Functional Characterization of the Disease-Associated N-Terminal Complement Factor H Mutation W198R.

Cserhalmi, Marcell; Uzonyi, Barbara; Merle, Nicolas S; Csuka, Dorottya; Meusburger, Edgar; Lhotta, Karl; Prohászka, Zoltán; Józsi, Mihály

Cserhalmi, Marcell; Uzonyi, Barbara; Merle, Nicolas S; Csuka, Dorottya; Meusburger, Edgar; Lhotta, Karl; Prohászka, Zoltán; Józsi, Mihály.

Afiliação

Cserhalmi M; MTA-ELTE "Lendület" Complement Research Group, Department of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Uzonyi B; MTA-ELTE Immunology Research Group, Department of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Merle NS; UMRS 1138, Cordeliers Research Center, Complement and Diseases Team, INSERM, Paris, France.
Csuka D; 3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
Meusburger E; Department of Nephrology and Dialysis, Academic Teaching Hospital Feldkirch, Feldkirch, Austria.
Lhotta K; Department of Nephrology and Dialysis, Academic Teaching Hospital Feldkirch, Feldkirch, Austria.
Prohászka Z; 3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
Józsi M; MTA-SE Immunology and Hematology Research Group, Semmelweis University, Budapest, Hungary.

Front Immunol ; 8: 1800, 2017.

Article em En | MEDLINE | ID: mdl-29321782

Palavras-chave

C3 glomerulopathy; atypical hemolytic uremic syndrome; complement dysregulation; factor H; kidney disease; mutation

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Immunol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Hungria

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