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3.4.2 Gene studies (23)

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20997 Transgenic mice expressing the Tyr437His mutant of human myocilin protein develop glaucoma
Zhou Y; Grinchuk O; Tomarev SI
Investigative Ophthalmology and Visual Science 2008; 49: 1932-1939
21002 Gene expression profiles of human trabecular meshwork cells induced by triamcinolone and dexamethasone
Fan BJ; Wang DY; Tham CC; Lam DS; Pang CP
Investigative Ophthalmology and Visual Science 2008; 49: 1886-1897
21167 Myocilin variations and familial glaucoma in Taxiarchis, a small Greek village
Wirtz MK; Konstas AGP; Samples JR; Kaltsos K; Economou A; Dimopoulos A; Georgiadou I; Petersen MB
Molecular Vision 2008; 14: 774-781
21371 The LOXL1 gene variations are not associated with primary open-angle and primary angle-closure glaucomas
Chakrabarti S; Rao KN; Kaur I; Parikh RS; Mandal AK; Chandrasekhar G; Thomas R
Investigative Ophthalmology and Visual Science 2008; 49: 2343-2347
21173 Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma
Aragon-Martin JA; Ritch R; Liebmann J; O'Brien C; Blaaow K; Mercieca F; Spiteri A; Cobb CJ; Damji KF; Tarkkanen A
Molecular Vision 2008; 14: 533-541
21165 Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma
Bhattacharjee A; Banerjee D; Mookherjee S; Acharya M; Banerjee A; Ray A; Sen A; Ray K
Molecular Vision 2008; 14: 841-850
21168 Presence of myocilin sequence variants in Japanese patients with open-angle glaucoma
Mengkegale MG; Fuse N; Miyazawa A; Takahashi K; Seimiya M; Yasui T; Tamai M; Nakazawa T; Nishida K
Molecular Vision 2008; 14: 413-417
21166 C677T polymorphism in the methylenetetrahydrofolate reductase gene is associated with primary closed-angle glaucoma
Michael S; Qamar R; Akhtar F; Khan WA; Ahmed A
Molecular Vision 2008; 14: 661-665
21172 Contributions of MYOC and CYP1B1 mutations to JOAG
Bayat B; Yazdani S; Alavi A; Chiani M; Chitsazian F; Tusi BK; Suri F; Narooie-Nejhad M; Sanati MH; Elahi E
Molecular Vision 2008; 14: 508-517
21175 Absence of optineurin (OPTN) gene mutations in Taiwanese patients with juvenile-onset open-angle glaucoma
Yen Y-C; Yang J-J; Chou M-C; Li S-Y
Molecular Vision 2008; 14: 487-494
21171 Lysyl oxidase-like protein 1 (LOXL1) gene polymorphisms and exfoliation glaucoma in a Central European population
Mossbock G; Renner W; Faschinger C; Schmut O; Wedrich A; Weger M
Molecular Vision 2008; 14: 857-861
21199 RETINOBASE: a web database, data mining and analysis platform for gene expression data on retina
Kalathur RK; Gagniere N; Berthommier G; Poidevin L; Raffelsberger W; Ripp R; Leveillard T; Poch O
BMC Genomics 2008; 9: 208
21170 Glutathione S-transferase M1 and T1 polymorphisms in Arab glaucoma patients
Abu-Amero KK; Morales J; Mohamed GH; Osman MN; Bosley TM
Molecular Vision 2008; 14: 425-430
21174 The role of mitochondrial haplogroups in glaucoma: A study in an Arab population
Abu-Amero KK; Morales J; Bosley TM; Mohamed GH; Cabrera VM
Molecular Vision 2008; 14: 518-522
21113 Phylogenetic evaluation of pathological gene mutations
Isashiki Y
Neuro-Ophthalmology Japan 2007; 24: 443-450
21122 Role of CYP1B1 in glaucoma
Vasiliou V; Gonzalez FJ
Annual review of pharmacology and toxicology 2008; 48: 333-358
21052 Enhanced binding of TBK1 by an optineurin mutant that causes a familial form of primary open-angle glaucoma
Morton S; Hesson L; Peggie M; Cohen P
FEBS Letters 2008; 582: 997-1002
21196 Gpnmb(R150X) allele must be present in bone marrow derived cells to mediate DBA/2J glaucoma
Anderson MG; Nair KS; Amonoo LA; Mehalow A; Trantow CM; Masli S; John SWM
BMC Genetics 2008; 9: 30
20991 Contribution of CYP1B1 mutations and founder effect to primary congenital glaucoma in mexico
Zenteno JC; Hernandez-Merino E; Mejia-Lopez H; Matías-Florentino M; Michel N; Elizondo-Olascoaga C; Korder-Ortega V; Casab-Rueda H; Garcia-Ortiz JE
Journal of Glaucoma 2008; 17: 189-192
21164 A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16
Lin Y; Liu T; Li J; Yang J; Du Q; Wang J; Yang Y; Liu X; Fan Y; Lu F
Molecular Vision 2008; 14: 739-744
20917 Aniridia with preserved visual function: A report of four cases with no mutations in PAX6
Traboulsi EI; Ellison J; Sears J; Maumenee IH; Avallone J; Mohney BG
American Journal of Ophthalmology 2008; 145: 760-764
21176 Deletion of G protein-coupled receptor 48 leads to ocular anterior segment dysgenesis (ASD) through down-regulation of Pitx2
Weng J; Luo J; Cheng X; Jin C; Zhou X; Qu J; Tu L; Ai D; Li D; Wang J
Proceedings of the National Academy of Sciences of the United States of America 2008; 105: 6081-6086
21201 DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity
Fan BJ; Pasquale L; Grosskreutz CL; Rhee D; Chen T; DeAngelis MM; Kim I; Del Bono E; Miller JW; Li T
BMC Medical Genetics 2008; 9: 5

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