Yüklüyor......

Human mitochondrial disease-like symptoms caused by a reduced tRNA aminoacylation activity in flies

The translation of genes encoded in the mitochondrial genome requires specific machinery that functions in the organelle. Among the many mutations linked to human disease that affect mitochondrial translation, several are localized to nuclear genes coding for mitochondrial aminoacyl-transfer RNA syn...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Guitart, Tanit, Picchioni, Daria, Piñeyro, David, Ribas de Pouplana, Lluís
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3711456/
https://ncbi.nlm.nih.gov/pubmed/23677612
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkt402
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!