RESPIRATORY MEDICINE, Reino Unido (2015, 2023)
  57. Lung, Estados Unidos America (1993)
  58. Matrix (stuttgart, Germany). Supplement, (1992)
  59. MATRIX BIOLOGY, Países Bajos (2018)
  60. MEDICAL HYPOTHESES, Reino Unido (1980)
  61. MOLECULAR BIOLOGY OF THE CELL, Estados Unidos America (2013, 2015, 2017)
  62. NATURE GENETICS, Estados Unidos America (2013)
  63. NATURE MEDICINE, Estados Unidos America (2008, 2017)
  64. Nature Reviews Disease Primers, Reino Unido (2017, 2020)
  65. Nature Reviews. Drug Discovery, Reino Unido (2017)
  66. Non-coding RNA Research, China (2024)
  67. Pathobiology, Suiza (1996)
  68. PLOS MEDICINE, Estados Unidos America (2005, 2008)
  69. PLOS ONE, Estados Unidos America (2007, 2011, 2016, 2017, 2018, 2019)
  70. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, Estados Unidos America (2002)
  71. RESPIRATORY MEDICINE, Reino Unido (1991)
  72. RESPIRATORY RESEARCH, Reino Unido (2001, 2011, 2016, 2018)
  73. REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION, México (1976, 2009, 2016)
  74. Revista Del Instituto Nacional De Enfermedades Respiratorias, México (2005)
  75. SARCOIDOSIS VASC DIF, Italia (2004, 2006)
  76. SCIENTIFIC REPORTS, Reino Unido (2019, 2024)
  77. SEMIN RESP CRIT CARE, Estados Unidos America (2010)
  78. Thorax, Reino Unido (2004, 2012, 2021)


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Documentos indexados (WoS y Scopus)

# Título del documento Autores Año Revista Fuente Citas WoS Citas Scopus
1Artificial intelligence in idiopathic pulmonary fibrosis: advances, challenges and future directionsCoautor y autor de correspondencia: Pardo A., Selman M., Buendia-Roldan I.2026EUROPEAN RESPIRATORY JOURNALWoS-id: 001682297500007
Scopus-id: 2-s2.0-105028659196
14
2Idiopathic pulmonary fibrosis risk loci in East Asian populations mirror those of European populationsCoautor: Pardo A., Peljto A.L., Furusawa H., Puthenvedu D., et al.2026AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEScopus-id: 2-s2.0-105043539814
01
3ATG-4B Deficiency and Impaired Autophagy Protects Mice From Experimental Hypersensitivity Pneumonitis Induced by Saccharopolyspora Rectivirgula ExposureCoautor: Pardo, A, Barajas, AMS, Gaxiola, M, Selman, M, et al.2025AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 001492206100050
00
4Decoding the complexity: mechanistic insights into comorbidities in idiopathic pulmonary fibrosisCoautor y autor de correspondencia: Pardo A., Selman M., Buendia-Roldan I.2025EUROPEAN RESPIRATORY JOURNALWoS-id: 001505182000023
Scopus-id: 2-s2.0-105006683970
1114
5Idiopathic Pulmonary Fibrosis: From Common Microscopy to Single-Cell Biology and Precision Medicine2ᵒ autor y autor de correspondencia: Pardo A., Selman M.2024AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 001212240600015
Scopus-id: 2-s2.0-85192028274
1113
6Increased ER Stress and Unfolded Protein Response Activation in Epithelial and Inflammatory Cells in Hypersensitivity PneumonitisCoautor: Pardo, A, Cabrera, S, Garcia-Vicente, A, Gutierrez, P, et al.2024JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRYWoS-id: 001219682200001
Scopus-id: 2-s2.0-85192551275
11
7Mir-155-5p targets TP53INP1 to promote proliferative phenotype in hypersensitivity pneumonitis lung fibroblastsCoautor: Pardo A., Espina-Ordoñez M., Balderas-Martínez Y.I., Torres-Machorro A.L., et al.2024Non-coding RNA ResearchWoS-id: 001225686000001
Scopus-id: 2-s2.0-85189770441
55
8Nuclear P62 Localization in Epithelial Cells From Idiopathic Pulmonary Fibrosis and Hypersensitivity Pneumonitis LungsCoautor: Pardo, A, Cabrera, S, Gutierrez, P, Sanchez, A, et al.2024AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 001277228902226
00
9Autophagy Induction After Lung Exposure to Saccharopolyspora Rectivirgula in a Mouse Model of Hypersensitivity PneumonitisCoautor: Pardo, A, Cabrera, S, Sanchez, A, Hererra, I, et al.2024AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 001277228902227
00
10Stress Fibers Are Present in Aberrant Senecent Epithelial Cells in Idiopathic Pulmonary Fibrosis, and Inhibition of Their Formation Prevents Cell Senescence In VitroCoautor: Pardo, A, Maldonado, M, Toscano-Marquez, F, Pérez-Calixto, D, et al.2024AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 001277228902276
00
11Altered expression pattern of immune response-related genes and isoforms in hypersensitivity pneumonitis lung fibroblastsCoautor: Pardo A., Torres-Machorro A.L., Becerril C., Hernández-Plata E., et al.2024SCIENTIFIC REPORTSWoS-id: 001341486300086
Scopus-id: 2-s2.0-85206277996
12
12Identification of MMP-7 as a prognostic biomarker of post-COVID persistent lung abnormalities.Coautor: Pardo, A, Roldán, IB, Chavez-Galan, L, Aguilar-Duran, H, et al.2024EUROPEAN RESPIRATORY JOURNALWoS-id: 001352764200013
00
13Determination of loss of chromosome Y in peripheral blood cells in males with idiopathic pulmonary fibrosisCoautor: Pardo A., Espinosa M., Herrera I., Buendía-Roldán I., et al.2024EUROPEAN RESPIRATORY JOURNALWoS-id: 001379762400023
Scopus-id: 2-s2.0-85209828403
43
14Matrix metalloprotease-7 is associated with post-COVID-19 persistent lung abnormalitiesCoautor: Pardo A., Buendia-Roldan I., Chavez-Galan L., Aguilar-Duran H., et al.2024ERJ Open ResearchWoS-id: 001390389900034
Scopus-id: 2-s2.0-85211361355
11
15Single-Cell Analysis Reveals Novel Immune Perturbations in Fibrotic Hypersensitivity PneumonitisCoautor: Pardo A., Zhao A.Y., Unterman A., Abu Hussein N.S., et al.2024AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 001417668900016
Scopus-id: 2-s2.0-85209828792
3936
16Usual interstitial pneumonia as a stand-alone diagnostic entity: the case for a paradigm shift?2ᵒ autor: Pardo, Annie, Selman, Moises, Wells, Athol U.2023LANCET RESPIRATORY MEDICINEWoS-id: 000927793000001
Scopus-id: 2-s2.0-85147389736
6469
17Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare VariantsCoautor: Pardo A., Peljto A.L., Blumhagen R.Z., Walts A.D., et al.2023AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000975601200016
Scopus-id: 2-s2.0-85149220360
6872
18Profibrotic Behavior of Lung Fibroblasts Derived From MMP8-MMP13 Double Knockout Mice Is Associated With a Delayed Fibrosis ResolutionCoautor: Pardo, A., Garcia, A., Gaxiola, M., Selman, M., et al.2023AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000995814701553
00
19Senescence or Autophagy, Divergent Mechanisms Driving Alveolar Regeneration in Accelerated Aging MiceCoautor: Pardo, A., Romero, Y., Camacho-Silverio, U., Valdivia-Herrera, T., et al.2023AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000995814702327
00
20Common and Distinct Bronchoalveolar Lavage and Lung Immune Signatures in Fibrotic Hypersensitivity Pneumonitis and Idiopathic Pulmonary FibrosisCoautor: Pardo, A., Zhao, A. Y., Yan, X., Sharma, P., et al.2023AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000995814704312
10
21Diagnostic unification of usual interstitial pneumonia is a step back ? Authors' reply2ᵒ autor: Pardo A., Selman M., Wells A.U.2023LANCET RESPIRATORY MEDICINEWoS-id: 001018923800001
Scopus-id: 2-s2.0-85153362790
00
22Fibroblasts From Idiopathic Pulmonary Fibrosis Induce Apoptosis and Reduce the Migration Capacity of T LymphocytesCoautor: Pardo, Annie, Chavez-Galan, Leslie, Becerril, Carina, Ruiz, Andy, et al.2022FRONTIERS IN IMMUNOLOGYWoS-id: 000760869700001
Scopus-id: 2-s2.0-85125267814
1416
23ZNF365 Downregulation Induces Senescence in Lung Fibroblasts and Epithelial CellsCoautor: Pardo, A., Huacuja Urista, J. M. Perez, Maldonado, M., Toscano-Marquez, F., et al.2022AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000792480401228
00
24Single-Cell RNA Sequencing of Peripheral Blood Mononuclear Cells Reveals That T Cell Composition, Gene Expression, and Clonotype Significantly Distinguish Fibrotic Hypersensitivity Pneumonitis and Idiopathic Pulmonary FibrosisCoautor: Pardo, A., Zhao, A. Y., Unterman, A., Adams, T., et al.2022AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000792480403396
10
25Latent Potential Regeneration of Alveolar Epithelial Cells from Aging Accelerated Mice Model (Zmpste24-/-)Coautor: Pardo, A., Romero, Y., Valdivia, T., Camacho, U., et al.2022AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000792480406028
00
26TGF-beta Signaling Is Implicated in the Initiation of Senescence in the Mouse Lung During AgingCoautor: Pardo, A., Calyeca, J., Balderas-Martinez, Y. I., Selman, M.2022AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000792480406029
00
27Changes in Immune Cell Populations in the Peripheral Blood of Individuals with Interstitial Lung AbnormalitiesCoautor: Pardo, A., Zhao, A. Y., Unterman, A., Adams, T. S., et al.2022AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000792480406080
00
28Single Nucleotide Polymorphisms (SNP) and SNP-SNP Interactions of the Surfactant Protein Genes Are Associated With Idiopathic Pulmonary Fibrosis in a Mexican Study Group; Comparison With Hypersensitivity PneumonitisCoautor: Pardo A., Abbasi A., Chen C., Gandhi C.K., et al.2022FRONTIERS IN IMMUNOLOGYWoS-id: 000812080200001
Scopus-id: 2-s2.0-85132286586
1415
29Lack of ZNF365 Drives Senescence and Exacerbates Experimental Lung FibrosisCoautor: Pardo, Annie, Urista, Juan, Maldonado, Mariel, Toscano-Marquez, Fernanda, et al.2022CellsWoS-id: 000859400200001
Scopus-id: 2-s2.0-85138367228
77
30SNP and Haplotype Interaction Models Reveal Association of Surfactant Protein Gene Polymorphisms With Hypersensitivity Pneumonitis of Mexican PopulationCoautor: PARDO, ANNIE, Gandhi, Chintan K., Chen, Chixiang, Amatya, Shaili, et al.2021Frontiers In MedicineWoS-id: 000608715200001
Scopus-id: 2-s2.0-85099660173
1720
31CD4+T cells in ageing-associated interstitial lung abnormalities show evidence of pro-inflammatory phenotypic and functional profileCoautor: PARDO, ANNIE, Machahua, Carlos, Buendia-Roldan, Ivette, Ocana-Guzman, Ranferi, et al.2021ThoraxWoS-id: 000610880000008
Scopus-id: 2-s2.0-85099657889
1414
32The Interplay of the Genetic Architecture, Aging, and Environmental Factors in the Pathogenesis of Idiopathic Pulmonary Fibrosis1ᵉʳ autor: Pardo, Annie, Selman, Moises2021AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000617344500005
Scopus-id: 2-s2.0-85101314075
100102
33One molecule, two opposite biological effects: The many faces of matrix metalloproteases in the pathogenesis of idiopathic pulmonary fibrosis1ᵉʳ autor: Pardo A., Selman M.2021AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000619666200006
