Potential involvement of DSCAML1 mutations in neurodevelopmental disorders.

Ogata, Shigehiro; Hashizume, Koichi; Hayase, Yoneko; Kanno, Yukie; Hori, Kei; Balan, Shabeesh; Yoshikawa, Takeo; Takahashi, Hidehiko; Taya, Shinichiro; Hoshino, Mikio

Ogata, Shigehiro; Hashizume, Koichi; Hayase, Yoneko; Kanno, Yukie; Hori, Kei; Balan, Shabeesh; Yoshikawa, Takeo; Takahashi, Hidehiko; Taya, Shinichiro; Hoshino, Mikio.

Afiliação

Ogata S; Department of Biochemistry and Cellular Biology, National Institute of Neuroscience, NCNP, Tokyo, Japan.
Hashizume K; Department of Psychiatry and Behavioral Sciences, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.
Hayase Y; Department of Biochemistry and Cellular Biology, National Institute of Neuroscience, NCNP, Tokyo, Japan.
Kanno Y; Department of Biochemistry and Cellular Biology, National Institute of Neuroscience, NCNP, Tokyo, Japan.
Hori K; Department of Biochemistry and Cellular Biology, National Institute of Neuroscience, NCNP, Tokyo, Japan.
Balan S; Department of Biochemistry and Cellular Biology, National Institute of Neuroscience, NCNP, Tokyo, Japan.
Yoshikawa T; Laboratory for Molecular Psychiatry, RIKEN Center for Brain Science, Saitama, Japan.
Takahashi H; Laboratory for Molecular Psychiatry, RIKEN Center for Brain Science, Saitama, Japan.
Taya S; Department of Psychiatry and Behavioral Sciences, Tokyo Medical and Dental University Graduate School, Tokyo, Japan.
Hoshino M; Department of Biochemistry and Cellular Biology, National Institute of Neuroscience, NCNP, Tokyo, Japan.

Genes Cells ; 26(3): 136-151, 2021 Mar.

Article em En | MEDLINE | ID: mdl-33501714

Assuntos

Moléculas de Adesão Celular/genética; Mutação/genética; Transtornos do Neurodesenvolvimento/genética; Animais; Transtorno do Espectro Autista/genética; Adesão Celular; Membrana Celular/metabolismo; Espinhas Dendríticas/metabolismo; Feminino; Glicosilação; Hipocampo/patologia; Humanos; Células L; Masculino; Camundongos; Anotação de Sequência Molecular; Proteínas Mutantes/metabolismo; Proteólise; Ratos Wistar; Esquizofrenia/genética; Sinapses/metabolismo

Palavras-chave

DSCAML1; mutations; neurodevelopmental disorder

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Moléculas de Adesão Celular / Transtornos do Neurodesenvolvimento / Mutação Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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