Φορτώνει......
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...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
National Academy of Sciences
2010
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| Θέματα: | |
| Διαθέσιμο Online: | 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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