Scopus-id: 2-s2.0-85101283129
01
34Mesenchymal?epithelial transition in fibroblasts of human normal lungs and interstitial lung diseasesCoautor: Pardo, Annie, Becerril, Carina, Montaño M., Cisneros, Jose, et al.2021BiomoleculesWoS-id: 000633432300001
Scopus-id: 2-s2.0-85101909558
1817
35Loss of MT1-MMP in Alveolar Epithelial Cells Exacerbates Pulmonary FibrosisCoautor: Pardo, Annie, Placido, Luis, Romero, Yair, Maldonado, Mariel, et al.2021INTERNATIONAL JOURNAL OF MOLECULAR SCIENCESWoS-id: 000645696100001
Scopus-id: 2-s2.0-85102356486
1920
36Transcriptomic profile of the mice aging lung is associated with inflammation and apoptosis as important pathwaysCoautor: PARDO, ANNIE, Calyeca, Jazmin, Balderas-Martinez, I, Yalbi, Selman, Moises2021Aging-UsWoS-id: 000651350800008
Scopus-id: 2-s2.0-85107087201
1011
37Development of a Diagnostic Biosensor Method of Hypersensitivity Pneumonitis towards a Point-of-Care BiosensorCoautor: Pardo A., Fiordelisio T., Buendia-Roldan I., Hautefeuille M., et al.2021BIOSENSORS-BASELWoS-id: 000665374000001
Scopus-id: 2-s2.0-85110258534
33
38Mitochondrial Dysfunction and Alterations in Mitochondrial Permeability Transition Pore (mPTP) Contribute to Apoptosis Resistance in Idiopathic Pulmonary Fibrosis FibroblastsCoautor: Pardo A., Rubi Luis-Garcia, Erika, Becerril C., Salgado-Aguayo A., et al.2021INTERNATIONAL JOURNAL OF MOLECULAR SCIENCESWoS-id: 000681888900001
Scopus-id: 2-s2.0-85110732347
3233
39Risk factors associated with the development of interstitial lung abnormalitiesCoautor: PARDO, ANNIE, Buendia-Roldan, Ivette, Fernandez, Rosario, Mejia, Mayra, et al.2021EUROPEAN RESPIRATORY JOURNALWoS-id: 000684220600007
Scopus-id: 2-s2.0-85112164657
3638
40Fibroageing: An ageing pathological feature driven by dysregulated extracellular matrix-cell mechanobiology2ᵒ autor y autor de correspondencia: Pardo, Annie, Selman, Moises2021AGEING RESEARCH REVIEWSWoS-id: 000684878000016
Scopus-id: 2-s2.0-85107927945
153155
41From pulmonary fibrosis to progressive pulmonary fibrosis a lethal pathobiological jump2ᵒ autor y autor de correspondencia: Pardo, Annie, Selman, Moises2021AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000697308700002
Scopus-id: 2-s2.0-85115083406
1922
42When things go wrong: exploring possible mechanisms driving the progressive fibrosis phenotype in interstitial lung diseases2ᵒ autor y autor de correspondencia: PARDO, ANNIE, Selman, Moises2021EUROPEAN RESPIRATORY JOURNALWoS-id: 000731853700015
Scopus-id: 2-s2.0-85115980887
7274
43The leading role of epithelial cells in the pathogenesis of idiopathic pulmonary fibrosis2ᵒ autor y autor de correspondencia: Pardo, Annie, Selman, Moises2020CELLULAR SIGNALLINGWoS-id: 000508747700028
Scopus-id: 2-s2.0-85075517628
188192
44Mitochondrial 8-oxoguanine DNA glycosylase mitigates alveolar epithelial cell PINK1 deficiency, mitochondrial DNA damage, apoptosis, and lung fibrosisCoautor: Pardo, Annie, Kim S.-J., Cheresh, Paul, Jablonski, Renea P., et al.2020AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000535408300033
Scopus-id: 2-s2.0-85084721183
4242
45Identification of Autophagy-related Proteins in Lungs From Hypersensitivity Pneumonitis PatientsCoautor: PARDO, ANNIE, Cabrera, Sandra, Rodriguez-Bobadilla, Carolina, Vazquez-Morales, Dulce, et al.2020JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRYWoS-id: 000538105800001
Scopus-id: 2-s2.0-85086005047
33
46IPA Software Analysis Reveals Inflammation and Apoptosis as Major Enrichment Functional Process in Normal Lung During AgingCoautor: PARDO, ANNIE, Calyeca, Jazmin, Balderas-Martinez, Yalbi, Mora, Ana, et al.2020FASEB JOURNALWoS-id: 000546107902181
00
47ZNF365 is overexpressed in Pulmonary FibrosisCoautor: PARDO, ANNIE, Urista, Juan, Maldonado, Mariel, Calyeca, Jazmin, et al.2020FASEB JOURNALWoS-id: 000546107904186
00
48Proteomic Evaluation of the Lungs of Senescence-Accelerated Prone 8 (SAMP8) MouseCoautor: Pardo, A., Balderas-Martinez, Y. I., Molina-Molina, M., Bech-Serra, J. J., et al.2020AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000556393505379
00
49Autophagy Biomarkers in Hypersensitivity PneumonitisCoautor: Pardo, A., Cabrera, S., Rodriguez-Bobadilla, C., Gaxiola, M., et al.2020AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000556622801516
00
50Protective Role of MMP14 in Alveolar Epithelial Cells in Pulmonary FibrosisCoautor: Pardo, A., Romero, Y., Maldonado, M., Placido, L. A., et al.2020AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000556622805424
00
51Hypersensitivity pneumonitisCoautor: PARDO, ANNIE, Costabel, Ulrich, Miyazaki, Yasunari, Koschel, Dirk, et al.2020Nature Reviews Disease PrimersWoS-id: 000561331600001
Scopus-id: 2-s2.0-85089142993
112129
52Update in Interstitial Lung Disease 2019Coautor: Pardo A., Montesi S.B., Fisher J.H., Martinez F.J., et al.2020AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000562950200012
Scopus-id: 2-s2.0-85089614591
2728
53Determination of the phenotypic age in residents of Mexico City: effect of accelerated ageing on lung function and structureCoautor: PARDO, ANNIE, Buendia-Roldan, Ivette, Fernandez-Plata, Rosario, Valdes-Bartolo, Abigail, et al.2020ERJ Open ResearchWoS-id: 000575353200009
90
54Why Does an Aging Smoker's Lung Develop Idiopathic Pulmonary Fibrosis and Not Chronic Obstructive Pulmonary Disease?Coautor y autor de correspondencia: Pardo A., Selman M., Martinez F.J.2019AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000457414800011
Scopus-id: 2-s2.0-85060943399
2530
55Role of ZNF365 in Pulmonary FibrosisCoautor: Pardo, A., Huacuja Urista, J. M. Perez, Maldonado, M., Calyeca, J., et al.2019AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000466776701430
00
56Homer1 Is Increased in Idiopathic Pulmonary Fibrosis and Affects Fibroblasts BehaviorCoautor: Pardo, A., Negreros, M., Maldonado, M., Balderas-Martinez, Y. I., et al.2019AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000466776701516
00
57Transcriptomic Profiling of Nasal Epithelial Brushings Identifies Signatures of AgingCoautor: Pardo, A., Reyfman, P. A., Sala, M., Verma, R., et al.2019AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000466776703123
00
58Changes of Lung Transcriptome During AgingCoautor: Pardo, A., Calyeca, M. J., Balderas-Martinez, Y. I., Selman, M.2019AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000466776705312
00
59Delayed resolution of bleomycin-induced pulmonary fibrosis in absence of MMP13 (collagenase 3)Coautor: Pardo, Annie, Cabrera, Sandra, Maciel, Mariana, Hernandez-Barrientos, Daniel, et al.2019AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000467997800021
Scopus-id: 2-s2.0-85065930631
3942
60PINK1 attenuates mtDNA release in alveolar epithelial cells and TLR9 mediated profibrotic responsesCoautor: Pardo, Annie, Bueno, Marta, Zank, Daniel, Buendia-Roldan, Ivette, et al.2019PLOS ONEWoS-id: 000470263700092
Scopus-id: 2-s2.0-85066749782
9093
61Resequencing study confirms that host defense and cell senescence gene variants contribute to the risk of idiopathic pulmonary fibrosisCoautor: Pardo, Annie, Moore, Camille, Blumhagent, Rachel Z., Yang, V, Ivana, et al.2019AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000475465500015
Scopus-id: 2-s2.0-85068860426
93102
62Lower levels of alpha-Klotho in serum are associated with decreased lung function in individuals with interstitial lung abnormalitiesCoautor: Pardo, Annie, Buendia-Roldan, Ivette, Machuca, Nancy, Mejia, Mayra, et al.2019SCIENTIFIC REPORTSWoS-id: 000477015300026
Scopus-id: 2-s2.0-85070606047
2425
63Alterations in mitochondrial permeability transition pore contribute to apoptosis resistance in IPF fibroblasts1ᵉʳ autor: Pardo Semo, Annie, Rubi Luis-Garcia, Erikal, Becerril, Carina, Mendoza, Criselda, et al.2019EUROPEAN RESPIRATORY JOURNALWoS-id: 000507372407217
00
64Transforming growth factor beta 1 induces methylation changes in lung fibroblastsCoautor: Pardo A., Negreros M., Hagood J.S., Espinoza C.R., et al.2019PLOS ONEWoS-id: 000532477400019
Scopus-id: 2-s2.0-85073165405
2426
65Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injuryCoautor: Pardo A., Valero-Jiménez A., Zúñiga J., Cisneros J., et al.2018PLOS ONEWoS-id: 000427189300009
Scopus-id: 2-s2.0-85043773930
1416
66R-Spondin-2 Is Upregulated in Idiopathic Pulmonary Fibrosis and Affects Fibroblast BehaviorCoautor: Pardo, Annie, Munguia-Reyes, Adrian, Balderas-Martinez, I, Yalbi, Becerril, Carina, et al.2018AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000437040100012
Scopus-id: 2-s2.0-85049668391
2120
67Upregulation and Nuclear Location of MMP28 in Alveolar Epithelium of Idiopathic Pulmonary FibrosisCoautor: Pardo, Annie, Maldonado, Mariel, Salgado-Aguayo, Alfonso, Herrera, Iliana, et al.2018AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000437040100013
Scopus-id: 2-s2.0-85048795784
2123
68Emerging insights into the role of matrix metalloproteases as therapeutic targets in fibrosisCoautor: Pardo A., Afratis N.A., Selman M., Sagi I.2018MATRIX BIOLOGYWoS-id: 000438480300011
Scopus-id: 2-s2.0-85042053457
5052
69Impaired autophagic activity and ATG4B deficiency are associated with increased endoplasmic reticulum stress-induced lung injuryCoautor: Pardo, Annie, Maciel, Mariana, Hernandez-Barrientos, Daniel, Herrera, Iliana, et al.2018Aging-UsWoS-id: 000443308900025
Scopus-id: 2-s2.0-85052590347
1617
70Identification of MMP28 as a biomarker for the differential diagnosis of idiopathic pulmonary fibrosisCoautor: Pardo A., Maldonado M., Buendía-Roldán I., Vicens-Zygmunt V., et al.2018PLOS ONEWoS-id: 000444683000076
Scopus-id: 2-s2.0-85053144840
2122
71R-Spondin 2 Is Upregulated in Idiopathic Pulmonary Fibrosis and Affects Fibroblasts BehaviorCoautor: Pardo, A., Munguia, A., Balderas-Martinez, Y. I., Becerril, L. C., et al.2018AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000449978902004
00
72Transforming Growth Factor Beta 1 (TGF-beta 1) Induced Profound Methylation Changes in Fibroblasts, and Revealed an Unexpected Role of Homer1 in Idiopathic Pulmonary FibrosisCoautor: Pardo, A., Negreros, M., Hagood, J. S., Espinoza, C., et al.2018AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000449978902005
00
