Carregant...

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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Gene Ther
Autors principals: Serfecz, Jacquelyn, Bazick, Hannah, Al Salihi, Mohammed Omar, Turner, Peter, Fields, Christopher, Cruz, Pedro, Renne, Rolf, Notterpek, Lucia
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2019
Matèries:
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!