204 related articles for article (PubMed ID: 23613724)
1. Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32.
Holmes LV; Strain L; Staniforth SJ; Moore I; Marchbank K; Kavanagh D; Goodship JA; Cordell HJ; Goodship TH
PLoS One; 2013; 8(4):e60352. PubMed ID: 23613724
[TBL] [Abstract][Full Text] [Related]
2. Contribution of copy number variation in the regulation of complement activation locus to development of age-related macular degeneration.
Schmid-Kubista KE; Tosakulwong N; Wu Y; Ryu E; Hecker LA; Baratz KH; Brown WL; Edwards AO
Invest Ophthalmol Vis Sci; 2009 Nov; 50(11):5070-9. PubMed ID: 19553609
[TBL] [Abstract][Full Text] [Related]
3. Copy number variation in the complement factor H-related genes and age-related macular degeneration.
Kubista KE; Tosakulwong N; Wu Y; Ryu E; Roeder JL; Hecker LA; Baratz KH; Brown WL; Edwards AO
Mol Vis; 2011; 17():2080-92. PubMed ID: 21850184
[TBL] [Abstract][Full Text] [Related]
4. Copy number variation analysis using next-generation sequencing identifies the
Park J; Yhim HY; Kang KP; Bae TW; Cho YG
Hematology; 2022 Dec; 27(1):603-608. PubMed ID: 35617302
[TBL] [Abstract][Full Text] [Related]
5. Variants in Complement Factor H and Complement Factor H-Related Protein Genes, CFHR3 and CFHR1, Affect Complement Activation in IgA Nephropathy.
Zhu L; Zhai YL; Wang FM; Hou P; Lv JC; Xu DM; Shi SF; Liu LJ; Yu F; Zhao MH; Novak J; Gharavi AG; Zhang H
J Am Soc Nephrol; 2015 May; 26(5):1195-204. PubMed ID: 25205734
[TBL] [Abstract][Full Text] [Related]
6. Fine Mapping Implicates a Deletion of CFHR1 and CFHR3 in Protection from IgA Nephropathy in Han Chinese.
Xie J; Kiryluk K; Li Y; Mladkova N; Zhu L; Hou P; Ren H; Wang W; Zhang H; Chen N; Gharavi AG
J Am Soc Nephrol; 2016 Oct; 27(10):3187-3194. PubMed ID: 26940089
[TBL] [Abstract][Full Text] [Related]
7. Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.
Zipfel PF; Edey M; Heinen S; Józsi M; Richter H; Misselwitz J; Hoppe B; Routledge D; Strain L; Hughes AE; Goodship JA; Licht C; Goodship TH; Skerka C
PLoS Genet; 2007 Mar; 3(3):e41. PubMed ID: 17367211
[TBL] [Abstract][Full Text] [Related]
8. An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD).
Fritsche LG; Lauer N; Hartmann A; Stippa S; Keilhauer CN; Oppermann M; Pandey MK; Köhl J; Zipfel PF; Weber BH; Skerka C
Hum Mol Genet; 2010 Dec; 19(23):4694-704. PubMed ID: 20843825
[TBL] [Abstract][Full Text] [Related]
9. The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.
Dragon-Durey MA; Blanc C; Marliot F; Loirat C; Blouin J; Sautes-Fridman C; Fridman WH; Frémeaux-Bacchi V
J Med Genet; 2009 Jul; 46(7):447-50. PubMed ID: 19435718
[TBL] [Abstract][Full Text] [Related]
10. Deletion Variants of
Jullien P; Laurent B; Claisse G; Masson I; Dinic M; Thibaudin D; Berthoux F; Alamartine E; Mariat C; Maillard N
J Am Soc Nephrol; 2018 Feb; 29(2):661-669. PubMed ID: 29114042
[TBL] [Abstract][Full Text] [Related]
11. Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration.
