116 related articles for article (PubMed ID: 25030427)
1. Mapping genetic variants in the CFH gene for association with leprosy in Han Chinese.
Zhang DF; Wang D; Li YY; Yao YG
Genes Immun; 2014 Oct; 15(7):506-10. PubMed ID: 25030427
[TBL] [Abstract][Full Text] [Related]
2. Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China.
Zhang DF; Huang XQ; Wang D; Li YY; Yao YG
Hum Genet; 2013 Jun; 132(6):629-40. PubMed ID: 23423485
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A genome-wide association study identifies key modulators of complement factor H binding to malondialdehyde-epitopes.
Alic L; Papac-Milicevic N; Czamara D; Rudnick RB; Ozsvar-Kozma M; Hartmann A; Gurbisz M; Hoermann G; Haslinger-Hutter S; Zipfel PF; Skerka C; Binder EB; Binder CJ
Proc Natl Acad Sci U S A; 2020 May; 117(18):9942-9951. PubMed ID: 32321835
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome.
Bernabéu-Herrero ME; Jiménez-Alcázar M; Anter J; Pinto S; Sánchez Chinchilla D; Garrido S; López-Trascasa M; Rodríguez de Córdoba S; Sánchez-Corral P
Mol Immunol; 2015 Oct; 67(2 Pt B):276-86. PubMed ID: 26163426
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. The mtDNA replication-related genes TFAM and POLG are associated with leprosy in Han Chinese from Southwest China.
Wang D; Li GD; Fan Y; Zhang DF; Bi R; Yu XF; Long H; Li YY; Yao YG
J Dermatol Sci; 2017 Dec; 88(3):349-356. PubMed ID: 28958595
[TBL] [Abstract][Full Text] [Related]
9. Missense Variants in HIF1A and LACC1 Contribute to Leprosy Risk in Han Chinese.
Wang D; Fan Y; Malhi M; Bi R; Wu Y; Xu M; Yu XF; Long H; Li YY; Zhang DF; Yao YG
Am J Hum Genet; 2018 May; 102(5):794-805. PubMed ID: 29706348
[TBL] [Abstract][Full Text] [Related]
10. Different hereditary contribution of the CFH gene between polypoidal choroidal vasculopathy and age-related macular degeneration in Chinese Han people.
Huang L; Li Y; Guo S; Sun Y; Zhang C; Bai Y; Li S; Yang F; Zhao M; Wang B; Yu W; Zhao M; Khor CC; Li X
Invest Ophthalmol Vis Sci; 2014 Apr; 55(4):2534-8. PubMed ID: 24692129
[TBL] [Abstract][Full Text] [Related]
11. Common variants of OPA1 conferring genetic susceptibility to leprosy in Han Chinese from Southwest China.
Xiang YL; Zhang DF; Wang D; Li YY; Yao YG
J Dermatol Sci; 2015 Nov; 80(2):133-41. PubMed ID: 26360011
[TBL] [Abstract][Full Text] [Related]
12. Association of the LRRK2 genetic polymorphisms with leprosy in Han Chinese from Southwest China.
Wang D; Xu L; Lv L; Su LY; Fan Y; Zhang DF; Bi R; Yu D; Zhang W; Li XA; Li YY; Yao YG
Genes Immun; 2015 Mar; 16(2):112-9. PubMed ID: 25521227
[TBL] [Abstract][Full Text] [Related]
13. Coding variant I62V in the complement factor H gene is strongly associated with polypoidal choroidal vasculopathy.
Kondo N; Honda S; Kuno S; Negi A
Ophthalmology; 2009 Feb; 116(2):304-10. PubMed ID: 19187823
[TBL] [Abstract][Full Text] [Related]
14. Common variants in the complement factor H gene confer genetic susceptibility to central serous chorioretinopathy.
Miki A; Kondo N; Yanagisawa S; Bessho H; Honda S; Negi A
Ophthalmology; 2014 May; 121(5):1067-72. PubMed ID: 24365176
[TBL] [Abstract][Full Text] [Related]
15. Competition between antagonistic complement factors for a single protein on N. meningitidis rules disease susceptibility.
Caesar JJ; Lavender H; Ward PN; Exley RM; Eaton J; Chittock E; Malik TH; Goiecoechea De Jorge E; Pickering MC; Tang CM; Lea SM
Elife; 2014 Dec; 3():. PubMed ID: 25534642
[TBL] [Abstract][Full Text] [Related]
16. Chronic central serous chorioretinopathy is associated with genetic variants implicated in age-related macular degeneration.
de Jong EK; Breukink MB; Schellevis RL; Bakker B; Mohr JK; Fauser S; Keunen JE; Hoyng CB; den Hollander AI; Boon CJ
Ophthalmology; 2015 Mar; 122(3):562-70. PubMed ID: 25439433
[TBL] [Abstract][Full Text] [Related]
17. Growth of geographic atrophy on fundus autofluorescence and polymorphisms of CFH, CFB, C3, FHR1-3, and ARMS2 in age-related macular degeneration.
Caire J; Recalde S; Velazquez-Villoria A; Garcia-Garcia L; Reiter N; Anter J; Fernandez-Robredo P; Alfredo García-Layana ;
JAMA Ophthalmol; 2014 May; 132(5):528-34. PubMed ID: 24557084
[TBL] [Abstract][Full Text] [Related]
18.
Yang MM; Sun HY; Meng T; Qiu SH; Zeng QQ; Ng TK; Jiang L; Deng TM; Zeng AN; Wang J; Luo XL
Front Immunol; 2021; 12():608723. PubMed ID: 33643312
[No Abstract] [Full Text] [Related]
19. Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation.
Schejbel L; Schmidt IM; Kirchhoff M; Andersen CB; Marquart HV; Zipfel P; Garred P
Genes Immun; 2011 Mar; 12(2):90-9. PubMed ID: 21270828
[TBL] [Abstract][Full Text] [Related]
20. Risk alleles in CFH and ARMS2 are independently associated with systemic complement activation in age-related macular degeneration.
Smailhodzic D; Klaver CC; Klevering BJ; Boon CJ; Groenewoud JM; Kirchhof B; Daha MR; den Hollander AI; Hoyng CB
Ophthalmology; 2012 Feb; 119(2):339-46. PubMed ID: 22133792
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