73Contribution of the Mitochondrial Intrinsic Pathway to the Apoptosis Resistance Exhibited by Fibroblasts from Idiopathic Pulmonary FibrosisCoautor: Pardo, A., Luis-Garcia, E. R., Becerril, C., Pedraza-Chaverri, J., et al.2018AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000449978902023
00
74MMP28 Is Upregulated in Idiopathic Pulmonary Fibrosis (IPF) Epithelium and Is a Promising Biomarker to Distinguish IPF from Non-IPF PatientsCoautor: Pardo, A., Maldonado, M., Buendia, I., Vicens Zygmunt, V., et al.2018AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000449978904451
00
75Absence of Zmpste24 Protects Aging Mice from the Development of Bleomycin Induced Pulmonary Fibrosis Through microRNAs ExpressionCoautor: Pardo, A., Calyeca, M. J., Olmos, R., Jasso, R., et al.2018AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000449980300242
00
76Proof of Concept of Eukaryotic Genetic Sensory Response Units in TGF-beta Signaling in Idiopathic Pulmonary FibrosisCoautor: Pardo, A., Balderas-Martinez, Y. I., Moreno-Quiroga, B., Negreros, M., et al.2018AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000449980302223
10
77Decreased Autophagy and Endoplasmic Reticulum (ER) Stress Induction During Aging, Is Associated with Aberrant Macrophage Recruitment and Lung Remodeling in MouseCoautor: Pardo, A., Maciel, M., McQuattie-Pimentel, A. C., Piseaux-Aillon, R., et al.2018AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000449980302225
00
78Unraveling the Role of MT1-mmp in Alveolar Epithelial Cells During Pulmonary FibrosisCoautor: Pardo, A., Placido, L., Maldonado, M., Toscano, F., et al.2018AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000449980302232
00
79Inflammatory pathways are upregulated in the nasal epithelium in patients with idiopathic pulmonary fibrosisCoautor: Pardo A., Sala M.A., Balderas-Martínez Y.I., Buendía-Roldan I., et al.2018RESPIRATORY RESEARCHWoS-id: 000451377700002
Scopus-id: 2-s2.0-85057158205
1313
80Accelerated aging induced by deficiency of Zmpste24 protects old mice to develop bleomycin-induced pulmonary fibrosisCoautor: Pardo, Annie, Calyeca, Jazmin, Balderas-Martinez, Yalbi I., Olmos, Raul, et al.2018Aging-UsWoS-id: 000454633200029
Scopus-id: 2-s2.0-85059328858
66
81Premature aging in Zmpste24 deficient mice protects them from bleomycin induced lung fibrosis through upregulation of antifibrotic microRNAs1ᵉʳ autor: Pardo, Annie, Calyeca, Jazmin, Olmos, Raul J., Jasso, Rogelio, et al.2018EUROPEAN RESPIRATORY JOURNALWoS-id: 000455567105386
00
82An official American thoracic society workshop report: Use of animal models for the preclinical assessment of potential therapies for pulmonary fibrosisCoautor: Pardo, A., Jenkins, R.G., Moore, B.B., Chambers, R.C., et al.2017AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000400259400017
Scopus-id: 2-s2.0-85018430587
368387
83Frequency And Risk Factors Associated To Interstitial Lung Abnormalities (ila) In Asymptomatic Older (> 60 Years) IndividualsCoautor: Pardo, A., Buendia-Roldan, I., Martinez-Espinosa, K., Mejia, M., et al.2017AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000400372500562
00
84Matrix Metalloproteinase (mmp)-28 Is Expressed In Alveolar Epithelial Cells In Idiopathic Pulmonary Fibrosis And Increases Their Proliferation And MigrationCoautor: Pardo, A., Maldonado, M., Ortiz-Quintero, B., Herrera, I., et al.2017AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000400372501628
10
85Decreased Autophagic Activity In Epithelial Cells Induces A Profibrotic PhenotypeCoautor: Pardo Cemo, A., Medina Perez, D. M., Cabrera, S., Selman Lama, M. E.2017AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000400372502446
00
86Adam10-Mediated Ephrin-B2 Shedding Drives Myofibroblast Activation And Tissue FibrosisCoautor: Pardo, A., Lagares, D., Ghassemi-Kakaroodi, P., Tremblay, C., et al.2017AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000400372504302
00
87Effect Of Cigarette Smoke In Lung Fibroblasts And Epithelial Cells Role Of Ccl2 In Development Of Idiopathic Pulmonary FibrosisCoautor: Pardo Cemo, A., Garcia Trejo, S. S., Checa Caratachea, M. A., Ruiz Lopez, V. M., et al.2017AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000400372506318
00
88Pink1 Deficiency In Aecii Triggers Release Of Mitochondrial Damps That Initiate Pro-Inflammatory And Pro-Fibrotic Responses In The LungCoautor: Pardo, A., Bueno, M., Fiedler, K. L., Alvarez, D., et al.2017AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000400372507013
10
89SIRT3 deficiency promotes lung fibrosis by augmenting alveolar epithelial cell mitochondrial DNA damage and apoptosisCoautor: Pardo, Annie, Jablonski, Renea P., Kim, Seok-Jo, Cheresh, Paul, et al.2017FASEB JOURNALWoS-id: 000401553400025
Scopus-id: 2-s2.0-85020241929
132140
90Improving biocuration of microRNAs in diseases: a case study in idiopathic pulmonary fibrosisCoautor: Pardo, Annie, Itzel Balderas-Martinez, Yalbi, Rinaldi, Fabio, Contreras, Gabriela, et al.2017DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATIONWoS-id: 000402291100001
Scopus-id: 2-s2.0-85015939383
34
91Rac2 is required for alternative macrophage activation and bleomycin induced pulmonary fibrosis; a macrophage autonomous phenotypeCoautor: Pardo A., Joshi S., Singh A.R., Wong S.S., et al.2017PLOS ONEWoS-id: 000407856600051
Scopus-id: 2-s2.0-85027716854
2828
92The Intersection of Aging Biology and the Pathobiology of Lung Diseases: A Joint NHLBI/NIA WorkshopCoautor: Pardo, A., Budinger, G.R.S., Kohanski, R.A., Gan, W., et al.2017JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCESWoS-id: 000412856300005
Scopus-id: 2-s2.0-85032637911
5464
93Idiopathic pulmonary fibrosisCoautor: Pardo A., Martinez F.J., Collard H.R., Raghu G., et al.2017Nature Reviews Disease PrimersWoS-id: 000413360700001
Scopus-id: 2-s2.0-85031926032
11751218
94Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related diseaseCoautor: Pardo, Annie, Mora, Ana L., Rojas, Mauricio, Selman, Moises2017Nature Reviews. Drug DiscoveryWoS-id: 000413919100014
Scopus-id: 2-s2.0-85032631839
68299
95Erratum: Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease (Nature reviews. Drug discovery (2017) 16 11 (755-772))Coautor: Pardo A., Mora A.L., Rojas M., Selman M.2017Nature Reviews. Drug DiscoveryWoS-id: 000413919100018
Scopus-id: 2-s2.0-85051243150
32096
96PINK1 deficiency in AECII triggers release of mitochondrial DAMPS that initiate pro-inflammatory and pro-fibrotic responses in the lungCoautor: Pardo, Anne, Bueno, Marta, Fiedler, Kaitlin, Alvarez, Diana, et al.2017FREE RADICAL BIOLOGY AND MEDICINEWoS-id: 000415805100076
00
97ADAM10-mediated ephrin-B2 shedding promotes myofibroblast activation and organ fibrosisCoautor: Pardo, Annie, Lagares, David, Ghassemi-Kakroodi, Parisa, Tremblay, Caroline, et al.2017NATURE MEDICINEWoS-id: 000417278200008
Scopus-id: 2-s2.0-85039065864
137137
98Corrigendum: ADAM10-mediated ephrin-B2 shedding promotes myofibroblast activation and organ fibrosisCoautor: Pardo A., Lagares D., Ghassemi-Kakroodi P., Tremblay C., et al.2017NATURE MEDICINEWoS-id: 000417278200010
Scopus-id: 2-s2.0-85065310562
55
99MMP28 is overexpressed in bronchial and alveolar epithelial cells in Idiopathic Pulmonary Fibrosis.Coautor: Pardo, A., Maldonado, M., Salgado-Aguayo, A., Herrera, I., et al.2017MOLECULAR BIOLOGY OF THE CELLWoS-id: 000426664301013
10
100Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis1ᵉʳ autor: Pardo A., Cabrera S., Maldonado M., Selman M.2016RESPIRATORY RESEARCHWoS-id: 000371294900001
Scopus-id: 2-s2.0-84962124806
245257
101Cigarette Smoke Enhances the Expression of Profibrotic Molecules in Alveolar Epithelial CellsCoautor: Pardo, Annie, Checa, Marco, Hagood, James S., Velazquez-Cruz, Rafael, et al.2016PLOS ONEWoS-id: 000371724200086
Scopus-id: 2-s2.0-84961123629
5964
102AGING AND PULMONARY FIBROSISCoautor y autor de correspondencia: Pardo, Annie, Selman, Moises, Buendia-Roldan, Ivette2016REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATIONWoS-id: 000375175300005
Scopus-id: 2-s2.0-84976515252
4547
103Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumoniaCoautor: Pardo, Annie, Fingerlin, Tasha E., Zhang, Weiming, Yang, Ivana V., et al.2016BMC GENETICSWoS-id: 000377578200001
Scopus-id: 2-s2.0-85008343470
9293
104Fibrogenic Lung Injury Induces Non-Cell-Autonomous Fibroblast InvasionCoautor: Pardo, Annie, Ahluwalia, Neil, Grasberger, Paula E., Mugo, Brian M., et al.2016AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000381702000009
Scopus-id: 2-s2.0-84988869832
2627
105Age-driven developmental drift in the pathogenesis of idiopathic pulmonary fibrosisCoautor y autor de correspondencia: Pardo, Annie, Selman, Moises, Lopez-Otin, Carlos2016EUROPEAN RESPIRATORY JOURNALWoS-id: 000385957400031
Scopus-id: 2-s2.0-84979988461
110116
106Fibroblast growth factor-1 attenuates TGF-beta 1-induced lung fibrosisCoautor: Pardo, Annie, Shimbori, Chiko, Bellaye, Pierre-Simon, Xia, Jiaji, et al.2016JOURNAL OF PATHOLOGYWoS-id: 000386691000008
Scopus-id: 2-s2.0-84988643127
8893
107Increased Expression of CC16 in Patients with Idiopathic Pulmonary FibrosisCoautor: Pardo, Annie, Buendia-Roldan, Ivette, Ruiz, Victor, Sierra, Patricia, et al.2016PLOS ONEWoS-id: 000391217400116
Scopus-id: 2-s2.0-85006372434
4745
108mTORC1 activation decreases autophagy in aging and idiopathic pulmonary fibrosis and contributes to apoptosis resistance in IPF fibroblastsCoautor: Pardo, Annie, Romero, Yair, Bueno, Marta, Ramirez, Remedios, et al.2016Aging CellWoS-id: 000392286200011
Scopus-id: 2-s2.0-84983437332
157173
109R-Spondin2 is upregulated in idiopathic pulmonary fibrosis and affects fibroblasts behaviorCoautor: Pardo, Annie, Munguia, Adrian, Becerril, Carina, Mendoza, Criselda, et al.2016FASEB JOURNALWoS-id: 000406444703442
00
110TMPRSS4: a novel serine protease involved in IPF development?Coautor: Pardo, Annie, Mayela Valero, Ana, Cisneros, Jose, Ramirez, Remedios, et al.2016FASEB JOURNALWoS-id: 000406444703443
10
111Lung Fibroblasts, Aging, and Idiopathic Pulmonary Fibrosis1ᵉʳ autor: Pardo, Annie, Selman, Moises2016ANNALS OF THE AMERICAN THORACIC SOCIETYWoS-id: 000419101500007
Scopus-id: 2-s2.0-85008395851
174179
112R-Spondin2 is upregulated in lungs and fibroblasts from idiopathic pulmonary fibrosisCoautor y autor de correspondencia: Pardo, A., Selman, M., Munguia, A.2015MOLECULAR BIOLOGY OF THE CELLWoS-id: 000209928402214
00
