Cargando…
A Large French Case-Control Study Emphasizes the Role of Rare Mc1R Variants in Melanoma Risk
Background. The MC1R gene implicated in melanogenesis and skin pigmentation is highly polymorphic. Several alleles are associated with red hair and fair skin phenotypes and contribute to melanoma risk. Objective. This work aims to assess the effect of different classes of MC1R variants, notably rare...
Autores principales: | Hu, Hui-Han, Benfodda, Mériem, Dumaz, Nicolas, Gazal, Steven, Descamps, Vincent, Bourillon, Agnès, Basset-Seguin, Nicole, Riffault, Angélique, Ezzedine, Khaled, Bagot, Martine, Bensussan, Armand, Saiag, Philippe, Grandchamp, Bernard, Soufir, Nadem |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003837/ https://www.ncbi.nlm.nih.gov/pubmed/24982914 http://dx.doi.org/10.1155/2014/925716 |
Ejemplares similares
-
PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study
por: Soufir, N, et al.
Publicado: (2006) -
Inhibition of the Proprotein Convertases Represses the Invasiveness of Human Primary Melanoma Cells with Altered p53, CDKN2A and N-Ras Genes
por: Lalou, Claude, et al.
Publicado: (2010) -
Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma
por: Soufir, N, et al.
Publicado: (2004) -
Frequency and Genomic Aspects of Intrinsic Resistance to Vismodegib in Locally Advanced Basal Cell Carcinoma
por: Yurchenko, Andrey A., et al.
Publicado: (2022) -
Extranodal NK/T-Cell Lymphoma: Toward the Identification of Clinical Molecular Targets
por: Schmitt, Christian, et al.
Publicado: (2011)