Annie Pardo

Q: What Schools Are Affiliated With Annie Pardo

Annie Pardo is affiliated with the following schools: University of California, Berkeley, National Autonomous University of Mexico, Stanford University, Baylor College of Medicine, University of California, San Francisco

Annie Pardo's AcademicInfluence.com Rankings

Annie Pardo

Computer Science

#8895

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#9351

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Machine Learning

#3762

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#3808

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Artificial Intelligence

#4081

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#4139

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Database

#5888

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#6107

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computer-science Degrees

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Computer Science

Annie Pardo's Degrees

PhD Computer Science Stanford University
Masters Computer Science University of California, Berkeley
Bachelors Computer Science University of California, Berkeley

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Annie Pardo's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Idiopathic Pulmonary Fibrosis: Prevailing and Evolving Hypotheses about Its Pathogenesis and Implications for Therapy (2001) (1723)
Idiopathic pulmonary fibrosis (2011) (1071)
The lysophosphatidic acid receptor LPA1 links pulmonary fibrosis to lung injury by mediating fibroblast recruitment and vascular leak (2008) (679)
Idiopathic pulmonary fibrosis (2012) (635)
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis (2013) (606)
Gene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humans (2002) (594)
Upregulation of gelatinases A and B, collagenases 1 and 2, and increased parenchymal cell death in COPD. (2000) (534)
MMP1 and MMP7 as Potential Peripheral Blood Biomarkers in Idiopathic Pulmonary Fibrosis (2008) (481)
Role of epithelial cells in idiopathic pulmonary fibrosis: from innocent targets to serial killers. (2006) (472)
Inhibition and role of let-7d in idiopathic pulmonary fibrosis. (2010) (464)
Gene expression profiles distinguish idiopathic pulmonary fibrosis from hypersensitivity pneumonitis. (2006) (418)
Up-Regulation and Profibrotic Role of Osteopontin in Human Idiopathic Pulmonary Fibrosis (2005) (414)
TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment? (2000) (390)
Hypersensitivity pneumonitis: insights in diagnosis and pathobiology. (2012) (379)
Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosis. (2008) (353)
Fibroblasts from idiopathic pulmonary fibrosis and normal lungs differ in growth rate, apoptosis, and tissue inhibitor of metalloproteinases expression. (2001) (342)
Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. an integral model. (2014) (327)
Idiopathic Pulmonary Fibrosis: Aberrant Recapitulation of Developmental Programs? (2008) (318)
Alveolar epithelial cell death adjacent to underlying myofibroblasts in advanced fibrotic human lung. (1998) (308)
Accelerated Variant of Idiopathic Pulmonary Fibrosis: Clinical Behavior and Gene Expression Pattern (2007) (273)
AMERICAN THORACIC SOCIETY; EUROPEAN RESPIRATORY SOCIETY; AMERICAN COLLEGE OF CHEST PHYSICIANS. IDIOPATHIC PULMONARY FIBROSIS: PREVAILING AND EVOLVING HYPOTHESES ABOUT ITS PATHOGENESIS AND IMPLICATIONS FOR THERAPY (2001) (247)
Matrix metalloproteases in aberrant fibrotic tissue remodeling. (2006) (245)
MMP-1: the elder of the family. (2005) (233)
Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease (2017) (223)
