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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.Annals of Neurology|September 30, 2004
A novel RAB7 mutation associated with ulcero-mutilating neuropathyHenry Houlden, Rosalind H M King, John R Muddle, et al.Journal of the Royal Society, Interface|January 1, 2015
β-Catenin is central to DUX4-driven network rewiring in facioscapulohumeral muscular dystrophyChristopher R S Banerji, Paul Knopp, Louise A Moyle, et al.Annals of the New York Academy of Sciences|July 10, 2003
Expression, desensitization, and internalization of the ACTH receptor (MC2R)Adrian J L Clark, Asma H Baig, Luke Noon, et al.American Journal of Medical Genetics. Part A|January 28, 2003
Chromosomal fragility in patients with triple A syndromeShalini Reshmi-Skarja, Angela Huebner, Katrin Handschug, et al.Nature Clinical Practice. Endocrinology & Metabolism|August 26, 2006
Endocrine assessment, molecular characterization and treatment of growth hormone insensitivity disordersMartin O Savage, Kenneth M Attie, Alessia David, et al.Endocrine Connections|June 13, 2019
ACTH signalling and adrenal development: lessons from mouse modelsTatiana V Novoselova, Peter J King, Leonardo Guasti, et al.The Journal of Biological Chemistry|April 2, 2002
Role of the proline-rich domain of dynamin-2 and its interactions with Src homology 3 domains during endocytosis of the AT1 angiotensin receptorMárta Szaszák, Zsuzsanna Gáborik, Gábor Turu, et al.Endocrinology|September 27, 2008
Distinct melanocortin 2 receptor accessory protein domains are required for melanocortin 2 receptor interaction and promotion of receptor traffickingTom R Webb, Li Chan, Sadani N Cooray, et al.FEBS Letters|May 29, 2007
The IGF-I splice variant MGF increases progenitor cells in ALS, dystrophic, and normal muscleKenan Ates, Shi Yu Yang, Richard W Orrell, et al.Pageof 13