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WGC-2021

3.4.2 Gene studies (142)

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90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
VanderWall KB
Stem cell reports 2020; 15: 52-66
90763 Glaucoma phenotype in a large Chinese family with myocilin Val251Ala mutation
Lu H
Genomics 2020; 112: 5129-5135
90582 No association between polymorphisms and normal-tension glaucoma
Lee JS
Ophthalmic Genetics 2020; 41: 427-431
90268 Lack of correlation between S1 RNA binding domain 1 SNP rs3213787/rs11884064 and normal-tension glaucoma in a population from the Republic of Korea
Jung SH
Medicine 2020; 99: e20066
90090 Expression profile analysis to predict potential biomarkers for glaucoma: BMP1, DMD and GEM
Zhang DW
PeerJ 2020; 8: e9462
90817 Characterization of a novel mutation in the MYOC gene in a Chinese family with primary open‑angle glaucoma
Fan W
Molecular medicine reports 2020; 22: 3263-3270
90180 Primary open angle glaucoma genetics: The common variants and their clinical associations (Review)
Trivli A
Molecular medicine reports 2020; 22: 1103-1110
89975 A comprehensive map of disease networks and molecular drug discoveries for glaucoma
Wang H
Scientific reports 2020; 10: 9719
90064 Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin
Kondkar AA
BMC Medical Genetics 2020; 21: 145
90081 FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma
Or L
Experimental Eye Research 2020; 200: 108220
90783 Updates on the molecular genetics of primary congenital glaucoma (Review)
Ling C
Experimental and therapeutic medicine 2020; 20: 968-977
90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
VanderWall KB
Stem cell reports 2020; 15: 52-66
90324 Coding Variants in and May Contribute to Risk of Primary Angle Closure Glaucoma
Qiao C
DNA and cell biology 2020; 39: 949-957
89943 EAAT1 variants associated with glaucoma
Yanagisawa M
Biochemical and Biophysical Research Communications 2020; 529: 943-949
90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Moschos MM
PLoS ONE 2020; 15: e0233692
90178 Insights into the regulatory molecules involved in glaucoma pathogenesis
Moazzeni H
American journal of medical genetics. Part C, Seminars in medical genetics 2020; 184: 782-827
90537 Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer
Minyaylo O
Data in brief 2020; 31: 106004
90247 Alteration of gene expression in mice after glaucoma filtration surgery
Adachi K
Scientific reports 2020; 10: 15036
90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Liu X
Experimental Eye Research 2020; 197: 108118
89947 Association of interleukin-6 gene polymorphisms and glaucoma: Systematic review and meta-analysis
Wu CL
European Journal of Ophthalmology 2020; 0: 1120672120940198
90271 Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma
Dettoraki M
PLoS ONE 2020; 15: e0233692
90783 Updates on the molecular genetics of primary congenital glaucoma (Review)
Zhang D
Experimental and therapeutic medicine 2020; 20: 968-977
90611 Retinal Ganglion Cells With a Glaucoma OPTN(E50K) Mutation Exhibit Neurodegenerative Phenotypes when Derived from Three-Dimensional Retinal Organoids
Huang KC
Stem cell reports 2020; 15: 52-66
89943 EAAT1 variants associated with glaucoma
Namekata K
Biochemical and Biophysical Research Communications 2020; 529: 943-949
90603 Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa
Li J
Experimental Eye Research 2020; 197: 108118

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