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3.4.2 Gene studies (217)
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Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies74499 Together JUN and DDIT3 (CHOP) control retinal ganglion cell death after axonal injury
Syc-Mazurek SB
Molecular Neurodegeneration 2017; 12: 71
74744 A Multi-Locus Genetic Risk Score for Primary Open-Angle Glaucoma (POAG) Variants Is Associated with POAG Risk in a Mediterranean Population: Inverse Correlations with Plasma Vitamin C and E Concentrations
Zanon-Moreno V
International journal of molecular sciences 2017; 18:
74528 A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Khalil A
Frontiers in cardiovascular medicine 2017; 4: 58
74718 FMNL2 with Functions Related to the Cytoskeleton is Partially Regulated by PAX6
Ghorbanpour E
Journal of ophthalmic & vision research 2017; 12: 407-412
74503 Axenfeld-Rieger syndrome
Seifi M
Clinical Genetics 2018; 93: 1123-1130
74367 Prdx6 retards senescence and restores trabecular meshwork cell health by regulating reactive oxygen species
Chhunchha B
Cell death discovery 2017; 3: 17060
74551 Integrated microarray analysis provided novel insights to the pathogenesis of glaucoma
Wang J
Molecular medicine reports 2017; 16: 8735-8746
74208 Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma
Mabuchi F
PLoS ONE 2017; 12: e0183709
74164 Genetic Association of the PARL-ABCC5-HTR3D-HTR3C Locus With Primary Angle-Closure Glaucoma in Chinese
Tang FY
Investigative Ophthalmology and Visual Science 2017; 58: 4384–4389
74674 Microarray expression profile analysis of long non-coding RNAs in optineurin E50K mutant transgenic mice
Li Y
Molecular medicine reports 2017; 16: 1255-1261
74488 Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate
Matovinovic E
Molecular Vision 2017; 23: 660-665
74745 An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Su HA
International journal of medical sciences 2017; 14: 1251-1256
74350 Identification of genes associated with primary open-angle glaucoma by bioinformatics approach
Qiu H
International Ophthalmology 2018; 38: 19-28
74634 A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma
Ghanbari M
Investigative Ophthalmology and Visual Science 2017; 58: 5368-5377
74198 Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population
Gong B
Ophthalmic Genetics 2018; 39: 35-40
74479 RIG-I-Like Receptor Signaling in Singleton-Merten Syndrome
Lu C
Frontiers in genetics 2017; 8: 118
74316 Caveolin-1 Protects Retinal Ganglion Cells against Acute Ocular Hypertension Injury via Modulating Microglial Phenotypes and Distribution and Activating AKT pathway
Zhang L
Scientific reports 2017; 7: 10716
74575 Polymorphism rs11656696 in GAS7 Is Not Associated with Primary Open Angle Glaucoma in a Saudi Cohort
Kondkar AA
Genetic testing and molecular biomarkers 2017; 21: 754-758
74514 Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery
Yu-Wai-Man C
JAMA ophthalmology 2017; 135: 1147-1155
74673 Identifying key genes in glaucoma based on a benchmarked dataset and the gene regulatory network
Chen X
Experimental and therapeutic medicine 2017; 14: 3651-3657
74249 RNA expression in human retina
Li M
Human Molecular Genetics 2017; 26: R68-R74
74739 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
Vande Perre P
European Journal of Medical Genetics 2018; 61: 72-78
74378 Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma
Protas ME
Human Molecular Genetics 2017; 26: 3630-3638
74827 Primary Open-Angle Glaucoma Genetics in African Americans
Restrepo NA
Current genetic medicine reports 2017; 5: 167-174
74547 Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndrome
Taskiran EZ
American Journal of Medical Genetics, Part A 2017; 173: 3143-3152
