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3.4.2 Gene studies (466)
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Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies60680 Calcium channel blockade reduces mechanical strain-induced extracellular matrix gene response in lamina cribrosa cells
Quill B
British Journal of Ophthalmology 2015; 99: 1009-1014
60605 Aggregate Effects of Intraocular Pressure and Cup-to-Disc Ratio Genetic Variants on Glaucoma in a Multiethnic Asian Population
Tham YC
Ophthalmology 2015; 122: 1149-1157
60141 Exome array analysis identifies CAV1/CAV2 as a susceptibility locus for intraocular pressure
Chen F
Investigative Ophthalmology and Visual Science 2015; 56: 544-551
60508 Association between SNPs of Metalloproteinases and Prostaglandin F2α Receptor Genes and Latanoprost Response in Open-Angle Glaucoma
Ussa F
Ophthalmology 2015; 122: 1040-8.e4
60802 Analysis of the Expression and Polymorphism of APOE, HSP, BDNF, and GRIN2B Genes Associated with the Neurodegeneration Process in the Pathogenesis of Primary Open Angle Glaucoma
Nowak A
BioMed research international 2015; 2015: 258281
60788 Charcot-Marie-Tooth 4B2 caused by a novel mutation in the MTMR13/SBF2 gene in two related Portuguese families
Negrão L
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2014; 33: 144-148
60591 Mutated myocilin and heterozygous Sod2 deficiency act synergistically in a mouse model of open-angle glaucoma
Joe MK
Human Molecular Genetics 2015; 24: 3322-3334
60305 Association between p53 codon 72 (Arg72Pro) polymorphism and primary open-angle glaucoma in Iranian patients
Neamatzadeh H
Iranian biomedical journal 2015; 19: 51-56
60527 Genetic variants associated with different risks for high tension glaucoma and normal tension glaucoma in a Chinese population
Chen Y
Investigative Ophthalmology and Visual Science 2015; 56: 2595-2600
60810 Molecular Analysis of NOTCH2 in Patients with Primary Open-Angle Glaucoma
Jakobsson C
Klinische Monatsblätter für Augenheilkunde 2015; 232: 427-431
60696 MicroRNAs that target RGS5
Banaei-Esfahani A
Iranian journal of basic medical sciences 2015; 18: 108-114
60487 Anirdia-like phenotype caused by 6p25 dosage aberrations
Sadagopan KA
American Journal of Medical Genetics, Part A 2015; 167: 524-528
60658 Hypo- and Hypermorphic FOXC1 Mutations in Dominant Glaucoma: Transactivation and Phenotypic Variability
Medina-Trillo C
PLoS ONE 2015; 10: e0119272
60816 The interactions of genes, age, and environment in glaucoma pathogenesis
Doucette LP
Survey of Ophthalmology 2015; 60: 310-326
60530 Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
Pfirrmann T
Human Molecular Genetics 2015; 24: 3119-3132
60528 A Novel Mgp-Cre Knock-in Mouse Reveals an Anti-calcification/anti-stiffness Candidate Gene in the Trabecular Meshwork and Scleral Peripapillary Region
Borras T
Investigative Ophthalmology and Visual Science 2015; 56: 2203-2214
60105 Detailed assessment of renal function in a proband with Harboyan syndrome caused by a novel homozygous SLC4A11 nonsense mutation
Liskova P
Ophthalmic Research 2015; 53: 30-35
60773 Functional analysis of optineurin and some of its disease-associated mutants
Bansal M
IUBMB Life 2015; 67: 120-128
60445 The genetics of POAG in black South Africans: a candidate gene association study
Williams SE
Scientific reports 2015; 5: 8378
60108 Association between CYP1A1m1 gene polymorphism and primary open-angle glaucoma
Costa NB
Genetics and Molecular Research 2014; 13: 10382-10389
60258 Phenotype and Genotype Correlation in Iranian Primary Congenital Glaucoma Patients
Yazdani S
Journal of Glaucoma 2016; 25: 33-38
60712 Visual impairment in an optineurin mouse model of primary open-angle glaucoma
Tseng HC
Neurobiology of Aging 2015; 36: 2201-2212
60574 Is the GSTM1 null polymorphism a risk factor for primary angle-closure glaucoma among Iranian population?
Safa FK
Acta Medica Iranica 2015; 53: 112-116
60462 Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia
Dubey SK
Molecular Vision 2015; 21: 88-97
60581 Genetic associations in PLEKHA7 and COL11A1 with primary angle closure glaucoma: a meta-analysis
Shuai P
Clinical and Experimental Ophthalmology 2015; 43: 523-530
