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A Single RET Mutation in Hirschsprung Disease Induces Intestinal Aganglionosis Via a Dominant-Negative Mechanism.
Sunardi, Mukhamad; Ito, Keisuke; Sato, Yuya; Uesaka, Toshihiro; Iwasaki, Mitsuhiro; Enomoto, Hideki.
Afiliação
  • Sunardi M; Division of Neural Differentiation and Regeneration, Department of Physiology and Cell Biology, Kobe University Graduate School of Medicine, Hyogo, Japan.
  • Ito K; Division of Neural Differentiation and Regeneration, Department of Physiology and Cell Biology, Kobe University Graduate School of Medicine, Hyogo, Japan.
  • Sato Y; Division of Neural Differentiation and Regeneration, Department of Physiology and Cell Biology, Kobe University Graduate School of Medicine, Hyogo, Japan.
  • Uesaka T; Division of Neural Differentiation and Regeneration, Department of Physiology and Cell Biology, Kobe University Graduate School of Medicine, Hyogo, Japan.
  • Iwasaki M; Division of Neural Differentiation and Regeneration, Department of Physiology and Cell Biology, Kobe University Graduate School of Medicine, Hyogo, Japan.
  • Enomoto H; Division of Neural Differentiation and Regeneration, Department of Physiology and Cell Biology, Kobe University Graduate School of Medicine, Hyogo, Japan. Electronic address: enomotoh@med.kobe-u.ac.jp.
Cell Mol Gastroenterol Hepatol ; 15(6): 1505-1524, 2023.
Article em En | MEDLINE | ID: mdl-36521661
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistema Nervoso Entérico / Doença de Hirschsprung Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistema Nervoso Entérico / Doença de Hirschsprung Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article