Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice

POGZ is an autism spectrum disorder risk gene. How POGZ mutations result in ASD is unclear and animal models are lacking. Here, the authors generate a brain specific Pogz deficient mouse presenting ASD-like behaviour and show the effects of Pogz deficiency in the cerebellum.

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Autores principales: Reut Suliman-Lavie, Ben Title, Yahel Cohen, Nanako Hamada, Maayan Tal, Nitzan Tal, Galya Monderer-Rothkoff, Bjorg Gudmundsdottir, Kristbjorn O. Gudmundsson, Jonathan R. Keller, Guo-Jen Huang, Koh-ichi Nagata, Yosef Yarom, Sagiv Shifman
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Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/14ea55860cc94204933e8e502705deac
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spelling oai:doaj.org-article:14ea55860cc94204933e8e502705deac2021-12-02T14:40:27ZPogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice10.1038/s41467-020-19577-02041-1723https://doaj.org/article/14ea55860cc94204933e8e502705deac2020-11-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-19577-0https://doaj.org/toc/2041-1723POGZ is an autism spectrum disorder risk gene. How POGZ mutations result in ASD is unclear and animal models are lacking. Here, the authors generate a brain specific Pogz deficient mouse presenting ASD-like behaviour and show the effects of Pogz deficiency in the cerebellum.Reut Suliman-LavieBen TitleYahel CohenNanako HamadaMaayan TalNitzan TalGalya Monderer-RothkoffBjorg GudmundsdottirKristbjorn O. GudmundssonJonathan R. KellerGuo-Jen HuangKoh-ichi NagataYosef YaromSagiv ShifmanNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Reut Suliman-Lavie
Ben Title
Yahel Cohen
Nanako Hamada
Maayan Tal
Nitzan Tal
Galya Monderer-Rothkoff
Bjorg Gudmundsdottir
Kristbjorn O. Gudmundsson
Jonathan R. Keller
Guo-Jen Huang
Koh-ichi Nagata
Yosef Yarom
Sagiv Shifman
Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
description POGZ is an autism spectrum disorder risk gene. How POGZ mutations result in ASD is unclear and animal models are lacking. Here, the authors generate a brain specific Pogz deficient mouse presenting ASD-like behaviour and show the effects of Pogz deficiency in the cerebellum.
format article
author Reut Suliman-Lavie
Ben Title
Yahel Cohen
Nanako Hamada
Maayan Tal
Nitzan Tal
Galya Monderer-Rothkoff
Bjorg Gudmundsdottir
Kristbjorn O. Gudmundsson
Jonathan R. Keller
Guo-Jen Huang
Koh-ichi Nagata
Yosef Yarom
Sagiv Shifman
author_facet Reut Suliman-Lavie
Ben Title
Yahel Cohen
Nanako Hamada
Maayan Tal
Nitzan Tal
Galya Monderer-Rothkoff
Bjorg Gudmundsdottir
Kristbjorn O. Gudmundsson
Jonathan R. Keller
Guo-Jen Huang
Koh-ichi Nagata
Yosef Yarom
Sagiv Shifman
author_sort Reut Suliman-Lavie
title Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
title_short Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
title_full Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
title_fullStr Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
title_full_unstemmed Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
title_sort pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/14ea55860cc94204933e8e502705deac
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