Zobrazeno 1 - 10
of 68
pro vyhledávání: '"C3 glomerulopathies"'
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Dense deposit disease (DDD) and C3 glomerulonephritis (C3GN) are types of membranoproliferative glomerulonephritis classified as C3 glomerulopathies. These conditions are characterized by an increased number of intraglomerular cells and diffuse thick
Externí odkaz:
https://doaj.org/article/b06c6593ed4d45b482db078caa7cadb5
Autor:
Sofiya Pisarenka, Nicole C. Meyer, Xue Xiao, Renee Goodfellow, Carla M. Nester, Yuzhou Zhang, Richard J. H. Smith
Publikováno v:
Frontiers in Immunology, Vol 13 (2023)
IntroductionC3 glomerulopathies (C3G) are ultra-rare complement-mediated diseases that lead to end-stage renal disease (ESRD) within 10 years of diagnosis in ~50% of patients. Overactivation of the alternative pathway (AP) of complement in the fluid
Externí odkaz:
https://doaj.org/article/278dc68f339840d88429924d9bfc4547
Autor:
Alicja Kuźniewska, Marcel Thiel, Daria Kowalska, Anna Felberg-Miętka, Patryk Szynkowski, Stanisław Ołdziej, Emilia Arjona, Ilse Jongerius, Santiago Rodriguez de Córdoba, Marcin Okrój, Aleksandra Urban
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The complement system is one of the first defense lines protecting from invading pathogens. However, it may turn offensive to the body’s own cells and tissues when deregulated by the presence of rare genetic variants that impair physiological regul
Externí odkaz:
https://doaj.org/article/8d3da185c518499ca4dbe1753d908751
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Monoclonal gammopathies result from neoplastic clones of the B-cell lineage and may cause kidney disease by various mechanisms. When the underlying clone does not meet criteria for a malignancy requiring treatment, the paraprotein is called a monoclo
Externí odkaz:
https://doaj.org/article/91d62179090740eab76980a4e0f6a9ab
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
C3 Glomerulopathy (C3G) is a renal disease mediated primarily by dysregulation of the alternative pathway of complement. Complement is the cornerstone of innate immunity. It targets infectious microbes for destruction, clears immune complexes, and ap
Externí odkaz:
https://doaj.org/article/c2ee36351c9c4e24872c8441dbc779ab
Autor:
Kuźniewska, Alicja, Thiel, Marcel, Kowalska, Daria, Felberg, Anna, Szynkowski, Patryk, Oldziej, Stanislaw, Arjona, Emilia, Jongerius, Ilse, Rodríguez de Córdoba, Santiago, Okrój, Marcin, Urban, Aleksandra
Publikováno v:
Frontiers in immunology, 13:1061696. Frontiers Media S.A.
8 p.-4 fig.
The complement system is one of the first defense lines protecting from invading pathogens. However, it may turn offensive to the body’s own cells and tissues when deregulated by the presence of rare genetic variants that impair ph
The complement system is one of the first defense lines protecting from invading pathogens. However, it may turn offensive to the body’s own cells and tissues when deregulated by the presence of rare genetic variants that impair ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::756bcd645090c0f49cebb096a323a414
https://pure.amc.nl/en/publications/substitutions-at-position-263-within-the-von-willebrand-factor-type-a-domain-determine-the-functionality-of-complement-c2-protein(25faa02a-f339-4886-8d92-2ee4f25fe53f).html
https://pure.amc.nl/en/publications/substitutions-at-position-263-within-the-von-willebrand-factor-type-a-domain-determine-the-functionality-of-complement-c2-protein(25faa02a-f339-4886-8d92-2ee4f25fe53f).html
Autor:
Sophie Chauvet, Lubka T. Roumenina, Pierre Aucouturier, Maria-Chiara Marinozzi, Marie-Agnès Dragon-Durey, Alexandre Karras, Yahsou Delmas, Moglie Le Quintrec, Dominique Guerrot, Noémie Jourde-Chiche, David Ribes, Pierre Ronco, Frank Bridoux, Véronique Fremeaux-Bacchi
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
C3 glomerulopathy (C3G) results from acquired or genetic abnormalities in the complement alternative pathway (AP). C3G with monoclonal immunoglobulin (MIg-C3G) was recently included in the spectrum of “monoclonal gammopathy of renal significance.
Externí odkaz:
https://doaj.org/article/45a54c4cddee40a79d7bc8371976ec81
Akademický článek
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Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 12 (2021)
Frontiers in Immunology, Vol 12 (2021)
Monoclonal gammopathies result from neoplastic clones of the B-cell lineage and may cause kidney disease by various mechanisms. When the underlying clone does not meet criteria for a malignancy requiring treatment, the paraprotein is called a monoclo
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.