FHIT, a Novel Modifier Gene in Pulmonary Arterial Hypertension-Reference-Cited by-同舟云学术

FHIT, a Novel Modifier Gene in Pulmonary Arterial Hypertension

Published:2019-01 Issue:1 Volume:199 Page:83-98
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:

Dannewitz Prosseda Svenja¹²^ORCID,Tian Xuefei¹²,Kuramoto Kazuya¹²,Boehm Mario¹²,Sudheendra Deepti¹,Miyagawa Kazuya²³⁴,Zhang Fan²,Solow-Cordero David⁵,Saldivar Joshua C.⁶,Austin Eric D.⁷,Loyd James E.⁷,Wheeler Lisa⁷,Andruska Adam¹,Donato Michele⁸,Wang Lingli¹²,Huebner Kay⁹,Metzger Ross J.²,Khatri Purvesh⁸,Spiekerkoetter Edda¹²³

Affiliation:

1. Division of Pulmonary and Critical Care, Department of Medicine

2. Wall Center for Pulmonary Vascular Disease

3. Cardiovascular Institute

4. Department of Pediatrics

5. High-Throughput Bioscience Center, and

6. Chemical and Systems Biology, Stanford University, Stanford, California

7. Vanderbilt University Medical Center, Nashville, Tennessee; and

8. Biomedical Informatics Research–Institute for Immunity, Transplantation, and Infection, Stanford University, Stanford, California

9. Molecular Genetics and Cancer Biology Program, Ohio State University, Columbus, Ohio

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.201712-2553OC

Reference91 articles.

1. Austin ED, Loyd JE, Phillips JA III. Heritable pulmonary arterial hypertension. 2002 Jul 18 [updated 2015 Jun 11; accessed 2018 Jun]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, et al., editors. GeneReviews. Seattle, WA: University of Washington, Seattle; 1993–2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1485/.

2. Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension

3. The Genetics of Pulmonary Arterial Hypertension in the Post‐BMPR2 Era

4. Primary Pulmonary Hypertension Is Associated With Reduced Pulmonary Vascular Expression of Type II Bone Morphogenetic Protein Receptor

5. Inaccuracy of Doppler Echocardiographic Estimates of Pulmonary Artery Pressures in Patients With Pulmonary Hypertension

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