m6AVar: a database of functional variants involved in m(6)A modification

Identifying disease-causing variants among a large number of single nucleotide variants (SNVs) is still a major challenge. Recently, N(6)-methyladenosine (m(6)A) has become a research hotspot because of its critical roles in many fundamental biological processes and a variety of diseases. Therefore,...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Nucleic Acids Res
Egile Nagusiak: Zheng, Yueyuan, Nie, Peng, Peng, Di, He, Zhihao, Liu, Mengni, Xie, Yubin, Miao, Yanyan, Zuo, Zhixiang, Ren, Jian
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2018
Gaiak:
Database Issue
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5753261/
https://ncbi.nlm.nih.gov/pubmed/29036329
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkx895
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