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Transcriptome analysis indicates dominant effects on ribosome and mitochondrial function of a premature termination codon mutation in the zebrafish gene psen2

PRESENILIN 2 (PSEN2) is one of the genes mutated in early onset familial Alzheimer’s disease (EOfAD). PSEN2 shares significant amino acid sequence identity with another EOfAD-related gene PRESENILIN 1 (PSEN1), and partial functional redundancy is seen between these two genes. However, the complete r...

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Pubblicato in:PLoS One
Autori principali: Jiang, Haowei, Pederson, Stephen Martin, Newman, Morgan, Dong, Yang, Barthelson, Karissa, Lardelli, Michael
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2020
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7357760/
https://ncbi.nlm.nih.gov/pubmed/32658922
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0232559
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