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Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin.
Hintze, Stefan; Möhl, Britta S; Beyerl, Jessica; Wulff, Karin; Wieser, Andreas; Bork, Konrad; Meinke, Peter.
Afiliação
  • Hintze S; Friedrich-Baur-Institute at the Department of Neurology, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
  • Möhl BS; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology, Infection and Pandemic Research, Munich, Germany.
  • Beyerl J; Institute of Virology, School of Medicine, Technical University of Munich/Helmholtz Zentrum München, Munich, Germany.
  • Wulff K; Division of Infectious Diseases and Tropical Medicine, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
  • Wieser A; Max-von-Pettenkofer Institute, Ludwig-Maximilians-University Munich, Munich, Germany.
  • Bork K; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology, Infection and Pandemic Research, Munich, Germany.
  • Meinke P; University Medicine, University of Greifswald, Greifswald, Germany.
Front Physiol ; 13: 1090732, 2022.
Article em En | MEDLINE | ID: mdl-36685169

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article