mTOR pathway repressing expression of FoxO3 is a potential mechanism involved in neonatal white matter dysplasia.

Liu, Xiuyun; Dong, Chen; Liu, Kaiyi; Chen, Huiyao; Liu, Bo; Dong, Xinran; Qian, Yanyan; Wu, Bingbing; Lin, Yifeng; Wang, Huijun; Yang, Lin; Zhou, Wenhao

Liu, Xiuyun; Dong, Chen; Liu, Kaiyi; Chen, Huiyao; Liu, Bo; Dong, Xinran; Qian, Yanyan; Wu, Bingbing; Lin, Yifeng; Wang, Huijun; Yang, Lin; Zhou, Wenhao.

Afiliação

Liu X; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Dong C; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Liu K; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Chen H; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Liu B; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Dong X; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Qian Y; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Wu B; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Lin Y; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Wang H; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Yang L; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
Zhou W; Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.

Hum Mol Genet ; 31(15): 2508-2520, 2022 08 17.

Article em En | MEDLINE | ID: mdl-35220433

Assuntos

Substância Branca; Diferenciação Celular/genética; Proteína Forkhead Box O3/genética; Proteína Forkhead Box O3/metabolismo; Humanos; Bainha de Mielina/metabolismo; Oligodendroglia/metabolismo; Transdução de Sinais; Sirolimo; Serina-Treonina Quinases TOR/genética; Serina-Treonina Quinases TOR/metabolismo; Substância Branca/metabolismo

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Substância Branca Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Substância Branca Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article