| scholarly article | Q13442814 |
| P50 | author | Eric S. White | Q38324814 |
| Jonathan Andrew Kropski | Q89503711 | ||
| Lorraine B. Ware | Q91134545 | ||
| P2093 | author name string | Lisa R Young | |
| Timothy S Blackwell | |||
| Joyce E Johnson | |||
| Jae Woo Lee | |||
| Pierre P Massion | |||
| Leena Choi | |||
| Jonathan D Kurtis | |||
| Steve D Groshong | |||
| James E Loyd | |||
| Joy D Cogan | |||
| Amber L Degryse | |||
| Frank B McMahon | |||
| Linda A Gleaves | |||
| Rinat Zaynagetdinov | |||
| Vasiliy V Polosukhin | |||
| Mark P Steele | |||
| Dong-Sheng Cheng | |||
| William E Lawson | |||
| Joseph F Solus | |||
| John A Worrell | |||
| Lisa H Lancaster | |||
| Errine T Garnett | |||
| Otis B Rickman | |||
| Cheryl Markin | |||
| Donald F Zoz | |||
| Daphne B Mitchell | |||
| Brittany R Jones | |||
| Melinda E McConaha | |||
| Peter F Crossno | |||
| Jason M Pritchett | |||
| John A Phillips Iii | |||
| P2860 | cites work | Clinical and pathologic features of familial interstitial pneumonia | Q36234581 |
| Transbronchial biopsy is useful in predicting UIP pattern | Q36402285 | ||
| High-resolution CT scan findings in familial interstitial pneumonia do not conform to those of idiopathic interstitial pneumonia | Q36447397 | ||
| Genetic studies provide clues on the pathogenesis of idiopathic pulmonary fibrosis | Q36485998 | ||
| Short telomeres are a risk factor for idiopathic pulmonary fibrosis | Q36861819 | ||
| Telomere shortening in familial and sporadic pulmonary fibrosis | Q36915503 | ||
| Generalized linear mixed models: a review and some extensions | Q37000464 | ||
| MUC5B promoter polymorphism and interstitial lung abnormalities | Q37105760 | ||
| Maternal infection with Schistosoma japonicum induces a profibrotic response in neonates | Q37548047 | ||
| Viral infection and aging as cofactors for the development of pulmonary fibrosis | Q37815487 | ||
| Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred | Q42675595 | ||
| Blood biomarkers MMP-7 and SP-A: predictors of outcome in idiopathic pulmonary fibrosis. | Q50954787 | ||
| Endoplasmic reticulum stress in alveolar epithelial cells is prominent in IPF: association with altered surfactant protein processing and herpesvirus infection. | Q53486707 | ||
| Familial idiopathic pulmonary fibrosis. Evidence of lung inflammation in unaffected family members | Q69497791 | ||
| Serum surfactant proteins A and D as prognostic factors in idiopathic pulmonary fibrosis and their relationship to disease extent | Q74316652 | ||
| Pulmonary fibrosis in families | Q79076907 | ||
| Characterization of fibroblast-specific protein 1 in pulmonary fibrosis | Q81196614 | ||
| Histopathologic findings of transbronchial biopsy in usual interstitial pneumonia | Q84343989 | ||
| VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing | Q24628978 | ||
| A surfactant protein C precursor protein BRICHOS domain mutation causes endoplasmic reticulum stress, proteasome dysfunction, and caspase 3 activation | Q24645087 | ||
| A mutation in the surfactant protein C gene associated with familial interstitial lung disease | Q28201394 | ||
| Familial pulmonary fibrosis is the strongest risk factor for idiopathic pulmonary fibrosis | Q28247967 | ||
| A novel dyskerin (DKC1) mutation is associated with familial interstitial pneumonia | Q28307444 | ||
| MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis | Q28472658 | ||
| Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis | Q28943334 | ||
| Epidemiology Standardization Project (American Thoracic Society) | Q29614936 | ||
| Telomerase mutations in families with idiopathic pulmonary fibrosis | Q29615671 | ||
| Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. | Q30374030 | ||
| Periostin promotes fibrosis and predicts progression in patients with idiopathic pulmonary fibrosis | Q30415751 | ||