Thy-1 promoter hypermethylation: a novel epigenetic pathogenic mechanism in pulmonary fibrosis. (2008) (221)
Loss of fibroblast Thy-1 expression correlates with lung fibrogenesis. (2005) (214)
An Official American Thoracic Society Workshop Report: Use of Animal Models for the Preclinical Assessment of Potential Therapies for Pulmonary Fibrosis (2017) (192)
Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis (2003) (171)
Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis (2016) (168)
Fibroblasts isolated after fibrotic lung injury induce apoptosis of alveolar epithelial cells in vitro. (1995) (165)
Surfactant protein genetic marker alleles identify a subgroup of tuberculosis in a Mexican population. (2000) (161)
Idiopathic pulmonary fibrosis: an epithelial/fibroblastic cross-talk disorder (2001) (153)
Functional diversity of T-cell subpopulations in subacute and chronic hypersensitivity pneumonitis. (2008) (149)
Idiopathic pulmonary fibrosis: pathogenesis and therapeutic approaches. (2004) (148)
Blue journal conference. Aging and susceptibility to lung disease. (2015) (146)
Role of Sonic Hedgehog in idiopathic pulmonary fibrosis. (2012) (135)
Idiopathic pulmonary fibrosis: new insights in its pathogenesis. (2002) (134)
Surfactant protein gene A, B, and D marker alleles in chronic obstructive pulmonary disease of a Mexican population. (2001) (133)
Increase of lung neutrophils in hypersensitivity pneumonitis is associated with lung fibrosis. (2000) (131)
The epithelial/fibroblastic pathway in the pathogenesis of idiopathic pulmonary fibrosis. (2003) (129)
FGF-1 reverts epithelial-mesenchymal transition induced by TGF-{beta}1 through MAPK/ERK kinase pathway. (2010) (127)
Lung Fibroblasts, Aging, and Idiopathic Pulmonary Fibrosis. (2016) (122)
Overexpression of MMP9 in macrophages attenuates pulmonary fibrosis induced by bleomycin. (2007) (119)
Unbalanced collagenases/TIMP-1 expression and epithelial apoptosis in experimental lung fibrosis. (2003) (118)
Matrix metalloproteinases inhibition attenuates tobacco smoke-induced emphysema in Guinea pigs. (2003) (118)
Idiopathic pulmonary fi brosis (2011) (116)
Gelatinases A and B are up-regulated in rat lungs by subacute hyperoxia: pathogenetic implications. (1998) (112)
mTORC1 activation decreases autophagy in aging and idiopathic pulmonary fibrosis and contributes to apoptosis resistance in IPF fibroblasts (2016) (112)
Essential role for the ATG4B protease and autophagy in bleomycin-induced pulmonary fibrosis (2015) (110)
Classification of usual interstitial pneumonia in patients with interstitial lung disease: assessment of a machine learning approach using high-dimensional transcriptional data. (2015) (107)
CCL18/DC‐CK‐1/PARC up‐regulation in hypersensitivity pneumonitis (2001) (104)
Human lung myofibroblast-derived inducers of alveolar epithelial apoptosis identified as angiotensin peptides. (1999) (101)
Genetic variants associated with severe pneumonia in A/H1N1 influenza infection (2011) (100)
Expression of matrix metalloproteases by fibrocytes: possible role in migration and homing. (2010) (99)
Matrix metalloproteinases 2, 9, and 13, and tissue inhibitors of metalloproteinases 1 and 2 in experimental lung silicosis. (1999) (99)
Tobacco smoke-induced lung emphysema in guinea pigs is associated with increased interstitial collagenase. (1996) (96)
The leading role of epithelial cells in the pathogenesis of idiopathic pulmonary fibrosis. (2019) (96)
Molecular mechanisms of pulmonary fibrosis. (2002) (94)
The MUC5B promoter polymorphism is associated with idiopathic pulmonary fibrosis in a Mexican cohort but is rare among Asian ancestries. (2015) (88)
