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Results: 9

1.

Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.

Maga TK, Nishimura CJ, Weaver AE, Frees KL, Smith RJ.

Hum Mutat. 2010 Jun;31(6):E1445-60. doi: 10.1002/humu.21256.

PMID:
20513133
[PubMed - indexed for MEDLINE]
2.

New genetic associations detected in a host response study to hepatitis B vaccine.

Davila S, Froeling FE, Tan A, Bonnard C, Boland GJ, Snippe H, Hibberd ML, Seielstad M.

Genes Immun. 2010 Apr;11(3):232-8. doi: 10.1038/gene.2010.1. Epub 2010 Mar 18.

PMID:
20237496
[PubMed - indexed for MEDLINE]
3.

Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome.

Sullivan M, Erlic Z, Hoffmann MM, Arbeiter K, Patzer L, Budde K, Hoppe B, Zeier M, Lhotta K, Rybicki LA, Bock A, Berisha G, Neumann HP.

Ann Hum Genet. 2010 Jan;74(1):17-26. doi: 10.1111/j.1469-1809.2009.00554.x.

PMID:
20059470
[PubMed - indexed for MEDLINE]
4.

Genetic analysis of complement factor H related 5, CFHR5, in patients with age-related macular degeneration.

Narendra U, Pauer GJ, Hagstrom SA.

Mol Vis. 2009;15:731-6. Epub 2009 Apr 10.

PMID:
19365580
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Risk of non-Hodgkin lymphoma in association with germline variation in complement genes.

Cerhan JR, Novak AJ, Fredericksen ZS, Wang AH, Liebow M, Call TG, Dogan A, Witzig TE, Ansell SM, Habermann TM, Kay NE, Slager SL.

Br J Haematol. 2009 Jun;145(5):614-23. doi: 10.1111/j.1365-2141.2009.07675.x. Epub 2009 Mar 30.

PMID:
19344414
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.

Zhang H, Morrison MA, Dewan A, Adams S, Andreoli M, Huynh N, Regan M, Brown A, Miller JW, Kim IK, Hoh J, Deangelis MM.

BMC Med Genet. 2008 Jun 9;9:51. doi: 10.1186/1471-2350-9-51.

PMID:
18541031
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: characterization, ethnic distribution and evolutionary implications.

Hageman GS, Hancox LS, Taiber AJ, Gehrs KM, Anderson DH, Johnson LV, Radeke MJ, Kavanagh D, Richards A, Atkinson J, Meri S, Bergeron J, Zernant J, Merriam J, Gold B, Allikmets R, Dean M; AMD Clinical Study Group.

Ann Med. 2006;38(8):592-604.

PMID:
17438673
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Genetic analysis of the complement factor H related 5 gene in haemolytic uraemic syndrome.

Monteferrante G, Brioschi S, Caprioli J, Pianetti G, Bettinaglio P, Bresin E, Remuzzi G, Noris M.

Mol Immunol. 2007 Mar;44(7):1704-8. Epub 2006 Sep 26.

PMID:
17000000
[PubMed - indexed for MEDLINE]
9.

Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease).

Abrera-Abeleda MA, Nishimura C, Smith JL, Sethi S, McRae JL, Murphy BF, Silvestri G, Skerka C, Józsi M, Zipfel PF, Hageman GS, Smith RJ.

J Med Genet. 2006 Jul;43(7):582-9. Epub 2005 Nov 18.

PMID:
16299065
[PubMed - indexed for MEDLINE]
Free PMC Article

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