Biochemical and Biophysical Research Communications
Volume 245, Issue 2, 17 April 1998, Pages 490-492
Regular ArticleHuman Pigmentation Phenotype: A Point Mutation Generates Nonfunctional MSH Receptor
References (12)
J. Invest. Dermatol.
(1991)- et al.
J. Invest. Dermatol.
(1995) - et al.
FEBS Letters
(1992) J. Biol. Chem.
(1993)- et al.
J. Invest. Dermatol.
(1986)
There are more references available in the full text version of this article.
Cited by (104)
MC1R Functions, Expression, and Implications for Targeted Therapy
2022, Journal of Investigative DermatologySkin aging and mitochondria
2021, Mitochondrial Dysfunction and Nanotherapeutics: Aging, Diseases, and Nanotechnology-Related Strategies in Mitochondrial MedicineMolecular signatures of human melanocortin receptors for ligand binding and signaling
2017, Biochimica et Biophysica Acta - Molecular Basis of DiseaseMC1R signaling. Intracellular partners and pathophysiological implications
2017, Biochimica et Biophysica Acta - Molecular Basis of DiseaseGermline melanoma susceptibility and prognostic genes: A review of the literature
2012, Journal of the American Academy of DermatologyPopulation-level genotyping of coat colour polymorphism in woolly mammoth (Mammuthus primigenius)
2011, Quaternary Science Reviews
- 1
Corresponding author: Fax: +4618501920.
Copyright © 1998 Academic Press. All rights reserved.