Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actin
about
The interaction of Piasy with Trim32, an E3-ubiquitin ligase mutated in limb-girdle muscular dystrophy type 2H, promotes Piasy degradation and regulates UVB-induced keratinocyte apoptosis through NFkappaBIntrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSomeTRIM32 is an E3 ubiquitin ligase for dysbindinHomozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Specific recognition and accelerated uncoating of retroviral capsids by the TRIM5alpha restriction factorThe TRIM-NHL protein TRIM32 activates microRNAs and prevents self-renewal in mouse neural progenitorsIncreased expression of the E3 ubiquitin ligase RNF5 is associated with decreased survival in breast cancerDeficiency of the E3 ubiquitin ligase TRIM32 in mice leads to a myopathy with a neurogenic componentThe beneficial role of proteolysis in skeletal muscle growth and stress adaptationLoss of muscle mass: current developments in cachexia and sarcopenia focused on biomarkers and treatmentRole of Inflammation in Muscle Homeostasis and MyogenesisRole of E2-Ub-conjugating enzymes during skeletal muscle atrophyThe ER-bound RING finger protein 5 (RNF5/RMA1) causes degenerative myopathy in transgenic mice and is deregulated in inclusion body myositisNitric oxide destabilizes Pias3 and regulates sumoylationUbiquitin ligase TRIM3 controls hippocampal plasticity and learning by regulating synaptic γ-actin levelsThe TRIM-NHL protein LIN-41 controls the onset of developmental plasticity in Caenorhabditis elegansThe Ubiquitin-Proteasome System and Molecular Chaperone Deregulation in Alzheimer's DiseaseMG53 regulates membrane budding and exocytosis in muscle cells.The E3 ubiquitin ligase specificity subunit ASB2beta is a novel regulator of muscle differentiation that targets filamin B to proteasomal degradationThe p97/VCP ATPase is critical in muscle atrophy and the accelerated degradation of muscle proteinsThe common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotypeDeficiency in ubiquitin ligase TRIM2 causes accumulation of neurofilament light chain and neurodegenerationThe neural stem cell fate determinant TRIM32 regulates complex behavioral traits.The dark side of EGFP: defective polyubiquitination.Ozz-E3 ubiquitin ligase targets sarcomeric embryonic myosin heavy chain during muscle development.Lentivirus-mediated RNA interference of tripartite motif 68 inhibits the proliferation of colorectal cancer cell lines SW1116 and HCT116 in vitroKelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathyLafora disease E3-ubiquitin ligase malin is related to TRIM32 at both the phylogenetic and functional levelSkeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx/atrogin-1TRIM32 protein modulates type I interferon induction and cellular antiviral response by targeting MITA/STING protein for K63-linked ubiquitinationMuscle wasting and cachexia in heart failure: mechanisms and therapies.SUMOylation of nuclear actinA novel actin mRNA splice variant regulates ACTG1 expression.TRIM32 protein sensitizes cells to tumor necrosis factor (TNFα)-induced apoptosis via its RING domain-dependent E3 ligase activity against X-linked inhibitor of apoptosis (XIAP).Proteomic survey of ubiquitin-linked nuclear proteins in interferon-stimulated macrophagesThe RNA helicase DDX6 regulates cell-fate specification in neural stem cells via miRNAs.TRIM32 Senses and Restricts Influenza A Virus by Ubiquitination of PB1 PolymeraseThe Schizophrenia-Related Protein Dysbindin-1A Is Degraded and Facilitates NF-Kappa B Activity in the NucleusLoss of muscle-specific RING-finger 3 predisposes the heart to cardiac rupture after myocardial infarction.Detection of TRIM32 deletions in LGMD patients analyzed by a combined strategy of CGH array and massively parallel sequencing
P2860
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P2860
Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actin
description
2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2005
@ast
im November 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2005/11/25)
@sk
vědecký článek publikovaný v roce 2005
@cs
wetenschappelijk artikel (gepubliceerd op 2005/11/25)
@nl
наукова стаття, опублікована в листопаді 2005
@uk
مقالة علمية (نشرت في 25-11-2005)
@ar
name
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@ast
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@en
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@nl
type
label
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@ast
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@en
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@nl
prefLabel
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@ast
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@en
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@nl
P2093
P3181
P1476
Trim32 is a ubiquitin ligase m ...... myosin and ubiquitinates actin
@en
P2093
Dmitri Kudryashov
Elena Kudryashova
Irina Kramerova
Melissa J. Spencer
P304
P3181
P356
10.1016/J.JMB.2005.09.068
P407
P577
2005-11-25T00:00:00Z