Showing results (31-40 of 476) with videos related to

Sort By:
Pageof 48
Journal of Molecular Endocrinology|December 16, 2006
Identification of a novel melanocortin 2 receptor splice variant in murine adipocytes: implications for post-transcriptional control of expression during adipogenesisLuke A Noon, Artem Bakmanidis, Adrian J L Clark, et al.
The International Journal of Biochemistry & Cell Biology|April 5, 2003
Endocytosis of the AT1A angiotensin receptor is independent of ubiquitylation of its cytoplasmic serine/threonine-rich regionBalázs Mihalik, Zsuzsanna Gáborik, Péter Várnai, et al.
Endocrine Development|March 19, 2009
Phenotypic aspects of growth hormone- and IGF-I-resistant syndromesMartin O Savage, Alessia David, Cecilia Camacho-Hubner, et al.
Endocrinology and Metabolism Clinics of North America|August 9, 2005
Diagnostic and therapeutic advances in growth hormone insensitivityAlessia David, Louise A Metherell, Adrian J L Clark, et al.
FEBS Letters|December 20, 2005
Differential beta-arrestin binding of AT1 and AT2 angiotensin receptorsGábor Turu, László Szidonya, Zsuzsanna Gáborik, et al.
Molecular Endocrinology (Baltimore, Md.)|July 2, 2011
The cytosolic chaperone Hsc70 promotes traffic to the cell surface of intracellular retained melanocortin-4 receptor mutantsEirini Meimaridou, Sakina B Gooljar, Nalini Ramnarace, et al.
Molecular and Cellular Endocrinology|May 12, 2004
Structural determinants of agonist-induced signaling and regulation of the angiotensin AT1 receptorLászló Hunyady, Zsuzsanna Gáborik, Bukhtiar H Shah, et al.
Biochemical Pharmacology|February 8, 2007
AT1 receptor blocker-insensitive mutant AT1A angiotensin receptors reveal the presence of G protein-independent signaling in C9 cellsLászló Szidonya, Katinka Süpeki, Eszter Karip, et al.
European Journal of Endocrinology|January 20, 2009
Functional consequence of a novel Y129C mutation in a patient with two contradictory melanocortin-2-receptor mutationsLi F Chan, Teng-Teng Chung, Ahmed F Massoud, et al.
Frontiers in Endocrinology|August 25, 2015
Whole-Exome Sequencing in the Differential Diagnosis of Primary Adrenal Insufficiency in ChildrenLi F Chan, Daniel C Campbell, Tatiana V Novoselova, et al.
Pageof 48