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3.4.2 Gene studies (25)

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26897 Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness
Lu Y
Twin Research and Human Genetics: the Official Journal of the International Society for Twin Studies 2010; 13: 274
26686 Increased optic atrophy type 1 expression protects retinal ganglion cells in a mouse model of glaucoma
Ju W-K; Kim K-Y; Duong-Polk KX; Lindsey JD; Ellisman MH; Weinreb RN
Molecular Vision 2010; 16: 1331-1342
26720 Prostaglandin E(2) receptor subtype EP2- and EP4-regulated gene expression profiling in human ciliary smooth muscle cells
Reitmair A; Lambrecht NWG; Yakubov I; Nieves A; Old D; Donde Y; Dinh D; Burk R; Sachs G; Im WB
Physiol Genomics 2010; 42: 348-360
26689 Screening of CYP1B1 and MYOC in moroccan families with primary congenital glaucoma: Three novel mutations in CYP1B1
Hilal L; Boutayeb S; Serrou A; Refass-Buret L; Shisseh H; Bencherifa F; El Mzibri M; Benazzouz B; Berraho A
Molecular Vision 2010; 16: 1215-1226
26805 The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness
Charlesworth J; Kramer PL; Dyer T; Diego V; Samples JR; Craig JE; Mackey DA; Hewitt AW; Blangero J; Wirtz MK
Investigative Ophthalmology and Visual Science 2010; 51: 3509-3514
26832 Expression of Nogo-A on the retina in rat model with chronic ocular hypertension
Nie Q-Z; Liu Z-L; Sha Q; Gao D-W
International Journal of Ophthalmology 2010; 10: 825-826
26902 Impairment of protein trafficking upon overexpression and mutation of optineurin
Park B; Ying H; Shen X; Park J-S; Qiu Y; Shyam R; Yue BYJT
PLoS ONE 2010; 5: 1-14
26688 Down-regulation of GRP78 in human glaucomatous trabecular meshwork cells
Chai F; Luo R; Li Y; Bai Y; He Y; Wei Y; Yan Z; Ge J; Zhuo Y
Molecular Vision 2010; 16: 1122-1131
26808 A genome-wide association study of optic disc parameters
Ramdas WD; van Koolwijk LME; Ikram MK; Jansonius NM; de Jong PTVM; Bergen AAB; Isaacs A; Amin N; Aulchenko YS; Wolfs RCW
PLoS Genetics 2010; 6: 1-12
26721 Quantitative trait loci associated with murine central corneal thickness
Lively GD; Koehn D; Hedberg-Buenz A; Wang K; Anderson MG
Physiol Genomics 2010; 42: 281-286
26798 Modulation of factors affecting optic nerve head astrocyte migration
Miao H; Crabb AW; Hernandez MR; Lukas TJ
Investigative Ophthalmology and Visual Science 2010; 51: 4096-4103
26625 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size
Macgregor S; Hewitt AW; Hysi PG; Ruddle JB; Medland SE; Henders AK; Gordon SD; Andrew T; McEvoy B; Sanfilippo PG
Human Molecular Genetics 2010; 19: 2716-2724
26800 Global gene expression changes in rat retinal ganglion cells in experimental glaucoma
Wang DY; Ray A; Rodgers K; Ergorul C; Hyman BT; Huang W; Grosskreutz CL
Investigative Ophthalmology and Visual Science 2010; 51: 4084-4095
26702 Genetics workshop: Part 1. The era of molecular ophthalmology
Young TL; Drack AV
Journal of AAPOS 2009; 13: 36-37
26769 Association of IL1A and IL1B loci with primary open angle glaucoma
Mookherjee S; Banerjee D; Chakraborty S; Banerjee A; Mukhopadhyay I; Sen A; Ray K
BMC Medical Genetics 2010; 11: 99
26773 Meta-analysis of association between optineurin gene and primary open-angle glaucoma
Cheng J-W; Li P; Wei R-L
Case Reports and Clinical Practice Review 2010; 16: CR369-377
26795 Amacrine cell gene expression and survival signaling: differences from neighboring retinal ganglion cells
Kunzevitzky NJ; Almeida MV; Goldberg JL
Investigative Ophthalmology and Visual Science 2010; 51: 3800-3812
26847 Role of HIF-1(alpha) and caspase-9 signal in rat retinal injure on chronic high ocular pressure
Gui D-M; Yang Y; Li X; Gao D-W
International Journal of Ophthalmology 2010; 10: 1269-1273
26803 Association of polymorphisms of tumor necrosis factor and tumor protein p53 with primary open-angle glaucoma
Fan BJ; Liu K; Wang DY; Tham CC; Tam PO; Lam DS; Pang CP
Investigative Ophthalmology and Visual Science 2010; 51: 4110-4116
26626 Reduced expression of Pax6 in lens and cornea of mutant mice leads to failure of chamber angle development and juvenile glaucoma
Kroeber M; Davis N; Holzmann S; Kritzenberger M; Shelah-Goraly M; Ofri R; Ashery-Padan R; Tamm ER
Human Molecular Genetics 2010; 19: 3332-3342
26753 Clinical characterization and proposed mechanism of juvenile glaucomaA patient with a chromosome 4p deletion, Wolf-Hirschhorn Syndrome
Curtin J; Moloney G; Grigg J; Sharota Franzco D
Ophthalmic Genetics 2010; 31: 135-138
26502 Genome-wide association study of normal tension glaucoma: Common variants in SRBD1 and ELOVL5 contribute to disease susceptibility
Writing Committee for the Normal Tension Glaucoma Genetic Study Group of Japan Glaucoma Society; Meguro A; Inoko H; Ota M; Mizuki N; Bahram S
Ophthalmology 2010; 117: 1331-1338
26693 Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population
Williams SEI; Whigham BT; Liu Y; Carmichael TR; Qin X; Schmidt S; Ramsay M; Hauser MA; Allingham RR
Molecular Vision 2010; 16: 705-712
26660 Apolipoprotein E genotypes in pseudoexfoliation syndrome and pseudoexfoliation glaucoma
Krumbiegel M; Pasutto F; Mardin CY; Weisschuh N; Paoli D; Gramer E; Weber BHF; Kruse FE; Schlotzer-Schrehardt U; Reis A
Journal of Glaucoma 2010; 19: 561-565
26646 Sturge-weber syndrome with congenital glaucoma and cytochrome P450 (CYP1B1) gene mutations
Tanwar M; Sihota R; Dada T; Gupta V; Das TK; Yadav U; Dada R
Journal of Glaucoma 2010; 19: 398-404

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