ロード中...
Tsc1 haploinsufficiency is sufficient to increase dendritic patterning and Filamin A levels
Most individuals with tuberous sclerosis complex (TSC) are born with a mutant allele of either TSC1 or TSC2 and a mosaic of psychological and cognitive defects. Tsc1 loss of heterozygosity contributes to severe dendritic abnormalities that are rescued by normalizing the levels of the actin-cross lin...
保存先:
| 出版年: | Neurosci Lett |
|---|---|
| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2016
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4983256/ https://ncbi.nlm.nih.gov/pubmed/27345385 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2016.06.037 |
| 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!
|