advertisement

Topcon

3.4.2 Gene studies (31)

Showing records 1 to 25

Display all abstracts in classification 3.4.2 Gene studies

Search within classification 3.4.2 Gene studies
55745 Cellular processing of myocilin
Qiu Y; Shen X; Shyam R; Yue BY; Ying H
PLoS ONE 2014; 9: e92845
55269 In silico analysis of the molecular machinery underlying aqueous humor production: potential implications for glaucoma
Janssen SF; Gorgels TG; van der Spek PJ; Jansonius NM; Bergen AA
Journal of clinical bioinformatics 2013; 3: 21
55258 Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation-differentiation balance early in life and optic nerve degeneration at old age
Iglesias AI; Springelkamp H; van der Linde H; Severijnen LA; Amin N; Oostra B; Kockx CE; van den Hout MC; van Ijcken WF; Hofman A; Uitterlinden AG; Verdijk RM; Klaver CC; Willemsen R; Van Duijn CM
Human Molecular Genetics 2014; 23: 1320-1332
55755 E50K-OPTN-Induced Retinal Cell Death Involves the Rab GTPase-Activating Protein, TBC1D17 Mediated Block in Autophagy
Chalasani ML; Kumari A; Radha V; Swarup G
PLoS ONE 2014; 9: e95758
55552 Susceptibility to glaucoma damage related to age and connective tissue mutations in mice
Steinhart MR; Cone-Kimball E; Nguyen C; Nguyen TD; Pease ME; Chakravarti S; Oglesby EN; Quigley HA
Experimental Eye Research 2014; 119: 54-60
55577 The role of the 148 Asp/Glu polymorphism of the APE1 gene in the development and progression of primary open angle glaucoma development in the Polish population
Cuchra M; Szaflik JP; Przybylowska-Sygut K; Gacek M; Kaminska A; Szaflik J; Majsterek I
Polish journal of pathology : official journal of the Polish Society of Pathologists 2013; 64: 296-302
55726 Effects of mutations and deletions in the human optineurin gene
Turturro S; Shen X; Shyam R; Yue BY; Ying H
SpringerPlus 2014; 3: 99
55610 Translating the ENCyclopedia Of DNA Elements Project findings to the clinic: ENCODE's implications for eye disease
Sanfilippo PG; Hewitt AW
Clinical and Experimental Ophthalmology 2014; 42: 78-83
55543 Comparison between axonal and retinal ganglion cell gene expression in various optic nerve injuries including glaucoma
Levkovitch-Verbin H; Makarovsky D; Vander S
Molecular Vision 2013; 19: 2526-2541
55676 Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss
Loomis SJ; Kang JH; Weinreb RN; Yaspan BL; Cooke Bailey JN; Gaasterland D; Gaasterland T; Lee RK; Lichter PR; Budenz DL; Liu Y; Realini T; Friedman DS; McCarty CA; Moroi SE; Olson L; Schuman JS; Singh K; Vollrath D; Wollstein G; Zack DJ; Brilliant M; Sit
Ophthalmology 2014; 121: 508-516
55403 Genetics of primary open angle glaucoma
Takamoto M; Araie M
Japanese Journal of Ophthalmology 2014; 58: 1-15
55718 Spatial and temporal localization of caveolin-1 protein in the developing retina
Gu X; Reagan A; Yen A; Bhatti F; Cohen AW; Elliott MH
Adv Exp Med Biol 2014; 801: 15-21
55449 Using the bipartite human phenotype network to reveal pleiotropy and epistasis beyond the gene
Darabos C; Harmon SH; Moore JH
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2014; 0: 188-199
55468 Role of the APOE ε2/ε3/ε4 polymorphism in the development of primary open-angle glaucoma: evidence from a comprehensive meta-analysis
Song Q; Chen P; Liu Q
PLoS ONE 2013; 8: e82347
55498 Genetic and environmental underpinnings to age-related ocular diseases
Seddon JM
Investigative Ophthalmology and Visual Science 2013; 54: ORSF28-30
55336 Analysis of catalase SNP rs1001179 in Saudi patients with primary open angle glaucoma
Abu-Amero KK; Kondkar AA; Mousa A; Osman EA; Al-Obeidan SA
Ophthalmic Genetics 2013; 34: 223-228
55338 Differential up-regulation of Vesl-1/Homer 1 protein isoforms associated with decline in visual performance in a preclinical glaucoma model
Kaja S; Naumchuk Y; Grillo SL; Borden PK; Koulen P
Vision Research 2014; 94: 16-23
55731 Spink2 modulates apoptotic susceptibility and is a candidate gene in the Rgcs1 QTL that affects retinal ganglion cell death after optic nerve damage
Dietz JA; Maes ME; Huang S; Yandell BS; Schlamp CL; Montgomery AD; Allingham RR; Hauser MA; Nickells RW
PLoS ONE 2014; 9: e93564
55412 Involvement of AP-1 and C/EBPβ in upregulation of endothelin B (ETB) receptor expression in a rodent model of glaucoma
He S; Minton AZ; Ma HY; Stankowska DL; Sun X; Krishnamoorthy RR
PLoS ONE 2013; 8: e79183
55766 Identification of genetic loci associated with primary angle-closure glaucoma in the basset hound
Ahram DF; Cook AC; Kecova H; Grozdanic SD; Kuehn MH
Molecular Vision 2014; 20: 497-510
55345 CYP1B1 genotype influences the phenotype in primary congenital glaucoma and surgical treatment
Chen X; Chen Y; Wang L; Jiang D; Wang W; Xia M; Yu L; Sun X
British Journal of Ophthalmology 2014; 98: 246-251
55173 CYP1B1 Mutations are a Major Contributor to Juvenile-Onset Open Angle Glaucoma in Saudi Arabia
Abu-Amero KK; Morales J; Aljasim LA; Edward DP
Ophthalmic Genetics 2015; 36: 184-187
55704 Anticipation, anti-glaucoma drug treatment response and phenotype of a Chinese family with glaucoma caused by the Pro370Leu myocilin mutation
Li CM; Zhang YH; Ye RH; Yi CX; Zhong YM; Cao D; Liu X
International Journal of Ophthalmology 2014; 7: 44-50
55323 Corneal enlargement without optic disk cupping in children with recessive CYP1B1 mutations
Khan AO; Aldahmesh MA; Mohamed JY; Alkuraya FS
Journal of AAPOS 2013; 17: 643-645
55330 Novel occurrence of axenfeld: Rieger syndrome in a patient with blepharophimosis ptosis epicanthus inversus syndrome
Shah BM; Dada T; Panda A; Tanwar M; Bhartiya S; Dada R
Indian Journal of Ophthalmology 2013; 0:

Issue 15-4

Change Issue


advertisement

Oculus