113Blue Journal Conference Aging and Susceptibility to Lung DiseaseCoautor: Pardo A., Thannickal V.J., Murthy M., Balch W.E., et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000348827000009
Scopus-id: 2-s2.0-84922287355
142151
114The MUC5B Promoter Polymorphism Is Associated With Idiopathic Pulmonary Fibrosis in a Mexican Cohort but Is Rare Among Asian AncestriesCoautor: Pardo A., Peljto A.L., Selman M., Kim D.S., et al.2015ChestWoS-id: 000349423200027
Scopus-id: 2-s2.0-84928329158
114126
115Fibrocytes Contribute to Inflammation and Fibrosis in Chronic Hypersensitivity Pneumonitis through Paracrine EffectsCoautor: Pardo A., de Alba, CG, Buendia-Roldán I., Salgado A., et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000350014500012
Scopus-id: 2-s2.0-84922874642
5865
116Matrix metalloproteinase (MMP)-19-deficient fibroblasts display a profibrotic phenotypeCoautor: Pardo A., Jara P., Calyeca J., Romero Y., et al.2015AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000351062100003
Scopus-id: 2-s2.0-84929050793
4346
117Lung-specific loss of a3 laminin worsens bleomycin-induced pulmonary fibrosisCoautor: Pardo A., Morales-Nebreda L.I., Rogel M.R., Eisenberg J.L., et al.2015AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000352208400011
Scopus-id: 2-s2.0-84929657150
3641
118Essential role for the ATG4B protease and autophagy in bleomycin-induced pulmonary fibrosisCoautor: Pardo A., Cabrera S., Maciel M., Herrera I., et al.2015AutophagyWoS-id: 000354185500009
Scopus-id: 2-s2.0-84942511008
142152
119Classification of usual interstitial pneumonia in patients with interstitial lung disease: Assessment of a machine learning approach using high-dimensional transcriptional dataCoautor: Pardo A., Kim S.Y., Diggans J., Pankratz D., et al.2015LANCET RESPIRATORY MEDICINEWoS-id: 000355558500024
Scopus-id: 2-s2.0-84930871576
120136
120Increased alveolar soluble annexin v promotes lung inflammation and fibrosisCoautor: Pardo A., Buckley S., Shi W., Xu W., et al.2015EUROPEAN RESPIRATORY JOURNALWoS-id: 000365454000028
Scopus-id: 2-s2.0-84946552488
1418
121Role Of R-Spondin2 In The Pathogenesis Of Idiopathic Pulmonary FibrosisCoautor: Pardo, A, Munguia, A, Ramirez, R, Mendoza, C, et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000377582801556
00
122Role Of Tmprss4 In Idiopathic Pulmonary FibrosisCoautor: Pardo, A, ValeroJimenez, A, Cisneros, J, Gaxiola, M, et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000377582801560
00
123Fibroblast Growth Factor-1 Attenuates Tgf-beta 1-Induced Lung Fibrosis By Regulating Tgf-beta 1 SignalingCoautor: Pardo, A, Shimbori, C, Bellaye, PS, Gauldie, J, et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000377582802141
10
124Mmp19 Expression Induces Er Stress Independent Of Catalytic Domain ActivityCoautor: Pardo, A, Yu, G, Vedagiri, K, Wang, R, et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000377582804502
00
125Soluble Ephrin-B2 Is A Novel Biomarker For Idiopathic Pulmonary Fibrosis2ᵒ autor: Pardo, A, Montesi, S, Selman, M, Shea, BS, et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000377582805433
00
126Tgf beta Induces Human Lung Fibroblasts Demethylation Downregulating Dna Methyltransferase-1 And Upregulating Ten-Eleven-Translocation 3Coautor: Pardo, A, Negreros, M, Hagood, J, Espinoza, C, et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000377582805435
00
127Failure Of Stress-Induced Responses In Aging And Ipf Fibroblasts Is Associated With Persistent Activation Of MtorCoautor: Pardo, A, Romero, Y, Bueno, M, Alvarez, D, et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000377582807128
00
128Lung Injury Induces Non-Cell-Autonomous Fibroblast Invasion During The Development Of FibrosisCoautor: Pardo, A, Ahluwalia, N, Mugo, BM, FeghaliBostwick, C, et al.2015AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000377582807153
00
129Fibroblast Growth Factor-1 Attenuates Tgf beta 1-Induced Lung Fibrosis Through Inhibition Of Smad2 PhosphorylationCoautor: Pardo, A., Shimbori, C., Xia, J., Gauldie, J., et al.2014AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000209838201134
00
130Fibroblasts From Ipf And From Lungs Of Old Mice Show Impaired AutophagyCoautor: Pardo, A., Romero, Y., Mora, A. L., Bueno, M., et al.2014AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000209838201160
00
131Diagnosis Of Interstitial Lung Diseases Using Machine Learning On High-Dimensional Transcriptional Data And Pathological And Clinical AssessmentCoautor: Pardo, A., Kennedy, G. C., Wilde, J. I., Velichko, S., et al.2014AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000209838203302
00
132Mmp8-Mmp13 Double Deficient Mouse Is More Sensitive To Experimental Pulmonary FibrosisCoautor: Pardo, A., Cabrera, S., Vergara, F., Nava, T., et al.2014AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000209838203359
00
133Genome-Wide Imputation Study Identifies New Genetic Loci For Pulmonary FibrosisCoautor: Pardo, A., Fingerlin, T. E., Zhang, W., Peljto, A. L., et al.2014AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000209838204747
00
134Genetic Variants Associated With Pulmonary Fibrosis In Asian And Hispanic PopulationsCoautor: Pardo, A., Peljto, A., Selman, M., Kim, D. S., et al.2014AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000209838205188
10
135Grainyhead-like 2 (GRHL2) distribution reveals novel pathophysiological differences between human idiopathic pulmonary fibrosis and mouse models of pulmonary fibrosisCoautor: Pardo A., Varma S., Mahavadi P., Sasikumar S., et al.2014AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000332389600003
Scopus-id: 2-s2.0-84900562074
1719
136Revealing the Pathogenic and Aging-related Mechanisms of the Enigmatic Idiopathic Pulmonary Fibrosis An Integral Model2ᵒ autor y autor de correspondencia: Pardo A., Selman M.2014AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000336017200007
Scopus-id: 2-s2.0-84901022861
381418
137Matrix metalloproteinase-19 deficient fibroblasts display a profibrotic phenotype1ᵉʳ autor: Pardo, A, Jara, P, Calyeca, J, Romero, Y, et al.2014FASEB JOURNALWoS-id: 000346651000317
00
138Stochastic Age-related Epigenetic Drift in the Pathogenesis of Idiopathic Pulmonary Fibrosis2ᵒ autor y autor de correspondencia: Pardo, A, Selman, M2014AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000346896000002
Scopus-id: 2-s2.0-84919402669
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139Dehydroepiandrosterone has strong antifibrotic effects and is decreased in idiopathic pulmonary fibrosisCoautor: Pardo, A., Mendoza-Milla, C., Montano, M., Becerril, C., et al.2014FEBS JOURNALWoS-id: 000359666801126
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140Fibrocytes participation in the pathogenesis of Hypersensitivity PneumonitisCoautor: Pardo, A, Garcia-deAlba, C, Salgado, A, Ramirez, R, et al.2013MOLECULAR BIOLOGY OF THE CELLWoS-id: 000209348703047
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141Does apoptosis evasion only affect fibroblasts from idiopathic pulmonary fibrosis?Coautor: Pardo, A, Zygmunt, VV, Mendoza, C, Olvera, G, et al.2013EUROPEAN RESPIRATORY JOURNALWoS-id: 000209370404075
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142Autophagy And Atg4b Protease Regulate Lung Homeostasis And Protects Mice From Experimental Pulmonary FibrosisCoautor: Pardo, A., Cabrera, S., Maciel, M., Vergara, F., et al.2013AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000209838401795
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143Is Resistance To Apoptosis A Unique Feature Of Fibroblasts From Idiopathic Pulmonary Fibrosis?Coautor: Pardo, A., Vicens Zygmunt, V., Mendoza-Milla, C., Romero Lopez, Y., et al.2013AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000209838401798
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144Novel Genetic Risk Loci For Pulmonary FibrosisCoautor: Pardo, A., Fingerlin, T. E., Murphy, E., Zhang, W., et al.2013AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000209838403048
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145Update in diffuse parenchymal lung disease 20122ᵒ autor y autor de correspondencia: Pardo A., Selman M.2013AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000318382700010
Scopus-id: 2-s2.0-84877151972
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146Gene expression profiles reveal molecular mechanisms involved in the progression and resolution of bleomycin-induced lung fibrosisCoautor: Pardo A., Cabrera S., Selman M., Lonzano-Bolaños A., et al.2013AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000318473900004
Scopus-id: 2-s2.0-84878640515
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147Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosisCoautor: Pardo A., Fingerlin T.E., Murphy E., Zhang W., et al.2013NATURE GENETICSWoS-id: 000319563900008
Scopus-id: 2-s2.0-84878686854
657698
148Telomerase and telomere length in pulmonary fibrosisCoautor: Pardo A., Liu T., Ullenbruch M., Choi Y.Y., et al.2013AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000322618300011
Scopus-id: 2-s2.0-84883175434
6873
149Erratum: Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis (Nature Genetics (2013) 45 (613-620))Coautor: Pardo A., Fingerlin T.E., Murphy E., Zhang W., et al.2013NATURE GENETICSWoS-id: 000326384100026
Scopus-id: 2-s2.0-84887032393
25
150Dehydroepiandrosterone has strong antifibrotic effects and is decreased in idiopathic pulmonary fibrosisCoautor: Pardo A., Mendoza-Milla C., Jiménez A.V., Rangel C., et al.2013EUROPEAN RESPIRATORY JOURNALWoS-id: 000326859100021
Scopus-id: 2-s2.0-84887314574
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151Matrix metalloproteinase (MMP)-1 induces lung alveolar epithelial cell migration and proliferation, protects from apoptosis, and represses mitochondrial oxygen consumptionCoautor: Pardo A., Herrera I., Cisneros J., Maldonado M., et al.2013JOURNAL OF BIOLOGICAL CHEMISTRYWoS-id: 000330623300027
Scopus-id: 2-s2.0-84883709167
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152Renin is an angiotensin-independent profibrotic mediator: role in pulmonary fibrosisCoautor: Pardo, A, Montes, E, Ruiz, V, Checa, M, et al.2012EUROPEAN RESPIRATORY JOURNALWoS-id: 000298636000021
Scopus-id: 2-s2.0-84855401264
3538
153Proteasomal inhibition after injury prevents fibrosis by modulating TGF-beta(1) signallingCoautor: Pardo A., Mutlu G.M., Budinger, GRS, Wu M., et al.2012ThoraxWoS-id: 000299321700010