Approaching the degradome in idiopathic pulmonary fibrosis. (2008) (88)
SIRT3 deficiency promotes lung fibrosis by augmenting alveolar epithelial cell mitochondrial DNA damage and apoptosis (2017) (83)
Matrix Metalloproteinase (MMP)-1 Induces Lung Alveolar Epithelial Cell Migration and Proliferation, Protects from Apoptosis, and Represses Mitochondrial Oxygen Consumption* (2013) (82)
Hypermethylation‐Mediated Silencing of p14ARF in Fibroblasts from Idiopathic Pulmonary Fibrosis (IPF) (2012) (81)
ADAM10-mediated ephrin-B2 shedding promotes myofibroblast activation and organ fibrosis (2017) (81)
Age-driven developmental drift in the pathogenesis of idiopathic pulmonary fibrosis (2016) (81)
Hypersensitivity pneumonitis caused by fungi. (2010) (79)
MMP-1 polymorphisms and the risk of idiopathic pulmonary fibrosis (2008) (79)
Increased expression of gelatinases and collagenase in rat lungs exposed to 100% oxygen. (1996) (78)
Role of matrix metaloproteases in idiopathic pulmonary fibrosis (2012) (77)
Matrix metalloproteinase-19 is a key regulator of lung fibrosis in mice and humans. (2012) (76)
Fibroblast growth factor‐1 attenuates TGF‐β1‐induced lung fibrosis (2016) (75)
Production of collagenase and tissue inhibitor of metalloproteinases by fibroblasts derived from normal and fibrotic human lungs. (1992) (75)
Telomerase and telomere length in pulmonary fibrosis. (2013) (74)
Absence of Thy-1 results in TGF-β induced MMP-9 expression and confers a profibrotic phenotype to human lung fibroblasts (2011) (73)
Activated MCTC mast cells infiltrate diseased lung areas in cystic fibrosis and idiopathic pulmonary fibrosis (2011) (72)
Proteasomal inhibition after injury prevents fibrosis by modulating TGF-β1 signalling (2011) (72)
Aging and interstitial lung diseases: unraveling an old forgotten player in the pathogenesis of lung fibrosis. (2010) (70)
Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia (2016) (66)
Resequencing Study Confirms Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis. (2019) (66)
MMP 1 and MMP 7 as Potential Peripheral Blood Biomarkers in Idiopathic Pulmonary Fibrosis (2008) (64)
Acidic fibroblast growth factor decreases alpha-smooth muscle actin expression and induces apoptosis in human normal lung fibroblasts. (2006) (63)
Bleomycin-induced pulmonary fibrosis is attenuated in γ-glutamyl transpeptidase-deficient mice (2003) (63)
Acidic fibroblast growth factor induces an antifibrogenic phenotype in human lung fibroblasts. (1999) (61)
Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease (2017) (59)
Transporter associated with antigen processing (TAP) 1 gene polymorphisms in patients with hypersensitivity pneumonitis. (2008) (54)
Cigarette Smoke Enhances the Expression of Profibrotic Molecules in Alveolar Epithelial Cells (2016) (53)
Membrane type-matrix metalloproteinases in idiopathic pulmonary fibrosis. (2006) (53)
Tumor necrosis factor receptor deficiency alters matrix metalloproteinase 13/tissue inhibitor of metalloproteinase 1 expression in murine silicosis. (2001) (52)
Increased surfactant protein-A levels in patients with newly diagnosed idiopathic pulmonary fibrosis. (2004) (50)
Cigarette smoke exposure potentiates bleomycin-induced lung fibrosis in guinea pigs. (2003) (49)
Fibrocytes contribute to inflammation and fibrosis in chronic hypersensitivity pneumonitis through paracrine effects. (2015) (49)
Major histocompatibility complex and alveolar epithelial apoptosis in idiopathic pulmonary fibrosis (2005) (47)
Proteinase-antiproteinase imbalance in the pathogenesis of emphysema: the role of metalloproteinases in lung damage. (1999) (46)
Leukotriene C4 upregulates collagenase expression and synthesis in human lung fibroblasts. (1994) (45)
