Pulmonary Hypertension and ATP-Sensitive Potassium Channels-Reference-Cited by-同舟云学术

Pulmonary Hypertension and ATP-Sensitive Potassium Channels

Published:2019-07 Issue:1 Volume:74 Page:14-22
ISSN:0194-911X
Container-title:Hypertension
language:en
Short-container-title:Hypertension

Author:

McClenaghan Conor¹,Woo Kel Vin²,Nichols Colin G.¹

Affiliation:

1. From the Department of Cell Biology and Physiology, and Center for the Investigation of Membrane Excitability Diseases (CIMED), Washington University, St Louis, MO (C.M., C.G.N.)

2. Department of Pediatrics, Division of Cardiology, Washington University School of Medicine, St Louis, MO (K.V.W.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

Reference142 articles.

1. Pulmonary Hypertension Surveillance

2. Clinical classification of pulmonary hypertension

3. Updated Clinical Classification of Pulmonary Hypertension

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

5. Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene

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