Scopus-id: 2-s2.0-84856049288
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154Genetic variants associated with severe pneumonia in A/H1N1 influenza infectionCoautor: Pardo A., Zuniga, J, Buendía-Roldán I., Zhao Y., et al.2012EUROPEAN RESPIRATORY JOURNALWoS-id: 000300883800015
Scopus-id: 2-s2.0-84860338151
8794
155Allele-specific transactivation of matrix metalloproteinase 7 by FOXA2 and correlation with plasma levels in idiopathic pulmonary fibrosisCoautor: Pardo A., Richards T.J., Park C., Chen Y., et al.2012AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000302918700005
Scopus-id: 2-s2.0-84859735765
3540
156Alveolar Epithelial Cell Disintegrity and Subsequent Activation A Key Process in Pulmonary Fibrosis2ᵒ autor y autor de correspondencia: Pardo A., Selman M.2012AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000306445300004
Scopus-id: 2-s2.0-84863899808
4244
157Hypersensitivity Pneumonitis Insights in Diagnosis and Pathobiology2ᵒ autor: Pardo A., Selman M., King Jr. T.E.2012AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000307600200006
Scopus-id: 2-s2.0-84865295963
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158Matrix Metalloproteinase-19 Is a Key Regulator of Lung Fibrosis in Mice and HumansCoautor: Pardo A., Yu G., Kovkarova-Naumovski E., Jara P., et al.2012AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000309898700013
Scopus-id: 2-s2.0-84867609706
9295
159Hypermethylation-Mediated Silencing of p14ARF in Fibroblasts from Idiopathic Pulmonary Fibrosis (IPF)Coautor: Pardo, A, Selman, M, Cisneros, J, Hagood, J, et al.2012FASEB JOURNALWoS-id: 000310711300716
Scopus-id: 2-s2.0-84865147542
8595
160Role of Sonic Hedgehog in idiopathic pulmonary fibrosisCoautor: Pardo A., Bolanos, AL, Milla C.M., Lira J.C., et al.2012AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000311905600005
Scopus-id: 2-s2.0-84870951352
126136
161Role of matrix metaloproteases in idiopathic pulmonary fibrosis1ᵉʳ autor: Pardo A., Selman M.2012Fibrogenesis and Tissue RepairScopus-id: 2-s2.0-84877043110
073
162Emerging drugs for idiopathic pulmonary fibrosis2ᵒ autor: Pardo A., Selman M., Richeldi L., Cerri S.2011EXPERT OPINION ON EMERGING DRUGSWoS-id: 000290965100009
Scopus-id: 2-s2.0-79957607779
2323
163Absence of Thy-1 results in TGF-beta induced MMP-9 expression and confers a profibrotic phenotype to human lung fibroblastsCoautor: Pardo, A, Ramirez, G, Hagood, JS, Sanders, Y, et al.2011LABORATORY INVESTIGATIONWoS-id: 000293214100009
Scopus-id: 2-s2.0-79960913880
7775
164Role of von Hippel-Lindau protein in fibroblast proliferation and fibrosis2ᵒ autor: Pardo A., Zhou Q., Konigshoff, M, Eickelberg O., et al.2011FASEB JOURNALWoS-id: 000294435200018
Scopus-id: 2-s2.0-80052669057
2222
165Inflammatory profiles in severe pneumonia associated with the pandemic influenza A/H1N1 virus isolated in Mexico CityCoautor: Pardo A., Zuniga, J, Torres M., Romo J., et al.2011AutoimmunityWoS-id: 000295694000006
Scopus-id: 2-s2.0-80053951786
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166Immunoglobulin Free Light Chains Are Increased in Hypersensitivity Pneumonitis and Idiopathic Pulmonary Fibrosis2ᵒ autor: Pardo A., Kormelink T.G., Knipping K., Buendía-Roldán I., et al.2011PLOS ONEWoS-id: 000295936900058
Scopus-id: 2-s2.0-80053326660
3640
167Activated MCTC mast cells infiltrate diseased lung areas in cystic fibrosis and idiopathic pulmonary fibrosisCoautor: Pardo A., Andersson C.K., Andersson-Sjöland A., Mori M., et al.2011RESPIRATORY RESEARCHWoS-id: 000296732100001
Scopus-id: 2-s2.0-80054700818
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168The effect of CTLA-4Ig, a CD28/B7 antagonist, on the lung inflammation and T cell subset profile during murine hypersensitivity pneumonitisCoautor: Pardo A., Jiménez-Alvarez L., Arreola J.L., Ramírez-Martínez G., et al.2011EXPERIMENTAL AND MOLECULAR PATHOLOGYWoS-id: 000297714700012
Scopus-id: 2-s2.0-80053531646
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169Idiopathic pulmonary fibrosis2ᵒ autor: Pardo A., King Jr. T.E., Selman M.2011LancetWoS-id: 000298136200029
Scopus-id: 2-s2.0-82755161052
17241821
170Antifibrotic effects of dehydroepiandrosterone (DHEA) in lung fibroblasts in vitroCoautor: Pardo, A, Milla, CM, Montano, M, Lozano, A, et al.2011FASEB JOURNALWoS-id: 000310708403430
00
171Immunoglobulin free light chains are increased in hypersensitivity pneumonitis and idiopathic pulmonary fibrosis patients2ᵒ autor: Pardo, A, Kormelink, TG, Knipping, K, Buendia-Roldan, I, et al.2011AllergyWoS-id: 000329462202383
00
172Fibrocytes express several matrix metalloproteinases. Possible role in migration and homingCoautor: Pardo, A, de Alba, CG, Becerril, C, Reyes, S, et al.2010FASEB JOURNALWoS-id: 000208675506721
00
173Role Of MMP19 In Epithelial-Mesenchymal Transition And Fibrosis2ᵒ autor: Pardo, A, Yu, G, Parwani, A, Selman, M, et al.2010AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000208771000220
00
174Altered Lung Mast Cell Populations Infiltrate Areas Of Inflammation And Remodeling In Patients With Cystic Fibrosis And Idiopathic Pulmonary FibrosisCoautor: Pardo, A, Andersson, C, Sjoland, AA, Mori, M, et al.2010AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000208771000427
10
175Inflammatory response and dynamics of lung T cell subsets in Th1, Th2 biased and Th2 deficient mice during the development of hypersensitivity pneumonitisCoautor: Pardo A., Jimenez-Alvarez L., Zuniga, J, Gaxiola M., et al.2010EXPERIMENTAL AND MOLECULAR PATHOLOGYWoS-id: 000277941900011
Scopus-id: 2-s2.0-77952560931
1416
176PDCD1 gene polymorphisms in different Mexican ethnic groups and their role in the susceptibility to hypersensitivity pneumonitisCoautor: Pardo A., Zuniga, J, Torres-García D., Jimenez L., et al.2010CLINICAL BIOCHEMISTRYWoS-id: 000279133100023
Scopus-id: 2-s2.0-77953693307
33
177Inhibition and Role of let-7d in Idiopathic Pulmonary FibrosisCoautor: Pardo A., Pandit K.V., Corcoran D., Yousef H., et al.2010AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000280206700013
Scopus-id: 2-s2.0-77955399498
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178FGF-1 reverts epithelial-mesenchymal transition induced by TGF-beta 1 through MAPK/ERK kinase pathwayCoautor: Pardo, A, Ramos, C, Becerril, C, Montano, M, et al.2010AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000281389000009
Scopus-id: 2-s2.0-77955633219
116124
179Aging and Interstitial Lung Diseases: Unraveling an Old Forgotten Player in the Pathogenesis of Lung FibrosisCoautor: Pardo A., Selman M., Rojas M., Mora A.L.2010SEMIN RESP CRIT CAREWoS-id: 000282232000010
Scopus-id: 2-s2.0-77958147116
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180Expression of Matrix Metalloproteases by Fibrocytes Possible Role in Migration and HomingCoautor: Pardo, A, Garcia-de-Alba, C, Becerril, C, Ruiz, V, et al.2010AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000283969700010
Scopus-id: 2-s2.0-78349303445
98107
181Hypersensitivity pneumonitis caused by fungiCoautor: Pardo A., Selman M., Lacasse Y., Cormier Y.2010ANNALS OF THE AMERICAN THORACIC SOCIETYScopus-id: 2-s2.0-77955480025
081
182Elevated levels of von Hippel-Lindau protein in human and mouse fibrotic lungs2ᵒ autor: Pardo, A, Zhou, GF, Koenigshoff, M, Dada, LA, et al.2009FASEB JOURNALWoS-id: 000208621500558
00
183The Absence of Thy-1 Expression by Human Lung Fibroblasts Is Associated with MMP-9 Expression.Coautor: Pardo, A, Ramirez, G, MacEwen, MW, Mendoza, F, et al.2009AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000208733102696
00
184Hypermethylation Mediated Silencing of p14ARF in Fibroblasts from Patients with Idiopathic Pulmonary Fibrosis (IPF): A Putative Role in Fibroblasts Resistance to Apoptosis.Coautor: Pardo, A, Cisneros, J, Checa, M, Ortiz-Quintero, B, et al.2009AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000208733102716
00
185MICA polymorphisms and decreased expression of the MICA receptor NKG2D contribute to idiopathic pulmonary fibrosis susceptibilityCoautor: Pardo A., Aquino-Galvez A., Pérez-Rodríguez M., Camarena Á., et al.2009HUMAN GENETICSWoS-id: 000266261600014
Scopus-id: 2-s2.0-67349165410
3741
186Idiopathic pulmonary fibrosisCoautor y autor de correspondencia: Pardo, A, Selman, M, Mejia, M2009REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATIONWoS-id: 000269347300007
Scopus-id: 2-s2.0-70349204030
00
187Matrix Metalloproteinase (MMP)-1 Induces Migration and Proliferation of Lung Epithelial CellsCoautor: Pardo, A, Herrera, I, Cisneros, J, Ramirez, R, et al.2008FASEB JOURNALWoS-id: 000208467801186
00
188Functional diversity of T-Cell Subpopulations in subacute and chronic hypersensitivity pneumonitisCoautor: Pardo A., Barrera L., Mendoza F., Zuniga, J, et al.2008AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000251982600008
Scopus-id: 2-s2.0-37849029903
134174
189The lysophosphatidic acid receptor LPA(1) links pulmonary fibrosis to lung injury by mediating fibroblast recruitment and vascular leakCoautor: Pardo A., Tager A.M., LaCamera P., Shea B.S., et al.2008NATURE MEDICINEWoS-id: 000252222400021
Scopus-id: 2-s2.0-38049091636
691751
190Idiopathic pulmonary fibrosis: Aberrant recapitulation of developmental programs?2ᵒ autor: Pardo, A, Selman, M, Kaminski, N2008PLOS MEDICINEWoS-id: 000254928900012
Scopus-id: 2-s2.0-41549108935
298307
191MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosisCoautor: Pardo, A, Rosas, IO, Richards, TJ, Konishi, K, et al.2008PLOS MEDICINEWoS-id: 000255369800017
Scopus-id: 2-s2.0-43249084804
484514
192Transporter associated with antigen processing (TAP) 1 gene polymorphisms in patients with hypersensitivity pneumonitisCoautor: Pardo A., Aquino-Galvez A., Camarena Á., Montano, M, et al.2008EXPERIMENTAL AND MOLECULAR PATHOLOGYWoS-id: 000255454000010
Scopus-id: 2-s2.0-41049093765
4166
193Approaching the degradome in idiopathic pulmonary fibrosis1ᵉʳ autor: Pardo, A, Selman, M, Kaminski, N2008INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGYWoS-id: 000256493300009
Scopus-id: 2-s2.0-43049084748
8389
194Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosisCoautor: Pardo A., Andersson-Sjöland A., de Alba C.G., Nihlberg K., et al.2008INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGYWoS-id: 000258479700019
Scopus-id: 2-s2.0-48949117344
298321