Surfactant components modulate fibroblast apoptosis and type I collagen and collagenase-1 expression. (2000) (45)
The Intersection of Aging Biology and the Pathobiology of Lung Diseases: A Joint NHLBI/NIA Workshop. (2017) (44)
Immunoglobulin Free Light Chains Are Increased in Hypersensitivity Pneumonitis and Idiopathic Pulmonary Fibrosis (2011) (44)
Idiopathic pulmonary fibrosis: misunderstandings between epithelial cells and fibroblasts? (2004) (44)
Lung collagenase inhibitors and spontaneous and latent collagenase activity in idiopathic pulmonary fibrosis and hypersensitivity pneumonitis. (1989) (43)
PINK1 attenuates mtDNA release in alveolar epithelial cells and TLR9 mediated profibrotic responses (2019) (43)
Allele-specific transactivation of matrix metalloproteinase 7 by FOXA2 and correlation with plasma levels in idiopathic pulmonary fibrosis. (2012) (41)
TISSUE INHIBITOR OF METALLOPROTEINASE-3 IS UP-REGULATED BY TRANSFORMING GROWTH FACTOR-β1 IN VITRO AND EXPRESSED IN FIBROBLASTIC FOCI IN VIVO IN IDIOPATHIC PULMONARY FIBROSIS (2006) (41)
Promoter variants in tissue inhibitor of metalloproteinase-3 (TIMP-3) protect against susceptibility in pigeon breeders’ disease (2004) (39)
Aging and Pulmonary Fibrosis. (2016) (39)
Matrix metalloproteinase (MMP)-19-deficient fibroblasts display a profibrotic phenotype. (2015) (39)
Human lung myofibroblast-derived inducers of alveolar epithelial apoptosis identified as angiotensin peptides. (1999) (38)
Gene expression profiles reveal molecular mechanisms involved in the progression and resolution of bleomycin-induced lung fibrosis. (2013) (37)
Hypersensitivity pneumonitis (2020) (37)
The Interplay of the Genetic Architecture, Aging, and Environmental Factors in the Pathogenesis of Idiopathic Pulmonary Fibrosis. (2020) (36)
Dehydroepiandrosterone has strong antifibrotic effects and is decreased in idiopathic pulmonary fibrosis (2012) (36)
Upregulation of acidic fibroblast growth factor during development of experimental lung fibrosis. (1997) (36)
Polymorphisms of surfactant protein gene A, B, D, and of SP-B-linked microsatellite markers in COPD of a Mexican population. (2000) (35)
Lung alveolar epithelial cells synthesize interstitial collagenase and gelatinases A and B in vitro. (1997) (35)
MICA polymorphisms and decreased expression of the MICA receptor NKG2D contribute to idiopathic pulmonary fibrosis susceptibility (2009) (35)
Increased Expression of CC16 in Patients with Idiopathic Pulmonary Fibrosis (2016) (33)
Cell size, cell cycle, and α-smooth muscle actin expression by primary human lung fibroblasts. (1998) (32)
Inflammatory profiles in severe pneumonia associated with the pandemic influenza A/H1N1 virus isolated in Mexico City (2011) (31)
Alveolar epithelial cell disintegrity and subsequent activation: a key process in pulmonary fibrosis. (2012) (29)
Emerging insights into the role of matrix metalloproteases as therapeutic targets in fibrosis. (2018) (29)
Renin is an angiotensin-independent profibrotic mediator: role in pulmonary fibrosis (2011) (28)
Matrix metalloproteinases and lung injury. (1996) (28)
When things go wrong: exploring possible mechanisms driving the progressive fibrosis phenotype in interstitial lung diseases (2021) (27)
Bleomycin-induced pulmonary fibrosis is attenuated in gamma-glutamyl transpeptidase-deficient mice. (2003) (23)
Fibroageing: An ageing pathological feature driven by dysregulated extracellular matrix-cell mechanobiology (2021) (22)
Fibrogenic Lung Injury Induces Non-Cell-Autonomous Fibroblast Invasion. (2016) (22)
Local and circulating microchimerism is associated with hypersensitivity pneumonitis. (2007) (22)
