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3.4.1 Linkage studies (16)
Showing records 1 to 16
Display all abstracts in classification 3.4.1 Linkage studies
Search within classification 3.4.1 Linkage studies12694 Evidence for a novel glaucoma locus at chromosome 3p21-22
Baird PN; Foote SJ; Mackey DA; Craig J; Speed TP; Bureau A
Human Genetics 2005; 117: 249-257
13055 A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma families
Baird PN; Richardson AJ; Mackey DA; Craig JE; Faucher M; Raymond V
American Journal of Ophthalmology 2005; 140: 760-762
12692 VAMP5 and VAMP8 are most likely not involved in primary open-angle glaucoma
Brinkmann JFF; Ottenheim CPE; de Jong LAMS; Zegers RHC; de Smet MD; de Jong PTVM; Bergen AAB
Molecular Vision 2005; 11: 582-586
12685 Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India
Chakrabarti S; Kaur K; Komatireddy S; Acharya M; Devi KR; Mukhopadhyay A; Mandal AK; Hasnain SE; Chandrasekhar G; Thomas R
Molecular Vision 2005; 11: 111-113
13155 Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree
Charlesworth JC; Dyer TD; Stankovich JM; Blangero J; Mackey DA; Craig JE; Green CM; Foote SJ; Baird PN; Sale MM
Investigative Ophthalmology and Visual Science 2005; 46: 3723-3729
12687 A compound heterozygous change found in Peters' anomaly
Churchill AJ; Yeung A
Molecular Vision 2005; 11: 66-70
12690 SNPs and interaction analyses of myocilin, optineurin, and apolipoprotein E in primary open angle glaucoma patients
Fan BJ; Wang DY; Fan DSP; Sin Tam PO; Lam DSC; Yung Tham CC; Lam CY; Lau TC; Pang CP
Molecular Vision 2005; 11: 625-631
12693 Association between glaucoma and gene polymorphism of endothelin type A receptor
Ishikawa K; Funayama T; Ohtake Y; Kimura I; Ideta H; Nakamoto K; Yasuda N; Fukuchi T; Fujimaki T; Murakami A
Molecular Vision 2005; 11: 431-437
12697 Analysis of rare variants and common haplotypes in the optineurin gene in Swedish glaucoma cases
Jansson M; Wadelius C; Rezaie T; Sarfarazi M
Ophthalmic Genetics 2005; 26: 85-89
13161 Evidence for association of endothelial nitric oxide synthase gene in subjects with glaucoma and a history of migraine
Logan JF; Chakravarthy U; Hughes AE; Patterson CC; Jackson JA; Rankin SJ
Investigative Ophthalmology and Visual Science 2005; 46: 3221-3226
12691 The apolipoprotein E gene polymorphism is associated with open angle glaucoma in the Japanese population
Mabuchi F; Tang S; Ando D; Yamakita M; Wang J; Kashiwagi K; Yamagata Z; Iijima H; Tsukahara S
Molecular Vision 2005; 11: 609-612
12686 Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma
Mukhopadhyay A; Komatireddy S; Acharya M; Bhattacharjee A; Mandal AK; Thakur SKD; Chandrasekhar G; Banerjee A; Thomas R; Chakrabarti S
Molecular Vision 2005; 11: 792-797
12689 A novel PAX6 gene mutation in a Chinese family with aniridia
Song S; Liu Y; Guo S; Zhang L; Zhang X; Wang S; Lu A; Li L
Molecular Vision 2005; 11: 335-337
12688 Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patients
Weisschuh N; Neumann D; Wolf C; Wissinger B; Gramer E
Molecular Vision 2005; 11: 284-287
12684 Autoimmunity against neurofilament protein and its possible association with HLA-DRB1
Yano T; Yamada K; Kimura A; Takeshita T; Minohara M; Kira JI; Senju S; Nishimura Y; Tanihara H
Immunology Letters 2005; 100: 164-169
13145 β1-adrenergic receptor polymorphisms and clinical efficacy of betaxolol hydrochloride in normal volunteers
Schwartz SG; Puckett BJ; Allen RC; Castillo IG; Leffler CT
Ophthalmology 2005; 112: 2131-2136
