advertisement
3.4.2 Gene studies (24)
Showing records 1 to 24
Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies21731 Glaucoma phenotype in a large Swiss pedigree with the myocilin Gly367Arg mutation
Iliev ME; Bodmer S; Gallati S; Lanz R; Sturmer J; Katsoulis K; Wolf S; Trittibach P; Sarra GM
Eye 2008; 22: 880-888
21578 Aqueous humor myocilin protein levels in normal, genetic carriers, and glaucoma Beagles
MacKay EO; Kallberg ME; Gelatt KN
Veterinary Ophthalmology 2008; 11: 177-185
21431 Role of the ETB receptor in retinal ganglion cell death in glaucoma
Krishnamoorthy RR; Rao VR; Dauphin R; Prasanna G; Johnson C; Yorio T
Canadian Journal of Physiology and Pharmacology 2008; 86: 380-393
21830 Microsatellite analysis of the GLC1B locus on chromosome 2 points to NCK2 as a new candidate gene for normal-tension glaucoma
Akiyama M; Yatsu K; Ota M; Katsuyama Y; Kashiwagi K; Mabuchi F; Iijima H; Kawase K; Yamamoto T; Nakamura M
British Journal of Ophthalmology 2008; 92: 1293-1296
21591 Rgcs1, a dominant QTL that affects retinal ganglion cell death after optic nerve crush in mice
Dietz JA; Li Y; Chung LM; Yandell BS; Schlamp CL; Nickells RW
BMC Neuroscience 2008; 9: 74
21568 Association between MYOC.mt1 promoter polymorphism and risk of primary open-angle glaucoma: A systematic review and meta-analysis
Liu T; Zeng D; Zeng C; He X
Medical Science Monitor 2008; 14: RA87-RA93
21766 Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations
Liu Y; Schmidt S; Qin X; Gibson J; Hutchins K; Santiago-Turla C; Wiggs JL; Budenz DL; Akafo S; Challa P
Investigative Ophthalmology and Visual Science 2008; 49: 3465-3468
21597 Susceptibility to glaucoma: Differential comparison of the astrocyte transcriptome from glaucomatous African American and Caucasian American donors
Lukas TJ; Miao H; Chen L; Riordan SM; Li W; Crabb AM; Wise A; Du P; Lin SM; Hernandez MR
Genome biology 2008; 9: R111
21810 Gillies Lecture: Dissecting glaucoma: Understanding the molecular risk factors
Mackey DA
Clinical and Experimental Ophthalmology 2008; 36: 403-409
21665 Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma
Mihelec M; St Heaps L; Flaherty M; Billson F; Rudduck C; Tam PPL; Grigg JR; Peters GB; Jamieson RV
Twin Research and Human Genetics: the Official Journal of the International Society for Twin Studies 2008; 11: 412-421
21814 Elevated amounts of myocilin in the aqueous humor of transgenic mice cause significant changes in ocular gene expression
Paper W; Kroeber M; Heersink S; Stephan DA; Fuchshofer R; Russell P; Tamm ER
Experimental Eye Research 2008; 87: 257-267
21506 The primary open-angle glaucoma gene WDR36 functions in ribosomal RNA processing and interacts with the p53 stress-response pathway
Skarie JM; Link BA
Human Molecular Genetics 2008; 17: 2474-2485
21646 Research advances in genes associated with primary open-angle glaucoma
Song W; Ren B-C
International Journal of Ophthalmology 2008; 8: 1426-1428
21539 Plasminogen activator inhibitor-1 4G/5G gene polymorphism and primary open-angle glaucoma
Mossbock G; Weger M; Faschinger C; Schmut O; Renner W
Molecular Vision 2008; 14: 1240-1244
21575 Heterozygous FOXC1 mutation (M161K) associated with congenital glaucoma and aniridia in an infant and a milder phenotype in her mother
Khan AO; Aldahmesh MA; Al-Amri A
Ophthalmic Genetics 2008; 29: 67-71
21550 Fine mapping of the GLC1K juvenile primary open-angle glaucoma locus and exclusion of candidate genes
Sud A; Del Bono EA; Haines JL; Wiggs JL
Molecular Vision 2008; 14: 1319-1326
21546 Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle-closure glaucoma and short axial length eyes
Aung T; Lim MCC; Wong TTL; Thalamuthu A; Yong VHK; Venkataraman D; Venkatraman A; Chew PTK; Vithana EN
Molecular Vision 2008; 14: 1313-1318
21686 Lack of association between the rs2664538 polymorphism in the MMP-9 gene and primary angle-closure glaucoma in Singaporean subjects
Aung T; Yong VH; Lim MC; Venkataraman D; Toh JY; Chew PT; Vithana EN
Journal of Glaucoma 2008; 17: 257-258
21549 Evaluation of LOXL1 polymorphisms in eyes with exfoliation glaucoma in Japanese
Fuse N; Miyazawa A; Nakazawa T; Mengkegale MG; Otomo T; Nishida K
Molecular Vision 2008; 14: 1338-1343
21544 Lysyl oxidase-like 1 gene polymorphisms in Japanese patients with primary open angle glaucoma and exfoliation syndrome
Mabuchi F; Sakurada Y; Kashiwagi K; Yamagata Z; Iijima H; Tsukahara S
Molecular Vision 2008; 14: 1303-1308
21542 LOXL1 genetic polymorphisms are associated with exfoliation glaucoma in the Japanese population
Mori K; Imai K; Matsuda A; Ikeda Y; Naruse S; Hitora-Takeshita H; Nakano M; Taniguchi T; Omi N; Tashiro K
Molecular Vision 2008; 14: 1037-1040
21815 Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese
Ozaki M; Lee KY; Vithana EN; Yong VH; Thalamuthu A; Mizoguchi T; Venkatraman A; Aung T
Investigative Ophthalmology and Visual Science 2008; 49: 3976-3980
21540 Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma
Rao KN; Ritch R; Dorairaj SK; Kaur I; Liebmann JM; Thomas R; Chakrabarti S
Molecular Vision 2008; 14: 1254-1262
21744 Intraocular pressure response to topical β-blockers associated with an ADRB2 single-nucleotide polymorphism
McCarty CA; Burmester JK; Mukesh BN; Patchett RB; Wilke RA
Archives of Ophthalmology 2008; 126: 959-963