Tissue inhibitor of metalloproteinase-3 is up-regulated by transforming growth factor-beta1 in vitro and expressed in fibroblastic foci in vivo in idiopathic pulmonary fibrosis. (2006) (21)
Role of von Hippel‐Lindau protein in fibroblast proliferation and fibrosis (2011) (21)
Cell size, cell cycle, and alpha-smooth muscle actin expression by primary human lung fibroblasts. (1998) (21)
Delayed resolution of bleomycin-induced pulmonary fibrosis in absence of MMP13 (collagenase 3). (2019) (21)
Rac2 is required for alternative macrophage activation and bleomycin induced pulmonary fibrosis; a macrophage autonomous phenotype (2017) (21)
Lung-specific loss of α3 laminin worsens bleomycin-induced pulmonary fibrosis. (2015) (20)
Inflammatory response and dynamics of lung T cell subsets in Th1, Th2 biased and Th2 deficient mice during the development of hypersensitivity pneumonitis. (2010) (20)
Why Does an Aging Smoker's Lung Develop Idiopathic Pulmonary Fibrosis and Not Chronic Obstructive Pulmonary Disease? (2019) (20)
The effect of CTLA-4Ig, a CD28/B7 antagonist, on the lung inflammation and T cell subset profile during murine hypersensitivity pneumonitis. (2011) (19)
Hypermethylation-mediated silencing of p14 in fibroblasts from idiopathic pulmonary fibrosis (2012) (19)
Upregulation and Nuclear Location of MMP28 in Alveolar Epithelium of Idiopathic Pulmonary Fibrosis (2018) (18)
Identification of the benign mesenchymal tumor gene HMGA2 in lymphangiomyomatosis. (2007) (17)
Grainyhead-like 2 (GRHL2) distribution reveals novel pathophysiological differences between human idiopathic pulmonary fibrosis and mouse models of pulmonary fibrosis. (2014) (17)
Use of oligonucleotide microarrays to analyze gene expression patterns in pulmonary fibrosis reveals distinct patterns of gene expression in mice and humans. (2002) (17)
Mitochondrial 8-Oxoguanine DNA Glycosylase Mitigates Alveolar Epithelial Cell PINK1 Deficiency, Mitochondrial DNA Damage, Apoptosis and Lung Fibrosis. (2020) (16)
Update in diffuse parenchymal lung disease 2012. (2013) (16)
Increased alveolar soluble annexin V promotes lung inflammation and fibrosis (2015) (16)
Lower levels of α-Klotho in serum are associated with decreased lung function in individuals with interstitial lung abnormalities (2019) (15)
Identification of MMP28 as a biomarker for the differential diagnosis of idiopathic pulmonary fibrosis (2018) (15)
Impaired autophagic activity and ATG4B deficiency are associated with increased endoplasmic reticulum stress-induced lung injury. (2018) (14)
Emerging drugs for idiopathic pulmonary fibrosis (2011) (14)
Purification of a procollagenase-activator present in medium of cultured guinea pig carrageenin granuloma. (1991) (14)
Stochastic age-related epigenetic drift in the pathogenesis of idiopathic pulmonary fibrosis. (2014) (14)
Expression of a 2.8-kb PDGF-B/c-sis transcript and synthesis of PDGF-like protein by human lung fibroblasts. (1995) (13)
Alveolar epithelial cell death adjacent to underlying myofibroblasts in advanced fibrotic human lung. (1998) (13)
Risk factors associated with the development of interstitial lung abnormalities (2021) (13)
Transforming growth factor beta 1 induces methylation changes in lung fibroblasts (2019) (13)
SNP and Haplotype Interaction Models Reveal Association of Surfactant Protein Gene Polymorphisms With Hypersensitivity Pneumonitis of Mexican Population (2021) (12)
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis (2013) (12)
Loss of MT1-MMP in Alveolar Epithelial Cells Exacerbates Pulmonary Fibrosis (2021) (12)
R‐Spondin‐2 Is Upregulated in Idiopathic Pulmonary Fibrosis and Affects Fibroblast Behavior (2018) (12)
