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RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis.
Wong, Samantha; Tan, Yu Xuan; Loh, Abigail Yi Ting; Tan, Kiat Yi; Lee, Hane; Aziz, Zainab; Nelson, Stanley F; Özkan, Engin; Kayserili, Hülya; Escande-Beillard, Nathalie; Reversade, Bruno.
Afiliação
  • Wong S; Institute of Molecular and Cellular Biology, A*STAR, Singapore, Singapore.
  • Tan YX; Experimental Drug Development Centre, A*STAR, Singapore, Singapore.
  • Loh AYT; Institute of Molecular and Cellular Biology, A*STAR, Singapore, Singapore.
  • Tan KY; Institute of Molecular and Cellular Biology, A*STAR, Singapore, Singapore.
  • Lee H; Genome Institute of Singapore, A*STAR, Singapore, Singapore.
  • Aziz Z; Institute of Molecular and Cellular Biology, A*STAR, Singapore, Singapore.
  • Nelson SF; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Özkan E; Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Kayserili H; 3billion, Inc, Seoul, South Korea.
  • Escande-Beillard N; Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL, USA.
  • Reversade B; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
EMBO Mol Med ; 15(5): e17078, 2023 05 08.
Article em En | MEDLINE | ID: mdl-37066513
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Proteína Tirosina Quinases / Síndrome de Noonan Tipo de estudo: Etiology_studies Limite: Humans / Newborn Idioma: En Revista: EMBO Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Singapura
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Proteína Tirosina Quinases / Síndrome de Noonan Tipo de estudo: Etiology_studies Limite: Humans / Newborn Idioma: En Revista: EMBO Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Singapura