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Impaired p53-Mediated DNA Damage Response Contributes to Microcephaly in Nijmegen Breakage Syndrome Patient-Derived Cerebral Organoids.
Martins, Soraia; Erichsen, Lars; Datsi, Angeliki; Wruck, Wasco; Goering, Wolfgang; Chatzantonaki, Eleftheria; de Amorim, Vanessa Cristina Meira; Rossi, Andrea; Chrzanowska, Krystyna H; Adjaye, James.
Afiliação
  • Martins S; Institute for Stem Cell Research and Regenerative Medicine, Medical Faculty, Heinrich-Heine University, 40225 Düsseldorf, Germany.
  • Erichsen L; Institute for Stem Cell Research and Regenerative Medicine, Medical Faculty, Heinrich-Heine University, 40225 Düsseldorf, Germany.
  • Datsi A; Institute for Transplantation Diagnostics and Cell Therapeutics, Heinrich-Heine University, 40225 Düsseldorf, Germany.
  • Wruck W; Institute for Stem Cell Research and Regenerative Medicine, Medical Faculty, Heinrich-Heine University, 40225 Düsseldorf, Germany.
  • Goering W; Institute for Pathology, Medical Faculty, Heinrich-Heine University, 40225 Düsseldorf, Germany.
  • Chatzantonaki E; Institute for Stem Cell Research and Regenerative Medicine, Medical Faculty, Heinrich-Heine University, 40225 Düsseldorf, Germany.
  • de Amorim VCM; Institute for Stem Cell Research and Regenerative Medicine, Medical Faculty, Heinrich-Heine University, 40225 Düsseldorf, Germany.
  • Rossi A; IUF-Leibniz Research Institute for Environmental Medicine, 40225 Düsseldorf, Germany.
  • Chrzanowska KH; Department of Medical Genetics, Children's Memorial Health Institute, 04-730 Warsaw, Poland.
  • Adjaye J; Institute for Stem Cell Research and Regenerative Medicine, Medical Faculty, Heinrich-Heine University, 40225 Düsseldorf, Germany.
Cells ; 11(5)2022 02 25.
Article em En | MEDLINE | ID: mdl-35269426

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Quebra de Nijmegen / Microcefalia Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Quebra de Nijmegen / Microcefalia Idioma: En Ano de publicação: 2022 Tipo de documento: Article