Expression and Localization of TIMP‐1, TIMP‐2, MMP‐13, MMP‐2, and MMP‐9 in Early and Advanced Experimental Lung Silicosis (1999) (12)
Mitochondrial Dysfunction and Alterations in Mitochondrial Permeability Transition Pore (mPTP) Contribute to Apoptosis Resistance in Idiopathic Pulmonary Fibrosis Fibroblasts (2021) (10)
Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury (2018) (10)
Inflammatory pathways are upregulated in the nasal epithelium in patients with idiopathic pulmonary fibrosis (2018) (9)
Increased expression of intercellular adhesion molecule 1, CD11/CD18 cell surface adhesion glycoproteins and alpha 4 beta 1 integrin in a rat model of chronic interstitial lung fibrosis. (1996) (9)
Production of platelet-derived growth factor by human lung cancer. (1991) (9)
Potential Role of Proteases in Pulmonary Fibrosis (1991) (9)
Update in Interstitial Lung Disease 2019. (2020) (8)
From pulmonary fibrosis to progressive pulmonary fibrosis - a lethal pathobiological jump. (2021) (8)
Problems encountered in high-level research in developing countries. (1998) (8)
Collagenase and collagenase inhibitors in bronchoalveolar lavage fluids. (1991) (8)
PDCD1 gene polymorphisms in different Mexican ethnic groups and their role in the susceptibility to hypersensitivity pneumonitis. (2010) (7)
Matrix Metalloproteinases and Tissue Inhibitors of Metalloproteinases in Pulmonary Fibrosis (2003) (6)
Fibroblast Senescence and Apoptosis. "One-Two Punch" to Slow Down Lung Fibrosis? (2017) (6)
Mesenchymal–Epithelial Transition in Fibroblasts of Human Normal Lungs and Interstitial Lung Diseases (2021) (6)
Pathogenic mechanisms in the development of diffuse pulmonary fibrosis. (1996) (6)
Accelerated aging induced by deficiency of Zmpste24 protects old mice to develop bleomycin-induced pulmonary fibrosis (2018) (6)
Extracellular Matrix Remodeling in Idiopathic Pulmonary Fibrosis (2001) (5)
Role of matrix metalloproteases in pulmonary fibrosis (2008) (5)
Decreased collagenase production by fibroblasts derived from idiopathic pulmonary fibrosis. (1992) (5)
Cloning and expression of guinea pig TIMP-2. Expression in normal and hyperoxic lung injury. (2000) (5)
Transcriptomic profile of the mice aging lung is associated with inflammation and apoptosis as important pathways (2021) (4)
Pigeon Breederʼs Disease: A Paradigm for Understanding Hypersensitivity Pneumonitis (1995) (4)
CD4+T cells in ageing-associated interstitial lung abnormalities show evidence of pro-inflammatory phenotypic and functional profile (2020) (4)
Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants. (2023) (4)
Improving biocuration of microRNAs in diseases: a case study in idiopathic pulmonary fibrosis (2017) (4)
Usual interstitial pneumonia as a stand-alone diagnostic entity: the case for a paradigm shift? (2023) (3)
Erratum: Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis (Nature Genetics (2013) 45 (613-620)) (2013) (3)
Determination of the phenotypic age in residents of Mexico City: effect of accelerated ageing on lung function and structure (2020) (3)
The Human Genome and Advances in Medicine: Limits and Future Prospects (2004) (2)
Corrigendum: ADAM10-mediated ephrin-B2 shedding promotes myofibroblast activation and organ fibrosis (2017) (2)
Aging and IPF: What Is the Link? (2014) (2)
Resequencing Study Con ﬁ rms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis (2019) (2)
Fibroblasts From Idiopathic Pulmonary Fibrosis Induce Apoptosis and Reduce the Migration Capacity of T Lymphocytes (2022) (2)
Club cell secretory protein-CC16 is increased in idiopathic pulmonary fibrosis (2016) (2)
