Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons

BACKGROUND: MBD5, encoding the methyl-CpG-binding domain 5 protein, has been proposed as a necessary and sufficient driver of the 2q23.1 microdeletion syndrome. De novo missense and protein-truncating variants from exome sequencing studies have directly implicated MBD5 in the etiology of autism spec...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Mol Autism
Päätekijät: Seabra, Catarina M., Aneichyk, Tatsiana, Erdin, Serkan, Tai, Derek J. C., De Esch, Celine E. F., Razaz, Parisa, An, Yu, Manavalan, Poornima, Ragavendran, Ashok, Stortchevoi, Alexei, Abad, Clemer, Young, Juan I., Maciel, Patricia, Talkowski, Michael E., Gusella, James F.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2020
Aiheet:
Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7275313/
https://ncbi.nlm.nih.gov/pubmed/32503625
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13229-020-00354-1
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