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Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus File File

Saito Ryo , Koebis Michinori , Nagai Taku , Shimizu Kimiko , Liao Jingzhu , Wulaer Bolati , Sugaya Yuki , Nagahama, Kenichiro , Uesaka Naofumi , Kushima Itaru , et al

Article Issue Date2020-02 View7
Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus File File

Saito, Ryo , Koebis, Michinori , Nagai, Taku , Shimizu, Kimiko , Liao, Jingzhu , Wulaer, Bolati , Sugaya, Yuki , Nagahama, Kenichiro , Uesaka, Naofumi , Kushima, Itaru , et al

Article Issue Date2020-02 View7
ERCC1 mutations impede DNA damage repair and cause liver and kidney dysfunction in patients File

Apelt, Katja , White, Susan M. , Kim, Hyun Suk , Yeo, Jung-Eun , Kragten, Angela , Wondergem, Annelotte P. , Rooimans, Martin A. , Gonzalez-Prieto, Roman , Wiegant, Wouter W. , Lunke, Sebastian , et al

Article Issue Date2021-03 View127
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