The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival.

Ma, Mengqi; Zhang, Xi; Zheng, Yiming; Lu, Shenzhao; Pan, Xueyang; Mao, Xiao; Pan, Hongling; Chung, Hyung-Lok; Wang, Hua; Guo, Hong; Bellen, Hugo J

Ma, Mengqi; Zhang, Xi; Zheng, Yiming; Lu, Shenzhao; Pan, Xueyang; Mao, Xiao; Pan, Hongling; Chung, Hyung-Lok; Wang, Hua; Guo, Hong; Bellen, Hugo J.

Afiliação

Ma M; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Zhang X; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
Zheng Y; National Health Commission Key Laboratory of Birth Defects Research, Prevention and Treatment, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan 410008, China.
Lu S; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Pan X; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Mao X; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
Pan H; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Chung HL; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
Wang H; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Guo H; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
Bellen HJ; National Health Commission Key Laboratory of Birth Defects Research, Prevention and Treatment, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan 410008, China.

Hum Mol Genet ; 32(6): 984-997, 2023 03 06.

Article em En | MEDLINE | ID: mdl-36255738

Assuntos

Encefalopatias; Epilepsia; Deficiência Intelectual; Transtornos do Neurodesenvolvimento; Animais; Sobrevivência Celular; Transtornos do Neurodesenvolvimento/genética; Deficiência Intelectual/genética; Mutação de Sentido Incorreto; Drosophila

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encefalopatias / Epilepsia / Transtornos do Neurodesenvolvimento / Deficiência Intelectual Tipo de estudo: Risk_factors_studies Limite: Animals Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

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