Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1-Reference-Cited by-同舟云学术

Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1

Published:2013-09 Issue:3 Volume:144 Page:794-804
ISSN:0012-3692
Container-title:Chest
language:en
Short-container-title:Chest

Author:

Hamvas Aaron,Deterding Robin R.,Wert Susan E.,White Frances V.,Dishop Megan K.,Alfano Danielle N.,Halbower Ann C.,Planer Benjamin,Stephan Mark J.,Uchida Derek A.,Williames Lee D.,Rosenfeld Jill A.,Lebel Robert Roger,Young Lisa R.,Cole F. Sessions,Nogee Lawrence M.

Funder

National Institutes of Health grants to Drs Hamvas and Cole

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Reference33 articles.

1. Diffuse lung disease in young children: application of a novel classification scheme;Deutsch;Am J Respir Crit Care Med,2007

2. Surfactant protein deficiency in familial interstitial lung disease;Amin;J Pediatr,2001

3. ABCA3 gene mutations in newborns with fatal surfactant deficiency;Shulenin;N Engl J Med,2004

4. Thyroid transcription factor-1 (TTF-1/Nkx2.1/TITF1) gene regulation in the lung;Boggaram;Clin Sci (Lond),2009

5. Mutations in TITF-1 are associated with benign hereditary chorea;Breedveld;Hum Mol Genet,2002

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