The S52F FOXF1 Mutation Inhibits STAT3 Signaling and Causes Alveolar Capillary Dysplasia-Reference-Cited by-同舟云学术

The S52F FOXF1 Mutation Inhibits STAT3 Signaling and Causes Alveolar Capillary Dysplasia

Published:2019-10-15 Issue:8 Volume:200 Page:1045-1056
ISSN:1073-449X
Container-title:American Journal of Respiratory and Critical Care Medicine
language:en
Short-container-title:Am J Respir Crit Care Med

Author:

Pradhan Arun¹²,Dunn Andrew¹²³,Ustiyan Vladimir¹²,Bolte Craig¹²,Wang Guolun¹²,Whitsett Jeffrey A.¹⁴,Zhang Yufang¹²,Porollo Alexey¹⁵,Hu Yueh-Chiang¹⁶,Xiao Rui⁷⁸,Szafranski Przemyslaw⁸,Shi Donglu³,Stankiewicz Pawel⁷⁸,Kalin Tanya V.¹⁴,Kalinichenko Vladimir V.¹²⁴

Affiliation:

1. Department of Pediatrics

2. Center for Lung Regenerative Medicine

3. The Materials Science and Engineering Program, College of Engineering and Applied Science, University of Cincinnati, Cincinnati, Ohio

4. Division of Pulmonary Biology

5. Center for Autoimmune Genomics and Etiology, and

6. Transgenic Animal and Genome Editing Core Facility, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio

7. Baylor Genetics, Houston, Texas; and

8. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Link

https://www.atsjournals.org/doi/pdf/10.1164/rccm.201810-1897OC

Reference50 articles.

1. Alveolar Capillary Dysplasia

2. Infants with Atypical Presentations of Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins Who Underwent Bilateral Lung Transplantation

3. Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

4. NovelFOXF1Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain

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