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Journal Abstract Search
239 related items for PubMed ID: 17003406
1. Analysis of the Y402H variant of the complement factor H gene in age-related macular degeneration. Baird PN, Islam FM, Richardson AJ, Cain M, Hunt N, Guymer R. Invest Ophthalmol Vis Sci; 2006 Oct; 47(10):4194-8. PubMed ID: 17003406 [Abstract] [Full Text] [Related]
2. Gene-environment interaction in progression of AMD: the CFH gene, smoking and exposure to chronic infection. Baird PN, Robman LD, Richardson AJ, Dimitrov PN, Tikellis G, McCarty CA, Guymer RH. Hum Mol Genet; 2008 May 01; 17(9):1299-305. PubMed ID: 18203751 [Abstract] [Full Text] [Related]
3. LOC387715/HTRA1 and complement factor H variants in patients with age-related macular degeneration seen at the mayo clinic. Pulido JS, Peterson LM, Mutapcic L, Bryant S, Highsmith WE. Ophthalmic Genet; 2007 Dec 01; 28(4):203-7. PubMed ID: 18161619 [Abstract] [Full Text] [Related]
4. Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population. Seitsonen S, Lemmelä S, Holopainen J, Tommila P, Ranta P, Kotamies A, Moilanen J, Palosaari T, Kaarniranta K, Meri S, Immonen I, Järvelä I. Mol Vis; 2006 Jul 20; 12():796-801. PubMed ID: 16885922 [Abstract] [Full Text] [Related]
5. Genotype-phenotype correlation of age-related macular degeneration: influence of complement factor H polymorphism. Droz I, Mantel I, Ambresin A, Faouzi M, Schorderet DF, Munier FL. Br J Ophthalmol; 2008 Apr 20; 92(4):513-7. PubMed ID: 18211923 [Abstract] [Full Text] [Related]
6. Association of complement factor H Y402H polymorphism with phenotype of neovascular age related macular degeneration in Israel. Chowers I, Cohen Y, Goldenberg-Cohen N, Vicuna-Kojchen J, Lichtinger A, Weinstein O, Pollack A, Axer-Siegel R, Hemo I, Averbukh E, Banin E, Meir T, Lederman M. Mol Vis; 2008 Apr 20; 14():1829-34. PubMed ID: 18852870 [Abstract] [Full Text] [Related]
10. A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration. Hughes AE, Orr N, Esfandiary H, Diaz-Torres M, Goodship T, Chakravarthy U. Nat Genet; 2006 Oct 20; 38(10):1173-7. PubMed ID: 16998489 [Abstract] [Full Text] [Related]
11. Elastin gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. Kondo N, Honda S, Ishibashi K, Tsukahara Y, Negi A. Invest Ophthalmol Vis Sci; 2008 Mar 20; 49(3):1101-5. PubMed ID: 18326737 [Abstract] [Full Text] [Related]
12. Evidence for association between multiple complement pathway genes and AMD. Dinu V, Miller PL, Zhao H. Genet Epidemiol; 2007 Apr 20; 31(3):224-37. PubMed ID: 17266113 [Abstract] [Full Text] [Related]
13. The common Y402H variant in complement factor H gene is not associated with susceptibility to myocardial infarction and its related risk factors. Stark K, Neureuther K, Sedlacek K, Hengstenberg W, Fischer M, Baessler A, Wiedmann S, Jeron A, Holmer S, Erdmann J, Schunkert H, Hengstenberg C. Clin Sci (Lond); 2007 Aug 20; 113(4):213-8. PubMed ID: 17472578 [Abstract] [Full Text] [Related]
14. Apolipoprotein (APOE) gene is associated with progression of age-related macular degeneration (AMD). Baird PN, Richardson AJ, Robman LD, Dimitrov PN, Tikellis G, McCarty CA, Guymer RH. Hum Mutat; 2006 Apr 20; 27(4):337-42. PubMed ID: 16453339 [Abstract] [Full Text] [Related]
15. 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 01; 17(7):971-7. PubMed ID: 18084039 [Abstract] [Full Text] [Related]
16. Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss. Francis PJ, Hamon SC, Ott J, Weleber RG, Klein ML. J Med Genet; 2009 May 01; 46(5):300-7. PubMed ID: 19015224 [Abstract] [Full Text] [Related]
18. Age-related macular degeneration: a perspective on genetic studies. Patel N, Adewoyin T, Chong NV. Eye (Lond); 2008 Jun 01; 22(6):768-76. PubMed ID: 17491602 [Abstract] [Full Text] [Related]
19. The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms. Liu J, Colville D, Wang YY, Baird PN, Guymer RH, Savige J. Br J Ophthalmol; 2009 Mar 01; 93(3):379-82. PubMed ID: 19019939 [Abstract] [Full Text] [Related]
20. 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 01; 50(11):5070-9. PubMed ID: 19553609 [Abstract] [Full Text] [Related] Page: [Next] [New Search]