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Delineating the role of MITF isoforms in pigmentation and tissue homeostasis
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 isoforms influence pigmentation in different tissues and...
Guardado en:
| Publicado en: | Pigment Cell Melanoma Res |
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| Autores principales: | , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7822220/ https://ncbi.nlm.nih.gov/pubmed/31562697 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/pcmr.12828 |
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