Spencer KL; Hauser MA; Olson LM; Schmidt S; Scott WK; Gallins P; Agarwal A; Postel EA; Pericak-Vance MA; Haines JL
Hum Mol Genet; 2008 Apr; 17(7):971-7. PubMed ID: 18084039
[TBL] [Abstract][Full Text] [Related]
12. A hybrid CFHR3-1 gene causes familial C3 glomerulopathy.
Malik TH; Lavin PJ; Goicoechea de Jorge E; Vernon KA; Rose KL; Patel MP; de Leeuw M; Neary JJ; Conlon PJ; Winn MP; Pickering MC
J Am Soc Nephrol; 2012 Jul; 23(7):1155-60. PubMed ID: 22626820
[TBL] [Abstract][Full Text] [Related]
13. Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome.
Moore I; Strain L; Pappworth I; Kavanagh D; Barlow PN; Herbert AP; Schmidt CQ; Staniforth SJ; Holmes LV; Ward R; Morgan L; Goodship TH; Marchbank KJ
Blood; 2010 Jan; 115(2):379-87. PubMed ID: 19861685
[TBL] [Abstract][Full Text] [Related]
14. Complement factor h autoantibodies and age-related macular degeneration.
Dhillon B; Wright AF; Tufail A; Pappworth I; Hayward C; Moore I; Strain L; Kavanagh D; Barlow PN; Herbert AP; Schmidt CQ; Armbrecht AM; Laude A; Deary IJ; Staniforth SJ; Holmes LV; Goodship TH; Marchbank KJ
Invest Ophthalmol Vis Sci; 2010 Nov; 51(11):5858-63. PubMed ID: 20592223
[TBL] [Abstract][Full Text] [Related]
15. Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration.
Cantsilieris S; White SJ; Richardson AJ; Guymer RH; Baird PN
PLoS One; 2012; 7(4):e35255. PubMed ID: 22558131
[TBL] [Abstract][Full Text] [Related]
16. Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent.
Raychaudhuri S; Ripke S; Li M; Neale BM; Fagerness J; Reynolds R; Sobrin L; Swaroop A; Abecasis G; Seddon JM; Daly MJ
Nat Genet; 2010 Jul; 42(7):553-5; author reply 555-6. PubMed ID: 20581873
[No Abstract] [Full Text] [Related]
17. Complement-Regulatory Proteins CFHR1 and CFHR3 and Patient Response to Anti-CD20 Monoclonal Antibody Therapy.
Rogers LM; Mott SL; Smith BJ; Link BK; Sahin D; Weiner GJ
Clin Cancer Res; 2017 Feb; 23(4):954-961. PubMed ID: 27528699
[No Abstract] [Full Text] [Related]
18. Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency.
Lee BH; Kwak SH; Shin JI; Lee SH; Choi HJ; Kang HG; Ha IS; Lee JS; Dragon-Durey MA; Choi Y; Cheong HI
Pediatr Res; 2009 Sep; 66(3):336-40. PubMed ID: 19531976
[TBL] [Abstract][Full Text] [Related]
19. Association of CFHR1 homozygous deletion with acute myelogenous leukemia in the European population.
Fratelli M; Bolis M; Kurosaki M; Dori M; Guarnaccia V; Spinelli O; Alberti M; Valoti E; Pileggi S; Noris M; Remuzzi G; Rambaldi A; Terao M; Garattini E
Leuk Lymphoma; 2016 May; 57(5):1234-7. PubMed ID: 26317246
[No Abstract] [Full Text] [Related]
20. Genome-wide association study identifies susceptibility loci for IgA nephropathy.
Gharavi AG; Kiryluk K; Choi M; Li Y; Hou P; Xie J; Sanna-Cherchi S; Men CJ; Julian BA; Wyatt RJ; Novak J; He JC; Wang H; Lv J; Zhu L; Wang W; Wang Z; Yasuno K; Gunel M; Mane S; Umlauf S; Tikhonova I; Beerman I; Savoldi S; Magistroni R; Ghiggeri GM; Bodria M; Lugani F; Ravani P; Ponticelli C; Allegri L; Boscutti G; Frasca G; Amore A; Peruzzi L; Coppo R; Izzi C; Viola BF; Prati E; Salvadori M; Mignani R; Gesualdo L; Bertinetto F; Mesiano P; Amoroso A; Scolari F; Chen N; Zhang H; Lifton RP
Nat Genet; 2011 Mar; 43(4):321-7. PubMed ID: 21399633
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
