Novel R634W c-kit mutation identified in familial mastocytosis.

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http://www.wikidata.org/entity/Q55071080

description

2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

@wuu

2014年学术文章

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2014年学术文章

@zh-cn

2014年学术文章

@zh-hans

2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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name

Novel R634W c-kit mutation identified in familial mastocytosis.

@en

Novel R634W c-kit mutation identified in familial mastocytosis.

@nl

type

Item

label

Novel R634W c-kit mutation identified in familial mastocytosis.

@en

Novel R634W c-kit mutation identified in familial mastocytosis.

@nl

prefLabel

Novel R634W c-kit mutation identified in familial mastocytosis.

@en

Novel R634W c-kit mutation identified in familial mastocytosis.

@nl

P1476

Novel R634W c-kit mutation identified in familial mastocytosis.

@en

P2093

Thomas M Beachkofsky

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Todd T Kobayashi

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Whitney L Pollard

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P2860

Phenotypic and genotypic characteristics of mastocytosis according to the age of onset.

Familial cutaneous mastocytosis.

A germline mutation in KIT in familial diffuse cutaneous mastocytosis.

Mutations in exons 9 and 13 of KIT gene are rare events in gastrointestinal stromal tumors. A study of 200 cases

Familial urticaria pigmentosa: report of a family and review of the role of KIT mutations.

KIT D816 mutation associates with adverse outcomes in core binding factor acute myeloid leukemia, especially in the subgroup with RUNX1/RUNX1T1 rearrangement.

Novel, activating KIT-N822I mutation in familial cutaneous mastocytosis.

Activation mutations of human c-KIT resistant to imatinib mesylate are sensitive to the tyrosine kinase inhibitor PKC412.

Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa.

Novel germline mutation of KIT associated with familial gastrointestinal stromal tumors and mastocytosis.

P304

267-270

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scholarly article

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10.1111/PDE.12381

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P433

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P478

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P577

2014-09-22T00:00:00Z

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P5875

265911580

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25243845

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