Exploring Missense Mutations in Tyrosine Kinases Implicated with Neurodegeneration.

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Exploring Missense Mutations in Tyrosine Kinases Implicated with Neurodegeneration.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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2016年學術文章

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Exploring Missense Mutations in Tyrosine Kinases Implicated with Neurodegeneration.

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Exploring Missense Mutations in Tyrosine Kinases Implicated with Neurodegeneration.

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Exploring Missense Mutations in Tyrosine Kinases Implicated with Neurodegeneration.

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P1476

Exploring Missense Mutations in Tyrosine Kinases Implicated with Neurodegeneration

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P2093

Neha Sami

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Sher Ali

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

Vijay Kumar

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ALK, the chromosome 2 gene locus altered by the t(2;5) in non-Hodgkin's lymphoma, encodes a novel neural receptor tyrosine kinase that is highly related to leukocyte tyrosine kinase (LTK)

Lethal congenital contractural syndrome type 2 (LCCS2) is caused by a mutation in ERBB3 (Her3), a modulator of the phosphatidylinositol-3-kinase/Akt pathway

The cytoplasmic adaptor protein Dok7 activates the receptor tyrosine kinase MuSK via dimerization

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P2888

s12035-016-0046-5

P304

5085-5106

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scholarly article

P356

10.1007/S12035-016-0046-5

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P433

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

P478

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

P50

Faizan Ahmad

Md Imtaiyaz Hassan

Asimul Islam

P577

2016-08-20T00:00:00Z

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P6179

1008842681

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27544236

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