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3.4.2 Gene studies (18)
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Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies17036 Aggregated myocilin induces Russell bodies and causes apoptosis: implications for the pathogenesis of myocilin-caused primary open-angle glaucoma
Yam GH; Gaplovska-Kysela K; Zuber C; Roth J
American Journal of Pathology 2007; 170: 100-109
17023 The optic nerve head in myocilin glaucoma
Hewitt AW; Bennett SL; Fingert JH; Cooper RL; Stone EM; Craig JE; Mackey DA
Investigative Ophthalmology and Visual Science 2007; 48: 238-243
16772 Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedigrees
Bennett SL; Hewitt AW; Poulsen JL; Kearns LS; Morgan JE; Craig JE; Mackey DA
Archives of Ophthalmology 2007; 125: 112-116
17044 Polymorphisms of DNA repair genes XRCC1 and XPD and risk of primary open angle glaucoma (POAG)
Guven M; Unal M; Batar B; Eroglu E; Devaroglu K; Tamcelik N; Ucar D; Sarici A
Molecular Vision 2007; 13: 12-17
16774 Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals
Hewitt AW; Bennett SL; Richards JE; Dimasi DP; Booth AP; Inglehearn C; Anwar R; Yamamoto T; Fingert JH; Heon E
Archives of Ophthalmology 2007; 125: 98-104
16769 The quest for genes causing complex traits in ocular medicine: successes, interpretations, and challenges
Iyengar SK
Archives of Ophthalmology 2007; 125: 11-18
16854 The OPA1 gene polymorphism is associated with normal tension and high tension glaucoma
Mabuchi F; Tang S; Kashiwagi K; Yamagata Z; Iijima H; Tsukahara S
American Journal of Ophthalmology 2007; 143: 125-130
16773 Evaluation of the β2-adrenergic receptor gene as a candidate glaucoma gene in 2 ancestral populations
McLaren N; Reed DM; Musch DC; Downs CA; Higashi ME; Santiago C; Radenbaugh PA; Allingham RR; Richards JE; Moroi SE
Archives of Ophthalmology 2007; 125: 105-111
16947 Molecular analysis of the CYP1B1 gene: identification of novel truncating mutations in patients with primary congenital glaucoma
Messina-Baas OM; Gonzalez-Huerta LM; Chima-Galan C; Kofman-Alfaro SH; Rivera-Vega MR; Babayan-Mena I; Cuevas-Covarrubias SA
Ophthalmic Research 2007; 9: 17-23
16771 Differential expression profile prioritization of positional candidate glaucoma genes: the GLC1C locus
Rozsa FW; Scott KM; Pawar H; Samples JR; Wirtz MK; Richards JE
Archives of Ophthalmology 2007; 125: 117-127
16775 A new locus (GLC1H) for adult-onset primary open-angle glaucoma maps to the 2p15-p16 region
Suriyapperuma SP; Child A; Desai T; Brice G; Kerr A; Crick RP; Sarfarazi M
Archives of Ophthalmology 2007; 125: 86-92
17055 Polymorphism in the IL-1(α) (-889) locus associated with elevated risk of primary open angle glaucoma
Wang C-Y; Shen Y-C; Lo F-Y; Su C-H; Lee S-H; Lin K-H; Tsai H-Y; Kuo N-W; Fan S-S
Molecular Vision 2006; 12: 1380-1385
16777 Genetic etiologies of glaucoma
Wiggs JL
Archives of Ophthalmology 2007; 125: 30-37
16920 A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG)
El-Ashry MF; Abd El-Aziz MM; Bhattacharya SS
Journal of Glaucoma 2007; 16: 104-111
17006 Glaucoma with aniridia and isolated congenital glaucoma in siblings: contribution and limits of genetics
Lise-Schneider B; Calvas P; Roche O; Lambert JC; Dufier JL; Costet-Fighiera C
Journal Français d'Ophtalmologie 2007; 30: 44-48
17015 Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations
Strungaru MH; Dinu I; Walter MA
Investigative Ophthalmology and Visual Science 2007; 48: 228-237
17189 Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome
Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF
Molecular Vision 2006; 12: 1448-1460
16846 Normal tension glaucoma is not associated with the interleukin -1α (-889) genetic polymorphism
Wang C-Y; Shen Y-C; Lo F-Y; Su C-H; Lee S-H; Tsai H-Y; Fan S-S
Journal of Glaucoma 2007; 16: 230-233