195Thy-1 Promoter Hypermethylation A Novel Epigenetic Pathogenic Mechanism in Pulmonary Fibrosis2ᵒ autor: Pardo A., Sanders Y.Y., Selman M., Nuovo G.J., et al.2008AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000260514300017
Scopus-id: 2-s2.0-55249123438
204227
196MMP-1 polymorphisms and the risk of idiopathic pulmonary fibrosisCoautor: Pardo A., Checa M., Ruiz V., Montano, M, et al.2008HUMAN GENETICSWoS-id: 000261178900003
Scopus-id: 2-s2.0-57049139310
6466
197Accelerated variant of idiopathic pulmonary fibrosis: Clinical behavior and gene expression patternCoautor: Pardo A., Selman M., Carrillo G., Estrada A., et al.2007PLOS ONEWoS-id: 000207448800012
Scopus-id: 2-s2.0-37549060070
216250
198Identification of the benign mesenchymal tumor gene HMGA2 in lymphangiomyomatosisCoautor: Pardo A., D'Armiento J., Imai K., Schiltz J., et al.2007CANCER RESEARCHWoS-id: 000244738100006
Scopus-id: 2-s2.0-33947238378
1615
199Local and circulating microchimerism is associated with hypersensitivity pneumonitisCoautor: Pardo A., Bustos M.L., Frías S., Ramos S., et al.2007AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000247549800014
Scopus-id: 2-s2.0-34447279648
2229
200Overexpression of MMP9 in macrophages attenuates pulmonary fibrosis induced by bleomycinCoautor: Pardo A., Cabrera S., Gaxiola M., Arreola J.L., et al.2007INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGYWoS-id: 000250899300016
Scopus-id: 2-s2.0-34748922290
107112
201Gene expression profiles distinguish idiopathic pulmonary fibrosis from hypersensitivity pneumonitis2ᵒ autor: Pardo A., Selman M., Barrera L., Estrada A., et al.2006AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000234520600008
Scopus-id: 2-s2.0-31944436620
359412
202Membrane type-matrix metalloproteinases in idiopathic pulmonary fibrosisCoautor: Pardo A., Garca-Alvarez J., Ramirez R., Sampieri C.L., et al.2006SARCOIDOSIS VASC DIFWoS-id: 000239684100002
Scopus-id: 2-s2.0-33747506955
4647
203Tissue inhibitor of metalloproteinase-3 is up-regulated by transforming growth factor-ß1 in vitro and expressed in fibroblastic foci in vivo in idiopathic pulmonary fibrosisCoautor: Pardo A., García-Alvarez J., Ramirez R., Checa M., et al.2006EXPERIMENTAL LUNG RESEARCHWoS-id: 000239759600003
Scopus-id: 2-s2.0-33747589649
4347
204Acidic fibroblast growth factor decreases a-smooth muscle actin expression and induces apoptosis in human normal lung fibroblastsCoautor: Pardo A., Ramos C., Montaño M., Becerril C., et al.2006AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000241103000004
Scopus-id: 2-s2.0-33751110893
6063
205Role of epithelial cells in idiopathic pulmonary fibrosis: From innocent targets to serial killers2ᵒ autor y autor de correspondencia: Pardo A., Selman M.2006ANNALS OF THE AMERICAN THORACIC SOCIETYScopus-id: 2-s2.0-33744924735
0473
206Matrix metalloproteases in aberrant fibrotic tissue remodeling1ᵉʳ autor: Pardo A., Selman M.2006ANNALS OF THE AMERICAN THORACIC SOCIETYScopus-id: 2-s2.0-33744938426
0231
207MMP-1: The elder of the family1ᵉʳ autor: Pardo A., Selman M.2005INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGYWoS-id: 000224909400008
Scopus-id: 2-s2.0-4944234428
234249
208Loss of fibroblast Thy-1 expression correlates with lung fibrogenesisCoautor: Pardo A., Hagood J.S., Prabhakaran P., Kumbla P., et al.2005AMERICAN JOURNAL OF PATHOLOGYWoS-id: 000230917600009
Scopus-id: 2-s2.0-25144471827
194197
209Up-regulation and profibrotic role of osteopontin in human idiopathic pulmonary fibrosis1ᵉʳ autor: Pardo A., Gibson K., Cisneros J., Richards T.J., et al.2005PLOS MEDICINEWoS-id: 000232433600018
Scopus-id: 2-s2.0-25644460419
407434
210Major histocompatibility complex and alveolar epithelial apoptosis in idiopathic pulmonary fibrosisCoautor: Pardo A., Falfén-Valencia R., Camarena A., Juárez A., et al.2005HUMAN GENETICSWoS-id: 000233996300009
Scopus-id: 2-s2.0-27944471041
3541
211Evaluation of osteopontin as a potential biological marker in idiopathic pulmonary fibrosis [Evaluación del posible papel de la osteopontina como marcador biológico en la fibrosis pulmonar idiopática]Coautor: Pardo A., De Alba C.G., Gaxiola M., Cisneros J., et al.2005Revista Del Instituto Nacional De Enfermedades RespiratoriasScopus-id: 2-s2.0-49649114845
00
212Increased Surfactant Protein-A Levels in Patients with Newly Diagnosed Idiopathic Pulmonary FibrosisCoautor: Pardo A., Phelps D.S., Umstead T.M., Mejia M., et al.2004ChestWoS-id: 000188978400040
Scopus-id: 2-s2.0-1242329140
3849
213Idiopathic pulmonary fibrosis: Pathogenesis and therapeutic approachesCoautor: Pardo A., Selman M., Thannickal V.J., Zisman D.A., et al.2004DrugsWoS-id: 000220196900005
Scopus-id: 2-s2.0-1542411333
193245
214Promoter variants in tissue inhibitor of metalloproteinase-3 (TIMP-3) protect against susceptibility in pigeon breeders' diseaseCoautor: Pardo A., Hill M.R., Briggs L., Montaño M.M., et al.2004ThoraxWoS-id: 000222329600010
Scopus-id: 2-s2.0-3142559718
3041
215Idiopathic pulmonary fibrosis: Misunderstandings between epithelial cells and fibroblasts?2ᵒ autor y autor de correspondencia: Pardo A., Selman M.2004SARCOIDOSIS VASC DIFWoS-id: 000224901900001
Scopus-id: 2-s2.0-8144226794
4755
216The Human Genome and Advances in Medicine: Limits and Future Prospects [El Genoma Humano. Límites y Perspectivas en el Avance de la Medicina]1ᵉʳ autor y autor de correspondencia: Pardo A.2004ARCHIVOS DE BRONCONEUMOLOGIAScopus-id: 2-s2.0-1842580288
01
217Bleomycin-induced pulmonary fibrosis is attenuated in ?-glutamyl transpeptidase-deficient mice1ᵉʳ autor: Pardo A., Ruiz V., Arreola J.L., Ramírez R., et al.2003AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000181439100020
Scopus-id: 2-s2.0-0037445289
5256
218Matrix metalloproteinases inhibition attenuates tobacco smoke-induced emphysema in guinea pigsCoautor: Pardo A., Selman M., Cisneros-Lira J., Gaxiola M., et al.2003ChestWoS-id: 000182773000048
Scopus-id: 2-s2.0-0037879047
89110
219The epithelial/fibroblastic pathway in the pathogenesis of idiopathic pulmonary fibrosis: Tying loose ends2ᵒ autor y autor de correspondencia: Pardo A., Selman M.2003AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000185132000019
Scopus-id: 2-s2.0-0041827226
111134
220Cigarette smoke exposure potentiates bleomycin-induced lung fibrosis in guinea pigsCoautor: Pardo A., Cisneros-Lira J., Gaxiola M., Ramos C., et al.2003AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000185178100022
Scopus-id: 2-s2.0-0141568026
3842
221Unbalanced collagenases/TIMIP-1 expression and epithelial apoptosis in experimental lung fibrosisCoautor: Pardo A., Ruiz V., Ordóñez R.Ma., Berumen J., et al.2003AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000185822300007
Scopus-id: 2-s2.0-0142182011
104116
222Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosisCoautor: Pardo A., Selman M., Lin H.-M., Montaño M., et al.2003HUMAN GENETICSWoS-id: 000186037500010
Scopus-id: 2-s2.0-0242690510
140159
223Gene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humansCoautor: Pardo A., Zuo F., Kaminski N., Eugui E., et al.2002PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAWoS-id: 000175377800098
Scopus-id: 2-s2.0-18344396051
517579
224Molecular mechanisms of pulmonary fibrosis.1ᵉʳ autor: Pardo A., Selman M.2002Frontiers in Bioscience-LandmarkWoS-id: 000177154700010
Scopus-id: 2-s2.0-4243944861
7586
225Idiopathic pulmonary fibrosis: New insights in its pathogenesis1ᵉʳ autor: Pardo A., Selman M.2002INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGYWoS-id: 000179096300005
Scopus-id: 2-s2.0-0036887578
114132
226Use of oligonucleotide microarrays to analyze gene expression patterns in pulmonary fibrosis reveals distinct patterns of gene expression in mice and humansCoautor: Pardo A., Kaminski N., Zuo F., Cojocaro G., et al.2002ChestScopus-id: 2-s2.0-0036130081
014
227Idiopathic pulmonary fibrosis: Prevailing and evolving hypotheses about its pathogenesis and implications for therapyCoautor y autor de correspondencia: Pardo A., Selman M., King T.E. Jr.2001ANNALS OF INTERNAL MEDICINEWoS-id: 000166356000008
Scopus-id: 2-s2.0-0035895243
14931702
228Tumor necrosis factor receptor deficiency alters matrix metalloproteinase 13/tissue inhibitor of metalloproteinase 1 expression in murine silicosisCoautor: Pardo A., Ortiz L.A., Lasky J., Gozal E., et al.2001AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000166540100041
Scopus-id: 2-s2.0-0035152071
4151
229Fibroblasts from idiopathic pulmonary fibrosis and normal lungs differ in growth rate, apoptosis, and tissue inhibitor of metalloproteinases expressionCoautor: Pardo A., Ramos C., Montaño M., García-Alvarez J., et al.2001AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYWoS-id: 000168913300012
Scopus-id: 2-s2.0-0035026949
306345
230Extracellular matrix remodeling in idiopathic pulmonary fibrosis1ᵉʳ autor: Pardo A., Selman M.2001ChestWoS-id: 000169917400069
Scopus-id: 2-s2.0-17944394802
22
231Surfactant protein gene A, B, and D marker alleles in chronic obstructive pulmonary disease of a Mexican populationCoautor: Pardo A., Guo X., Lin H.-M., Lin Z., et al.2001EUROPEAN RESPIRATORY JOURNALWoS-id: 000171073700008
Scopus-id: 2-s2.0-17944363930
106128
232CCL18/DC-CK-1/PARC up-regulation in hypersensitivity pneumonitis1ᵉʳ autor: Pardo A., Smith K.M., Abrams J., Coffman R., et al.2001JOURNAL OF LEUKOCYTE BIOLOGYWoS-id: 000171467500016
Scopus-id: 2-s2.0-0034800653
8597
233Idiopathic pulmonary fibrosis: An epithelial/fibroblastic cross-talk disorder2ᵒ autor y autor de correspondencia: Pardo A., Selman M.2001RESPIRATORY RESEARCHWoS-id: 000176756600001
Scopus-id: 2-s2.0-25444478849
344148
234Tumor necrosis factor receptor deficiency protects mice from silica-induced lung fibrosis by altering lung matrix metalloproteinase-13/tissue inhibitor of metalloproteinase-1 RNA expression and decreasing activating protein-1 activationCoautor: Pardo A., Ortiz L.A., Lasky J.A., Gozal E., et al.2001ChestScopus-id: 2-s2.0-0034926096
00
235Cloning and expression of guinea pig TIMP-2. Expression in normal and hyperoxic lung injuryCoautor: Pardo A., Meléndez J., Maldonado V., Bingle C.D., et al.2000AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000086487300013
Scopus-id: 2-s2.0-0034008782
55
236Increase of lung neutrophils in hypersensitivity pneumonitis is associated with lung fibrosis1ᵉʳ autor: Pardo A., Barrios R., Gaxiola M., Segura-Valdez L., et al.2000AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000086945400051
