Citations for
1C3
Fibrinogen interaction with complement C3: a potential therapeutic target to reduce thrombosis risk.
King RJ, Schuett K, Tiede C, Jankowski V, John V, Trehan A, Simmons K, Ponnambalam S, Storey RF, Fishwick CWG, McPherson MJ, Tomlinson DC, Ajjan RA.
Haematologica un 1;106(6):1616-1623. doi: 10.3324/haematol.2019.239558 2021
2C3
Complement C3 deficiency ameliorates aging related changes in the kidney.
Wu X, Lin L, Cui J, Chen Y, Yang L, Wan J.
Life Sci. Nov 1;260:118370. doi: 10.1016/j.lfs.2020.118370. Epub 2020 Aug 31. 2020
3C3
Complement Components, C3 and C4, and the Metabolic Syndrome
Copenhaver M, Yu CY, Hoffman RP.
Curr Diabetes Rev. 15(1):44-48. doi: 10.2174/1573399814666180417122030 2019
4ATG16L1, C3
Complement Component C3 Is Highly Expressed in Human Pancreatic Islets and Prevents β Cell Death via ATG16L1 Interaction and Autophagy Regulation.
King BC, Kulak K, Krus U, Rosberg R, Golec E, Wozniak K, Gomez MF, Zhang E, O'Connell DJ, Renström E, Blom AM
Cell Metab. Jan 8;29(1):202-210.e6. doi: 10.1016/j.cmet.2018.09.009. Epub 2018 Oct 4. 2019
5C3
Complement C3 Affects Rac1 Activity in the Developing Brain.
Gorelik A, Sapir T, Ben-Reuven L, Reiner O.
Front Mol Neurosci. May 7;11:150. doi: 10.3389/fnmol.2018.00150. 2018
6C3, CFH, CFHR1
Mapping the Complement Factor H-Related Protein 1 (CFHR1):C3b/C3d Interactions
Hannan JP, Laskowski J, Thurman JM, Hageman GS, Holers VM.
PLoS One. Nov 4;11(11):e0166200. doi: 10.1371/journal.pone.0166200 2016
7C3
Complement inhibition in C3 glomerulopathy
Nester CM, Smith RJ.
Semin Immunol. Jun;28(3):241-9. doi: 10.1016/j.smim.2016.06.002. Epub 2016 Jul 9. 2016
8C3, GRIN1
Neuroprotective effects of C3 exoenzyme in excitotoxic retinopathy. 2014 PMID:
Wang Y, Wang Y, Yang Q, Guo L, Yin Y, Fan N, Zhou X, Cai SP, Kaufman PL, Liu X.
Exp Eye Res. Aug;125:128-34. doi: 10.1016/j.exer.2014.05.018. Epub 2014 Jun 11. 2014
9C3
Complement C3: an emerging risk factor in cardiometabolic disease.
Hertle E, van Greevenbroek MM, Stehouwer CD.
Diabetologia. Apr;55(4):881-4. doi: 10.1007/s00125-012-2462-z. Epub 2012 Jan 27 2012
10APOE, ARMD1, ARMD2, ARMD3, ARMD7, ARMD8, ARMDA, ARMDC, ARMS2, C2, C3, CFB, CFH, HTRA1
Multilocus analysis of age-related macular degeneration.
Bergeron-Sawitzke J, Gold B, Olsh A, Schlotterbeck S, Lemon K, Visvanathan K, Allikmets R, Dean M.
Eur J Hum Genet ur J Hum Genet. 2009 Mar 4. [Epub ahead of print] 2009
11C3
C3 R102G polymorphism increases risk of age-related macular degeneration.
Spencer KL, Olson LM, Anderson BM, Schnetz-Boutaud N, Scott WK, Gallins P, Agarwal A, Postel EA, Pericak-Vance MA, Haines JL.
Hum Mol Genet 17(12):1821-4. Epub 2008 Mar 6. 2008
12C3
Variation in complement factor 3 is associated with risk of age-related macular degeneration.
Maller JB, Fagerness JA, Reynolds RC, Neale BM, Daly MJ, Seddon JM.
Nat Genet 39(10):1200-1. Epub 2007 Sep 2. 2007
13C3, C3D
Molecular analysis of a novel hereditary C3 deficiency with systemic lupus erythematosus.
Tsukamoto H, Horiuchi T, Kokuba H, Nagae S, Nishizaka H, Sawabe T, Harashima S, Himeji D, Koyama T, Otsuka J, Mitoma H, Kimoto Y, Hashimura C, Kitano E, Kitamura H, Furue M, Harada M.
Biochem Biophys Res Commun 330(1):298-304. 2005
14C3
Inherited human complement C3 deficiency.
Singer L, et al.
J Biol Chem 269 : 28494-28499. 1994
15C3
EcoRI polymorphism in the human third complement component (C3) gene.
Botto M, et al.
Nucleic Acids Res 18 : 2833. 1990
16C3
Genomic organization of human complement component C3.
Fong KY, Botto M, Walport MJ, So AK.
Genomics 7(4):579-86. 1990
17FUT1, C3
New linkage data on chromosome 19 with particular reference to the H (FUT1) locus.
Ball SP, et al.
(HGM10) Cytogenet Cell Genet 51 : 956. 1989
18LDLR, C3, APOC2, LW, BCAM , FUT2
The chromosome 19 linkage group LDLR, C3, LW, APOC2, LU, SE in man.
Lewis M, et al.
Ann Hum Genet 52 : 137-144. 1988
19LW, C3
The LW:C3 recombination fraction in female meioses.
Lewis M, et al.
Ann Hum Genet 51 : 201-203. 1987
20APOC1, APOC2, APOE, C3, LDLR, PEPD, GPI
Regional mapping of human chromosome 19 : Organisation of genes for plasma lipid transport (APOC1,-C2, and -E and LDLR) and the genes C3, PEPD, and GPI.
Lusis AJ, et al.
Proc Natl Acad Sci U S A 83 : 3929-3933. 1986
21C3, LPCN
Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19.
Shaw DJ, et al.
Hum Genet 74 : 267-269. 1986
22C3
Human complement component C3: cDNA coding sequence and derived primary structure.
De Bruijn MHL, et al.
Proc Natl Acad Sci U S A 82 : 708-712. 1985
23C3, LW
Linkage of the LW blood group locus with the complement C3 and Lutheran blood group loci.
Sistonen P.
Ann Hum Genet 48 : 239-242. 1984
24C3, PEPD, GPI, APOE
Mapping studies with peptidase D (PEPD).
Ball S, et al.
(HGM7) Cytogenet Cell Genet 37 : 411-412. 1984
25C3, FUT2, LE, PEPD, BCAM
Genetics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19.
Eiberg H, et al.
Clin Genet 24 : 159-170. 1983
26C3
Assignment of the gene for the third component of human complement (C3) to chromosome 19 using human-mouse somatic cell hybrids.
Whitehead AS, et al.
Cytogenet Cell Genet 32 : 326-327. 1982
27C3
Assignment of a structural gene for the third component of human complement to chromosome 19.
Whitehead AS, et al.
Proc Natl Acad Sci U S A 79 : 5021-5025. 1982
28C3, LDLR
Probable linkage between essential familial hypercholesterolemia and third complement component (C3).
Elston RC, et al.
Cytogenet Cell Genet 16 : 294-297. 1976