Roles of FGFR in oral carcinogenesis. - Wikidata - wikimedia - TriplyDB

Roles of FGFR in oral carcinogenesis.

Roles of FGFR in oral carcinogenesis.

http://www.wikidata.org/entity/Q38842890

about

Roles of FGFR in oral carcinogenesis.

http://www.wikidata.org/entity/Q38842890

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Roles of FGFR in oral carcinogenesis.

@en

type

label

Roles of FGFR in oral carcinogenesis.

@en

prefLabel

Roles of FGFR in oral carcinogenesis.

@en

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Cell Proliferation

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Roles of FGFR in oral carcinogenesis

@en

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Fangman Chen

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

Jiayi Wang

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

Qianming Chen

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

Rui Liu

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

Xiaoyan Xie

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

Yao Yuan

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

Zhiyong Wang

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

P2860

Global cancer statistics

FGF receptor-4 (FGFR4) polymorphism acts as an activity switch of a membrane type 1 matrix metalloproteinase-FGFR4 complex

Cellular signaling by fibroblast growth factor receptors

Determination of ligand-binding specificity by alternative splicing: two distinct growth factor receptors encoded by a single gene

Inhibition of tumor angiogenesis and growth by a small-molecule multi-FGF receptor blocker with allosteric properties

Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family

Molecular pathways: fibroblast growth factor signaling: a new therapeutic opportunity in cancer

Antibody-based targeting of FGFR3 in bladder carcinoma and t(4;14)-positive multiple myeloma in mice

Discovery of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (NVP-BGJ398), a potent and selective inhibitor of the fibroblast growth factor receptor family of receptor tyrosine kinase

PKC412 inhibits the zinc finger 198-fibroblast growth factor receptor 1 fusion tyrosine kinase and is active in treatment of stem cell myeloproliferative disorder.

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261-269

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scholarly article

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10.1111/CPR.12260

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3

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49

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2016-06-01T00:00:00Z

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27218663

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6495773

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