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3.4.2 Gene studies (34)
Showing records 1 to 25
Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies57298 Ultrastructural Abnormalities of the Trabecular Meshwork Extracellular Matrix in Cyp1b1-Deficient Mice
Teixeira LB; Zhao Y; Dubielzig RR; Sorenson CM; Sheibani N
Veterinary pathology 2015; 52: 397-403
57344 Peroxidasin is essential for eye development in the mouse
Yan X; Sabrautzki S; Horsch M; Fuchs H; Gailus-Durner V; Beckers J; Hrabě de Angelis M; Graw J
Human Molecular Genetics 2014; 23: 5597-5614
57464 Lack of association between lysyl oxidase-like 1 polymorphisms and primary open angle glaucoma: a meta-analysis
Sun W; Sheng Y; Weng Y; Xu CX; Williams SE; Liu YT; Hauser MA; Allingham RR; Jin MJ; Chen GD
International Journal of Ophthalmology 2014; 7: 550-556
57196 Mutation analysis of seven known glaucoma-associated genes in Chinese patients with glaucoma
Huang X; Li M; Guo X; Li S; Xiao X; Jia X; Liu X; Zhang Q
Investigative Ophthalmology and Visual Science 2014; 55: 3594-3602
57325 Apolipoprotein E gene ε4ε4 is associated with elevated risk of primary open angle glaucoma in Asians: a meta-analysis
Wang Y; Zhou YF; Zhao BY; Gu ZY; Li SL
BMC Medical Genetics 2014; 15: 60
57220 Myocilin modulates programmed cell death during retinal development
Koch MA; Rosenhammer B; Koschade SE; Braunger BM; Volz C; Jägle H; Tamm ER
Experimental Eye Research 2014; 125: 41-52
57288 Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma
Carnes MU; Liu YP; Allingham RR; Whigham BT; Havens S; Garrett ME; Qiao C; ; Katsanis N; Wiggs JL; Pasquale LR; Ashley-Koch A; Oh EC; Hauser MA
PLoS Genetics 2014; 10: e1004372
57527 Developments in Ocular Genetics: 2013 Annual Review
Aboobakar IF; Allingham RR
Asia-Pacific journal of ophthalmology (Philadelphia, Pa.) 2014; 3: 181-193
57245 Bibliometric network analysis of glaucoma
Dong LY; Yin M; Kang XL
Genetics and Molecular Research 2014; 13: 3577-3585
57482 Differential gene expression in glaucoma
Jakobs TC
Cold Spring Harbor perspectives in medicine 2014; 4: a020636
57091 Identification of a novel MYOC mutation, p.(Trp373), in a family with open angle glaucoma
Crawford A; Souzeau E; Agar A; Ridge B; Dubowsky A; Burdon KP; Craig JE
Gene 2014; 545: 271-275
57289 Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population
Vishal M; Sharma A; Kaurani L; Chakraborty S; Ray J; Sen A; Mukhopadhyay A; Ray K
Scientific reports 2014; 4: 5115
57224 Mechanosensitive release of adenosine 5'-triphosphate through pannexin channels and mechanosensitive upregulation of pannexin channels in optic nerve head astrocytes: A mechanism for purinergic involvement in chronic strain
Beckel JM; Argall AJ; Lim JC; Xia J; Lu W; Coffey EE; Macarak EJ; Shahidullah M; Delamere NA; Zode GS; Sheffield VC; Shestopalov VI; Laties AM; Mitchell CH
GLIA 2014; 62: 1486-1501
57077 Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian origins
Kaurani L; Vishal M; Kumar D; Sharma A; Mehani B; Sharma C; Chakraborty S; Jha P; Ray J; Sen A; Dash D; Ray K; Mukhopadhyay A
Investigative Ophthalmology and Visual Science 2014; 55: 3258-3264
57175 A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LBD1-mediated dimerisation
Cross SH; MacAlinao DG; McKie L; Rose L; Kearney AL; Rainger J; Thaung C; Keighren M; Jadeja S; West K; Kneeland SC; Smith RS; Howell GR; Young F; Robertson M; van T' Hof R; John SW; Jackson IJ
PLoS Genetics 2014; 10: e1004359
57459 Glutathione s-transferase M1 and T1 genetic polymorphisms in Iranian patients with glaucoma
Safa FK; Shahsavari G; Abyaneh RZ
Iranian journal of basic medical sciences 2014; 17: 332-336
57054 Myocilin is involved in NgR1/Lingo-1-mediated oligodendrocyte differentiation and myelination of the optic nerve
Kwon HS; Nakaya N; Abu-Asab M; Kim HS; Tomarev SI
Journal of Neuroscience 2014; 34: 5539-5551
57461 Association of apolipoprotein E-219T>G promoter polymorphism with primary open angle glaucoma in Turkish population
Saglar E; Bozkurt B; Irkec M
International Journal of Ophthalmology 2014; 7: 426-430
57480 Oligomerization of optineurin and its oxidative stress- or E50K mutation-driven covalent cross-linking: possible relationship with glaucoma pathology
Gao J; Ohtsubo M; Hotta Y; Minoshima S
PLoS ONE 2014; 9: e101206
57423 Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study
Al-Haddad C; Abdulaal M; Badra R; Barikian A; Noureddine B; Farra C
Ophthalmic Genetics 2014; 0: 1-6
57368 Molecular Karyotyping of a Dysmorphic Girl from Saudi Arabia with CYP1B1-negative Primary Congenital Glaucoma
Abu-Amero KK; Kondkar AA; Khan AO
Ophthalmic Genetics 2014; 0: 1-4
57425 CYP1B1 gene mutations causing primary congenital glaucoma in Tunisia
Bouyacoub Y; Ben Yahia S; Abroug N; Kahloun R; Kefi R; Khairallah M; Abdelhak S
Annals of Human Genetics 2014; 78: 255-263
57019 Axenfeld-Rieger syndrome: further clinical and array delineation of four unrelated patients with a 4q25 microdeletion
Titheradge H; Togneri F; McMullan D; Brueton L; Lim D; Williams D
American Journal of Medical Genetics, Part A 2014; 164: 1695-1701
57419 Novel mutations in PXDN cause microphthalmia and anterior segment dysgenesis
Choi A; Lao R; Ling-Fung Tang P; Wan E; Mayer W; Bardakjian T; Shaw GM; Kwok PY; Schneider A; Slavotinek A
European Journal of Human Genetics 2015; 23: 337-341
56997 TBK1 gene duplication and normal-tension glaucoma
Ritch R; Darbro B; Menon G; Khanna CL; Solivan-Timpe F; Roos BR; Sarfarzi M; Kawase K; Yamamoto T; Robin AL; Lotery AJ; Fingert JH
JAMA ophthalmology 2014; 132: 544-548
