Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension.
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Novel crosstalk to BMP signalling: cGMP-dependent kinase I modulates BMP receptor and Smad activityBMPR2 spruces up the endothelium in pulmonary hypertensionThe molecular genetics and cellular mechanisms underlying pulmonary arterial hypertensionThe Wnt and BMP families of signaling morphogens at the vertebrate neuromuscular junctionDisruption of axonal transport perturbs bone morphogenetic protein (BMP)--signaling and contributes to synaptic abnormalities in two neurodegenerative diseasesStructural and thermodynamic characterization of a cytoplasmic dynein light chain intermediate chain complexDynein light chain Tctex-type 1 modulates orexin signaling through its interaction with orexin 1 receptorBMP type II receptor regulates positioning of outflow tract and remodeling of atrioventricular cushion during cardiogenesisG protein beta gamma subunit interaction with the dynein light-chain component Tctex-1 regulates neurite outgrowthBone morphogenetic protein 2 induces pulmonary angiogenesis via Wnt-beta-catenin and Wnt-RhoA-Rac1 pathways.Relay of retrograde synaptogenic signals through axonal transport of BMP receptors.Endoglin-mediated suppression of prostate cancer invasion is regulated by activin and bone morphogenetic protein type II receptors.Requirement of a dynein light chain in TGFbeta/Smad3 signaling.The dynamic interaction of AMBRA1 with the dynein motor complex regulates mammalian autophagy.Dynein Light Chain 1 (DYNLT1) Interacts with Normal and Oncogenic Nucleoporins.Rescuing the BMPR2 signaling axis in pulmonary arterial hypertensionRequirement of a dynein light chain in transforming growth factor β signaling in zebrafish ovarian follicle cells.The genetics of pulmonary arterial hypertension in the post-BMPR2 era.Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expression.Cytoskeletal defects in Bmpr2-associated pulmonary arterial hypertensionMetabolomic analysis of bone morphogenetic protein receptor type 2 mutations in human pulmonary endothelium reveals widespread metabolic reprogramming.Connectivity map analysis of nonsense-mediated decay-positive BMPR2-related hereditary pulmonary arterial hypertension provides insights into disease penetrance.Control of phenotypic plasticity of smooth muscle cells by bone morphogenetic protein signaling through the myocardin-related transcription factors.Novel biochemical pathways of endoglin in vascular cell physiology.Raf/ERK drives the proliferative and invasive phenotype of BMPR2-silenced pulmonary artery endothelial cells.A New Era in Medical Management of Severe Pediatric Pulmonary Arterial Hypertension.Aberrant Expression of Dynein light chain 1 (DYNLT1) is Associated with Human Male Factor Infertility.Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects.Mice expressing BMPR2R899X transgene in smooth muscle develop pulmonary vascular lesions.Genetics and genomics of pulmonary arterial hypertension.SMAD1 deficiency in either endothelial or smooth muscle cells can predispose mice to pulmonary hypertensionA potential role for insulin resistance in experimental pulmonary hypertensionGender, sex hormones and pulmonary hypertension.Rho-kinase inhibition alleviates pulmonary hypertension in transgenic mice expressing a dominant-negative type II bone morphogenetic protein receptor gene.Defective pulmonary vascular remodeling in Smad8 mutant miceMechanisms of disease: pulmonary arterial hypertension.Bone Morphogenetic Protein functions as a context-dependent angiogenic cue in vertebrates.Diversity is in my veins: role of bone morphogenetic protein signaling during venous morphogenesis in zebrafish illustrates the heterogeneity within endothelial cellsDifferential regulation of translation and endocytosis of alternatively spliced forms of the type II bone morphogenetic protein (BMP) receptorModulation of Rho guanine exchange factor Lfc activity by protein kinase A-mediated phosphorylation.
P2860
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P2860
Functional interaction between BMPR-II and Tctex-1, a light chain of Dynein, is isoform-specific and disrupted by mutations underlying primary pulmonary hypertension.
description
2003 nî lūn-bûn
@nan
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Functional interaction between ...... rimary pulmonary hypertension.
@ast
Functional interaction between ...... rimary pulmonary hypertension.
@en
Functional interaction between ...... rimary pulmonary hypertension.
@nl
type
label
Functional interaction between ...... rimary pulmonary hypertension.
@ast
Functional interaction between ...... rimary pulmonary hypertension.
@en
Functional interaction between ...... rimary pulmonary hypertension.
@nl
prefLabel
Functional interaction between ...... rimary pulmonary hypertension.
@ast
Functional interaction between ...... rimary pulmonary hypertension.
@en
Functional interaction between ...... rimary pulmonary hypertension.
@nl
P2093
P50
P356
P1476
Functional interaction between ...... rimary pulmonary hypertension.
@en
P2093
Carl Atkinson
Julia A Flanagan
Nung Rudarakanchana
Rachel Harrison
P304
P356
10.1093/HMG/DDG365
P577
2003-10-28T00:00:00Z