Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Rolando Ruiz"'
Autor:
Elyse K. Paterson‐Coleman, Jonathan Neumann, Eric Pearlman, Michaela E. Marshall, Grant R. MacGregor, Anand K. Ganesan, Jessica L. Flesher, Priya Vasudeva, Rolando Ruiz-Vega
Publikováno v:
Pigment Cell Melanoma Res
MITF, a gene that is mutated in familial melanoma and Waardenburg syndrome, encodes multiple isoforms expressed from alternative promoters that share common coding exons but have unique amino termini. It is not completely understood how these isoform
Autor:
Emaad Razzak, Jessica Shiu, John Lowengrub, Arthur D. Lander, Priya Vasudeva, Tatiana B. Krasieva, Rolando Ruiz-Vega, Anand K. Ganesan, Michael G. Caldwell, Huaming Yan, Chi-Fen Chen
Publikováno v:
eLife, Vol 9 (2020)
Mutational activation of the BRAF proto-oncogene in melanocytes reliably produces benign nevi (pigmented ‘moles’), yet the same change is the most common driver mutation in melanoma. The reason nevi stop growing, and do not progress to melanoma,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62336ac1d40bcbdb502c9697b2d1e3c0
https://doi.org/10.1101/2020.07.14.203018
https://doi.org/10.1101/2020.07.14.203018