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A mechanism in agrin signaling revealed by a prevalent Rapsyn mutation in congenital myasthenic syndrome.
Xing, Guanglin; Jing, Hongyang; Zhang, Lei; Cao, Yu; Li, Lei; Zhao, Kai; Dong, Zhaoqi; Chen, Wenbing; Wang, Hongsheng; Cao, Rangjuan; Xiong, Wen-Cheng; Mei, Lin.
Afiliação
  • Xing G; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
  • Jing H; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
  • Zhang L; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
  • Cao Y; Department of Neuroscience and Regenerative Medicine, Augusta University, Augusta, United States.
  • Li L; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
  • Zhao K; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
  • Dong Z; Department of Neuroscience and Regenerative Medicine, Augusta University, Augusta, United States.
  • Chen W; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
  • Wang H; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
  • Cao R; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
  • Xiong WC; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
  • Mei L; Department of Neurosciences, School of Medicine, Case Western Reserve University, Cleveland, United States.
Elife ; 82019 09 24.
Article em En | MEDLINE | ID: mdl-31549961
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Agrina / Mutação de Sentido Incorreto / Síndromes Miastênicas Congênitas / Proteínas Mutantes / Proteínas Musculares Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Agrina / Mutação de Sentido Incorreto / Síndromes Miastênicas Congênitas / Proteínas Mutantes / Proteínas Musculares Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos