Cargando…
Using iPS cell-derived neurons to uncover cellular phenotypes associated with Timothy Syndrome
Monogenic neurodevelopmental disorders provide key insights into the pathogenesis of disease and help us understand how specific genes control the development of the human brain. Timothy syndrome is caused by a missense mutation in the L-type calcium channel Ca(v)1.2 that is associated with developm...
Autores principales: | Paşca, Sergiu P., Portmann, Thomas, Voineagu, Irina, Yazawa, Masayuki, Shcheglovitov, Oleksandr, Paşca, Anca M., Cord, Branden, Palmer, Theo D., Chikahisa, Sachiko, Seiji, Nishino, Bernstein, Jonathan A., Hallmayer, Joachim, Geschwind, Daniel H., Dolmetsch, Ricardo E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517299/ https://www.ncbi.nlm.nih.gov/pubmed/22120178 http://dx.doi.org/10.1038/nm.2576 |
Ejemplares similares
-
Using iPS cells to investigate cardiac phenotypes in patients with Timothy Syndrome
por: Yazawa, Masayuki, et al.
Publicado: (2011) -
Timothy Syndrome is associated with activity-dependent dendritic retraction in rodent and human neurons
por: Krey, Jocelyn F., et al.
Publicado: (2013) -
Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome
por: Tian, Yuan, et al.
Publicado: (2014) -
Aberrant calcium channel splicing drives defects in cortical differentiation in Timothy syndrome
por: Panagiotakos, Georgia, et al.
Publicado: (2019) -
A Promoter in the Coding Region of the Calcium Channel Gene CACNA1C Generates the Transcription Factor CCAT
por: Gomez-Ospina, Natalia, et al.
Publicado: (2013)