Scopus-id: 2-s2.0-0034027869
111136
237Polymorphisms of surfactant protein gene A, B, D, and of SP-B-linked microsatellite markers in COPD of a Mexican populationCoautor: Pardo A., Guo X., Lin H.-M., Lin Z., et al.2000ChestWoS-id: 000087178200020
Scopus-id: 2-s2.0-0034035293
2227
238TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment?Coautor: Pardo A., Selman M., Ruiz V., Cabrera S., et al.2000AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000088906900020
Scopus-id: 2-s2.0-0033830350
350393
239Surfactant components modulate fibroblast apoptosis and type I collagen and collagenase-1 expressionCoautor: Pardo A., Vázquez De Lara L., Becerril C., Montaño M., et al.2000AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000090056200022
Scopus-id: 2-s2.0-0033681307
4247
240Surfactant protein genetic marker alleles identify a subgroup of tuberculosis in a Mexican populationCoautor: Pardo A., Floros J., Lin H.-M., Garcia A., et al.2000JOURNAL OF INFECTIOUS DISEASESWoS-id: 000090106000024
Scopus-id: 2-s2.0-0033790682
132144
241Upregulation of gelatinases A and B, collagenases 1 and 2, and increased parenchymal cell death in COPD2ᵒ autor: Pardo A., Segura-Valdez L., Gaxiola M., Uhal B.D., et al.2000ChestScopus-id: 2-s2.0-0034101866
0443
242Proteinase-antiproteinase imbalance in the pathogenesis of Emphysema: The role of metalloproteinases in lung damage1ᵉʳ autor y autor de correspondencia: Pardo A.1999HISTOLOGY AND HISTOPATHOLOGYWoS-id: 000078017300024
Scopus-id: 2-s2.0-0033005427
3746
243Expression of matrix metalloproteinase 1 in rodents: Comment on the article by Huebner et al [5] (multiple letters)2ᵒ autor: Pardo A., Selman M., Huebner J.L., Kraus V.B.1999ARTHRITIS AND RHEUMATISMWoS-id: 000079123700036
Scopus-id: 2-s2.0-0033020048
00
244Expression and localization of TIMP-1, TIMP-2, MMP-13, MMP-2, and MMP-9 in early and advanced experimental lung silicosis1ᵉʳ autor: Pardo A., Pérez-Ramos J., Segura-Valdez L., Ramírez R., et al.1999ANNALS OF THE NEW YORK ACADEMY OF SCIENCESWoS-id: 000081587000066
Scopus-id: 2-s2.0-0032838245
1012
245Matrix metalloproteinases 2, 9, and 13, and tissue inhibitors of metalloproteinases 1 and 2 in experimental lung silicosisCoautor: Pardo A., Pérez-Ramos J., Segura-Valdez M.D.L., Vanda B., et al.1999AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: 000083071000029
Scopus-id: 2-s2.0-0032847673
8796
246Human lung myofibroblast-derived inducers of alveolar epithelial apoptosis identified as angiotensin peptidesCoautor: Pardo A., Wang R., Ramos C., Joshi I., et al.1999AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000084234800011
Scopus-id: 2-s2.0-0033372934
115134
247Acidic fibroblast growth factor induces an antifibrogenic phenotype in human lung fibroblasts2ᵒ autor: Pardo A., Becerril C., Montaño M., Ramos C., et al.1999AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGYScopus-id: 2-s2.0-0033124588
050
248Problems encountered in high-level research in developing countriesCoautor y autor de correspondencia: Pardo A., Selman M., Pérez-Padilla R.1998ChestWoS-id: 000075367700044
Scopus-id: 2-s2.0-0031841270
75
249Gelatinases A and B are up-regulated in rat lungs by subacute hyperoxia: Pathogenetic implications1ᵉʳ autor: Pardo A., Barrios R., Maldonado V., Meléndez J., et al.1998AMERICAN JOURNAL OF PATHOLOGYWoS-id: 000075745500019
Scopus-id: 2-s2.0-0031659907
95106
250Cell size, cell cycle, and a-smooth muscle actin expression by primary human lung fibroblastsCoautor: Pardo A., Uhal B.D., Ramos C., Joshi I., et al.1998AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000076855700020
Scopus-id: 2-s2.0-0031792068
4750
251Alveolar epithelial cell death adjacent to underlying myofibroblasts in advanced fibrotic human lungCoautor: Pardo A., Uhal B.D., Joshi I., Hughes W.F., et al.1998AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: 000077747100021
Scopus-id: 2-s2.0-0032437815
211301
252Upregulation of acidic fibroblast growth factor during development of experimental lung fibrosis2ᵒ autor: Pardo A., Barrios R., Ramos C., Montaño M., et al.1997AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: A1997XP58900021
Scopus-id: 2-s2.0-0030821779
2839
253Lung alveolar epithelial cells synthesize interstitial collagenase and gelatinases A and B in vitro1ᵉʳ autor: Pardo A., Ridge K., Uhal B., Iasha Sznajder J., et al.1997INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGYWoS-id: A1997XW22600007
Scopus-id: 2-s2.0-0030855716
2731
254Tobacco smoke-induced lung emphysema in guinea pigs is associated with increased interstitial collagenaseCoautor: Pardo A., Selman M., Montaño M., Ramos C., et al.1996AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: A1996VR96500007
Scopus-id: 2-s2.0-0029902493
6676
255Increased expression of gelatinases and collagenase in rat lungs exposed to 100% oxygen1ᵉʳ autor: Pardo A., Selman M., Ridge K., Barrios R., et al.1996AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEWoS-id: A1996VN22100040
Scopus-id: 2-s2.0-0029999515
6682
256Matrix metalloproteinases and lung injury1ᵉʳ autor: Pardo A., Selman M.1996Brazilian Journal Of Medical And Biological ResearchWoS-id: A1996VF23100004
Scopus-id: 2-s2.0-0030224342
1718
257Pathogenic mechanisms in the development of diffuse pulmonary fibrosis2ᵒ autor y autor de correspondencia: Pardo A., Selman M.1996Brazilian Journal Of Medical And Biological ResearchWoS-id: A1996VF23100005
Scopus-id: 2-s2.0-0030225225
68
258Increased expression of intercellular adhesion molecule 1,CD11/CD18 cell surface adhesion glycoproteins and a4ß1 integrin in a rat model of chronic interstitial lung fibrosisCoautor: Pardo A., Barquín N., Chou P., Ramos C., et al.1996PathobiologyWoS-id: A1996WF93100003
Scopus-id: 2-s2.0-0030465604
89
259Pigeon breeder's disease: A paradigm for understanding hypersensitivity pneumonitisCoautor: Pardo A., Selman M., Salas J., Perez-Padilla R.1995Clinical Pulmonary MedicineScopus-id: 2-s2.0-0028916454
04
260Expression of a 2.8-kb PDGF-B/c-sis transcript and synthesis of PDGF-like protein by human lung fibroblastsCoautor: Pardo A., Rojas-Valencia L., Montiel F., Montano M., et al.1995ChestWoS-id: A1995RJ22200045
Scopus-id: 2-s2.0-0029071077
1113
261Fibroblasts isolated after fibrotic lung injury induce apoptosis of alveolar epithelial cells in vitroCoautor: Pardo A., Uhal B.D., Joshi I., True A.L., et al.1995AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGYWoS-id: A1995TL81800012
Scopus-id: 2-s2.0-0029177813
127159
262Cellular source of collagenase and TIMP-1 in carrageenin-induced granulomaCoautor: Pardo A., Jimenez-Garcia J.F., Pérez-Ramos J., Selman M.1994EXPERIMENTAL AND MOLECULAR PATHOLOGYWoS-id: A1994PF29400006
Scopus-id: 2-s2.0-0028041028
11
263Leukotriene C4 upregulates collagenase expression and synthesis in human lung fibroblastsCoautor: Pardo A., Medina L., Pérez-Ramos J., Ramírez R., et al.1994BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCHWoS-id: A1994PR79000002
Scopus-id: 2-s2.0-0028044213
3338
264Comparison between lung parenchyma and bronchoalveolar lavage collagenolytic activityCoautor: Pardo A., Montaño M., Ramos C., Selman M.1993LungWoS-id: A1993KH46700003
Scopus-id: 2-s2.0-0027473493
23
265Collagenase-inhibitory activity in deposit and resorption phases of Guinea pig carrageenin granuloma1ᵉʳ autor: Pardo A., Ramirez R., Ramos C., Martha, et al.1992CONNECTIVE TISSUE RESEARCHWoS-id: A1992KV17600005
Scopus-id: 2-s2.0-0027014275
11
266Production of collagenase and tissue inhibitor of metalloproteinases by fibroblasts derived from normal and fibrotic human lungs1ᵉʳ autor: Pardo A., Selman M., Ramirez R., Ramos C., et al.1992ChestWoS-id: A1992JR49500022
Scopus-id: 2-s2.0-0026701007
7473
267Decreased collagenase production by fibroblasts derived from idiopathic pulmonary fibrosis.1ᵉʳ autor: Pardo A., Selman M.1992Matrix (stuttgart, Germany). SupplementScopus-id: 2-s2.0-0027015338
05
268Collagenase and collagenase inhibitors in bronchoalveolar lavage fluids2ᵒ autor: Pardo A., Selman M., Barquin N., Sansores R., et al.1991ChestWoS-id: A1991FV61000032
Scopus-id: 2-s2.0-0025910175
86
269Potential role of proteases in pulmonary fibrosis2ᵒ autor y autor de correspondencia: PARDO A., SELMAN M.1991ANNALS OF THE NEW YORK ACADEMY OF SCIENCESWoS-id: A1991FZ45400029
Scopus-id: 2-s2.0-0026391502
07
270Purification of a procollagenase-acttvator present in medium of cultured Guinea pig carrageenin granuloma1ᵉʳ autor: Pardo A., Ramirez R., Gutierrez-Kobeh L., Mendoza F., et al.1991CONNECTIVE TISSUE RESEARCHWoS-id: A1991GL08500003
Scopus-id: 2-s2.0-0026301638
1010
271Production of platelet-derived growth factor by human lung cancerCoautor: Pardo A., Bravo M., Vasquez R., Rubio H., et al.1991RESPIRATORY MEDICINEWoS-id: A1991GQ02900007
Scopus-id: 2-s2.0-0026001677
109
272Lung collagenase inhibitors and spontaneous and latent collagenase activity in idiopathic pulmonary fibrosis and hypersensitivity pneumonitisCoautor: Pardo A., Montano M., Ramos C., Gonzales G., et al.1989ChestWoS-id: A1989AY07900036
Scopus-id: 2-s2.0-0024469253
4439
273Carrageenin-stimulated peritoneal macrophages release in vitro collagenase and gelatinase.2ᵒ autor y autor de correspondencia: Pardo A., López-Escalera R.1987Collagen And Related ResearchWoS-id: A1987J979000002
Scopus-id: 2-s2.0-0023411995
32
274Collagen biosynthesis and degradation during deposit and resorptive phases of carrageenin granuloma2ᵒ autor y autor de correspondencia: Pardo A., Figueras T.1986Collagen And Related ResearchScopus-id: 2-s2.0-0022879023
06
275Immunohistochemical identification of collagenase in carrageenin granuloma1ᵉʳ autor: Pardo A., Rosenstein I., Montfort I., Perez Tamayo R.1983JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRYWoS-id: A1983QP10500009
Scopus-id: 2-s2.0-0020508022
1612
276Collagen-bound collagenase1ᵉʳ autor: Pardo A., Soto H., Montfort I., Tamayo R.P.1980CONNECTIVE TISSUE RESEARCHWoS-id: A1980KM08800006
Scopus-id: 2-s2.0-0018938286
1915
277What controls collagen resorption in vivo?Coautor y autor de correspondencia: Pardo A., Perez Tamayo R., Montfort I.1980MEDICAL HYPOTHESESWoS-id: A1980KA37600003
Scopus-id: 2-s2.0-0018964652
77
278Mammalian collagenases. A review of recent advances [Colagenasas de mamíferos. Revisión de algunos avances recientes.]Coautor: Pardo A., Pérez Tamayo R., Montfort I., Rosenstein I., et al.1976REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATIONScopus-id: 2-s2.0-0016971114
