The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleus. - Wikidata - wikimedia - TriplyDB

The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleus.

The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleus.

http://www.wikidata.org/entity/Q30476859

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Drosophila NMNAT maintains neural integrity independent of its NAD synthesis activity Axon degeneration: Molecular mechanisms of a self-destruction pathway Wallerian degeneration, wld(s), and nmnat.Targeting anti-inflammatory treatment can ameliorate injury-induced neuropathic pain.Reducing expression of NAD+ synthesizing enzyme NMNAT1 does not affect the rate of Wallerian degeneration.Local axonal protection by WldS as revealed by conditional regulation of protein stability.Differential proteomics analysis of synaptic proteins identifies potential cellular targets and protein mediators of synaptic neuroprotection conferred by the slow Wallerian degeneration (Wlds) gene.UBE4B: a promising regulatory molecule in neuronal death and survival.Modified cell cycle status in a mouse model of altered neuronal vulnerability (slow Wallerian degeneration; Wlds).p97 Composition Changes Caused by Allosteric Inhibition Are Suppressed by an On-Target Mechanism that Increases the Enzyme's ATPase Activity.Wld S requires Nmnat1 enzymatic activity and N16-VCP interactions to suppress Wallerian degeneration.Wld S protein requires Nmnat activity and a short N-terminal sequence to protect axons in mice Transgenic mice expressing the Nmnat1 protein manifest robust delay in axonal degeneration in vivo.NEDD8 ultimate buster-1 long (NUB1L) protein promotes transfer of NEDD8 to proteasome for degradation through the P97UFD1/NPL4 complex.NAD and axon degeneration: from the Wlds gene to neurochemistry.Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia.Wld(S), Nmnats and axon degeneration--progress in the past two decades.Intrinsic axonal degeneration pathways are critical for glaucomatous damage.Signaling mechanisms regulating Wallerian degeneration.Molecular mechanisms in the initiation phase of Wallerian degeneration.Evolutionary divergence of valosin-containing protein/cell division cycle protein 48 binding interactions among endoplasmic reticulum-associated degradation proteins.

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The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleus.

http://www.wikidata.org/entity/Q30476859

description

2005 nî lūn-bûn

@nan

2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2005年の論文

@ja

2005年論文

@yue

2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

@wuu

name

The slow Wallerian degeneratio ...... ributes it within the nucleus.

@ast

The slow Wallerian degeneratio ...... ributes it within the nucleus.

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type

label

The slow Wallerian degeneratio ...... ributes it within the nucleus.

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The slow Wallerian degeneratio ...... ributes it within the nucleus.

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prefLabel

The slow Wallerian degeneratio ...... ributes it within the nucleus.

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The slow Wallerian degeneratio ...... ributes it within the nucleus.

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MBC.E05-04-0375

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Molecular Biology of the Cell

P1476

The slow Wallerian degeneratio ...... ributes it within the nucleus.

@en

P2093

Arzu Celik

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

Bogdan Beirowski

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

Daniela Grumme

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

Diana Wagner

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

Georg Haase

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

Heike Laser

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

Jane E Haley

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Laura Conforti

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

Markus Plomann

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

Michael P Coleman

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

P2860

Molecular cloning, chromosomal localization, tissue mRNA levels, bacterial expression, and enzymatic properties of human NMN adenylyltransferase

U box proteins as a new family of ubiquitin-protein ligases

Valosin-containing protein is a multi-ubiquitin chain-targeting factor required in ubiquitin-proteasome degradation

The human homologue of the yeast polyubiquitination factor Ufd2p is cleaved by caspase 6 and granzyme B during apoptosis

Involvement of valosin-containing protein, an ATPase Co-purified with IkappaBalpha and 26 S proteasome, in ubiquitin-proteasome-mediated degradation of IkappaBalpha

A complex of mammalian ufd1 and npl4 links the AAA-ATPase, p97, to ubiquitin and nuclear transport pathways

Characterization of the transforming activity of p80, a hyperphosphorylated protein in a Ki-1 lymphoma cell line with chromosomal translocation t(2;5)

A local mechanism mediates NAD-dependent protection of axon degeneration

Ataxin-3 interactions with rad23 and valosin-containing protein and its associations with ubiquitin chains and the proteasome are consistent with a role in ubiquitin-mediated proteolysis

Protein dislocation from the ER requires polyubiquitination and the AAA-ATPase Cdc48.

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1075-1084

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scholarly article

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10.1091/MBC.E05-04-0375

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3

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17

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Giacomo Morreale

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2005-12-21T00:00:00Z

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16371511

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