Cardiac malformations and midline skeletal defects in mice lacking filamin A. - Wikidata - wikimedia - TriplyDB

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

http://www.wikidata.org/entity/Q51796683

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A meckelin-filamin A interaction mediates ciliogenesis RhoD regulates cytoskeletal dynamics via the actin nucleation-promoting factor WASp homologue associated with actin Golgi membranes and microtubules RefilinB (FAM101B) targets filamin A to organize perinuclear actin networks and regulates nuclear shape.Structure of three tandem filamin domains reveals auto-inhibition of ligand binding Nuclear actin and actin-binding proteins in the regulation of transcription and gene expression Allelic diversity in human developmental neurogenetics: insights into biology and disease Genetics of valvular heart disease 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 Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders Generation of intestinal surface: an absorbing tale A novel interaction between FlnA and Syk regulates platelet ITAM-mediated receptor signaling and function Filamin B mutations cause chondrocyte defects in skeletal development A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development Genetic disruption of the sh3pxd2a gene reveals an essential role in mouse development and the existence of a novel isoform of tks5 FLN-1/filamin is required for maintenance of actin and exit of fertilized oocytes from the spermatheca in C. elegans Filamin structure, function and mechanics: are altered filamin-mediated force responses associated with human disease?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.A neuron autonomous role for the familial dysautonomia gene ELP1 in sympathetic and sensory target tissue innervation.Structural basis of filamin A functions New insights into the versatile roles of platelet FlnA.Filamins in mechanosensing and signaling.Expression of the familial cardiac valvular dystrophy gene, filamin-A, during heart morphogenesis.The role of pygopus in the differentiation of intracardiac valves in Drosophila.Normal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseases Filamin A regulates focal adhesion disassembly and suppresses breast cancer cell migration and invasion.Targeting filamin B induces tumor growth and metastasis via enhanced activity of matrix metalloproteinase-9 and secretion of VEGF-A.Combined cardiological and neurological abnormalities due to filamin A gene mutation.Developmental basis for filamin-A-associated myxomatous mitral valve disease.The filamins: organizers of cell structure and function Filamin-A regulates neutrophil uropod retraction through RhoA during chemotaxis.The E3 ubiquitin ligase specificity subunit ASB2α targets filamins for proteasomal degradation by interacting with the filamin actin-binding domain Binding of pro-prion to filamin A: by design or an unfortunate blunder The dual role of filamin A in cancer: can't live with (too much of) it, can't live without it.Cytoskeletal proteins in cortical development and disease: actin associated proteins in periventricular heterotopia.Whole exome sequence analysis of Peters anomaly.Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement.

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P2860

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

http://www.wikidata.org/entity/Q51796683

description

2006 nî lūn-bûn

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2006年の論文

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2006年学术文章

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2006年学术文章

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2006年学术文章

@zh-cn

2006年学术文章

@zh-hans

2006年学术文章

@zh-my

2006年学术文章

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2006年學術文章

@yue

2006年學術文章

@zh-hant

name

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

@en

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

@nl

type

label

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

@en

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

@nl

prefLabel

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

@en

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

@nl

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Human Molecular Genetics

P1476

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

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P2093

Alan W Hart

http://www.w3.org/2001/XMLSchema#string

Joanne E Morgan

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Jürgen Schneider

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Katrine West

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Lisa McKie

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Sally H Cross

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P2860

FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated manner

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

Human endothelial actin-binding protein (ABP-280, nonmuscle filamin): a molecular leaf spring

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye

Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique

Filamins as integrators of cell mechanics and signalling

Neural crest and cardiovascular development: a 20-year perspective

Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development

Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development

Actin-binding and dimerization domains of HeLa cell filamin

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2457-2467

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scholarly article

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10.1093/HMG/DDL168

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16

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15

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Shoumo Bhattacharya

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2006-07-06T00:00:00Z

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6960430

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16825286

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