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Downregulation of the human peripheral myelin protein 22 gene by miR-29a in cellular models of Charcot–Marie–Tooth disease

The majority of hereditary neuropathies are caused by duplication of the peripheral myelin protein 22 (PMP22) gene. Therefore, mechanisms to suppress the expression of the PMP22 gene have high therapeutic significance. Here we asked whether the human PMP22 gene is a target for regulation by microRNA...

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Détails bibliographiques
Publié dans:Gene Ther
Auteurs principaux: Serfecz, Jacquelyn, Bazick, Hannah, Al Salihi, Mohammed Omar, Turner, Peter, Fields, Christopher, Cruz, Pedro, Renne, Rolf, Notterpek, Lucia
Format: Artigo
Langue:Inglês
Publié: Nature Publishing Group UK 2019
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6920087/
https://ncbi.nlm.nih.gov/pubmed/31455873
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41434-019-0098-z
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