Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development - Wikidata - awgldk - TriplyDB

Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development

Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development

http://www.wikidata.org/entity/Q35676707

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Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia Structure of three tandem filamin domains reveals auto-inhibition of ligand binding Common variants in FLNB/CRTAP, not ARHGEF3 at 3p, are associated with osteoporosis in southern Chinese women Epidemiology and pathophysiology of mitral valve prolapse: new insights into disease progression, genetics, and molecular basis Evidence for the mechanosensor function of filamin in tissue development.Filamin and phospholipase C-ε are required for calcium signaling in the Caenorhabditis elegans spermatheca Filamins regulate cell spreading and initiation of cell migration Molecular Basis of Filamin A-FilGAP Interaction and Its Impairment in Congenital Disorders Associated with Filamin A Mutations Atomic Structures of Two Novel Immunoglobulin-like Domain Pairs in the Actin Cross-linking Protein Filamin Filamin B mutations cause chondrocyte defects in skeletal development F-actin clustering and cell dysmotility induced by the pathological W148R missense mutation of filamin B at the actin-binding domain FLN-1/filamin is required for maintenance of actin and exit of fertilized oocytes from the spermatheca in C. elegans Transcript diversification in the nervous system: a to I RNA editing in CNS function and disease development Filamin B plays a key role in vascular endothelial growth factor-induced endothelial cell motility through its interaction with Rac-1 and Vav-2.Extended Field Laser Confocal Microscopy (EFLCM): combining automated Gigapixel image capture with in silico virtual microscopy Gene expression profiles of colonic mucosa in healthy young adult and senior dogs.Filamins in mechanosensing and signaling.Formin 1 and filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plate Disease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severity.Targeting filamin B induces tumor growth and metastasis via enhanced activity of matrix metalloproteinase-9 and secretion of VEGF-A.High-molecular-weight hyaluronan is a novel inhibitor of pulmonary vascular leakiness The filamins: organizers of cell structure and function Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal.Filamin-A regulates neutrophil uropod retraction through RhoA during chemotaxis.Filamin B regulates chondrocyte proliferation and differentiation through Cdk1 signaling Type XVII collagen regulates lamellipod stability, cell motility, and signaling to Rac1 by targeting bullous pemphigoid antigen 1e to alpha6beta4 integrin Assembly of a filamin four-domain fragment and the influence of splicing variant-1 on the structure.Filamin depletion blocks endoplasmic spreading and destabilizes force-bearing adhesions.Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients Critical role of filamin-binding LIM protein 1 (FBLP-1)/migfilin in regulation of bone remodeling.Targeting filamin A reduces K-RAS-induced lung adenocarcinomas and endothelial response to tumor growth in mice.Hypoxia-induced expression of VE-cadherin and filamin B in glioma cell cultures and pseudopalisade structures Auxiliary and autonomous proteoglycan signaling networks Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome Cell biology of embryonic migration.Animal models of scoliosis.Snail promotes cell migration through PI3K/AKT-dependent Rac1 activation as well as PI3K/AKT-independent pathways during prostate cancer progression.Characterization of two ENU-induced mutations affecting mouse skeletal morphology.Cyclosporine does not reduce myocardial infarct size in a porcine ischemia-reperfusion model.Protein disulfide isomerase increases in myocardial endothelial cells in mice exposed to chronic hypoxia: a stimulatory role in angiogenesis.

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P2860

Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development

http://www.wikidata.org/entity/Q35676707

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2007 nî lūn-bûn

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Filamin B deficiency in mice r ...... ired microvascular development

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Filamin B deficiency in mice r ...... ired microvascular development

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type

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Filamin B deficiency in mice r ...... ired microvascular development

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Filamin B deficiency in mice r ...... ired microvascular development

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Filamin B deficiency in mice r ...... ired microvascular development

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Filamin B deficiency in mice r ...... ired microvascular development

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Emilie Flaberg

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Fei Tian

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Johan Sandzén

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Levent M Akyürek

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Martin O Bergo

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Renhai Cao

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Xianghua Zhou

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Yihai Cao

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P2860

The small GTPase RalA targets filamin to induce filopodia

FilGAP, a Rho- and ROCK-regulated GAP for Rac binds filamin A to control actin remodelling

Human beta-filamin is a new protein that interacts with the cytoplasmic tail of glycoprotein Ibalpha

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact

A novel human actin-binding protein homologue that binds to platelet glycoprotein Ibalpha

Mutations in FLNB cause boomerang dysplasia

Interaction of presenilins with the filamin family of actin-binding proteins

Akt1 in endothelial cell and angiogenesis

Filamins as integrators of cell mechanics and signalling

N-myristoyltransferase 1 is essential in early mouse development

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