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3.4.2 Gene studies (143)
Showing records 1 to 25
Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies91693 Clinical and genetic analysis of Ser341Pro variant in a Korean family with primary open angle glaucoma
Moon S
International Journal of Ophthalmology 2020; 13: 1689-1696
91382 Genetic pre-screening for glaucoma in population-based epidemiology: protocol for a double-blind prospective screening study within Lifelines (EyeLife)
Neustaeter A
BMC Ophthalmology 2021; 21: 18
91156 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
Yamamoto Y
Scientific reports 2020; 10: 20936
91387 Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis
Thakur N
BMC Medical Genomics 2021; 14: 1
91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
Canut MI
Scientific reports 2021; 11: 1583
91099 CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix
Bonet-Fernández JM
Human Genetics 2020; 139: 1209-1231
91504 Predicting the Future of Genetic Risk Profiling of Glaucoma: A Narrative Review
Han X
JAMA ophthalmology 2021; 139: 224-231
91555 Association of gene polymorphisms with primary open angle glaucoma in Brazilian patients
Occhiutto ML
Ophthalmic Genetics 2021; 42: 53-61
91259 Prevalence of MYOC risk variants for glaucoma in different populations
Liuska PJ
Acta Ophthalmologica 2021; 99: e1090-e1097
91768 A novel mutation in the aspartate beta-hydroxylase () gene is associated with a rare form of Traboulsi syndrome
Senthil S
Ophthalmic Genetics 2021; 42: 28-34
91040 Polygenetic-Risk Scores for A Glaucoma Risk Interact with Blood Pressure, Glucose Control, and Carbohydrate Intake
Jee D
Nutrients 2020; 12:
91397 Coinheritance of and variants in a Chinese family with juvenile-onset primary open-angle glaucoma: A case report
Yang X
World journal of clinical cases 2021; 9: 697-706
91085 Evaluation of silent information regulator T (SIRT) 1 and Forkhead Box O (FOXO) transcription factor 1 and 3a genes in glaucoma
Yaman D
Molecular Biology Reports 2020; 47: 9337-9344
91280 MYOC Gene Sequencing Analysis in Primary Open-Angle Glaucoma Patients from the Centre Region of Portugal
Silva F
Acta medica portuguesa 2020; 0:
91224 Disruption of 24-Hour Rhythm in Intraocular Pressure Correlates with Retinal Ganglion Cell Loss in Glaucoma
Neroev V
International journal of molecular sciences 2020; 22:
91727 A clinical characteristics and genetic analysis of a case of Rubinstein-Taybi syndrome with glaucoma
Huang FR
European review for medical and pharmacological sciences 2021; 25: 1447-1454
91826 Ganglion cells apoptosis in diabetic rats as early prediction of glaucoma: a study of Brn3b gene expression and association with change of quantity of NO, caspase-3, NF-κB, and TNF-α
Tjandra I
International Journal of Ophthalmology 2020; 13: 1872-1879
91808 A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home Tonometry
Qassim A
Ophthalmology. Glaucoma 2021; 4: 411-420
91423 Long Non-coding RNA MALAT1 Alleviates the Elevated Intraocular Pressure (Eiop)-induced Glaucoma Progression via Sponging miR-149-5p
Wang L
Current Eye Research 2020; 0: 1-9
91164 The loss of microglia activities facilitates glaucoma progression in association with CYP1B1 gene mutation (p.Gly61Glu)
Alghamdi A
PLoS ONE 2020; 15: e0241902
91634 In-depth analysis of eight susceptibility loci of primary angle closure glaucoma in Han Chinese
Shi H
Experimental Eye Research 2021; 202: 108350
91825 MLIP genotype as a predictor of pharmacological response in primary open-angle glaucoma and ocular hypertension
Villa O
Scientific reports 2021; 11: 1583
91826 Ganglion cells apoptosis in diabetic rats as early prediction of glaucoma: a study of Brn3b gene expression and association with change of quantity of NO, caspase-3, NF-κB, and TNF-α
Soeharso P
International Journal of Ophthalmology 2020; 13: 1872-1879
91768 A novel mutation in the aspartate beta-hydroxylase () gene is associated with a rare form of Traboulsi syndrome
Sharma S
Ophthalmic Genetics 2021; 42: 28-34
91040 Polygenetic-Risk Scores for A Glaucoma Risk Interact with Blood Pressure, Glucose Control, and Carbohydrate Intake
Huang S
Nutrients 2020; 12:
