Načítá se...
GSE4 peptide suppresses oxidative and telomere deficiencies in ataxia telangiectasia patient cells
Ataxia telangiectasia (AT) is a genetic disease caused by mutations in the ATM gene but the mechanisms underlying AT are not completely understood. Key functions of the ATM protein are to sense and regulate cellular redox status and to transduce DNA double-strand break signals to downstream effector...
Uloženo v:
| Vydáno v: | Cell Death Differ |
|---|---|
| Hlavní autoři: | , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group UK
2019
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6748109/ https://ncbi.nlm.nih.gov/pubmed/30670828 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41418-018-0272-7 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|