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Prostaglandins & Other Lipid Mediators|May 27, 2008
Lack of a significant role of P-Rex1, a major regulator of macrophage Rac1 activation and chemotaxis, in atherogenesisZhenglong Wang, Xuemei Dong, Zhong Li, et al.
The Journal of Biological Chemistry|April 3, 2014
Hepatocyte growth factor (Hgf) stimulates low density lipoprotein receptor-related protein (Lrp) 5/6 phosphorylation and promotes canonical Wnt signalingFarrukh M Koraishy, Cynthia Silva, Sherene Mason, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 1, 2022
Pazopanib Is a Potential Treatment for Coronavirus-Induced Lung InjuriesYi Luan, Qianying Yuan, Qijun Wang, et al.
Current Biology : CB|October 26, 2005
P-Rex1 is a primary Rac2 guanine nucleotide exchange factor in mouse neutrophilsXuemei Dong, Zhicheng Mo, Gary Bokoch, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2002
Neutrophils lacking phosphoinositide 3-kinase gamma show loss of directionality during N-formyl-Met-Leu-Phe-induced chemotaxisMichael Hannigan, Lijun Zhan, Zhong Li, et al.
The Journal of Cell Biology|February 13, 2013
Clathrin and AP2 are required for PtdIns(4,5)P2-mediated formation of LRP6 signalosomesIngyu Kim, Weijun Pan, Sara A Jones, et al.
Journal of Leukocyte Biology|January 18, 2007
Signaling requirements for translocation of P-Rex1, a key Rac2 exchange factor involved in chemoattractant-stimulated human neutrophil functionTieming Zhao, Perihan Nalbant, Mikio Hoshino, et al.
The Journal of Biological Chemistry|June 8, 2010
Different roles of G protein subunits beta1 and beta2 in neutrophil function revealed by gene expression silencing in primary mouse neutrophilsYong Zhang, Wenwen Tang, Matthew C Jones, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 12, 2020
Small GTPase ARF6 Is a Coincidence-Detection Code for RPH3A Polarization in Neutrophil PolarizationChunguang Ren, Qianying Yuan, Xiaoying Jian, et al.
Bone Reports|March 21, 2020
Corrigendum to "Skeletal disease in a father and daughter with a novel monoallelic WNT1 mutation" [Bone Rep. 9 (2018) 154-158]Kathleen Timme, Elizabeth Sanchez Rangel, Qianying Yuan, et al.
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