Human pigmentation genes: identification, structure and consequences of polymorphic variation
Top Cited Papers
- 9 October 2001
- Vol. 277 (1-2) , 49-62
- https://doi.org/10.1016/s0378-1119(01)00694-1
Abstract
No abstract availableKeywords
This publication has 73 references indexed in Scilit:
- Melanosomal pH, Pink Locus Protein and their Roles in MelanogenesisJournal of Investigative Dermatology, 2001
- Initial sequencing and analysis of the human genomeNature, 2001
- Regulation of the Catalytic Activity of Preexisting Tyrosinase in Black and Caucasian Human Melanocyte Cell CulturesExperimental Cell Research, 2001
- Aberrant pH of Melanosomes in Pink-Eyed Dilution (p) Mutant MelanocytesJournal of Investigative Dermatology, 2000
- The Underwhite (uw) Locus Acts Autonomously and Reduces the Production of MelaninJournal of Investigative Dermatology, 2000
- Loss of Function Mutations of the Human Melanocortin 1 Receptor Are Common and Are Associated with Red HairBiochemical and Biophysical Research Communications, 1999
- Human Pigmentation Phenotype: A Point Mutation Generates Nonfunctional MSH ReceptorBiochemical and Biophysical Research Communications, 1998
- Tyrosinase and related proteins in mammalian pigmentationFEBS Letters, 1996
- Chromosomal Structure of the Human TYRP1 and TYRP2 Loci and Comparison of the Tyrosinase-Related Protein Gene FamilyGenomics, 1995
- nmb, a novel gene, is expressed in low‐metastatic human melanoma cell lines and xenograftsInternational Journal of Cancer, 1995