טוען...
Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader–Willi syndromes
Angelman syndrome (AS) and Prader–Willi syndrome (PWS) are neurodevelopmental disorders of genomic imprinting. AS results from loss of function of the ubiquitin protein ligase E3A (UBE3A) gene, whereas the genetic defect in PWS is unknown. Although induced pluripotent stem cells (iPSCs) provide inva...
שמור ב:
| Main Authors: | , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
National Academy of Sciences
2010
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2955112/ https://ncbi.nlm.nih.gov/pubmed/20876107 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1004487107 |
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