Genetic and Morphological Features of Human iPSC-Derived Neurons with Chromosome 15q11.2 (BP1-BP2) Deletions

BACKGROUND: Copy number variation on chromosome 15q11.2 (BP1-BP2) causes a deletion of CYFIP1, NIPA1, NIPA2 and TUBGCP5. Furthermore, it also affects brain structure and elevates the risk for several neurodevelopmental disorders that are associated with dendritic spine abnormalities. In rodents, alt...

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Bibliografski detalji
Izdano u:Mol Neuropsychiatry
Glavni autori: Das, Dhanjit K., Tapias, Victor, D'Aiuto, Leonardo, Chowdari, Kodavali V., Francis, Lily, Zhi, Yun, Ghosh, Ayantika, Surti, Urvashi, Tischfield, Jay, Sheldon, Michael, Moore, Jennifer C., Fish, Ken, Nimgaonkar, Vishwajit L.
Format: Artigo
Jezik:Inglês
Izdano: S. Karger AG 2015
Teme:
Preliminary Study
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4627696/
https://ncbi.nlm.nih.gov/pubmed/26528485
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000430916
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