RMDisease V2.0: an updated database of genetic variants that affect RNA modifications with disease and trait implication

Recent advances in epitranscriptomics have unveiled functional associations between RNA modifications (RMs) and multiple human diseases, but distinguishing the functional or disease-related single nucleotide variants (SNVs) from the majority of ‘silent’ variants remains a major challenge. We previou...

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Detalles Bibliográficos
Autores principales: Song, Bowen, Wang, Xuan, Liang, Zhanmin, Ma, Jiongming, Huang, Daiyun, Wang, Yue, de Magalhães, João Pedro, Rigden, Daniel J, Meng, Jia, Liu, Gang, Chen, Kunqi, Wei, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Database Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825452/
https://www.ncbi.nlm.nih.gov/pubmed/36062570
http://dx.doi.org/10.1093/nar/gkac750

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825452/
https://www.ncbi.nlm.nih.gov/pubmed/36062570
http://dx.doi.org/10.1093/nar/gkac750

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