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The Journal of Clinical Endocrinology and Metabolism|October 22, 2010
Loss of the C terminus of melanocortin receptor 2 (MC2R) results in impaired cell surface expression and ACTH insensitivityAndrea Hirsch, Eirini Meimaridou, Monica Fernandez-Cancio, et al.
Endocrinology|February 26, 2010
Angiotensin II-induced expression of brain-derived neurotrophic factor in human and rat adrenocortical cellsMária Szekeres, György L Nádasy, Gábor Turu, et al.
Hormone Research in Paediatrics|March 2, 2010
Familial isolated primary pigmented nodular adrenocortical disease associated with a novel low penetrance PRKAR1A gene splice site mutationHelen L Storr, Louise A Metherell, Renuka Dias, et al.
The Journal of Clinical Endocrinology and Metabolism|October 15, 2003
Association between insulin-like growth factor I (IGF-I) polymorphisms, circulating IGF-I, and pre- and postnatal growth in two European small for gestational age populationsLinda B Johnston, Jovanna Dahlgren, Juliane Leger, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 2013
Ligand-specific conformational change of the G-protein-coupled receptor ALX/FPR2 determines proresolving functional responsesSadani N Cooray, Thomas Gobbetti, Trinidad Montero-Melendez, et al.
Molecular Endocrinology (Baltimore, Md.)|October 27, 2009
Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanismHelen L Storr, Barbara Kind, David A Parfitt, et al.
Clinical Endocrinology|August 31, 2002
Spontaneous growth hormone secretory characteristics in children with partial growth hormone insensitivityRagnar Bjarnason, Kausik Banerjee, Steven J Rose, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 8, 2018
MRAP deficiency impairs adrenal progenitor cell differentiation and gland zonationTatiana V Novoselova, Mashal Hussain, Peter J King, et al.
Molecular Endocrinology (Baltimore, Md.)|October 3, 2013
Melanocortin 4 receptor becomes an ACTH receptor by coexpression of melanocortin receptor accessory protein 2Maria Josep Agulleiro, Raúl Cortés, Begoña Fernández-Durán, et al.
Human Genetics|October 18, 2002
Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneityEmmanuelle Génin, Angela Huebner, Christine Jaillard, et al.
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