An amyotrophic lateral sclerosis-linked mutation in GLE1 alters the cellular pool of human Gle1 functional isoforms.

Aditi , Glass L, Dawson TR, Wente SR
Adv Biol Regul. 2016 62: 25-36

PMID: 26776475 · PMCID: PMC4864155 · DOI:10.1016/j.jbior.2015.11.001

MeSH Terms (15)

Amyotrophic Lateral Sclerosis Animals Cytoplasm Cytoplasmic Granules Gene Expression HeLa Cells Humans Mutagenesis, Insertional Nuclear Envelope Nucleocytoplasmic Transport Proteins Phytic Acid Point Mutation Protein Aggregates Protein Isoforms RNA, Small Interfering

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