Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
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SHARPIN is an endogenous inhibitor of β1-integrin activationStructural Analysis of SHARPIN, a Subunit of a Large Multi-protein E3 Ubiquitin Ligase, Reveals a Novel Dimerization Function for the Pleckstrin Homology SuperfoldPolyglucosan body myopathy caused by defective ubiquitin ligase RBCK1Balancing cell numbers during organogenesis: Six1a differentially affects neurons and sensory hair cells in the inner ear.BOR-syndrome-associated Eya1 mutations lead to enhanced proteasomal degradation of Eya1 proteinSystems analysis identifies an essential role for SHANK-associated RH domain-interacting protein (SHARPIN) in macrophage Toll-like receptor 2 (TLR2) responses.Mutually Exclusive Roles of SHARPIN in Integrin Inactivation and NF-κB Signaling.The Eyes Absent proteins in development and disease.Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes.Sharpin promotes hepatocellular carcinoma progression via transactivation of Versican expression.The EYA-SO/SIX complex in development and disease.Linear ubiquitination-mediated NF-κB regulation and its related disorders.The multifaceted role of the E3 ubiquitin ligase HOIL-1: beyond linear ubiquitination.The Sharpin interactome reveals a role for Sharpin in lamellipodium formation via the Arp2/3 complex.SHARPIN regulates collagen architecture and ductal outgrowth in the developing mouse mammary gland.Identification of RBCK1 as a novel regulator of FKBPL: implications for tumor growth and response to tamoxifen.Genetic Syndromes Affecting Kidney Development.Loss of mtch2 function impairs early development of liver, intestine and visceral adipocytes in zebrafish larvae.Novel partial duplication of EYA1 causes branchiootic syndrome in a large Brazilian family.A Firefly Luciferase Dual Color Bioluminescence Reporter Assay Using Two Substrates To Simultaneously Monitor Two Gene Expression Events.Microtia: epidemiology and genetics.
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P2860
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
description
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2010
@ast
im Dezember 2010 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2010/12/01)
@sk
vědecký článek publikovaný v roce 2010
@cs
wetenschappelijk artikel (gepubliceerd op 2010/12/01)
@nl
наукова стаття, опублікована в грудні 2010
@uk
مقالة علمية (نشرت في ديسمبر 2010)
@ar
name
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@ast
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@en
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@nl
type
label
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@ast
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@en
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@nl
prefLabel
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@ast
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@en
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@nl
P2093
P2860
P921
P356
P1476
Sipl1 and Rbck1 are novel Eya1-binding proteins with a role in craniofacial development
@en
P2093
Andreas Kispert
Birgit Besenbeck
Christina Ebert
Dagmar Kruspe
Frank Bollig
Frank Hänel
Kathrin Landgraf
Mark-Oliver Trowe
P2860
P304
P356
10.1128/MCB.01645-09
P407
P577
2010-10-18T00:00:00Z