Annie Pardo
#158,358
Most Influential Person Now
Researcher
Annie Pardo's AcademicInfluence.com Rankings
Annie Pardocomputer-science Degrees
Computer Science
#8895
World Rank
#9351
Historical Rank
Machine Learning
#3762
World Rank
#3808
Historical Rank
Artificial Intelligence
#4081
World Rank
#4139
Historical Rank
Database
#5888
World Rank
#6107
Historical Rank

Download Badge
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
Similar Degrees You Can Earn
Why Is Annie Pardo Influential?
(Suggest an Edit or Addition)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)
This paper list is powered by the following services:
What Schools Are Affiliated With Annie Pardo?
Annie Pardo is affiliated with the following schools: