Beuschlein F, Fassnacht M, Klink A, Allolio B, Reincke M. ACTH-receptor expression, regulation and role in adrenocortial tumor formation. „Eur J Endocrinol”. 144 (3), s. 199–206, 2001. DOI: 10.1530/eje.0.1440199. PMID: 11248736. (ang.).
Raikhinstein M, Zohar M, Hanukoglu I. cDNA cloning and sequence analysis of the bovine adrenocorticotropic hormone (ACTH) receptor. „Biochim Biophys Acta”. 1220 (3), s. 329–32, 1994. DOI: 10.1016/0167-4889(94)90157-0. PMID: 8305507. (ang.).
Hanukoglu I, Feuchtwanger R, Hanukoglu A. Mechanism of corticotropin and cAMP induction of mitochondrial cytochrome P450 system enzymes in adrenal cortex cells. „J Biol Chem”. 265 (33), s. 20602–8, 1990. DOI: 10.1590/S0100-879X2000001000015. PMID: 2173715. (ang.).
Clark AJ, McLoughlin L, Grossman A. Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor. „Lancet”. 341 (8843), s. 461–2, 1993. DOI: 10.1016/0140-6736(93)90208-X. PMID: 8094489. (ang.).
Tsigos C, Arai K, Hung W, Chrousos GP. Hereditary isolated glucocorticoid deficiency is associated with abnormalities of the adrenocorticotropin receptor gene. „J Clin Invest”. 92 (5), s. 2458–61, 1993. DOI: 10.1172/JCI116853. PMID: 8227361. (ang.).
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Beuschlein F, Fassnacht M, Klink A, Allolio B, Reincke M. ACTH-receptor expression, regulation and role in adrenocortial tumor formation. „Eur J Endocrinol”. 144 (3), s. 199–206, 2001. DOI: 10.1530/eje.0.1440199. PMID: 11248736. (ang.).
Raikhinstein M, Zohar M, Hanukoglu I. cDNA cloning and sequence analysis of the bovine adrenocorticotropic hormone (ACTH) receptor. „Biochim Biophys Acta”. 1220 (3), s. 329–32, 1994. DOI: 10.1016/0167-4889(94)90157-0. PMID: 8305507. (ang.).
Hanukoglu I, Feuchtwanger R, Hanukoglu A. Mechanism of corticotropin and cAMP induction of mitochondrial cytochrome P450 system enzymes in adrenal cortex cells. „J Biol Chem”. 265 (33), s. 20602–8, 1990. DOI: 10.1590/S0100-879X2000001000015. PMID: 2173715. (ang.).
Clark AJ, McLoughlin L, Grossman A. Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor. „Lancet”. 341 (8843), s. 461–2, 1993. DOI: 10.1016/0140-6736(93)90208-X. PMID: 8094489. (ang.).
Tsigos C, Arai K, Hung W, Chrousos GP. Hereditary isolated glucocorticoid deficiency is associated with abnormalities of the adrenocorticotropin receptor gene. „J Clin Invest”. 92 (5), s. 2458–61, 1993. DOI: 10.1172/JCI116853. PMID: 8227361. (ang.).