Genetic and Methylation Analysis of CTNNB1 in Benign and Malignant Melanocytic Lesions

SIMPLE SUMMARY: Recurrent CTNNB1 exon 3 mutations have been recognized in the distinct group of melanocytic tumors showing deep penetrating nevus-like morphology and in 1–2% of advanced melanoma. We performed a detailed genetic analysis of difficult-to-classify nevi and melanomas with CTNNB1 mutatio...

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Detalles Bibliográficos
Autores principales: Zaremba, Anne, Jansen, Philipp, Murali, Rajmohan, Mayakonda, Anand, Riedel, Anna, Krahl, Dieter, Burkhardt, Hans, John, Stefan, Géraud, Cyrill, Philip, Manuel, Kretz, Julia, Möller, Inga, Stadtler, Nadine, Sucker, Antje, Paschen, Annette, Ugurel, Selma, Zimmer, Lisa, Livingstone, Elisabeth, Horn, Susanne, Plass, Christoph, Schadendorf, Dirk, Hadaschik, Eva, Lutsik, Pavlo, Griewank, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454999/
https://www.ncbi.nlm.nih.gov/pubmed/36077603
http://dx.doi.org/10.3390/cancers14174066

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454999/
https://www.ncbi.nlm.nih.gov/pubmed/36077603
http://dx.doi.org/10.3390/cancers14174066

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