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3.4.2 Gene studies (12)
Showing records 1 to 12
Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies14456 Correlation between genotype and phenotype in primary open angle glaucoma of Brazilian families with mutations in exon 3 of the TIGR/MYOC gene
Povoa CA; Santiago Malta RF; de Moraes Rezende M; Santana de Melo KF; Giannella Neto D
Arquivos Brasileiros de Oftalmologia 2006; 69: 289-297
14498 Screening and sequence analysis of TIGR gene mutation in patients with primary open angle glaucoma
Su Y; Wang F; Wang J-Q; Shan Y-C; Liu P; Chen J
Chinese Journal of Clinical Rehabilitation 2006; 10: 114-115
15096 SNPs and interaction analyses of noelin 2, myocilin, and optineurin genes in Japanese patients with open-angle glaucoma
Funayama T; Mashima Y; Ohtake Y; Ishikawa K; Fuse N; Yasuda N; Fukuchi T; Murakami A; Hotta Y; Shimada N
Investigative Ophthalmology and Visual Science 2006; 47: 5368-5375
15019 Low penetrance of His26Asp mutation in the optineurin gene in a Japanese family with normal-tension glaucoma
Yasuda N; Nakamoto K; Funayama T; Mashima Y
Nippon Ganka Gakkai Zasshi 2006; 110: 594-600
15008 OPTN gene: profile of patients with glaucoma from India
Sripriya S; Nirmaladevi J; George R; Hemamalini A; Baskaran M; Prema R; Ve Ramesh S; Karthiyayini T; Amali J; Job S
Molecular Vision 2006; 12: 816-820
15252 Genotype and phenotype correlations in congenital glaucoma: CYP1B1 mutations, goniodysgenesis, and clinical characteristics
Hollander DA; Sarfarazi M; Stoilov I; Wood IS; Fredrick DR; Alvarado JA
American Journal of Ophthalmology 2006; 142: 993-1004
15143 Reduced human and murine corneal thickness in an Axenfeld-Rieger syndrome subtype
Asai-Coakwell M; Backhouse C; Casey RJ; Gage PJ; Lehmann OJ
Investigative Ophthalmology and Visual Science 2006; 47: 4905-4909
15200 Novel CYP1B1 and known PAX6 mutations in anterior segment dysgenesis (ASD)
Chavarria-Soley G; Michels-Rautenstrauss K; Caliebe A; Kautza M; Mardin CY; Rautenstrauss B
Journal of Glaucoma 2006; 15: 499-504
15177 Distribution of optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United States
Hauser MA; Sena DF; Flor J; Walter J; Auguste J; Larocque-Abramson K; Graham F; Delbono E; Haines JL; Pericak-Vance MA
Journal of Glaucoma 2006; 15: 358-363
14759 Investigations on the association between normal tension glaucoma and single nucleotide polymorphisms of the endothelin-1 and endothelin receptor genes
Kim SH; Kim JY; Kim DM; Ko HS; Kim SY; Yoo T; Hwang SS; Park SS
Molecular Vision 2006; 12: 1016-1021
14468 Genetic context determines susceptibility to intraocular pressure elevation in a mouse pigmentary glaucoma
Anderson MG; Libby RT; Mao M; Cosma IM; Wilson LA; Smith RS; John SWM
BMC Biology 2006; 4: 20
14758 Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene
Challa P; Hauser MA; Luna CC; Freedman SF; Pericak Vance M; Yang J; McDonald MT; Allingham RR
Molecular Vision 2006; 12: 1009-1015
