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The DYT6 Dystonia Protein THAP1 Regulates Myelination Within The Oligodendrocyte Lineage
The childhood-onset motor disorder DYT6 dystonia is caused by loss-of-function mutations in the transcription factor THAP1, but the neurodevelopmental processes in which THAP1 participates are unknown. We find that THAP1 is essential for the timing of myelination initiation during CNS maturation. Co...
שמור ב:
| הוצא לאור ב: | Dev Cell |
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| Main Authors: | , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2017
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5847273/ https://ncbi.nlm.nih.gov/pubmed/28697333 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.devcel.2017.06.009 |
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