Ufl1 deficiency causes skin pigmentation by up-regulation of Endothelin-1

Ufmylation (UFM1 modification) is a newly identified ubiquitin-like modification system involved in numerous cellular processes. However, the regulatory mechanisms and biological functions of this modification remain mostly unknown. We have recently reported that Ufmylation family genes have frequen...

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Detalles Bibliográficos
Autores principales: Wang, Ke, Xu, Hu-Ning, Wang, Yi-Wen, Mao, Jian, Liu, Da, Zhu, Xiao-Jing, Cong, Yu-Sheng, Wang, Miao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478483/
https://www.ncbi.nlm.nih.gov/pubmed/36120581
http://dx.doi.org/10.3389/fcell.2022.961675

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478483/
https://www.ncbi.nlm.nih.gov/pubmed/36120581
http://dx.doi.org/10.3389/fcell.2022.961675

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