An antiproliferative BMP-2/PPARγ/apoE axis in human and murine SMCs and its role in pulmonary hypertension-Reference-Cited by-同舟云学术

An antiproliferative BMP-2/PPARγ/apoE axis in human and murine SMCs and its role in pulmonary hypertension

Published:2008-05-01 Issue:5 Volume:118 Page:1846-1857
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Hansmann Georg,de Jesus Perez Vinicio A.,Alastalo Tero-Pekka,Alvira Cristina M.,Guignabert Christophe,Bekker Janine M.,Schellong Stefan,Urashima Takashi,Wang Lingli,Morrell Nicholas W.,Rabinovitch Marlene

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference54 articles.

1. Epidermal Growth Factor Receptor Blockade Mediates Smooth Muscle Cell Apoptosis and Improves Survival in Rats With Pulmonary Hypertension

2. Reversal of experimental pulmonary hypertension by PDGF inhibition

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

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

5. Genetic basis of pulmonary arterial hypertension

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