Zobrazeno 1 - 10
of 410
pro vyhledávání: '"Dorin Bogdan"'
Autor:
Kuang, Huang, Shen, Cong-rong, Jia, Xiao-yu, Tan, Meng, Yang, Xue-fen, Cui, Zhao, Borza, Dorin-Bogdan, Zhao, Ming-hui
Publikováno v:
In Kidney International December 2023 104(6):1124-1134
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Externí odkaz:
https://doaj.org/article/1c239ded24924da690b554ce58567272
Autor:
Odiatis, Christoforos, Savva, Isavella, Pieri, Myrtani, Ioannou, Pavlos, Petrou, Petros, Papagregoriou, Gregory, Antoniadou, Kyriaki, Makrides, Neoklis, Stefanou, Charalambos, Ljubanović, Danica Galešić, Nikolaou, Georgios, Borza, Dorin-Bogdan, Stylianou, Kostas, Gross, Oliver, Deltas, Constantinos
Publikováno v:
In Matrix Biology Plus February 2021 9
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Membranous nephropathy (MN) is an immune kidney disease characterized by glomerular subepithelial immune complexes (ICs) containing antigen, IgG, and products of complement activation. Whereas proteinuria is caused by complement-mediated podocyte inj
Externí odkaz:
https://doaj.org/article/223d251b77014a9db9bdead97e672c12
Publikováno v:
ACS ES&T Water. 3:1150-1160
Autor:
Christoforos Odiatis, Isavella Savva, Myrtani Pieri, Pavlos Ioannou, Petros Petrou, Gregory Papagregoriou, Kyriaki Antoniadou, Neoklis Makrides, Charalambos Stefanou, Danica Galešić Ljubanović, Georgios Nikolaou, Dorin-Bogdan Borza, Kostas Stylianou, Oliver Gross, Constantinos Deltas
Publikováno v:
Matrix Biology Plus, Vol 9, Iss , Pp 100053- (2021)
Alport syndrome (AS) is a severe inherited glomerulopathy caused by mutations in the genes encoding the α-chains of type-IV collagen, the most abundant component of the extracellular glomerular basement membrane (GBM). Currently most AS mouse models
Externí odkaz:
https://doaj.org/article/38be1c9bdd2b47dd9ba217ef68279c4b
Autor:
Dorin-Bogdan Borza, Pallavi Manral
Publikováno v:
Journal of the American Society of Nephrology : JASN.
Autor:
Wentian Luo, Florina Olaru, Jeffrey H. Miner, Laurence H. Beck, Johan van der Vlag, Joshua M. Thurman, Dorin-Bogdan Borza
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Membranous nephropathy is an immune kidney disease caused by IgG antibodies that form glomerular subepithelial immune complexes. Proteinuria is mediated by complement activation, as a result of podocyte injury by C5b-9, but the role of specific compl
Externí odkaz:
https://doaj.org/article/da88cfb1dd4f4f22b43292fd24893f34
Autor:
Fidler, Aaron L., Vanacore, Roberto M., Chetyrkin, Sergei V., Pedchenko, Vadim K., Bhave, Gautam, Yin, Viravuth P., Stothers, Cody L., Rose, Kristie Lindsey, McDonald, W. Hayes, Clark, Travis A., Borz, Dorin-Bogdan, Steele, Robert E., Ivy, Michael T., Aspirnauts, The, Hudson, Julie K., Hudson, Billy G.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2014 Jan 01. 111(1), 331-336.
Externí odkaz:
https://www.jstor.org/stable/23770544
Autor:
Dorin-Bogdan Borza, Xiao-yu Jia, Wentian Luo, Zhao Cui, Cong-Rong Shen, Florina Olaru, Ming-Hui Zhao
Publikováno v:
J Am Soc Nephrol
Background Antiglomerular basement membrane (anti-GBM) disease is characterized by GN and often pulmonary hemorrhage, mediated by autoantibodies that typically recognize cryptic epitopes within α345(IV) collagen-a major component of the glomerular a