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Self-damage caused by dysregulation of the complement alternative pathway: Relevance of the factor H protein family

Sanchez-Corral, P. and Pouw, R. B. and Lopez-Trascasa, M. and Józsi, Mihály (2018) Self-damage caused by dysregulation of the complement alternative pathway: Relevance of the factor H protein family. FRONTIERS IN IMMUNOLOGY, 9 (7). ISSN 1664-3224

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Item Type: Article
Uncontrolled Keywords: COMPLEMENT ACTIVATION; opsonization; Hemolytic-Uremic Syndrome; Dense deposit disease; Copy number variation; GENOME-WIDE ASSOCIATION; age-related macular degeneration; C-REACTIVE-PROTEIN; atypical hemolytic uremic syndrome; SHORT CONSENSUS REPEAT; Factor H; C3 glomerulopathy; LONG PENTRAXIN PTX3; HEPARIN-BINDING DOMAIN; SURFACE-RECOGNITION DOMAINS; TRANSLATIONAL MINIREVIEW SERIES; factor H-related protein; complement de-regulation;
Subjects: Q Science / természettudomány > QR Microbiology / mikrobiológia > QR180 Immunology / immunológia
SWORD Depositor: MTMT SWORD
Depositing User: MTMT SWORD
Date Deposited: 25 Nov 2019 09:43
Last Modified: 25 Nov 2019 09:43
URI: http://real.mtak.hu/id/eprint/103725

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