ロード中...
Huntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice
Mutations in the X‐linked MECP2 gene are responsible for Rett syndrome (RTT), a severe neurological disorder for which there is no treatment. Several studies have linked the loss of MeCP2 function to alterations of brain‐derived neurotrophic factor (BDNF) levels, but non‐specific overexpression of B...
保存先:
| 出版年: | EMBO Mol Med |
|---|---|
| 主要な著者: | , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2020
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7005633/ https://ncbi.nlm.nih.gov/pubmed/31913581 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/emmm.201910889 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|