Subclinical lung disease, macrocytosis, and premature graying in kindreds with telomerase (TERT) mutations.
about
A roadmap to promote clinical and translational research in rheumatoid arthritis-associated interstitial lung diseaseMitochondria in the spotlight of aging and idiopathic pulmonary fibrosisShort telomeres, telomeropathy, and subclinical extrapulmonary organ damage in patients with interstitial lung disease.Functional impact of a spectrum of interstitial lung abnormalities in rheumatoid arthritis.Interstitial lung disease: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases.Effect of telomere length on survival in patients with idiopathic pulmonary fibrosis: an observational cohort study with independent validation.Bone marrow failure and the telomeropathies.Genetics and early detection in idiopathic pulmonary fibrosisRed blood cell size is inversely associated with leukocyte telomere length in a large multi-ethnic population.Decreasing initial telomere length in humans intergenerationally understates age-associated telomere shortening.Subclinical interstitial lung disease: why you should care.Lung fibrosis, premature graying, and macrocytosis.Genetic studies provide clues on the pathogenesis of idiopathic pulmonary fibrosis.Quantifying heterogeneity in emphysema from high-resolution computed tomography: a lung tissue research consortium study.Anemia of Central Origin.MUC5B promoter polymorphism and interstitial lung abnormalities.Differential telomerase expression in idiopathic pulmonary fibrosis and non-small cell lung cancer.Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) genePulmonary fibrosis in the era of stratified medicine.Interstitial Lung Disease in Werner Syndrome: A Case Report of a 55-Year-Old Male Patient.Transforming growth factor β1 regulates the expression of CCN2 in human keratinocytes via Smad-ERK signalling.Running short on time: lung transplant evaluation for telomere-related pulmonary fibrosis.Insights from human genetic studies of lung and organ fibrosis.Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease.Idiopathic pulmonary fibrosis a rare disease with severe bone fragility.Clinical Genetics in Interstitial Lung Disease.Emerging therapies for idiopathic pulmonary fibrosis, a progressive age-related disease.
P2860
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P2860
Subclinical lung disease, macrocytosis, and premature graying in kindreds with telomerase (TERT) mutations.
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
name
Subclinical lung disease, macr ...... h telomerase (TERT) mutations.
@ast
Subclinical lung disease, macr ...... h telomerase (TERT) mutations.
@en
type
label
Subclinical lung disease, macr ...... h telomerase (TERT) mutations.
@ast
Subclinical lung disease, macr ...... h telomerase (TERT) mutations.
@en
prefLabel
Subclinical lung disease, macr ...... h telomerase (TERT) mutations.
@ast
Subclinical lung disease, macr ...... h telomerase (TERT) mutations.
@en
P2093
P2860
P356
P1433
P1476
Subclinical lung disease, macr ...... h telomerase (TERT) mutations.
@en
P2093
Alberto Diaz de Leon
Cecelia Brewington
Christine Kim Garcia
Connie C W Hsia
Cuneyt Yilmaz
Jennifer T Cronkhite
Richard Wang
P2860
P304
P356
10.1378/CHEST.10-2865
P407
P50
P577
2011-02-24T00:00:00Z