Mutated SASH1 promotes Mitf expression in a heterozygous mutated SASH1 knock-in mouse model

The SAM and SH3 domain-containing 1 (SASH1) genes have been identified as the causal genes of dyschromatosis universalis hereditaria (DUH); these genes cause the pathological phenotypes of DUH, and SASH1 variants have been shown to regulate the abnormal pigmentation phenotype in human skin in variou...

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Detalles Bibliográficos
Autores principales: Xu, Zexi, Li, Yadong, Wang, Dahong, Wu, Daoqiu, Wang, Jinyun, Chen, Lian, Deng, Yinqian, Zhang, Jing, Wu, Zhixiong, Wan, Xin, Liu, Qianfan, Huang, Hai, Hu, Pingsheng, Zeng, Jiawei, Zhou, Ding'an
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387086/
https://www.ncbi.nlm.nih.gov/pubmed/32582980
http://dx.doi.org/10.3892/ijmm.2020.4652

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387086/
https://www.ncbi.nlm.nih.gov/pubmed/32582980
http://dx.doi.org/10.3892/ijmm.2020.4652

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