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3.4.2 Gene studies (19)
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Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies17505 Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change
Acharya M; Mookherjee S; Bhattacharjee A; Thakur SK; Bandyopadhyay AK; Sen A; Chakrabarti S; Ray K
BMC molecular biology 2007; 8: 21
18060 Myocilin variants in Indian patients with open-angle glaucoma
Bhattacharjee A; Acharya M; Mukhopadhyay A; Mookherjee S; Banerjee D; Bandopadhyay AK; Thakur SK; Sen A; Ray K
Archives of Ophthalmology 2007; 125: 823-829
18232 A glaucoma-associated mutant of optineurin selectively induces death of retinal ganglion cells which is inhibited by antioxidants
Chalasani ML; Radha V; Gupta V; Agarwal N; Balasubramanian D; Swarup G
Investigative Ophthalmology and Visual Science 2007; 48: 1607-1614
17545 Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds
Hewitt AW; Samples JR; Allingham RR; Jarvela I; Kitsos G; Krishnadas SR; Richards JE; Lichter PR; Petersen MB; Sundaresan P
Molecular Vision 2007; 13: 487-492
18182 Lack of association between interleukin-1 gene cluster polymorphisms and glaucoma in Chinese subjects
How AC; Aung T; Chew X; Yong VH; Lim MC; Lee KY; Toh JY; Li Y; Liu J; Vithana EN
Investigative Ophthalmology and Visual Science 2007; 48: 2123-2126
17436 Role of CYP1B1, MYOC, OPTN and OPTC genes in adult-onset primary open-angle glaucoma: Predominance of CYP1B1 mutations in Indian patients
Kumar A; Basavaraj MG; Gupta SK; Qamar I; Ali AM; Bajaj V; Ramesh TK; Prakash RD; Shetty JS; Dorairaj SK
Molecular Vision 2007; 13: 667-676
17438 Novel LMX1B mutation in familial nail-patella syndrome with variable expression to open angle glaucoma
Milla E; Hernan I; Gamundi MJ; Martinez-Gimeno M; Carballo M
Molecular Vision 2007; 13: 639-648
17539 Molecular genetic analysis of a consanguineous south Indian family with congenital glaucoma: Relevance of genetic testing and counseling
Ramprasad VL; George RJ; Sripriya S; Nirmaladevi J; Vijaya L; Kumaramanickavel G
Ophthalmic Genetics 2007; 28: 17-24
18061 Effects of APOE and CHRNA4 genotypes on retinal nerve fibre layer thickness at the optic disc and on risk for developing exfoliation syndrome
Ritland JS; Utheim TP; Utheim OA; Espeseth T; Lydersen S; Semb SO; Rootwelt H; Elsås T
Acta Ophthalmologica Scandinavica 2007; 85: 257-261
17580 Myocilin mutations among primary open angle glaucoma patients of Kanyakumari district, South India
Rose R; Karthikeyan M; Anandan B; Jayaraman G
Molecular Vision 2007; 13: 497-503
18160 Association between genetic polymorphisms of the prostaglandin F2α receptor gene and response to latanoprost
Sakurai M; Higashide T; Takahashi M; Sugiyama K
Ophthalmology 2007; 114: 1039-1045
17504 Glaucoma-causing myocilin mutants require the peroxisomal targeting signal-1 receptor (PTS1R) to elevate intraocular pressure
Shepard AR; Jacobson N; Millar JC; Pang I-H; Steely HT; Searby CC; Sheffield VC; Stone EM; Clark AF
Human Molecular Genetics 2007; 16: 609-617
17618 Genetic testing for inherited eye disease
Stone EM
Archives of Ophthalmology 2007; 125: 205-212
17631 Molecular genetics of inherited neuropathies
Takashima H
Rinshō shinkeigaku (Clinical neurology) 2006; 46: 760-767
18065 Glutathione S transferase M1 and T1 genetic polymorphisms are related to the risk of primary open-angle glaucoma: a study in a Turkish population
Unal M; Güven M; Devranoğlu K; Ozaydin A; Batar B; Tamçelik N; Görgün EE; Uçar D; Sarici A
British Journal of Ophthalmology 2007; 91: 527-530
18044 Apolipoprotein E polymorphisms in patients with primary open-angle glaucoma
Zetterberg M; Tasa G; Palmér MS; Juronen E; Teesalu P; Blennow K; Zetterberg H
American Journal of Ophthalmology 2007; 143: 1059-1060
17641 Genotype and phenotype correlations in congenital glaucoma
Hollander DA; Sarfarazi M; Stoilov I; Wood IS; Fredrick DR; Alvarado JA
Transactions of the American Ophthalmological Society 2006; 104: 183-193
17957 Study of genetic mutation locus in a family with congenital aniridia
Cong RC; Song SJ; Liu YZ
Chinese Journal of Ophthalmology 2006; 42: 1113-1117
17437 The variant N363S of glucocorticoid receptor in steroid-induced ocular hypertension in Hungarian patients treated with photorefractive keratectomy
Szabo V; Borgulya G; Filkorn T; Majnik J; Banyasz I; Nagy ZZ
Molecular Vision 2007; 13: 659-666
