| scholarly article | Q13442814 |
| P50 | author | Joseph R Arron | Q61147913 |
| Brian L. Yaspan | Q61264929 | ||
| Jonathan Andrew Kropski | Q89503711 | ||
| P2093 | author name string | Jan Vogel | |
| Jens Reeder | |||
| Timothy S Blackwell | |||
| William F Forrest | |||
| Harold R Collard | |||
| Tushar R Bhangale | |||
| Thirumalai R Ramalingam | |||
| Alexander R Abbas | |||
| Karen Cuenco | |||
| Paul J Wolters | |||
| Kiran Mukhyala | |||
| Matthew J Brauer | |||
| Lisa H Lancaster | |||
| Julie Hunkapiller | |||
| Margaret Neighbors | |||
| Jennifer Tom | |||
| Amy Cowgill | |||
| Amy Dressen | |||
| Christopher Cabanski | |||
| Janina Reeder | |||
| P2860 | cites work | A mutation in the surfactant protein C gene associated with familial interstitial lung disease | Q28201394 |
| Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): two randomised trials | Q28237583 | ||
| Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis | Q28240230 | ||
| A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis | Q28240241 | ||
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| Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancer | Q40081417 | ||
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| Regulation of MUC5B Expression in Idiopathic Pulmonary Fibrosis | Q48150087 | ||
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| Mice with Pulmonary Fibrosis Driven by Telomere Dysfunction. | Q54261111 | ||
| Surfactant protein C mutations are the basis of a significant portion of adult familial pulmonary fibrosis in a dutch cohort. | Q54418482 | ||
| SFTPA2 Mutations in Familial and Sporadic Idiopathic Interstitial Pneumonia | Q86700271 | ||
| Idiopathic pulmonary fibrosis | Q87721963 | ||
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| Shelterin: the protein complex that shapes and safeguards human telomeres | Q28272546 | ||
| Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis | Q28291143 | ||
| An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management | Q28308246 | ||
| Ensembl 2016 | Q28603093 | ||
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| Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. | Q30374030 | ||
| Alveolar progenitor and stem cells in lung development, renewal and cancer. | Q33579149 | ||
| Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive | Q33692595 | ||
| Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis. | Q33869660 | ||
| The role of senescent cells in ageing | Q34041036 | ||
| Effect of telomere length on survival in patients with idiopathic pulmonary fibrosis: an observational cohort study with independent validation. | Q34060344 | ||
| Reconstructing lineage hierarchies of the distal lung epithelium using single-cell RNA-seq | Q34094294 | ||
| The idiopathic pulmonary fibrosis honeycomb cyst contains a mucocilary pseudostratified epithelium | Q34634190 | ||
| Increased and prolonged pulmonary fibrosis in surfactant protein C-deficient mice following intratracheal bleomycin | Q35085416 | ||
| Rare variants in RTEL1 are associated with familial interstitial pneumonia | Q35262015 | ||
| Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF | Q35536294 | ||
| Telomere dysfunction causes alveolar stem cell failure | Q35549158 | ||
| Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening | Q35554660 | ||
| Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis. | Q35645765 | ||
| Adult-onset pulmonary fibrosis caused by mutations in telomerase | Q35759839 | ||
| Incorporating genetics into the identification and treatment of Idiopathic Pulmonary Fibrosis | Q35786160 | ||
| A common MUC5B promoter polymorphism and pulmonary fibrosis. | Q36048530 | ||
| Short telomeres are a risk factor for idiopathic pulmonary fibrosis | Q36861819 | ||
| Telomeres and age-related disease: how telomere biology informs clinical paradigms | Q36904429 | ||
| Telomere dysfunction in alveolar epithelial cells causes lung remodeling and fibrosis | Q37277301 | ||
| Epidemiology of idiopathic pulmonary fibrosis | Q37359126 | ||
| Alternate-locus aware variant calling in whole genome sequencing | Q37501768 | ||
| Clinical course and prediction of survival in idiopathic pulmonary fibrosis | Q37799183 | ||
| Hyaluronan and TLR4 promote surfactant-protein-C-positive alveolar progenitor cell renewal and prevent severe pulmonary fibrosis in mice. | Q38735180 | ||
| Idiopathic Pulmonary Fibrosis: A Genetic Disease That Involves Mucociliary Dysfunction of the Peripheral Airways | Q38821078 | ||
| P433 | issue | 8 | |
| P921 | main subject | pulmonary fibrosis | Q32446 |
| idiopathic pulmonary fibrosis | Q2290446 | ||
| P304 | page(s) | 603-614 | |
| P577 | publication date | 2018-06-18 | |
| P1433 | published in | The Lancet. Respiratory medicine | Q27724908 |
| P1476 | title | Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study | |
| P478 | volume | 6 |
| Q64084585 | Acute Exacerbation of Idiopathic Pulmonary Fibrosis |
| Q91605838 | Association between FCGR2A rs1801274 and MUC5B rs35705950 variations and pneumonia susceptibility |
| Q89503712 | Development and Progression of Radiologic Abnormalities in Individuals at Risk for Familial ILD |
| Q90606561 | Familial pulmonary fibrosis: a world without frontiers |
| Q92741862 | GDF15 is an epithelial-derived biomarker of idiopathic pulmonary fibrosis |
| Q91651595 | Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosis |
| Q57173045 | Prognostic and predictive biomarkers for patients with idiopathic pulmonary fibrosis treated with pirfenidone: post-hoc assessment of the CAPACITY and ASCEND trials |
| Q92965420 | Telomerase Variants in Patients with Cirrhosis Awaiting Liver Transplantation |
| Q92701873 | Telomere Abnormalities in the Pathobiology of Idiopathic Pulmonary Fibrosis |
| Q90638451 | Telomere Length and Use of Immunosuppressive Medications in Idiopathic Pulmonary Fibrosis |
| Q102071847 | Telomere length and risk of idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease: a mendelian randomisation study |
| Q90428685 | Telomeres in Interstitial Lung Disease: The Short and the Long of It |
| Q97646086 | The Diverse Roles of the Mucin Gene Cluster Located on Chromosome 11p15.5 in Colorectal Cancer |
| Q89929991 | The Search for Molecular Markers in a Gene-Orphan Case Study of a Pediatric Spinal Cord Pilocytic Astrocytoma |
| Q89067946 | Towards genetic reclassification of idiopathic pulmonary fibrosis |
| Q99572138 | Unique roles of rare variants in the genetics of complex diseases in humans |
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