Leukotriene C 4 upregulates collagenase expression and synthesis in human lung fibroblasts (2002) (2)
MMP-8 Is A Central Player In Fibrocytes Transmigration (2010) (2)
Pulmonary Perspective (2012) (2)
Lung-Speci fi c Loss of a 3 Laminin Worsens Bleomycin-Induced Pulmonary Fibrosis (2015) (1)
Idiopathic Pulmonary Fibrosis: Clinical Behavior, Pathogenic Mechanisms and Therapeutic Approach (2015) (1)
Matrix Metalloproteinase (MMP-1) Induces Alveolar Epithelial Cell Migration And Proliferation, Protects From Apoptosis And Represses Mitochondrial Oxygen Consumption (2012) (1)
Increased Of Lung Matrix-Metalloproteinase (MMP)-9 Distinguishes Combined Pulmonary Fibrosis With Emphysema (CPFE) From Idiopathic Pulmonary Fibrosis (IPF) Alone (2011) (1)
TMPRSS4: a novel serine protease involved in IPF development? (2016) (1)
Development of a Diagnostic Biosensor Method of Hypersensitivity Pneumonitis towards a Point-of-Care Biosensor (2021) (1)
Hypermethylation Mediated Silencing of p14ARF in Fibroblasts from Patients with Idiopathic Pulmonary Fibrosis (IPF): A Putative Role in Fibroblasts Resistance to Apoptosis. (2009) (1)
Fibrocytes express several matrix metalloproteinases. Possible role in migration and homing (2010) (1)
Single 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 Pneumonitis (2022) (1)
Altered Lung Mast Cell Populations Infiltrate Areas Of Inflammation And Remodeling In Patients With Cystic Fibrosis And Idiopathic Pulmonary Fibrosis (2010) (1)
Hematopoietic Derived Fibrocytes: Emerging Effector Cells in Fibrotic Disorders (2012) (1)
Cellular source of collagenase and TIMP-1 in carrageenin-induced granuloma. (1994) (1)
Translational Research in Acute Lung Injury and Pulmonary Fibrosis Grainyhead-like 2 ( GRHL 2 ) distribution reveals novel pathophysiological differences between human idiopathic pulmonary fibrosis and mouse models of pulmonary fibrosis (2014) (1)
Premature aging in Zmpste24 deficient mice protects them from bleomycin induced lung fibrosis through upregulation of antifibrotic microRNAs (2018) (1)
Protective Role of MMP14 in Alveolar Epithelial Cells in Pulmonary Fibrosis (2020) (0)
Molecules in focus MMP-1 : the elder of the family (2004) (0)
Elevated levels of von Hippel‐Lindau protein in human and mouse fibrotic lungs (2009) (0)
Proteomic Evaluation of the Lungs of Senescence-Accelerated Prone 8 (SAMP8) Mouse (2020) (0)
Identification of Unfolded Protein Response Related Proteins in Lungs From Hypersensitivity Pneumonitis Patients (2023) (0)
Diagnostic unification of usual interstitial pneumonia is a step back - Authors' reply. (2023) (0)
Homer1 Is Increased in Idiopathic Pulmonary Fibrosis and Affects Fibroblasts Behavior (2019) (0)
Common and Distinct Bronchoalveolar Lavage and Lung Immune Signatures in Fibrotic Hypersensitivity Pneumonitis and Idiopathic Pulmonary Fibrosis (2023) (0)
CRITICAL CARE UPDATE Update in Interstitial Lung Disease 2019 (2020) (0)
Senescence or Autophagy, Divergent Mechanisms Driving Alveolar Regeneration in Accelerated Aging Mice (2023) (0)
R‐Spondin2 is upregulated in idiopathic pulmonary fibrosis and affects fibroblasts behavior (2016) (0)
Profibrotic Behavior of Lung Fibroblasts Derived From MMP8-MMP13 Double Knockout Mice Is Associated With a Delayed Fibrosis Resolution (2023) (0)
Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia (2016) (0)
Lower levels of α-Klotho in serum are associated with decreased lung function in individuals with interstitial lung abnormalities (2019) (0)
Determination of the phenotypic age of the residents of Mexico City. Effect of accelerated aging on lung function and structure (2020) (0)
Identification of Autophagy-related Proteins in Lungs From Hypersensitivity Pneumonitis Patients (2020) (0)
