Modeling of Fibrotic Lung Disease Using 3D Organoids Derived from Human Pluripotent Stem Cells-Reference-Cited by-同舟云学术

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Modeling of Fibrotic Lung Disease Using 3D Organoids Derived from Human Pluripotent Stem Cells

Published:2019-06 Issue:12 Volume:27 Page:3709-3723.e5
ISSN:2211-1247
Container-title:Cell Reports
language:en
Short-container-title:Cell Reports

Author:

Strikoudis Alexandros,Cieślak Anna,Loffredo Lucas,Chen Ya-Wen,Patel Nina,Saqi Anjali,Lederer David J.,Snoeck Hans-Willem

Funder

NIH

Thomas R Kully IPF Research Fund

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference95 articles.

1. Short telomeres are a risk factor for idiopathic pulmonary fibrosis;Alder;Proc. Natl. Acad. Sci. USA,2008

2. Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis;Alder;PLoS Genet.,2011

3. Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis;Alder;Chest,2015

4. Telomere dysfunction causes alveolar stem cell failure;Alder;Proc. Natl. Acad. Sci. USA,2015

5. American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias

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