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Trends in Endocrinology and Metabolism: TEM|November 8, 2005
Inherited ACTH insensitivity illuminates the mechanisms of ACTH actionAdrian J L Clark, Louise A Metherell, Michael E Cheetham, et al.Molecular and Cellular Endocrinology|April 6, 2004
Constitutive activation of the human ACTH receptor resulting from a synergistic interaction between two naturally occurring missense mutations in the MC2R geneFrancesca M Swords, Luke A Noon, Peter J King, et al.The Journal of Clinical Endocrinology and Metabolism|April 30, 2010
Repair of aberrant splicing in growth hormone receptor by antisense oligonucleotides targeting the splice sites of a pseudoexonAlessia David, Umasuthan Srirangalingam, Louise A Metherell, et al.Best Practice & Research. Clinical Endocrinology & Metabolism|June 9, 2009
The genetics of familial glucocorticoid deficiencyAdrian J L Clark, Li F Chan, Teng-Teng Chung, et al.Endocrinology|September 26, 2006
A CCAAT/enhancer-binding protein site at -87 is required for the activation of a novel murine melanocortin 2-receptor promoter at late stages during adipogenesisLuke A Noon, Adrian J L Clark, Peter J O'Shaughnessy, et al.Endocrinology|December 24, 2010
Bioluminescence resonance energy transfer reveals the adrenocorticotropin (ACTH)-induced conformational change of the activated ACTH receptor complex in living cellsSadani N Cooray, Teng-Teng Chung, Khansa Mazhar, et al.Circulation Research|January 27, 2007
Epigenetic modification of the renin-angiotensin system in the fetal programming of hypertensionIrina Bogdarina, Simon Welham, Peter J King, et al.Endocrinology|January 5, 2008
Mechanisms of adrenocorticotropin-induced activation of extracellularly regulated kinase 1/2 mitogen-activated protein kinase in the human H295R adrenal cell lineMandy E Janes, K M Emily Chu, Adrian J L Clark, et al.Plos One|January 7, 2014
Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acidGioia Altobelli, Irina G Bogdarina, Elia Stupka, et al.Clinical Endocrinology|June 30, 2009
Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2Teng-Teng L L Chung, Li F Chan, Louise A Metherell, et al.Pageof 48