about
X-linked disorders with cerebellar dysgenesisNovel interactors and a role for supervillin in early cytokinesis.Platelet proteome analysis reveals integrin-dependent aggregation defects in patients with myelodysplastic syndromes.Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA geneAllelic diversity in human developmental neurogenetics: insights into biology and diseaseSpecificity of ADAR-mediated RNA editing in newly identified targetsResearch advances on structure and biological functions of integrinsGenes and brain malformations associated with abnormal neuron positioningMolecular Basis of Filamin A-FilGAP Interaction and Its Impairment in Congenital Disorders Associated with Filamin A MutationsA novel interaction between FlnA and Syk regulates platelet ITAM-mediated receptor signaling and functionIdentification and characterization of multiple similar ligand-binding repeats in filamin: implication on filamin-mediated receptor clustering and cross-talkA trans-acting protein effect causes severe eye malformation in the Mp mouseLoss of FilaminC (FLNc) results in severe defects in myogenesis and myotube structureCurrent themes in molecular pediatrics: molecular medicine and its applications.Macrophage mesenchymal migration requires podosome stabilization by filamin AStructural basis of filamin A functionsProteomic analysis permits the identification of new biomarkers of arterial wall remodeling in hypertension.Filamins in mechanosensing and signaling.Formin 1 and filamin B physically interact to coordinate chondrocyte proliferation and differentiation in the growth plateDisease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severity.Expansion of the Spectrum of FLNA Mutations Associated with Melnick-Needles SyndromeNormal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseasesGenome-wide screening for DNA variants associated with reading and language traitsXq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance.Diverse functions for the semaphorin receptor PlexinD1 in development and disease.Cell type-specific filamin complex regulation by a novel class of HECT ubiquitin ligase is required for normal cell motility and patterning.The filamins: organizers of cell structure and functionBinding of pro-prion to filamin A: by design or an unfortunate blunderThe dual role of filamin A in cancer: can't live with (too much of) it, can't live without it.Whole exome sequence analysis of Peters anomaly.Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement.A switch of G protein-coupled receptor binding preference from phosphoinositide 3-kinase (PI3K)-p85 to filamin A negatively controls the PI3K pathway.47 patients with FLNA associated periventricular nodular heterotopiaIdentification of CAP as a costameric protein that interacts with filamin C.Brefeldin A-inhibited guanine exchange factor 2 regulates filamin A phosphorylation and neuronal migration.Monoubiquitination of filamin B regulates vascular endothelial growth factor-mediated trafficking of histone deacetylase 7.Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A.ASB2 targets filamins A and B to proteasomal degradation.ASB2α, an E3 ubiquitin ligase specificity subunit, regulates cell spreading and triggers proteasomal degradation of filamins by targeting the filamin calponin homology 1 domainGenetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder.
P2860
Q21202871-95C32174-3EEA-46A4-B473-C8EFB5ED56D6Q24304327-4B7F1B87-B42A-4246-8E31-B26138556062Q24314265-C0979EDB-1E0D-49ED-B24B-A3B168BE9438Q24620559-61B3EC5B-57C6-467B-82B8-CC1CE0270C70Q24620889-5C9B9F52-7D71-45A4-83EC-51A2F5C4D5EDQ24652694-F27C6B46-E08F-49F0-9E7E-7A7D6219F359Q26741077-A035242A-8597-47FB-A255-5E26D38824B7Q26779045-E583AC18-33BC-499E-A023-8C68E456D0C4Q27654191-691F8BBE-2624-42E1-B1C4-FE3993EA58BBQ28115628-06045B44-C59D-4843-9EA0-D12289DE8681Q28119187-1B162BB7-CC5B-4435-83C6-388BEFAD5EF8Q28508709-24F8B33C-23E9-41D6-B444-21AFABED0BC3Q28594543-A91892CE-D5A0-4A5E-BFDE-1A8AC00D45B9Q30397005-88B628F2-D9BE-4B7C-B159-032393F2A0E4Q30513877-281CC765-7632-41E2-B980-C7E6602EF89BQ33308469-38E89900-3D62-4FE8-BD73-38B3FFE8ECB8Q33337003-D33158CC-3914-400E-A59C-34EED7F64E79Q33900830-96DA2BF9-20F8-4C2F-A594-7F72826A4631Q33991787-A63D7484-EB0F-41CE-921B-D6D33CAF3F32Q34108318-FD066F4B-1A56-4F30-9C2D-D9E2F333AD01Q34146747-FE3D9998-A44F-40BF-950E-322AE8E55DECQ34173783-D67CA6EC-AF2A-4FD4-A281-5971ED9AE594Q34195610-1702AF5D-394F-477C-8E16-A6BE90019F54Q34326039-63565028-0D21-463E-A97E-85F67FC5B32FQ34361068-470FA152-DBCB-4CFF-B3BD-8260981A613CQ34707679-F3978DFA-1111-4AFF-BF3B-48C4D8ECCD1CQ34891266-07829E31-8939-4703-87BF-C0C216CDEC16Q35173852-33599F4C-79D6-46AE-A371-397863BF567FQ35223554-9D219F9D-FE98-4624-8D03-B258FEBA5B3FQ35395210-C3C8A9D9-9CC7-4008-A1BA-234270951786Q35752546-C41F2407-1665-4DD0-8F2E-26E1B305AA0CQ35807246-E4D29E1C-7C24-4570-B962-E5EC4A16A6B5Q36168967-2AD09D58-AD44-4FA6-8EE3-4BAB677A2656Q36173940-2E228ED5-E6B7-4724-8811-5BB9E0634938Q36340949-0F7B1D8F-DA66-4AFA-A375-6DA78BF9676FQ36759844-3C4B4752-6141-45B3-AB21-BE1DAA536DFFQ36809682-75006330-7BCF-49F6-B214-585D14E91C48Q37003539-EBFDF892-BDBB-4143-904E-96601FE74283Q37272236-46CC9AB0-853F-4EE4-AA8D-2EDD628C2CDCQ37322350-5F31CD44-3C62-4075-A8B8-F3C4DBD41BFC
P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Filamin A: phenotypic diversity.
@ast
Filamin A: phenotypic diversity.
@en
type
label
Filamin A: phenotypic diversity.
@ast
Filamin A: phenotypic diversity.
@en
prefLabel
Filamin A: phenotypic diversity.
@ast
Filamin A: phenotypic diversity.
@en
P1476
Filamin A: phenotypic diversity.
@en
P2093
Stephen P Robertson
P304
P356
10.1016/J.GDE.2005.04.001
P577
2005-06-01T00:00:00Z