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Metabolic adaptation of human skin fibroblasts to ER stress caused by glycosylation defect in PMM2-CDG.
Zdrazilova, L; Rakosnikova, T; Himmelreich, N; Ondruskova, N; Pasak, M; Vanisova, M; Volfova, N; Honzik, T; Thiel, C; Hansikova, H.
Afiliação
  • Zdrazilova L; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Rakosnikova T; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Himmelreich N; Centre for Child and Adolescent Medicine Heidelberg, Department 1, Heidelberg, Germany.
  • Ondruskova N; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Pasak M; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Vanisova M; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Volfova N; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Honzik T; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
  • Thiel C; Centre for Child and Adolescent Medicine Heidelberg, Department 1, Heidelberg, Germany.
  • Hansikova H; Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic. Electronic address: hana.hansikova@lf1.cuni.cz.
Mol Genet Metab ; 139(4): 107629, 2023 08.
Article em En | MEDLINE | ID: mdl-37392701
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfotransferases (Fosfomutases) / Defeitos Congênitos da Glicosilação Limite: Humans Idioma: En Revista: Mol Genet Metab Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Ano de publicação: 2023 Tipo de documento: Article País de afiliação: República Tcheca
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfotransferases (Fosfomutases) / Defeitos Congênitos da Glicosilação Limite: Humans Idioma: En Revista: Mol Genet Metab Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Ano de publicação: 2023 Tipo de documento: Article País de afiliação: República Tcheca