Professor | 王海坤 | 数字化转型顾问

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Name

王海坤

Contact Information

hkwang@ips.ac.cn

Language ability

中文, 英语

Province

上海

University/Lab Affiliation and Title	中国科学院大学
Faculty	Life Sciences
Academic Background & Achievements	2004-09--2007-07 博士: 北京协和医学院 2000-09--2003-07 硕士: 北京大学 1996-09--2000-06 学士: 北京大学
Work Experience	2014-12~现在 - 中国科学院上海巴斯德研究所 - 研究员 2013-08~2014-05 - Wistar研究所（美国） - 助理研究员 2009-01~2013-07 - Wistar研究所（美国） - 博士后 2007-12~2008-12 - 宾夕法尼亚大学 - 博士后 2003-08~2004-08 - 北京华大基因研究所 - 研究助理
Awards	The Ching Jer Chern Memorial Award (2012): 研究所

University/Lab Affiliation and Title

中国科学院大学

Faculty

Life Sciences

Academic Background & Achievements

Work Experience

Awards

Areas of Focus	TFH细胞分化的转录调节机制成熟B细胞分化的转录调节研究
Publications	Foxp1 controls naive CD8+ T cell quiescence by simultaneously repressing key pathways in cellular metabolism and cell cycle progression., The Journal of Immunology, 2016 The transcription factor Foxp1 is a critical negative regulator of T follicular helper cell differentiation, Nature Immunology, 2014 Transcription factor Foxp1 exerts essential cell-intrinsic regulation of the quiescence of naive T cells, Nature Immunology, 2011 Extracellular Calcium Controls Background Current and Neuronal Excitability via an UNC79-UNC80-NALCN Cation Channel Complex, Neuron, 2010 UNC-80 functions as a scaffold for Src kinase in NALCN channel function, Channels, 2009 A novel, single, transmembrane protein CATSPERG is associated with CATSPER1 channel protein, Biology of Reproduction, 2009 Peptide neurotransmitters activate a cation channel complex of NALCN and UNC-80, Nature, 2009 TAM receptors and the regulation of erythropoiesis in mice, Haematologica, 2009 Expression patterns and functions of Toll-like receptors in mouse sertoli cells, Endocrinology, 2008

Areas of Focus

TFH细胞分化的转录调节机制
成熟B细胞分化的转录调节研究

Publications

Foxp1 controls naive CD8+ T cell quiescence by simultaneously repressing key pathways in cellular metabolism and cell cycle progression., The Journal of Immunology, 2016
The transcription factor Foxp1 is a critical negative regulator of T follicular helper cell differentiation, Nature Immunology, 2014
Transcription factor Foxp1 exerts essential cell-intrinsic regulation of the quiescence of naive T cells, Nature Immunology, 2011
Extracellular Calcium Controls Background Current and Neuronal Excitability via an UNC79-UNC80-NALCN Cation Channel Complex, Neuron, 2010
UNC-80 functions as a scaffold for Src kinase in NALCN channel function, Channels, 2009
A novel, single, transmembrane protein CATSPERG is associated with CATSPER1 channel protein, Biology of Reproduction, 2009
Peptide neurotransmitters activate a cation channel complex of NALCN and UNC-80, Nature, 2009
TAM receptors and the regulation of erythropoiesis in mice, Haematologica, 2009
Expression patterns and functions of Toll-like receptors in mouse sertoli cells, Endocrinology, 2008

Tfh细胞 B细胞分化转录调节 Foxp1 Cxcr5 Pd-1 Icos Bcl-6 Il-21

刘小龙 - 中国科学院大学

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