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Methyl-CpG Binding Protein 2 (Mecp2) Regulates Sensory Function Through Sema5b and Robo2

Mutations in the gene encoding the MECP2 underlies Rett syndrome, a neurodevelopmental disorder in young females. Although reduced pain sensitivity in Rett syndrome patients and in partial MeCP2 deficient mice had been reported, these previous studies focused predominantly on motor impairments. Ther...

詳細記述

保存先:
書誌詳細
出版年:Front Cell Neurosci
主要な著者: Leong, Wan Y., Lim, Zhi H., Korzh, Vladimir, Pietri, Thomas, Goh, Eyleen L. K.
フォーマット: Artigo
言語:Inglês
出版事項: Frontiers Media S.A. 2015
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4685056/
https://ncbi.nlm.nih.gov/pubmed/26733807
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2015.00481
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