| Epithelial endoplasmic reticulum stress and apoptosis in sporadic idiopathic pulmonary fibrosis | Q30484036 | ||
| Epstein-Barr virus replication within pulmonary epithelial cells in cryptogenic fibrosing alveolitis. | Q33605234 | ||
| C-X-C motif chemokine 13 (CXCL13) is a prognostic biomarker of idiopathic pulmonary fibrosis | Q33901646 | ||
| The elevation of serum napsin A in idiopathic pulmonary fibrosis, compared with KL-6, surfactant protein-A and surfactant protein-D. | Q34410117 | ||
| Comparative study of KL-6, surfactant protein-A, surfactant protein-D, and monocyte chemoattractant protein-1 as serum markers for interstitial lung diseases. | Q34520692 | ||
| Schistosoma japonicum soluble egg antigens attenuate invasion in a first trimester human placental trophoblast model | Q34766888 | ||
| Natural history of pulmonary fibrosis in two subjects with the same telomerase mutation | Q34923419 | ||
| The MUC5B variant is associated with idiopathic pulmonary fibrosis but not with systemic sclerosis interstitial lung disease in the European Caucasian population | Q34935466 | ||
| Genetics in pulmonary fibrosis--familial cases provide clues to the pathogenesis of idiopathic pulmonary fibrosis | Q35010171 | ||
| Herpesvirus DNA is consistently detected in lungs of patients with idiopathic pulmonary fibrosis | Q35027515 | ||
| A variant in the promoter of MUC5B and idiopathic pulmonary fibrosis | Q35083039 | ||
| Viral infection in acute exacerbation of idiopathic pulmonary fibrosis | Q35107245 | ||
| Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis | Q35683018 | ||
| Adult-onset pulmonary fibrosis caused by mutations in telomerase | Q35759839 | ||
| Telomere length assessment in human archival tissues: combined telomere fluorescence in situ hybridization and immunostaining | Q35788945 | ||
| Right place, right time: the evolving role of herpesvirus infection as a "second hit" in idiopathic pulmonary fibrosis | Q35850237 | ||
| Early interstitial lung disease in familial pulmonary fibrosis | Q36013730 | ||
| A common MUC5B promoter polymorphism and pulmonary fibrosis. | Q36048530 | ||
| Transbronchial biopsy in usual interstitial pneumonia | Q36168852 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | pneumonia | Q12192 |
| P304 | page(s) | 417-426 | |
| P577 | publication date | 2015-02-01 | |
| P1433 | published in | American Journal of Respiratory and Critical Care Medicine | Q4744267 |
| P1476 | title | Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease | |
| P478 | volume | 191 |
| Q43178545 | A first glimpse at the early origins of idiopathic pulmonary fibrosis |
| Q90693925 | Alveolar Epithelial Type II Cells as Drivers of Lung Fibrosis in Idiopathic Pulmonary Fibrosis |
| Q47815265 | An Official American Thoracic Society Workshop Report: Translational Research in Rare Respiratory Diseases. |
| Q47937434 | Are newly launched pharmacotherapies efficacious in treating idiopathic pulmonary fibrosis? Or is there still more work to be done? |
| Q36790758 | Association Between Interstitial Lung Abnormalities and All-Cause Mortality |
| Q35758535 | CD8+ T Cell Response to Gammaherpesvirus Infection Mediates Inflammation and Fibrosis in Interferon Gamma Receptor-Deficient Mice |
| Q89503712 | Development and Progression of Radiologic Abnormalities in Individuals at Risk for Familial ILD |
| Q52642205 | Endoplasmic reticulum stress in pulmonary fibrosis. |
| Q47239353 | Endoplasmic reticulum stress in the pathogenesis of fibrotic disease |
| Q90606561 | Familial pulmonary fibrosis: a world without frontiers |
| Q48037972 | Genetic Evaluation and Testing of Patients and Families with Idiopathic Pulmonary Fibrosis |
| Q40502107 | High attenuation areas on chest computed tomography in community-dwelling adults: the MESA study. |
