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3.4.2 Gene studies (187)
Showing records 1 to 25
Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies67569 The 6p25 deletion syndrome: An update on a rare neurocristopathy
de Vos IJ
Ophthalmic Genetics 2016; 0: 1-7
67148 A Novel Luciferase Assay For Sensitively Monitoring Myocilin Variants in Cell Culture
Zadoo S
Investigative Ophthalmology and Visual Science 2016; 57: 1939-1950
66829 Genetic Associations of Primary Angle-Closure Disease: A Systematic Review and Meta-analysis
Rong SS
Ophthalmology 2016; 123: 1211-1221
67599 PLEKHA7 Recruits PDZD11 to Adherens Junctions to Stabilize Nectins
Guerrera D
Journal of Biological Chemistry 2016; 291: 11016-11029
67169 Advance in molecular genetic research on primary congenital glaucoma
Li X
Chinese Journal of Medical Genetics 2016; 33: 256-260
67565 PLEKHA7: Cytoskeletal adaptor protein at center stage in junctional organization and signaling
Shah J
International Journal of Biochemistry and Cell Biology 2016; 75: 112-116
67283 Effects of optineurin mutants on SH-SY5Y cell survival
Zhu M
Molecular and Cellular Neurosciences 2016; 74: 18-24
67230 Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma
Vishal M
BMC Medical Genomics 2016; 9: 15
66876 Vascular and autonomic dysregulation in primary open-angle glaucoma
Pasquale LR
Current Opinions in Ophthalmology 2016; 27: 94-101
67232 Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome
Sharma S
Experimental Eye Research 2016; 146: 212-223
67126 ABCB1 variants confer susceptibility to primary open-angle glaucoma and predict individual differences to latanoprost treatment
Liu H
Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie 2016; 80: 115-120
66644 Risk of open angle glaucoma due to tumor necrosis factor alpha gene polymorphisms
Hamid MA
Electronic physician 2016; 8: 1978-1983
67141 An integrative data mining approach to identifying adverse outcome pathway signatures
Oki NO
Toxicology 2016; 350: 49-61
66677 CYP1B1-mediated Pathobiology of Primary Congenital Glaucoma
Faiq MA
Journal of Current Glaucoma Practice 2015; 9: 77-80
66777 Mice Homozygous for a Deletion in the Glaucoma Susceptibility Locus INK4 Show Increased Vulnerability of Retinal Ganglion Cells to Elevated Intraocular Pressure
Gao S
American Journal of Pathology 2016; 186: 985-1005
67113 Polymorphism of CYP46A1 and PPARγ2 Genes in Risk Prediction of Primary Open Angle Glaucoma Among North Indian Population
Chandra A
Middle East African Journal of Ophthalmology 2016; 23: 172-176
67573 Analysis of toll-like receptor rs4986790 polymorphism in Saudi patients with primary open angle glaucoma
Abu-Amero KK
Ophthalmic Genetics 2016; 0: 1-5
67432 Toward Novel Diagnostics for Primary Open-Angle Glaucoma? An Association Study of Polymorphic Variation in Ras Homolog Family Member (A, B, C, D) Genes RHOA, RHOB, RHOC, and RHOD
Saracaloglu A
Omics : a journal of integrative biology 2016; 20: 290-295
67558 Novel BEST1 Mutations and Special Clinical Features of Best Vitelliform Macular Dystrophy
Liu J
Ophthalmic Research 2016; 0:
66802 Association of MMP-9 Gene Polymorphisms with Glaucoma: A Meta-Analysis
Zhang Y
Ophthalmic Research 2016; 55: 172-179
67499 Correlation of Aqueous Humor Lysyl Oxidase Activity with TGF-ß Levels and LOXL1 Genotype in Pseudoexfoliation
Gayathri R
Current Eye Research 2016; 0: 1-8
67050 Epigenetic Mechanisms of the Aging Human Retina
Pennington KL
Journal of experimental neuroscience 2015; 9: 51-79
66812 Analysis of Toll-Like Receptor 2 Polymorphism (rs5743704) in Saudi Patients with Primary Open-Angle Glaucoma
Kondkar AA
Genetic testing and molecular biomarkers 2016; 20: 216-219
67491 An examination of the regulatory mechanism of Pxdn mutation-induced eye disorders using microarray analysis
Yang Y
International Journal of Molecular Medicine 2016; 37: 1449-1456
67553 A novel de novo Myocilin variant in a patient with sporadic juvenile open angle glaucoma
Souzeau E
BMC Medical Genetics 2016; 17: 30
