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3.4.2 Gene studies (29)

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25854 Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts
Ayub H; Khan MI; Micheal S; Akhtar F; Ajmal M; Shafique S; Ali SH; den Hollander AI; Ahmed A; Qamar R
Molecular Vision 2010; 16: 18-25
25850 Ethnicity-based subgroup meta-analysis of the association of LOXL1 polymorphisms with glaucoma
Chen H; Chen LJ; Zhang M; Gong W; Tam PO; Lam DS; Pang CP
Molecular Vision 2010; 16: 167-177
26215 Ophthalmological features associated with COL4A1 mutations
Coupry I; Sibon I; Mortemousque B; Rouanet F; Mine M; Goizet C
Archives of Ophthalmology 2010; 128: 483-489
26067 VAV2 and VAV3 as candidate disease genes for spontaneous glaucoma in mice and humans
Fujikawa K; Iwata T; Inoue K; Akahori M; Kadotani H; Fukaya M; Watanabe M; Chang Q; Barnett EM; Swat W
PLoS ONE 2010; 5:2: e9050
25676 Genetic bases for glaucoma
Fuse N
Tohoku Journal of Experimental Medicine 2010; 221: 1-10
25824 KMeyeDB: A graphical database of mutations in genes that cause eye diseases
Kawamura T; Ohtsubo M; Mitsuyama S; Ohno-Nakamura S; Shimizu N; Minoshima S
Human Mutation 2010; 31: 667-674
25885 Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern Greece
Kitsos G; Petrou Z; Grigoriadou M; Samples JR; Hewitt AW; Kokotas H; Giannoulia-Karantana A; Mackey DA; Wirtz MK; Moschou M
Clinical Ophthalmology 2010; 4: 171-178
25843 AQP1 and SLC4A10 as candidate genes for primary open-angle glaucoma
Liu W; Liu Y; Qin XJ; Schmidt S; Hauser MA; Allingham RR
Molecular Vision 2010; 16: 93-97
26202 Estrogen receptor beta gene polymorphism and intraocular pressure elevation in female patients with primary open-angle glaucoma
Mabuchi F; Sakurada Y; Kashiwagi K; Yamagata Z; Iijima H; Tsukahara S
American Journal of Ophthalmology 2010; 149: 826-830
25654 Genetic variants of CYP1B1 and WDR36 in the patients with primary congenital glaucoma and primary open angle glaucoma from Saint-Petersburg
Motushchuk AE; Komarova TI; Grudinina NA; Rakhmanov VV; Mandel'shtam MI; Astakhov IS; Vasil'ev VB
Genetika 2009; 45: 1659-1667
25730 New mutation in the MYOC gene and its association with primary open-angle glaucoma in a Chinese family
Qu X; Zhou X; Zhou K; Xie X; Tian Y
Molecular Biology Reports 2010; 37: 255-261
25861 Wnt gene expression in human trabecular meshwork cells
Shyam R; Shen X; Yue BY; Wentz-Hunter KK
Molecular Vision 2010; 16: 122-129
26174 Little evidence for association of the glaucoma gene MYOC with open-angle glaucoma
Sohn S; Hur W; Choi YR; Chung YS; Ki CS; Kee C
British Journal of Ophthalmology 2010; 94: 639-642
26105 Association of POAG risk factors and the Thr377Met MYOC mutation in an isolated Greek population
Wirtz MK; Samples JR; Toumanidou V; Charlesworth J; Mikropoulos DG; Kaltsos K; Economou A; Dimopoulos A; Georgiadou IN; Moumtzis G
Investigative Ophthalmology and Visual Science 2010; 51: 3055-3060
25946 Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population
Wolf C; Gramer E; Muller-Myhsok B; Pasutto F; Wissinger B; Weisschuh N
BMC Genetics 2010; 11: 8
25855 A novel optineurin genetic mutation associated with open-angle glaucoma in a Chinese family
Xiao Z; Meng Q; Tsai JC; Yuan H; Xu N; Li Y
Molecular Vision 2009; 15: 1649-1654
26068 Posttranslational modifications, localization, and protein interactions of optineurin, the product of a glaucoma gene
Ying H; Shen X; Park B; Yue BYJT
PLoS ONE 2010; 5:2: e9168
26110 Retinal cell responses to elevated intraocular pressure: a gene array comparison between the whole retina and retinal ganglion cell layer
Guo Y; Cepurna WO; Dyck JA; Doser TA; Johnson EC; Morrison JC
Investigative Ophthalmology and Visual Science 2010; 51: 3003-3018
25859 Analysis of microsatellite polymorphisms within the GLC1F locus in Japanese patients with normal tension glaucoma
Murakami K; Meguro A; Ota M; Shiota T; Nomura N; Kashiwagi K; Mabuchi F; Iijima H; Kawase K; Yamamoto T
Molecular Vision 2010; 16: 462-466
25786 Molecular complexity of primary open angle glaucoma: current concepts
Ray K; Mookherjee S
Journal of genetics 2009; 88: 451-467
25929 ASK1 deficiency attenuates neural cell death in GLAST-deficient mice, a model of normal tension glaucoma
Harada C; Namekata K; Guo X; Yoshida H; Mitamura Y; Matsumoto Y; Tanaka K; Ichijo H; Harada T
Cell Death and Differentiation ;
26069 SPARC deficiency results in improved surgical survival in a novel mouse model of glaucoma filtration surgery
Seet L-F; Su R; Barathi VA; Lee WS; Poh R; Heng YM; Manser E; Vithana EN; Aung T; Weaver M
PLoS ONE 2010; 5:2: e9415
26073 CYP1B1 Gene Analysis in Primary Congenital Glaucoma Brazilian Patients: Novel Mutations and Association With Poor Prognosis
Paolera MD; Cabral de Vasconcellos JP; Umbelino CC; Kasahara N; Rocha MN; Richeti F; Costa VP; Tavares A; de Melo MB
Journal of Glaucoma 2010; 19: 176-182
25852 Identification of four novel cytochrome P4501B1 mutations (p.I94X, p.H279D, p.Q340H, and p.K433K) in primary congenital glaucoma patients
Tanwar M; Dada T; Sihota R; Dada R
Molecular Vision 2009; 15: 2926-2937
25848 Association of toll-like receptor 2 gene polymorphisms with normal tension glaucoma
Nakamura J; Meguro A; Ota M; Nomura E; Nishide T; Kashiwagi K; Mabuchi F; Iijima H; Kawase K; Yamamoto T
Molecular Vision 2009; 15: 2905-2910

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