Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Teng-Teng Chung"'
Publikováno v:
Endocrinology
Bioluminescence resonance energy transfer analysis is used to study the interaction between melanocortin 2 receptor (MC2R) accessory protein and the MC2R and provides evidence for protein kinase A-dependent conformational changes in the receptor comp
Publikováno v:
European Journal of Endocrinology
ContextFamilial glucocorticoid deficiency (FGD) is a rare autosomal recessive disease, characterised by isolated glucocorticoid deficiency in the absence of mineralocorticoid deficiency. Inactivating mutations in the ACTH receptor (melanocortin-2-rec
Publikováno v:
Best Practice & Research Clinical Endocrinology & Metabolism. 23:159-165
Familial glucocorticoid deficiency is an autosomal recessive disorder resulting from defects in the action of adrenocorticotropic hormone (ACTH) to stimulate glucocorticoid synthesis in the adrenal. Production of mineralocorticoids by the adrenal is
Autor:
Adrian J. L. Clark, Peter J. King, Li F. Chan, Louise A. Metherell, Tom R. Webb, J. P. Chapple, Sadani N. Cooray, Teng-Teng Chung
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 93:4948-4954
Context: There are at least 24 missense, nonconservative mutations found in the ACTH receptor [melanocortin 2 receptor (MC2R)] that have been associated with the autosomal recessive disease familial glucocorticoid deficiency (FGD) type 1. The charact