Publications by authors named "Matthieu Raveau"

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Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairment.
Hideo Hagihara, Hirotaka Shoji, Satoko Hattori, Giovanni Sala, Yoshihiro Takamiya, Matthieu Raveau

Elife· March 2024

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CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate.
Toshimitsu Suzuki, Tetsuya Tatsukawa, Genki Sudo, Caroline Delandre, Yun Jin Pai, Matthieu Raveau

Sci Rep· May 2022

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Impairment of spatial memory accuracy improved by Cbr1 copy number resumption and GABA receptor-dependent enhancement of synaptic inhibition in Down syndrome model mice.
Fumiko Arima-Yoshida, Matthieu Raveau, Atsushi Shimohata, Kenji Amano, Akihiro Fukushima

Sci Rep· August 2020

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CRISPR/dCas9-based Scn1a gene activation in inhibitory neurons ameliorates epileptic and behavioral phenotypes of Dravet syndrome model mice.
Tetsushi Yamagata, Matthieu Raveau, Kenta Kobayashi, Hiroyuki Miyamoto, Tetsuya Tatsukawa

Neurobiol Dis· July 2020

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A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders.
Toshimitsu Suzuki, Toshifumi Suzuki, Matthieu Raveau, Noriko Miyake, Genki Sudo

Ann Clin Transl Neurol· July 2020

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Airway Ciliary Beating Affected by the Dose-Dependent [Ca] Increase in Down Syndrome Mice, Ts1Rhr.
Haruka Kogiso, Matthieu Raveau, Kazuhiro Yamakawa, Daichi Saito, Yukiko Ikeuchi

Int J Mol Sci· March 2020

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haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity.
Tetsuya Tatsukawa, Matthieu Raveau, Ikuo Ogiwara, Satoko Hattori, Hiroyuki Miyamoto

Mol Autism· May 2019

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Impaired cortico-striatal excitatory transmission triggers epilepsy.
Hiroyuki Miyamoto, Tetsuya Tatsukawa, Atsushi Shimohata, Tetsushi Yamagata, Toshimitsu Suzuki, Matthieu Raveau

Nat Commun· April 2019

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DYRK1A-haploinsufficiency in mice causes autistic-like features and febrile seizures.
Matthieu Raveau, Atsushi Shimohata, Kenji Amano, Hiroyuki Miyamoto, Kazuhiro Yamakawa

Neurobiol Dis· February 2018

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Alterations of in vivo CA1 network activity in Dp(16)1Yey Down syndrome model mice.
Matthieu Raveau, Denis Polygalov, Roman Boehringer, Kenji Amano, Kazuhiro Yamakawa

Elife· February 2018

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Ts1Cje Down syndrome model mice exhibit environmental stimuli-triggered locomotor hyperactivity and sociability concurrent with increased flux through central dopamine and serotonin metabolism.
Atsushi Shimohata, Keiichi Ishihara, Satoko Hattori, Hiroyuki Miyamoto, Hiromasa Morishita, Matthieu Raveau

Exp Neurol· July 2017

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Brain ventriculomegaly in Down syndrome mice is caused by Pcp4 dose-dependent cilia dysfunction.
Matthieu Raveau, Takashi Nakahari, Sachie Asada, Keiichi Ishihara, Kenji Amano

Hum Mol Genet· March 2017

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Deletion of the App-Runx1 region in mice models human partial monosomy 21.
Thomas Arbogast, Matthieu Raveau, Claire Chevalier, Valérie Nalesso, Doulaye Dembele

Dis Model Mech· June 2015

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The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model.
Matthieu Raveau, Jacques M Lignon, Valérie Nalesso, Arnaud Duchon, Yoram Groner

PLoS Genet· May 2012

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Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome.
Arnaud Duchon, Matthieu Raveau, Claire Chevalier, Valérie Nalesso, Andrew J Sharp

Mamm Genome· December 2011

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Controlled somatic and germline copy number variation in the mouse model.
Yann Hérault, Arnaud Duchon, Damien Maréchal, Matthieu Raveau, Patricia L Pereira

Curr Genomics· September 2010

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