Transgenic rescue of ataxia mice reveals a male-specific sterility defect. - Wikidata - wikimedia - TriplyDB

Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

http://www.wikidata.org/entity/Q37118359

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Deubiquitination of Dishevelled by Usp14 is required for Wnt signaling Enhancement of proteasome activity by a small-molecule inhibitor of USP14 Knobbed acrosome defect is associated with a region containing the genes STK17b and HECW2 on porcine chromosome 15.Possible role of ZPAC, zygote-specific proteasome assembly chaperone, during spermatogenesis in the mouse.Deubiquitylation of deubiquitylases Molecular chaperones, cochaperones, and ubiquitination/deubiquitination system: involvement in the production of high quality spermatozoa.Trimming of ubiquitin chains by proteasome-associated deubiquitinating enzymes.Genetic background alters the severity and onset of neuromuscular disease caused by the loss of ubiquitin-specific protease 14 (usp14)The proteasome-associated deubiquitinating enzyme Usp14 is essential for the maintenance of synaptic ubiquitin levels and the development of neuromuscular junctions Ubiquitination regulates the morphogenesis and function of sperm organelles The role of deubiquitinating enzymes in spermatogenesis.Concise Review: Fate Determination of Stem Cells by Deubiquitinating Enzymes.Neurotoxic mechanisms by which the USP14 inhibitor IU1 depletes ubiquitinated proteins and Tau in rat cerebral cortical neurons: Relevance to Alzheimer's disease.Meddling with Fate: The Proteasomal Deubiquitinating Enzymes.

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Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

http://www.wikidata.org/entity/Q37118359

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 27 September 2008

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

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name

Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

@en

Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

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type

label

Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

@en

Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

@nl

prefLabel

Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

@en

Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

@nl

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J.YDBIO.2008.09.021

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Developmental Biology

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Transgenic rescue of ataxia mice reveals a male-specific sterility defect.

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Alexis Huffman

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Crystal Wheeler

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Deborah A Swing

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Julie Wilson

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Kevin Roth

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Miriam Sutovsky

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Peter Sutovsky

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Ping-Chung Chen

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Scott Wilson

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Stephen Crimmins

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P2860

The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction

Structure and mechanisms of the proteasome-associated deubiquitinating enzyme USP14

Multiple associated proteins regulate proteasome structure and function.

Deubiquitinating enzyme Ubp6 functions noncatalytically to delay proteasomal degradation.

Interaction of the Doa4 deubiquitinating enzyme with the yeast 26S proteasome.

Global mapping of the yeast genetic interaction network.

Role of Rpn11 metalloprotease in deubiquitination and degradation by the 26S proteasome.

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y

Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease

Targeted disruption of the murine Fanconi anemia gene, Fancg/Xrcc9

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33-42

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10.1016/J.YDBIO.2008.09.021

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