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3.4.2 Gene studies (28)
Showing records 1 to 25
Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies48614 Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations
Cornes BK; Khor CC; Nongpiur ME; Xu L; Tay WT; Zheng Y; Lavanya R; Li Y; Wu R; Sim X; Wang YX; Chen P; Teo YY; Chia KS; Seielstad M; Liu J; Hibberd ML; Cheng CY; Saw SM; Tai ES; Jonas JB; Vithana EN; Wong TY; Aung T
Human Molecular Genetics 2012; 21: 437-445
49195 Evaluation of SNPs on Chromosome 2p with Primary Open Angle Glaucoma in the South Indian Cohort
Balasubbu S; Krishnadas SR; Jiao X; Hejtmancik JF; Sundaresan P
Investigative Ophthalmology and Visual Science 2012; 53: 1861-1864
49236 Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese
Nakano M; Ikeda Y; Tokuda Y; Fuwa M; Omi N; Ueno M; Imai K; Adachi H; Kageyama M; Mori K; Kinoshita S; Tashiro K
PLoS ONE 2012; 7: e33389
48809 Genome-wide association studies in the hunt for genes causing primary open angle glaucoma
Burdon KP
Clinical and Experimental Ophthalmology 2012; 40: 358-363
48509 A detailed meta-analysis shows no association between TNF-α -308G/A polymorphism and different forms of glaucoma
Yu QQ; Yao Y
Ophthalmic Research 2012; 47: 47-51
48872 Interactive effects of ATOH7 and RFTN1 in association with adult-onset primary open-angle glaucoma
Chen JH; Wang D; Huang C; Zheng Y; Chen H; Pang CP; Zhang M
Investigative Ophthalmology and Visual Science 2012; 53: 779-785
48764 Variants in ASB10 are associated with open-angle glaucoma
Pasutto F; Keller KE; Weisschuh N; Sticht H; Samples JR; Yang YF; Zenkel M; Schlö,tzer-Schrehardt U; Mardin CY; Frezzotti P; Edmunds B; Kramer PL; Gramer E; Reis A; Acott TS; Wirtz MK
Human Molecular Genetics 2012; 21: 1336-1349
48834 Myocilin mutations among POAG patients from two populations of Tamil Nadu, South India, a comparative analysis
Rose R; Balakrishnan A; Muthusamy K; Arumugam P; Shanmugam S; Gopalswamy J
Molecular Vision 2011; 17: 3243-3253
49214 Lack of association between the C677T single nucleotide polymorphism of the MTHFR gene and glaucoma in Iranian patients
Nilforoushan N; Aghapour S; Raoofian R; Saee Rad S; Greene WK; Fakhraie G; Heidari M
Acta Medica Iranica 2012; 50: 208-212
49321 Polymorphism in the TNF-α(-863) locus associated with reduced risk of primary open angle glaucoma
Wang CY; Shen YC; Wei LC; Lin KH; Feng SC; Yang YY; Chiu CH; Tsai HY
Molecular Vision 2012; 18: 779-785
49322 No association of genetic polymorphisms in CYP1B1 with primary open-angle glaucoma: a meta- and gene-based analysis
Dong S; Yang J; Yu W; Kota P; Xia X; Xu H
Molecular Vision 2012; 18: 786-796
48836 Effects of optineurin siRNA on apoptotic genes and apoptosis in RGC-5 cells
Li H; Ao X; Jia J; Wang Q; Zhang Z
Molecular Vision 2011; 17: 3314-3325
48905 Substratum stiffness and latrunculin B regulate matrix gene and protein expression in human trabecular meshwork cells
Thomasy SM; Wood JA; Kass PH; Murphy CJ; Russell P
Investigative Ophthalmology and Visual Science 2012; 53: 952-958
49006 Non-housekeeping genes expressed in human trabecular meshwork cell cultures
Paylakhi SH; Yazdani S; April C; Fan JB; Moazzeni H; Ronaghi M; Elahi E
Molecular Vision 2012; 18: 241-254
48741 Mitochondrial dysfunction in glaucoma: understanding genetic influences
Lascaratos G; Garway-Heath DF; Willoughby CE; Chau KY; Schapira AH
Mitochondrion 2012; 12: 202-212
49052 Serum levels and H/L gene polymorphism of mannose-binding lectin in primary open angle glaucoma
Dursun O; Yilmaz A; Ayaz L; Tamer L
Current Eye Research 2012; 37: 212-217
48810 Current concepts on primary open-angle glaucoma genetics: a contribution to disease pathophysiology and future treatment
Gemenetzi M; Yang Y; Lotery AJ
Eye 2012; 26: 355-369
48986 Silencing of Fem1cR3 gene expression in the DBA/2J mouse precedes retinal ganglion cell death and is associated with histone deacetylase activity
Pelzel HR; Schlamp CL; Waclawski M; Shaw MK; Nickells RW
Investigative Ophthalmology and Visual Science 2012; 53: 1428-1435
49224 Flt1 and Flk1 mediate regulation of intraocular pressure and their double heterozygosity causes the buphthalmia in mice
Sano K; Katsuta O; Shirae S; Kubota Y; Ema M; Suda T; Nakamura M; Hirashima M
Biochemical and Biophysical Research Communications 2012; 420: 422-427
49319 Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma
Mao M; Solivan-Timpe F; Roos BR; Mullins RF; Oetting TA; Kwon YH; Brzeskiewicz PM; Stone EM; Alward WL; Anderson MG; Fingert JH
Molecular Vision 2012; 18: 705-713
48866 Analysis of copy number variation using whole genome exon-focused array CGH in Korean patients with primary congenital glaucoma
Lee JH; Ki CS; Kim HJ; Suh W; Lee ST; Kim JW; Kee C
Molecular Vision 2011; 17: 3583-3590
48615 PAX6 3' deletion in a family with aniridia
Wawrocka A; Budny B; Debicki S; Jamsheer A; Sowinska A; Krawczynski MR
Ophthalmic Genetics 2012; 33: 44-48
49149 A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family
Jin C; Wang Q; Li J; Zhu Y; Shentu X; Yao K
Molecular Vision 2012; 18: 465-470
48595 Prevalence of high-risk alleles in the LOXL1 gene and its association with pseudoexfoliation syndrome and exfoliation glaucoma in a Latin American population
Jaimes M; Rivera-Parra D; Miranda-Duarte A; Valdé,s G; Zenteno JC
Ophthalmic Genetics 2012; 33: 12-17
49032 Variations in LOXL1 associated with exfoliation glaucoma do not affect amine oxidase activity
Kim S; Kim Y
Molecular Vision 2012; 18: 265-270
