SASH1 promotes melanin synthesis and migration via suppression of TGF-β1 secretion in melanocytes resulting in pathologic hyperpigmentation

Dyschromatosis universalis hereditaria (DUH) is an autosomal dominant pigmentary genodermatosis characterized by the presence of patches of hyperpigmentation and hypopigmented macules distributed over the body, with most cases reported in Asia. DUH is a heterogeneous disease and a small portion of p...

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Detalles Bibliográficos
Autores principales: Cui, Hongzhou, Guo, Shuping, He, Hongxia, Guo, Huina, Zhang, Yuliang, Wang, Binquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053321/
https://www.ncbi.nlm.nih.gov/pubmed/32174800
http://dx.doi.org/10.7150/ijbs.38415

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053321/
https://www.ncbi.nlm.nih.gov/pubmed/32174800
http://dx.doi.org/10.7150/ijbs.38415

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