טוען...
Modeling xeroderma pigmentosum associated neurological pathologies with patients-derived iPSCs
Xeroderma pigmentosum (XP) is a group of genetic disorders caused by mutations of XP-associated genes, resulting in impairment of DNA repair. XP patients frequently exhibit neurological degeneration, but the underlying mechanism is unknown, in part due to lack of proper disease models. Here, we gene...
שמור ב:
| הוצא לאור ב: | Protein Cell |
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| Main Authors: | , , , , , , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Higher Education Press
2016
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4791426/ https://ncbi.nlm.nih.gov/pubmed/26874523 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13238-016-0244-y |
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