Molecular genetics of the ACTH and melanocyte-stimulating hormone receptors
- 1 September 1993
- journal article
- review article
- Published by Elsevier in Trends in Endocrinology & Metabolism
- Vol. 4 (7), 242-247
- https://doi.org/10.1016/1043-2760(93)90129-3
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptorThe Lancet, 1993
- Molecular cloning and expression of the human melanocyte stimulating hormone receptor cDNAFEBS Letters, 1992
- A point mutation of the rhodopsin gene in one form of retinitis pigmentosaNature, 1990
- UVB-Induced Melanogenesis May Be Mediated Through the MSH-Receptor System.Journal of Investigative Dermatology, 1989
- Identification and Characterization of Melanotropin Binding Proteins from M2R Melanoma Cells by Covalent Photoaffinity Labeling*Endocrinology, 1988
- Molecular biology of the visual pigmentsVision Research, 1986
- Melanocyte-stimulating hormone, tyrosinase activity and the regulation of eumelanogenesis and phaeomelanogenesis in the hair follicular melanocytes of the mouseJournal of Endocrinology, 1986
- Up regulation of corticotrophin receptors by ACTH1–24 in normal and hypophysectomized rabbitsBiochemical and Biophysical Research Communications, 1980
- FAMILIAL GLUCOCORTICOID DEFICIENCY WITH ACHALASIA OF THE CARDIA AND DEFICIENT TEAR PRODUCTIONThe Lancet, 1978
- SOMBRE, A VIABLE DOMINANT MUTANT IN THE HOUSE MOUSEJournal of Heredity, 1961