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Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors

BACKGROUND: Rett syndrome (RTT) is a progressive neurodevelopmental disease that is characterized by abnormalities in cognitive, social, and motor skills. RTT is often caused by mutations in the X-linked gene encoding methyl-CpG binding protein 2 (MeCP2). The mechanism by which impaired MeCP2 induce...

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Detalhes bibliográficos
Publicado no:Mol Autism
Main Authors: Varderidou-Minasian, Suzy, Hinz, Lisa, Hagemans, Dominique, Posthuma, Danielle, Altelaar, Maarten, Heine, Vivi M.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7251722/
https://ncbi.nlm.nih.gov/pubmed/32460858
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13229-020-00344-3
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