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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Detalles Bibliográficos
Autores principales: Pulos-Holmes, Mia C, Srole, Daniel N, Juarez, Maria G, Lee, Amy S-Y, McSwiggen, David T, Ingolia, Nicholas T, Cate, Jamie H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Biochemistry and Chemical Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721798/
https://www.ncbi.nlm.nih.gov/pubmed/31414986
http://dx.doi.org/10.7554/eLife.48193

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721798/
https://www.ncbi.nlm.nih.gov/pubmed/31414986
http://dx.doi.org/10.7554/eLife.48193

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