Genomic Organization and Sequence of D12S53E (Pmel 17), the Human Homologue of the Mouse Silver (si) Locus
- 1 January 1996
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 106 (1) , 24-27
- https://doi.org/10.1111/1523-1747.ep12326976
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- Mapping of the human gene for a melanocyte protein Pmel 17 (D12S53E) to chromosome 12q13–q14Genomics, 1995
- Mousesilver.mutation is caused by a single base insertion in the putative cytoplasmic domain of Pmel 17Nucleic Acids Research, 1995
- Cloning and Expression of the Gene for the Melanoma-Associated ME20 AntigenDNA and Cell Biology, 1994
- Genetic Disorders of PigmentationPublished by Springer Nature ,1994
- Pigmentation Genes: the Tyrosinase Gene Family and the pmel 17 Gene FamilyJournal of Investigative Dermatology, 1993
- The cDNA RPE1 and monoclonal antibody HMB-50 define gene products preferentially expressed in retinal pigment epitheliumExperimental Eye Research, 1992
- A melanocyte-specific gene, Pmel 17, maps near the silver coat color locus on mouse chromosome 10 and is in a syntenic region on human chromosome 12.Proceedings of the National Academy of Sciences, 1991
- Complete Sequence and Expression of a cDNA Encoding a Chicken 115‐kDa Melanosomal Matrix ProteinPigment Cell Research, 1991
- Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus.Proceedings of the National Academy of Sciences, 1987