Transcriptome clarifies mechanisms of lesion genesis versus progression in models of Ccm3 cerebral cavernous malformations

Cerebral cavernous malformations (CCMs) are dilated capillaries causing epilepsy and stroke. Inheritance of a heterozygous mutation in CCM3/PDCD10 is responsible for the most aggressive familial form of the disease. Here we studied the differences and commonalities between the transcriptomes of micr...

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Detalhes bibliográficos
Publicado no:Acta Neuropathol Commun
Main Authors: Koskimäki, Janne, Zhang, Dongdong, Li, Yan, Saadat, Laleh, Moore, Thomas, Lightle, Rhonda, Polster, Sean P., Carrión-Penagos, Julián, Lyne, Seán B., Zeineddine, Hussein A., Shi, Changbin, Shenkar, Robert, Romanos, Sharbel, Avner, Kenneth, Srinath, Abhinav, Shen, Le, Detter, Matthew R., Snellings, Daniel, Cao, Ying, Lopez-Ramirez, Miguel A., Fonseca, Gregory, Tang, Alan T., Faber, Pieter, Andrade, Jorge, Ginsberg, Mark, Kahn, Mark L., Marchuk, Douglas A., Girard, Romuald, Awad, Issam A.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6699077/
https://ncbi.nlm.nih.gov/pubmed/31426861
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-019-0789-0
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