PubMed (OMIM) for id: 712

Year	Number of Results
1974	1
1979	1
1980	2
1982	1
1984	1
1986	1
1988	1
1991	1
1992	1
1995	1
1996	1
1997	1
1998	1
2002	1
2007	2
2009	1
2011	2
2014	1
2016	1
2018	1
2024	0

1

C1q restrains autoimmunity and viral infection by regulating CD8⁺ T cell metabolism.

Ling GS, Crawford G, Buang N, Bartok I, Tian K, Thielens NM, Bally I, Harker JA, Ashton-Rickardt PG, Rutschmann S, Strid J, Botto M. Ling GS, et al. Science. 2018 May 4;360(6388):558-563. doi: 10.1126/science.aao4555. Science. 2018. PMID: 29724957 Free PMC article.

2

Complement and microglia mediate early synapse loss in Alzheimer mouse models.

Hong S, Beja-Glasser VF, Nfonoyim BM, Frouin A, Li S, Ramakrishnan S, Merry KM, Shi Q, Rosenthal A, Barres BA, Lemere CA, Selkoe DJ, Stevens B. Hong S, et al. Science. 2016 May 6;352(6286):712-716. doi: 10.1126/science.aad8373. Epub 2016 Mar 31. Science. 2016. PMID: 27033548 Free PMC article.

3

Complement is activated by IgG hexamers assembled at the cell surface.

Diebolder CA, Beurskens FJ, de Jong RN, Koning RI, Strumane K, Lindorfer MA, Voorhorst M, Ugurlar D, Rosati S, Heck AJ, van de Winkel JG, Wilson IA, Koster AJ, Taylor RP, Saphire EO, Burton DR, Schuurman J, Gros P, Parren PW. Diebolder CA, et al. Science. 2014 Mar 14;343(6176):1260-3. doi: 10.1126/science.1248943. Science. 2014. PMID: 24626930 Free PMC article.

4

Disease-causing mutations in genes of the complement system.

Degn SE, Jensenius JC, Thiel S. Degn SE, et al. Am J Hum Genet. 2011 Jun 10;88(6):689-705. doi: 10.1016/j.ajhg.2011.05.011. Am J Hum Genet. 2011. PMID: 21664996 Free PMC article. Review.

5

Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutations.

Schejbel L, Skattum L, Hagelberg S, Åhlin A, Schiller B, Berg S, Genel F, Truedsson L, Garred P. Schejbel L, et al. Genes Immun. 2011 Dec;12(8):626-34. doi: 10.1038/gene.2011.39. Epub 2011 Jun 9. Genes Immun. 2011. PMID: 21654842

6

Immunoglobulin M is required for protection against atherosclerosis in low-density lipoprotein receptor-deficient mice.

Lewis MJ, Malik TH, Ehrenstein MR, Boyle JJ, Botto M, Haskard DO. Lewis MJ, et al. Circulation. 2009 Aug 4;120(5):417-26. doi: 10.1161/CIRCULATIONAHA.109.868158. Epub 2009 Jul 20. Circulation. 2009. PMID: 19620499 Free PMC article.

7

The classical complement cascade mediates CNS synapse elimination.

Stevens B, Allen NJ, Vazquez LE, Howell GR, Christopherson KS, Nouri N, Micheva KD, Mehalow AK, Huberman AD, Stafford B, Sher A, Litke AM, Lambris JD, Smith SJ, John SW, Barres BA. Stevens B, et al. Cell. 2007 Dec 14;131(6):1164-78. doi: 10.1016/j.cell.2007.10.036. Cell. 2007. PMID: 18083105 Free article.

8

Clinical variability and characteristic autoantibody profile in primary C1q complement deficiency.

Vassallo G, Newton RW, Chieng SE, Haeney MR, Shabani A, Arkwright PD. Vassallo G, et al. Rheumatology (Oxford). 2007 Oct;46(10):1612-4. doi: 10.1093/rheumatology/kem207. Rheumatology (Oxford). 2007. PMID: 17890276

9

Non-redundant role of the long pentraxin PTX3 in anti-fungal innate immune response.

Garlanda C, Hirsch E, Bozza S, Salustri A, De Acetis M, Nota R, Maccagno A, Riva F, Bottazzi B, Peri G, Doni A, Vago L, Botto M, De Santis R, Carminati P, Siracusa G, Altruda F, Vecchi A, Romani L, Mantovani A. Garlanda C, et al. Nature. 2002 Nov 14;420(6912):182-6. doi: 10.1038/nature01195. Nature. 2002. PMID: 12432394

10

Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies.

Botto M, Dell'Agnola C, Bygrave AE, Thompson EM, Cook HT, Petry F, Loos M, Pandolfi PP, Walport MJ. Botto M, et al. Nat Genet. 1998 May;19(1):56-9. doi: 10.1038/ng0598-56. Nat Genet. 1998. PMID: 9590289

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