A Rare Missense Variant in Telomerase Reverse Transcriptase is Associated with Idiopathic Pulmonary Fibrosis in a Chinese Han Family

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A Rare Missense Variant in Telomerase Reverse Transcriptase is Associated with Idiopathic Pulmonary Fibrosis in a Chinese Han Family is …
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scholarly articleQ13442814

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P356DOI10.4103/0366-6999.240802
P932PMC publication ID6144832
P698PubMed publication ID30203795

P2093author name stringTao Jiang
Xi Zhan
Yong Lu
Qiao Ye
Yuan-Hua Yang
Chun-Ming Zheng
P2860cites workThe genetic basis of idiopathic pulmonary fibrosisQ40777090
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 FamiliesQ47914471
Finding the missing heritability of complex diseasesQ22122198
The telomere syndromesQ24632444
Familial pulmonary fibrosis is the strongest risk factor for idiopathic pulmonary fibrosisQ28247967
An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and managementQ28308246
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosisQ28943334
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association studyQ28943525
Telomerase mutations in families with idiopathic pulmonary fibrosisQ29615671
Genetic characterization of a Chinese family with familial idiopathic pulmonary fibrosisQ30420251
Telomerase gene mutations and telomere length shortening in patients with idiopathic pulmonary fibrosis in a Chinese populationQ33418402
Pathogenesis of idiopathic pulmonary fibrosisQ33976506
Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomeraseQ35030917
Rare variants in RTEL1 are associated with familial interstitial pneumoniaQ35262015
Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shorteningQ35554660
Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosisQ35570923
Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.Q35645765
Ethnic and racial differences in the presence of idiopathic pulmonary fibrosis at deathQ35803056
Telomerase activity is required for bleomycin-induced pulmonary fibrosis in mice.Q36138013
Short telomeres are a risk factor for idiopathic pulmonary fibrosisQ36861819
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 PopulationsQ37149994
IDIOPATHIC PULMONARY FIBROSIS IS A COMPLEX GENETIC DISORDER.Q37563857
P433issue18
P407language of work or nameEnglishQ1860
P921main subjectpulmonary fibrosisQ32446
idiopathic pulmonary fibrosisQ2290446
P304page(s)2205-2209
P577publication date2018-09-20
P1433published inChinese Medical JournalQ5100534
P1476titleA Rare Missense Variant in Telomerase Reverse Transcriptase is Associated with Idiopathic Pulmonary Fibrosis in a Chinese Han Family
P478volume131

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