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3.4.2 Gene studies (13)
Showing records 1 to 13
Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies22938 Multiple gene polymorphisms analysis revealed a different profile of genetic polymorphisms of primary open-angle glaucoma in northern Chinese
Jia L-Y; Tam PO-S; Chiang SW-Y; Ding N; Chen LJ; Yam GH-F; Pang C-P; Wang N-L
Molecular Vision 2009; 15: 89-98
22937 Heterozygous expression of myocilin glaucoma mutants increases secretion of the mutant forms and reduces extracellular processed myocilin
Aroca-Aguilar J-D; Sanchez-Sanchez F; Martinez-Redondo F; Coca-Prados M; Escribano J
Molecular Vision 2008; 14: 2097-2108
22935 Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese
Gong WF; Chiang SWY; Chen LJ; Tam POS; Jia LY; Leung DYL; Geng YQ; Tham CCY; Lam DSC; Ritch R
Molecular Vision 2008; 14: 2381-2389
22932 LOXL1 variants in elderly Japanese patients with exfoliation syndrome/glaucoma, primary open-angle glaucoma, normal tension glaucoma, and cataract
Tanito M; Minami M; Akahori M; Kaidzu S; Takai Y; Ohira A; Iwata T
Molecular Vision 2008; 14: 1898-1905
22929 Optineurin coding variants in Ghanaian patients with primary open-angle glaucoma
Liu Y; Akafo S; Santiago-Turla C; Cohen CS; Larocque-Abramson KR; Qin X; Herndon LW; Challa P; Schmidt S; Hauser MA
Molecular Vision 2008; 14: 2367-2372
22934 Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol
Suri F; Kalhor R; Zargar SJ; Nilforooshan N; Yazdani S; Nezari H; Paylakhi SH; Narooie-Nejhad M; Bayat B; Sedaghati T
Molecular Vision 2008; 14: 2349-2356
22930 Myocilin polymorphisms and high myopia in subjects of European origin
Zayats T; Yanovitch T; Creer RC; McMahon G; Li Y-J; Young TL; Guggenheim JA
Molecular Vision 2009; 15: 213-222
22933 Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma
Firasat S; Riazuddin SA; Khan SN; Riazuddin S
Molecular Vision 2008; 14: 2002-2009
22715 The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma
Chakrabarti S; Kaur K; Rao KN; Mandal AK; Kaur I; Parikh RS; Thomas R
Investigative Ophthalmology and Visual Science 2009; 50: 75-83
23000 Mutation analysis of B3GALTL in Peters Plus syndrome
Reis LM; Tyler RC; Abdul-Rahman O; Trapane P; Wallerstein R; Broome D; Hoffman J; Khan A; Paradiso C; Ron N
American Journal of Medical Genetics, Part A 2008; 146: 2603-2610
22576 A new autosomal dominant Peters' anomaly phenotype expanding the anterior segment dysgenesis spectrum
Berker N; Alanay Y; Elgin U; Volkan-Salanci B; Simsek T; Akarsu N; Alikasifoglu M
Acta Ophthalmologica 2009; 87: 52-57
22498 Investigation of the association between 677C>T and 1298A>C 5,10-methylenetetra- hydrofolate reductase gene polymorphisms and normal-tension glaucoma
Woo SJ; Kim JY; Kim DM; Park SS; Ko HS; Yoo T
Eye 2009; 23: 17-24
22761 Genotype-correlated expression of lysyl oxidase-like 1 in ocular tissues of patients with pseudoexfoliation syndrome/glaucoma and normal patients
Schlotzer-Schrehardt U; Pasutto F; Sommer P; Hornstra I; Kruse FE; Naumann GOH; Reis A; Zenkel M
American Journal of Pathology 2008; 173: 1724-1735