scholarly article | Q13442814 |
P2093 | author name string | Tao Jiang | |
Xi Zhan | |||
Yong Lu | |||
Qiao Ye | |||
Yuan-Hua Yang | |||
Chun-Ming Zheng | |||
P2860 | cites work | The genetic basis of idiopathic pulmonary fibrosis | Q40777090 |
Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. | Q46125322 | ||
Prevalence and characteristics of TERT and TERC mutations in suspected genetic pulmonary fibrosis. | Q47699201 | ||
Diagnostic criteria for idiopathic pulmonary fibrosis: a Fleischner Society White Paper. | Q47706610 | ||
Rare Genetic Variants in PARN Are Associated with Pulmonary Fibrosis in Families | Q47914471 | ||
Finding the missing heritability of complex diseases | Q22122198 | ||
The telomere syndromes | Q24632444 | ||
Familial pulmonary fibrosis is the strongest risk factor for idiopathic pulmonary fibrosis | Q28247967 | ||
An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management | Q28308246 | ||
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis | Q28943334 | ||
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study | Q28943525 | ||
Telomerase mutations in families with idiopathic pulmonary fibrosis | Q29615671 | ||
Genetic characterization of a Chinese family with familial idiopathic pulmonary fibrosis | Q30420251 | ||
Telomerase gene mutations and telomere length shortening in patients with idiopathic pulmonary fibrosis in a Chinese population | Q33418402 | ||
Pathogenesis of idiopathic pulmonary fibrosis | Q33976506 | ||
Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase | Q35030917 | ||
Rare variants in RTEL1 are associated with familial interstitial pneumonia | Q35262015 | ||
Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening | Q35554660 | ||
Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis | Q35570923 | ||
Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis. | Q35645765 | ||
Ethnic and racial differences in the presence of idiopathic pulmonary fibrosis at death | Q35803056 | ||
Telomerase activity is required for bleomycin-induced pulmonary fibrosis in mice. | Q36138013 | ||
Short telomeres are a risk factor for idiopathic pulmonary fibrosis | Q36861819 | ||
TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements. | Q37041915 | ||
Association Between the MUC5B Promoter Polymorphism rs35705950 and Idiopathic Pulmonary Fibrosis: A Meta-analysis and Trial Sequential Analysis in Caucasian and Asian Populations | Q37149994 | ||
IDIOPATHIC PULMONARY FIBROSIS IS A COMPLEX GENETIC DISORDER. | Q37563857 | ||
P433 | issue | 18 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | pulmonary fibrosis | Q32446 |
idiopathic pulmonary fibrosis | Q2290446 | ||
P304 | page(s) | 2205-2209 | |
P577 | publication date | 2018-09-20 | |
P1433 | published in | Chinese Medical Journal | Q5100534 |
P1476 | title | A Rare Missense Variant in Telomerase Reverse Transcriptase is Associated with Idiopathic Pulmonary Fibrosis in a Chinese Han Family | |
P478 | volume | 131 |
Search more.