Inhibition of KDM1A activity restores adult neurogenesis and improves hippocampal memory in a mouse model of Kabuki syndrome

Kabuki syndrome (KS) is a rare cause of intellectual disability primarily caused by loss-of-function mutations in lysine-specific methyltransferase 2D (KMT2D), which normally adds methyl marks to lysine 4 on histone 3. Previous studies have shown that a mouse model of KS (Kmt2d(+/βGeo)) demonstrates...

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Detalles Bibliográficos
Autores principales: Zhang, Li, Pilarowski, Genay, Pich, Emilio Merlo, Nakatani, Atsushi, Dunlop, John, Baba, Rina, Matsuda, Satoru, Daini, Masaki, Hattori, Yasushi, Matsumoto, Shigemitsu, Ito, Mitsuhiro, Kimura, Haruhide, Bjornsson, Hans Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940709/
https://www.ncbi.nlm.nih.gov/pubmed/33738331
http://dx.doi.org/10.1016/j.omtm.2021.02.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940709/
https://www.ncbi.nlm.nih.gov/pubmed/33738331
http://dx.doi.org/10.1016/j.omtm.2021.02.011

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