| Q30838920 | Hsp90 regulation of fibroblast activation in pulmonary fibrosis |
| Q48032800 | IPF in 2016: towards a better diagnosis |
| Q93091814 | Idiopathic Pulmonary Fibrosis Is a Genetic Disease Involving Mucus and the Peripheral Airways |
| Q38821078 | Idiopathic Pulmonary Fibrosis: A Genetic Disease That Involves Mucociliary Dysfunction of the Peripheral Airways |
| Q46134058 | Idiopathic interstitial pneumonias in 2015: A new era. |
| Q87721963 | Idiopathic pulmonary fibrosis |
| Q89691744 | Idiopathic pulmonary fibrosis |
| Q52721106 | Idiopathic pulmonary fibrosis: Epithelial-mesenchymal interactions and emerging therapeutic targets. |
| Q35786160 | Incorporating genetics into the identification and treatment of Idiopathic Pulmonary Fibrosis |
| Q38913044 | Influences of innate immunity, autophagy, and fibroblast activation in the pathogenesis of lung fibrosis |
| Q89503728 | Interstitial Lung Disease in Relatives of Patients with Pulmonary Fibrosis |
| Q97568165 | Interstitial lung abnormalities detected incidentally on CT: a Position Paper from the Fleischner Society |
| Q64232728 | Interstitial lung abnormalities: erecting fences in the path towards advanced pulmonary fibrosis |
| Q36066466 | Lost after translation: insights from pulmonary surfactant for understanding the role of alveolar epithelial dysfunction and cellular quality control in fibrotic lung disease |
| Q90316654 | MUC5B variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis |
| Q29248145 | Mitochondria in the spotlight of aging and idiopathic pulmonary fibrosis |
| Q60044254 | Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in mice |
| Q39791661 | Plasma Surfactant Protein-D, Matrix Metalloproteinase-7, and Osteopontin Index Distinguishes Idiopathic Pulmonary Fibrosis from Other Idiopathic Interstitial Pneumonias. |
| Q33714064 | Precision Medicine: The New Frontier in Idiopathic Pulmonary Fibrosis |
| Q26745905 | Recent advances in understanding idiopathic pulmonary fibrosis |
| Q38751135 | Serum Matrix Metalloproteinase-7, Respiratory Symptoms, and Mortality in Community-dwelling Adults: The Multi-Ethnic Study of Atherosclerosis |
| Q48342417 | Short telomere length in IPF lung associates with fibrotic lesions and predicts survival. |
| Q37277301 | Telomere dysfunction in alveolar epithelial cells causes lung remodeling and fibrosis |
| Q90428685 | Telomeres in Interstitial Lung Disease: The Short and the Long of It |
| Q42378740 | Telomeres revisited: RTEL1 variants in pulmonary fibrosis |
| Q40146154 | The MUC5B promoter polymorphism and telomere length in patients with chronic hypersensitivity pneumonitis: an observational cohort-control study. |
| Q47124422 | The MUC5B promoter polymorphism is associated with specific interstitial lung abnormality subtypes |
| Q26786969 | The Role of Mitochondrial DNA in Mediating Alveolar Epithelial Cell Apoptosis and Pulmonary Fibrosis |
| Q33924950 | The diagnosis of idiopathic pulmonary fibrosis: current and future approaches |
| Q40777090 | The genetic basis of idiopathic pulmonary fibrosis |
| Q33871544 | The respiratory microbiome in idiopathic pulmonary fibrosis |
| Q50056514 | Time for a change: is idiopathic pulmonary fibrosis still idiopathic and only fibrotic? |
| Q51532190 | To Suppress the Radicals We Must Have Biomarkers of Oxidative Stress. |
| Q26779192 | Understanding Idiopathic Interstitial Pneumonia: A Gene-Based Review of Stressed Lungs |
| Q47804444 | Validation of the prognostic value of MMP-7 in idiopathic pulmonary fibrosis |
| Q28081676 | Viruses in Idiopathic Pulmonary Fibrosis. Etiology and Exacerbation |
| Q36064954 | miR-34 miRNAs Regulate Cellular Senescence in Type II Alveolar Epithelial Cells of Patients with Idiopathic Pulmonary Fibrosis |
Search more.