Shp2 is dispensable in the formation and maintenance of the neuromuscular junction. - Wikidata - wikimedia - TriplyDB

Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

http://www.wikidata.org/entity/Q52012657

about

To build a synapse: signaling pathways in neuromuscular junction assembly Impaired neurodevelopment by the low complexity domain of CPEB4 reveals a convergent pathway with neurodegeneration.Tyrosine phosphatases such as SHP-2 act in a balance with Src-family kinases in stabilization of postsynaptic clusters of acetylcholine receptors.The function of Shp2 tyrosine phosphatase in the dispersal of acetylcholine receptor clusters.Distinct roles of muscle and motoneuron LRP4 in neuromuscular junction formation.HSP90 beta regulates rapsyn turnover and subsequent AChR cluster formation and maintenance.alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering.Protein tyrosine phosphatases: functional inferences from mouse models and human diseases.The proteasome-associated deubiquitinating enzyme Usp14 is essential for the maintenance of synaptic ubiquitin levels and the development of neuromuscular junctions Nestin negatively regulates postsynaptic differentiation of the neuromuscular synapse.The mechanism of acetylcholine receptor in binding MuSK in myasthenia gravis and the role of HSP90 molecular chaperone.Neuregulin1 fine-tunes pre-, post-, and perisynaptic neuromuscular junction development.Enzymatic Activity of the Scaffold Protein Rapsyn for Synapse Formation.Preclinical Comparison of Mechanistically Different Antiseizure, Antinociceptive, and/or Antidepressant Drugs in a Battery of Rodent Models of Nociceptive and Neuropathic Pain.

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Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

http://www.wikidata.org/entity/Q52012657

description

2006 nî lūn-bûn

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2006年の論文

@ja

2006年学术文章

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2006年学术文章

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2006年学术文章

@zh-cn

2006年学术文章

@zh-hans

2006年学术文章

@zh-my

2006年学术文章

@zh-sg

2006年學術文章

@yue

2006年學術文章

@zh-hant

name

Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

@en

Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

@nl

type

label

Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

@en

Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

@nl

prefLabel

Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

@en

Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

@nl

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Shp2 is dispensable in the formation and maintenance of the neuromuscular junction.

@en

P2093

Gen-Sheng Feng

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Lin Mei

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

Tian-Ming Gao

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

Wen C Xiong

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Xian-Ping Dong

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Xiao-Ming Li

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P2860

Ligand-specific activation of HER4/p180erbB4, a fourth member of the epidermal growth factor receptor family

Isolation and characterization of ERBB3, a third member of the ERBB/epidermal growth factor receptor family: evidence for overexpression in a subset of human mammary tumors

Molecular cloning and expression of an additional epidermal growth factor receptor-related gene

Identification of a human src homology 2-containing protein-tyrosine-phosphatase: a putative homolog of Drosophila corkscrew

Distinct domains of MuSK mediate its abilities to induce and to associate with postsynaptic specializations

Development of the vertebrate neuromuscular junction

The 'Shp'ing news: SH2 domain-containing tyrosine phosphatases in cell signaling

Distinct roles of nerve and muscle in postsynaptic differentiation of the neuromuscular synapse

Characterization of hematopoietic intracellular protein tyrosine phosphatases: description of a phosphatase containing an SH2 domain and another enriched in proline-, glutamic acid-, serine-, and threonine-rich sequences

Induction, assembly, maturation and maintenance of a postsynaptic apparatus

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53-63

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10.1159/000094484

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2

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15

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