Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
about
hSiah2 is a new Vav binding protein which inhibits Vav-mediated signaling pathwaysRING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitinationThe ubiquitin-conjugating enzymes UbcH7 and UbcH8 interact with RING finger/IBR motif-containing domains of HHARI and H7-AP1Stabilization and activation of p53 by the coactivator protein TAFII31Regulation of BOB.1/OBF.1 stability by SIAHAn RBCC protein implicated in maintenance of steady-state neuregulin receptor levelsMediation of the DCC apoptotic signal by DIP13 alphaPolycystin-1 regulates the stability and ubiquitination of transcription factor Jade-1Staring, a novel E3 ubiquitin-protein ligase that targets syntaxin 1 for degradationComparative analysis of apoptosis and inflammation genes of mice and humansMEX is a testis-specific E3 ubiquitin ligase that promotes death receptor-induced apoptosisMOR is not enough: identification of novel mu-opioid receptor interacting proteins using traditional and modified membrane yeast two-hybrid screensRNF5, a RING finger protein that regulates cell motility by targeting paxillin ubiquitination and altered localizationSiah1 interacts with the scaffold protein POSH to promote JNK activation and apoptosisp53-inducible human homologue of Drosophila seven in absentia (Siah) inhibits cell growth: suppression by BAG-1.LNX functions as a RING type E3 ubiquitin ligase that targets the cell fate determinant Numb for ubiquitin-dependent degradationBiological models and genes of tumor reversion: cellular reprogramming through tpt1/TCTP and SIAH-1Stress-induced decrease in TRAF2 stability is mediated by Siah2The RING finger protein Siah-1 regulates the level of the transcriptional coactivator OBF-1Siah-1 N-terminal RING domain is required for proteolysis function, and C-terminal sequences regulate oligomerization and binding to target proteinsSiah-1 binds and regulates the function of NumbUbiquitin-protein ligase activity of X-linked inhibitor of apoptosis protein promotes proteasomal degradation of caspase-3 and enhances its anti-apoptotic effect in Fas-induced cell deathNetrin induces down-regulation of its receptor, Deleted in Colorectal Cancer, through the ubiquitin-proteasome pathway in the embryonic cortical neuronSIAH-1 promotes apoptosis and tumor suppression through a network involving the regulation of protein folding, unfolding, and trafficking: identification of common effectors with p53 and p21(Waf1)Pw1/Peg3 is a potential cell death mediator and cooperates with Siah1a in p53-mediated apoptosisA role for Seven in Absentia Homolog (Siah1a) in metabotropic glutamate receptor signalingA family of structurally related RING finger proteins interacts specifically with the ubiquitin-conjugating enzyme UbcM4SIAH-1 interacts with alpha-tubulin and degrades the kinesin Kid by the proteasome pathway during mitosisThe coiled-coil domain is the structural determinant for mammalian homologues of Drosophila Sina-mediated degradation of promyelocytic leukemia protein and other tripartite motif proteins by the proteasomePathogenesis of colorectal carcinoma and therapeutic implications: the roles of the ubiquitin-proteasome system and Cox-2Myosin X regulates netrin receptors and functions in axonal path-findingPresenilin-dependent "gamma-secretase" processing of deleted in colorectal cancer (DCC)Proteolysis of AKAP121 regulates mitochondrial activity during cellular hypoxia and brain ischaemiaThe ubiquitin ligase component Siah1a is required for completion of meiosis I in male miceA genetic strategy to eliminate self-activator baits prior to high-throughput yeast two-hybrid screens.Covalent modification of the transcriptional repressor tramtrack by the ubiquitin-related protein Smt3 in Drosophila fliessiah-1 Protein is necessary for high glucose-induced glyceraldehyde-3-phosphate dehydrogenase nuclear accumulation and cell death in Muller cellsDistinct expression patterns of the E3 ligase SIAH-1 and its partner Kid/KIF22 in normal tissues and in the breast tumoral processes.Direct ubiquitination of beta-catenin by Siah-1 and regulation by the exchange factor TBL1.The ubiquitin ligase Siah2 and the hypoxia response.
P2860
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P248
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P2860
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
description
1997 nî lūn-bûn
@nan
1997 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@ast
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@en
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@en-gb
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@nl
type
label
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@ast
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@en
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@en-gb
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@nl
prefLabel
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@ast
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@en
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@en-gb
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@nl
P2093
P2860
P921
P356
P1433
P1476
Mammalian homologs of seven in absentia regulate DCC via the ubiquitin-proteasome pathway
@en
P2093
P2860
P304
P356
10.1101/GAD.11.20.2701
P407
P577
1997-10-15T00:00:00Z