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3.4.2 Gene studies (10)
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Display all abstracts in classification 3.4.2 Gene studies
Search within classification 3.4.2 Gene studies19257 A novel single nucleotide polymorphism, IVS2 -97A>T, in the prostaglandin F2α receptor gene was identified among the Malaysian patients with glaucoma
Hoh BP; Zahary MN; Tajudin LSA; Chieng LL; Cheong MT; Sidek MR; Zulkifli A; Zilfalil BA
Kobe Journal of Medical Sciences 2007; 53: 49-52
19653 Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma
Thorleifsson G; Magnusson KP; Sulem P; Walters GB; Gudbjartsson DF; Stefansson H; Jonsson T; Jonasdottir A; Stefansdottir G
Science 2007; 317: 1397-1400
19282 Disease gene candidates revealed by expression profiling of retinal ganglion cell development
Wang JT; Kunzevitzky NJ; Dugas JC; Cameron M; Barres BA; Goldberg JL
Journal of Neuroscience 2007; 27: 8593-8603
19379 A report of a SNP EX3 1209A>G of prostaglandin F receptor gene among Malaysians
Zahari MN; Peng HB; Ling CL; Tet CM; Tajudin LSA; Alwi Z
International Medical Journal 2007; 14: 89-91
19381 Methylenetetrahydrofolate reductase genetic polymorphisms in patients with primary open-angle glaucoma
Zetterberg M; Tasa G; Palmer MS; Juronen E; Toover E; Blennow K; Zetterberg H
Ophthalmic Genetics 2007; 28: 47-50
19390 Absence of glaucoma in DBA/2J mice homozygous for wild-type versions of Gpnmb and Tyrp1
Howell GR; Libby RT; Marchant JK; Wilson LA; Cosma IM; Smith RS; Anderson MG; John SW
BMC Genetics 2007; 8: 45
19382 Chromosomal abnormalities and glaucoma: A case of congenital glaucoma associated with 9p deletion syndrome
Saha K; Lloyd IC; Russell-Eggitt IM; Taylor DSI
Ophthalmic Genetics 2007; 28: 69-72
19366 Fine mapping of new glaucoma locus GLC1M and exclusion of neuregulin 2 as the causative gene
Fan BJ; Ko WC; Wang DY; Canlas O; Ritch R; Lam DSC; Pang CP
Molecular Vision 2007; 13: 779-784
19367 Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome
Fuse N; Takahashi K; Yokokura S; Nishida K
Molecular Vision 2007; 13: 1005-1009
19334 Col4a1 mutation causes endoplasmic reticulum stress and genetically modifiable ocular dysgenesis
Gould DB; Marchant JK; Savinova OV; Smith RS; John SWM
Human Molecular Genetics 2007; 16: 798-807
