Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene.
about
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasiaFunctional changes in pulmonary arterial endothelial cells associated with BMPR2 mutationsNotch3 signaling promotes the development of pulmonary arterial hypertensionBMP4 induces HO-1 via a Smad-independent, p38MAPK-dependent pathway in pulmonary artery myocytesBone morphogenetic protein (BMP) and activin type II receptors balance BMP9 signals mediated by activin receptor-like kinase-1 in human pulmonary artery endothelial cellsALK1 signaling regulates early postnatal lymphatic vessel developmentMolecular pathogenesis of pulmonary arterial hypertensionNew insights into the pathogenesis and treatment of primary pulmonary hypertensionBone morphogenetic proteins, genetics and the pathophysiology of primary pulmonary hypertensionGenomic approaches to research in pulmonary hypertensionAnorexigen-induced pulmonary hypertension and the serotonin (5-HT) hypothesis: lessons for the future in pathogenesisEffects of ADMA upon gene expression: an insight into the pathophysiological significance of raised plasma ADMA.Challenges and Current Efforts in the Development of Biomarkers for Chronic Inflammatory and Remodeling Conditions of the LungsTargeting BMP signalling in cardiovascular disease and anaemiaOveractive bone morphogenetic protein signaling in heterotopic ossification and Duchenne muscular dystrophyMolecular mechanisms of pulmonary arterial remodelingThe molecular genetics and cellular mechanisms underlying pulmonary arterial hypertensionApelin-APJ signaling: a potential therapeutic target for pulmonary arterial hypertensionThe genetics of pulmonary arterial hypertensionStructure analysis of bone morphogenetic protein-2 type I receptor complexes reveals a mechanism of receptor inactivation in juvenile polyposis syndromePulmonary arterial hypertension associated with congenital heart disease and Eisenmenger syndrome: current practice in pediatricsBone morphogenetic protein receptor type II is a receptor for growth differentiation factor-9Whole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertensionLinking a serotonin transporter polymorphism to vascular smooth muscle proliferation in patients with primary pulmonary hypertensionSerotonin transporter overexpression is responsible for pulmonary artery smooth muscle hyperplasia in primary pulmonary hypertensionMutations of NOTCH3 in childhood pulmonary arterial hypertensionBone morphogenetic protein 4 enhances canonical transient receptor potential expression, store-operated Ca2+ entry, and basal [Ca2+]i in rat distal pulmonary arterial smooth muscle cellsHypoxia induces alteration of bone morphogenetic protein receptor signaling in pulmonary artery endothelial cellDownregulation of type II bone morphogenetic protein receptor in hypoxic pulmonary hypertensionPGC1α-mediated mitofusin-2 deficiency in female rats and humans with pulmonary arterial hypertensionWnt signaling regulates smooth muscle precursor development in the mouse lung via a tenascin C/PDGFR pathwayInflammation, endothelial injury, and persistent pulmonary hypertension in heterozygous BMPR2-mutant miceNoggin inhibits hypoxia-induced proliferation by targeting store-operated calcium entry and transient receptor potential cation channels.Pulmonary Arterial Hypertension and the Sex Hormone Paradox.Pulmonary Hypertension in Children.Bone morphogenetic protein 2 induces pulmonary angiogenesis via Wnt-beta-catenin and Wnt-RhoA-Rac1 pathways.Pulmonary arterial hypertension: the clinical syndrome.Gene profiling techniques and their application in angiogenesis and vascular development.BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta-analysisEndoglin-mediated suppression of prostate cancer invasion is regulated by activin and bone morphogenetic protein type II receptors.
P2860
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P2860
Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene.
description
2000 nî lūn-bûn
@nan
2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Familial primary pulmonary hyp ...... etic protein receptor-II gene.
@ast
Familial primary pulmonary hyp ...... etic protein receptor-II gene.
@en
Familial primary pulmonary hypertension
@nl
type
label
Familial primary pulmonary hyp ...... etic protein receptor-II gene.
@ast
Familial primary pulmonary hyp ...... etic protein receptor-II gene.
@en
Familial primary pulmonary hypertension
@nl
prefLabel
Familial primary pulmonary hyp ...... etic protein receptor-II gene.
@ast
Familial primary pulmonary hyp ...... etic protein receptor-II gene.
@en
Familial primary pulmonary hypertension
@nl
P2093
P2860
P356
P1476
Familial primary pulmonary hyp ...... etic protein receptor-II gene.
@en
P2093
J A Knowles
S G Fischer
S Kalachikov
P2860
P304
P356
10.1086/303059
P407
P577
2000-07-20T00:00:00Z