Repression of ferritin light chain translation by human eIF3

A central problem in human biology remains the discovery of causal molecular links between mutations identified in genome-wide association studies (GWAS) and their corresponding disease traits. This challenge is magnified for variants residing in non-coding regions of the genome. Single-nucleotide p...

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Bibliografske podrobnosti
izdano v:eLife
Main Authors: Pulos-Holmes, Mia C, Srole, Daniel N, Juarez, Maria G, Lee, Amy S-Y, McSwiggen, David T, Ingolia, Nicholas T, Cate, Jamie H
Format: Artigo
Jezik:Inglês
Izdano: eLife Sciences Publications, Ltd 2019
Teme:
Biochemistry and Chemical Biology
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6721798/
https://ncbi.nlm.nih.gov/pubmed/31414986
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.48193
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