00
279The presence of collagenase in collagen preparations1ᵉʳ autor: Pardo A., Pérez Tamayo R.1975BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTSWoS-id: A1975AB35100013
Scopus-id: 2-s2.0-0016693453
2214
280The collagenase of carrageenin granuloma1ᵉʳ autor: Pardo A., Pérez-Tamayo R.1974CONNECTIVE TISSUE RESEARCHWoS-id: A1974V035700010
Scopus-id: 2-s2.0-0016370669
127
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Documentos no indexados (Humanindex)

# Título del documento ISSN Revista Año Fuente
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Capítulos de libros (WoS y Scopus)

# Título del capítulo Título del libro Autores Alcance Año ISBN Fuente
1Hypersensitivity pneumonitisInterstitial Pulmonary And Bronchiolar DisordersSelman M., Pardo A., Mejía M., Capítulo de un Libro20169781420053449Scopus-id: 2-s2.0-85051689504
2Foreword: Contemporary approaches to idiopathic pulmonary fibrosisContemporary Approaches To Idiopathic Pulmonary FibrosisPardo A., Selman M., Editorial Material20159781780845135Scopus-id: 2-s2.0-84958696864
3Epithelial biology in idiopathic pulmonary fibrosisContemporary Approaches To Idiopathic Pulmonary FibrosisPardo A., Selman M., Capítulo de un Libro20159781780845135Scopus-id: 2-s2.0-84958689330
4Aging and IPF: What Is the Link?Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical GuideSelman, Moises, Pardo, Annie, Romero, Yair, et al.Article20149781627036818WoS-id: 000328150500013
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Obras con ISBN (Indautor)

# Título del documento Autores Alcance Año ISBN Fuente
1Cuaderno De Viaje. María Fernanda Campa Uranga, La ChataANNIE, PARDO CEMO, ELISA, FITZ DÍAZ, Libro Completo20239786078877768INDAUTOR
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Proyectos

# Nombre Participantes Convocatoria Fecha Inicio Fecha Fin
1Mecanismos epigenéticos asociados al efecto del TGF beta en fibroblastos de Fibrosis Pulmonar Idiopática.ANNIE PARDO CEMO,
Presupuesto de la UNAM asignado a la Dependencia01-01-200031-12-2020
2Efecto de la expresión de MMP-28 sobre diferentes funciones del epitelio alveolar y mecanismos involucrados en su posible localización nuclear.ANNIE PARDO CEMO,
Presupuesto de la UNAM asignado a la Dependencia05-11-200031-12-2020
3Evaluación de Biomarcadores de Envejecimiento pulmonar aceleradoANNIE PARDO CEMO,
Presupuesto de la UNAM asignado a la Dependencia, Otras Universidades, Centros o Institutos Nacionales08-02-201508-02-2018
4Modificaciones pulmonares y respuesta ante el daño fibrosante en ratones con envejecimiento acelerado.ANNIE PARDO CEMO,
Presupuesto de la UNAM asignado a la Dependencia01-01-201531-12-2020
5Papel de la metaloproteasa de matriz asociada a membrana tipo-1 (MT1-MMP) en la fibrosis pulmonar. Papel de la MTMMP1ANNIE PARDO CEMO,
Presupuesto de la UNAM asignado a la Dependencia, Otras Universidades, Centros o Institutos Nacionales03-05-201630-12-2018
6Efecto de la expresión de MMP-28 sobre diferentes funciones del epitelio alveolar pulmonar, mecanismos involucrados en su localización nuclear y papel en la fibrosis pulmonarANNIE PARDO CEMO,
Recursos PAPIIT01-01-201631-12-2018
7Efecto de la expresión de ZNF-365 en fibroblastos y células epiteliales pulmonares y evaluación de su papel en la fibrosis pulmonar.ANNIE PARDO CEMO,
Recursos PAPIIT01-01-202031-12-2022
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Participación en Comités de Tesis

# Título del documento Tipo de Tesis Sinodales Autores Año Entidad Url
1La ausencia de ZNF365 promueve la senescencia y exacerba la fibrosis pulmonar experimentalTesis de DoctoradoANNIE PARDO CEMO; FELIX RECILLAS TARGA; JORGE MELENDEZ ZAJGLA; Pérez Huacuja Urista, Juan Manuel; 2023Facultad de Ciencias, Instituto de Fisiología Celular,
2Papel del TGF-ß1 en el perfil de expresión y metilación del ADN de fibroblastos de pulmón humano normal y de pulmones con FPITesis de DoctoradoANNIE PARDO CEMO; Negreros Amaya, Miguel Ángel; 2020Facultad de Ciencias,
3Modificaciones pulmonares y respuesta ante el daño fibrosante en ratones con envejecimiento aceleradoTesis de DoctoradoANNIE PARDO CEMO; Calyeca Gómez, María del Jazmín; 2019Facultad de Ciencias,
4Efecto de la rigidez de la matriz en fibroblastos pulmonares normales huanosTesis de MaestríaANNIE PARDO CEMO; González Mora, Andrea Magali; 2018Facultad de Ciencias,
5Efecto de la expresión de MMP-28 sobre diferentes funciones del epitelio alveolar y mecanismos involucrados en su posible localización nuclearTesis de DoctoradoANNIE PARDO CEMO; Maldonado Bonilla, Mariel Sofía; 2018Facultad de Ciencias,
6Análisis de la respuesta al daño en un modelo tridimensional de fibroblastos humanosTesis de MaestríaFERNANDO EDGAR KROTZSCH GOMEZ; ANNIE PARDO CEMO; ANDRES ELIU CASTELL RODRIGUEZ; Gómez Rosas, Ana Laura; 2017Facultad de Ciencias, Facultad de Medicina,
7Evaluación de autofagia y del sistema ubiquitina-proteosoma en fibroblastos normales y derivados de pacientes con fibrosis pulmonar idiopáticaTesis de DoctoradoANNIE PARDO CEMO; Romero López, Yair; 2016Facultad de Ciencias,
8Regulación epigenética de bmp2 por acetilación de histonas en fibroblastos humanos de pulmón normalTesis de LicenciaturaANNIE PARDO CEMO; Pérez Huacuja Urista, Juan Manuel; 2015Facultad de Ciencias,
9Posibles mecanismos antifibrogenicos de la mmp19Tesis de DoctoradoANNIE PARDO CEMO; Jara Pelaez, Paul Daniel; 2015Facultad de Ciencias,
10Efecto de la MMP1 en el comportamiento de células epiteliales alveolares de ratónTesis de DoctoradoANNIE PARDO CEMO; Herrera Fuentes, Iliana; 2014Facultad de Ciencias,
11Evaluación de ppar-γ-1 en la fibrosis pulmonar inducida en un ratón deficiente de la mmp-19Tesis de MaestríaANNIE PARDO CEMO; Placido Méndez, Luis Antonio; 2013Facultad de Ciencias,
12Efecto de la expresión de thy-1 en fibroblastos pulmonares humanos en su comunicación con las células epiteliales alveolaresTesis de MaestríaANNIE PARDO CEMO; Calyeca Gómez, María del Jazmín; 2013Facultad de Ciencias,
13Análisis de la expresión de la ADAMTS-5 en fibrosis pulmonar idiopáticaTesis de LicenciaturaANNIE PARDO CEMO; Calyeca Gómez, María del Jazmín; 2011Facultad de Ciencias,
14Expresión de ADAMTS-9 en fibrosis pulmonar idiopática (FPI)Tesis de LicenciaturaANNIE PARDO CEMO; Rizo Pastrana, Ivette; 2011Facultad de Ciencias,
15Efecto de la matriz extracelular en la diferenciación del trofoblasto de ratónTesis de DoctoradoFELIPE VADILLO ORTEGA; ANNIE PARDO CEMO; LUIS FELIPE JIMENEZ GARCIA; LUIS ARTURO BAIZA GUTMAN; et al.Martínez Hernández, María Guadalupe; 2011Facultad de Ciencias, Facultad de Estudios Superiores "Iztacala", Facultad de Medicina,
16Mecanismos moleculares en el desarrollo de enfisema en pacientes con fibrosis pulmonar idiopáticaTesis de MaestríaANNIE PARDO CEMO; MOISES EDUARDO SELMAN LAMA; Munguía Reyes, Adrián; 2011Facultad de Ciencias, Facultad de Medicina,
17Altas concentraciones de glucosa inducen un fenotipo profibrótico en células del epitelio alveolar pulmonarTesis de MaestríaANNIE PARDO CEMO; Cid Soto, Miguel Ángel; 2011Facultad de Ciencias,
18Papel del receptor Thy-1 (CD90) en el comportamiento de fibroblastos pulmonares humanosTesis de DoctoradoANNIE PARDO CEMO; FERNANDO LOPEZ CASILLAS; Ramírez Martínez, Gustavo; 2011Facultad de Ciencias, Instituto de Fisiología Celular,
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Docencia Impartida

# Entidad Nivel Asignatura Año Semestre Alumnos
1Facultad de CienciasLicenciaturaTALLER NIVEL 220252025-23
2Facultad de CienciasLicenciaturaTALLER NIVEL I20242025-17
3Facultad de CienciasLicenciaturaTALLER NIVEL 420242025-18
4Facultad de CienciasLicenciaturaTALLER NIVEL 320242024-28
5Facultad de CienciasLicenciaturaTALLER NIVEL 220232024-18
6Facultad de CienciasLicenciaturaTALLER NIVEL I20232023-27
7Facultad de CienciasLicenciaturaTALLER NIVEL 420212021-25
8Facultad de CienciasLicenciaturaTALLER NIVEL 420202021-11
9Facultad de CienciasLicenciaturaTALLER NIVEL 320202021-15
10Facultad de CienciasLicenciaturaTALLER NIVEL 220202020-25
11Facultad de CienciasLicenciaturaTALLER NIVEL 320202020-21
12Facultad de CienciasLicenciaturaTALLER NIVEL 420202020-22
13Facultad de CienciasLicenciaturaTALLER NIVEL I20192020-15
14Facultad de CienciasLicenciaturaTALLER NIVEL 220192020-11
15Facultad de CienciasLicenciaturaTALLER NIVEL 320192020-12
16Facultad de CienciasLicenciaturaTALLER NIVEL 420192019-22
17Facultad de CienciasLicenciaturaTALLER NIVEL 220192019-22
18Facultad de CienciasLicenciaturaTALLER NIVEL 320182019-12
19Facultad de CienciasLicenciaturaTALLER NIVEL I20182019-14
20Facultad de CienciasLicenciaturaTALLER NIVEL 420182018-21
21Facultad de CienciasLicenciaturaTALLER NIVEL 220182018-24
22Facultad de CienciasLicenciaturaTALLER NIVEL 320172018-11
23Facultad de CienciasLicenciaturaTALLER NIVEL I20172018-15
24Facultad de CienciasLicenciaturaTALLER NIVEL 220172017-21
25Facultad de CienciasLicenciaturaTALLER NIVEL I20162017-14
26Facultad de CienciasLicenciaturaBIOL.MOLEC.DE LA CELULA II20132014-124
27Facultad de CienciasLicenciaturaTALLER NIVEL 420132014-13
28Facultad de CienciasLicenciaturaTALLER NIVEL 320132013-23
29Facultad de CienciasLicenciaturaBIOLOGIA MOLEC DE LA CELUL I20132013-225
30Facultad de CienciasLicenciaturaTALLER NIVEL 420132013-21
31Facultad de CienciasLicenciaturaTALLER NIVEL 220122013-14
32Facultad de CienciasLicenciaturaTALLER NIVEL 320122013-11
33Facultad de CienciasLicenciaturaBIOLOGIA MOLEC DE LA CELUL I20122012-224
34Facultad de CienciasLicenciaturaTALLER NIVEL I20122012-24
35Facultad de CienciasLicenciaturaBIOL.MOLEC.DE LA CELULA II20112012-124
36Facultad de CienciasLicenciaturaBIOLOGIA MOLEC DE LA CELUL I20112011-226
37Facultad de CienciasLicenciaturaTALLER NIVEL 420112011-23
38Facultad de CienciasLicenciaturaTALLER NIVEL 320102011-13
39Facultad de CienciasLicenciaturaTALLER NIVEL 220102010-23
40Facultad de CienciasLicenciaturaTALLER NIVEL I20092010-13
41Facultad de CienciasLicenciaturaTALLER NIVEL 420092009-23
42Facultad de CienciasLicenciaturaTALLER NIVEL 320082009-13
43Facultad de CienciasLicenciaturaTALLER NIVEL 220082008-23
44Facultad de CienciasLicenciaturaTALLER NIVEL 420082008-24
45Facultad de CienciasLicenciaturaTALLER NIVEL I20072008-13
46Facultad de CienciasLicenciaturaTALLER NIVEL 320072008-14
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