Autophagy Biomarkers in Hypersensitivity Pneumonitis (2020) (0)
Human lung myoﬁbroblast-derived inducers of alveolar epithelial apoptosis identiﬁed as angiotensin peptides (1999) (0)
Association of Surfactant Protein Gene Polymorphisms with Hypersensitivity Pneumonitis in a Mexican Population (2020) (0)
Patients With Idiopathic Pulmonary Fibrosis (IPF) Exhibit A Remarkable Decrease Of Dehydroepiandrosterone (DHEA). Putative Antifibrotic Effects Of DHEA On Lung Fibroblasts In Vitro (2010) (0)
MatrixMetalloproteinase(MMP)-1InducesLungAlveolar EpithelialCellMigrationandProliferation,Protectsfrom Apoptosis,andRepressesMitochondrialOxygenConsumption * (2013) (0)
PINK1 deficiency in AECII triggers release of mitochondrial DAMPS that initiate pro-inflammatory and pro-fibrotic responses in the lung (2017) (0)
Epithelial biology in idiopathic pulmonary fibrosis (2015) (0)
ZNF365 is overexpressed in Pulmonary Fibrosis (2020) (0)
Matrix metalloproteinase‐19 deficient fibroblasts display a profibrotic phenotype (1046.4) (2014) (0)
Expression of matrix metalloproteinase 1 in rodents: comment on the article by Huebner et al. (1999) (0)
Changes of Lung Transcriptome During Aging (2019) (0)
OP0209 Soluble Ephrin-B2 Ectodomain Contributes to the Pathogenesis of Systemic Sclerosis (2015) (0)
eScholarship Title Blue Journal Conference Aging and Susceptibility to Lung Disease Permalink (2015) (0)
EXPRESSION OF MATRIX METALLOPROTEINASE 1 IN RODENTS : COMMENT ON THE ARTICLE BY HUEBNER ET AL. AUTHORS' REPLY (1999) (0)
One Molecule, Two Opposite Biological Effects: The Many Faces of Matrix Metalloproteases in the Pathogenesis of Idiopathic Pulmonary Fibrosis (2020) (0)
Increased Levels of Matrix Metalloproteinase (MMP)-9 and TGF-β and Lower Levels of IL-8 Differentiate Combined Pulmonary Fibrosis With Emphysema (CPFE) From Idiopathic Pulmonary Fibrosis (IPF) Alone (2011) (0)
Antifibrotic effects of dehydroepiandrosterone (DHEA) in lung fibroblasts in vitro (2011) (0)
ALUNG December 21/6 (1999) (0)
P057 Soluble Ephrin-B2 is a Prognostic Biomarker of Pulmonary Fibrosis (2016) (0)
Contemporary Approaches to Idiopathic Pulmonary Fibrosis (2015) (0)
Collagenase-inhibitory activity in deposit and resorption phases of guinea pig carrageenin granuloma. (1992) (0)
Fibroblast Growth Factor-1 attenuates TGFβ1-induced lung fibrosis through inhibition of Smad2/3 phosphorylation (2014) (0)
Comparison between lung parenchyma and bronchoalveolar lavage collagenolytic activity (2004) (0)
Matrix Metalloproteinase (MMP)‐1 Induces Migration and Proliferation of Lung Epithelial Cells (2008) (0)
The Absence of Thy-1 Expression by Human Lung Fibroblasts Is Associated with MMP-9 Expression. (2009) (0)
Does apoptosis evasion only affect fibroblasts from idiopathic pulmonary fibrosis (2013) (0)
Tumor 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 Activation (2001) (0)
Frequency and risk factors associated to Interstitial Lung Abnormalities (ILA) in asymptomatic older (>60 years) individuals (2017) (0)
Why a smoker-aging lung develops IPF and not COPD? (2015) (0)
IPA Software Analysis Reveals Inflammation and Apoptosis as Major Enrichment Functional Process in Normal Lung During Aging (2020) (0)
Lack of ZNF365 Drives Senescence and Exacerbates Experimental Lung Fibrosis (2022) (0)
Evaluation of osteopontin as a potential biological marker in idiopathic pulmonary fibrosis (2005) (0)
Matrix metalloproteinase ( MMP )-19 deficient fibroblasts display a profibrotic 2 phenotype 3 4 * (2015) (0)
MMP19 is Sustaining in Pulmonary Fibrosis through Induction of ER Stress (2014) (0)

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