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Molecular and Cellular Endocrinology|May 2, 2018
Deletion of fetoplacental Fshr inhibits fetal vessel angiogenesis in the mouse placentaJulie A W Stilley, Deborah L SegaloffEndocrine Reviews|April 12, 2002
The lutropin/choriogonadotropin receptor, a 2002 perspectiveMario Ascoli, Francesca Fanelli, Deborah L SegaloffMolecular Endocrinology (Baltimore, Md.)|March 10, 2012
Revisiting and questioning functional rescue between dimerized LH receptor mutantsMeilin Zhang, Rongbin Guan, Deborah L SegaloffMolecular Endocrinology (Baltimore, Md.)|July 30, 2002
Chimeras of the rat and human FSH receptors (FSHRs) identify residues that permit or suppress transmembrane 6 mutation-induced constitutive activation of the FSHR via rearrangements of hydrophobic interactions between helices 6 and 7Ya-Xiong Tao, Dario Mizrachi, Deborah L SegaloffThe Journal of Biological Chemistry|May 24, 2005
The formation of a salt bridge between helices 3 and 6 is responsible for the constitutive activity and lack of hormone responsiveness of the naturally occurring L457R mutation of the human lutropin receptorMeilin Zhang, Dario Mizrachi, Francesca Fanelli, et al.Endocrinology|July 5, 2013
Heterodimerization between the lutropin and follitropin receptors is associated with an attenuation of hormone-dependent signalingXiuyan Feng, Meilin Zhang, Rongbin Guan, et al.The Journal of Biological Chemistry|November 5, 2003
Constitutive and agonist-dependent self-association of the cell surface human lutropin receptorYa-Xiong Tao, Nathan B Johnson, Deborah L SegaloffEndocrinology|December 29, 2007
An intracellular loop (IL2) residue confers different basal constitutive activities to the human lutropin receptor and human thyrotropin receptor through structural communication between IL2 and helix 6, via helix 3Xiuyan Feng, Thomas Müller, Dario Mizrachi, et al.The Journal of Clinical Endocrinology and Metabolism|February 18, 2014
Signaling through FSH receptors on human umbilical vein endothelial cells promotes angiogenesisJulie A Stilley, Rongbin Guan, Diane M Duffy, et al.Cellular Signalling|July 21, 2009
A cell surface inactive mutant of the human lutropin receptor (hLHR) attenuates signaling of wild-type or constitutively active receptors via heterodimerizationMeilin Zhang, Xiuyan Feng, Rongbin Guan, et al.Pageof 4