134 related articles for article (PubMed ID: 2575258)
1. Molecular genetics of ornithine aminotransferase defect in gyrate atrophy.
Inana G; Hotta Y; Zintz C; Nakajima A; Shiono T; Kennaway NG; Weleber RG
Prog Clin Biol Res; 1989; 314():99-111. PubMed ID: 2575258
[No Abstract] [Full Text] [Related]
2. Molecular basis of ornithine aminotransferase defect in gyrate atrophy.
Inana G; Hotta Y; Zintz C; Chambers C; Kennaway NG; Weleber RG; Nakajima A; Shiono T
Prog Clin Biol Res; 1991; 362():191-219. PubMed ID: 1672235
[No Abstract] [Full Text] [Related]
3. Expression of human ornithine aminotransferase (OAT) in OAT-deficient Chinese hamster ovary cells and fibroblasts of gyrate atrophy patient.
Hotta Y; Inana G
Jpn J Ophthalmol; 1992; 36(1):28-32. PubMed ID: 1635292
[TBL] [Abstract][Full Text] [Related]
4. [Molecular genetics of gyrate atrophy].
Inana G; Inoue I; Totsuka S; Zintz C; Hotta Y; Shiono T; Nakayasu K; Nakajima A; Ohura T; Kominami E
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):518-22. PubMed ID: 3270857
[No Abstract] [Full Text] [Related]
5. Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency.
Ramesh V; Gusella JF; Shih VE
Mol Biol Med; 1991 Feb; 8(1):81-93. PubMed ID: 1682785
[TBL] [Abstract][Full Text] [Related]
6. Expression defect of ornithine aminotransferase gene in gyrate atrophy.
Inana G; Hotta Y; Zintz C; Takki K; Weleber RG; Kennaway NG; Nakayasu K; Nakajima A; Shiono T
Invest Ophthalmol Vis Sci; 1988 Jul; 29(7):1001-5. PubMed ID: 3417397
[TBL] [Abstract][Full Text] [Related]
7. Gene transfer and expression of human ornithine aminotransferase.
Hotta Y; Inana G
Invest Ophthalmol Vis Sci; 1989 Jun; 30(6):1024-31. PubMed ID: 2732018
[TBL] [Abstract][Full Text] [Related]
8. Three novel mutations of the ornithine aminotransferase (OAT) gene in gyrate atrophy.
Park JK; Herron BJ; O'Donnell JJ; Shih VE; Ramesh V
Genomics; 1992 Oct; 14(2):553-4. PubMed ID: 1427882
[No Abstract] [Full Text] [Related]
9. A 15-bp deletion in exon 5 of the ornithine aminotransferase (OAT) locus associated with gyrate atrophy.
Park JK; O'Donnell JJ; Shih VE; Gusella JF; Ramesh V
Hum Mutat; 1992; 1(4):293-7. PubMed ID: 1301936
[TBL] [Abstract][Full Text] [Related]
10. The ornithine aminotransferase gene in gyrate atrophy of the retina: analysis of expression and gross structure of this gene in cultured fibroblasts.
Shull JD; Pitot HC
In Vitro Cell Dev Biol; 1989 Oct; 25(10):971-6. PubMed ID: 2808228
[TBL] [Abstract][Full Text] [Related]
11. Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences.
Brody LC; Mitchell GA; Obie C; Michaud J; Steel G; Fontaine G; Robert MF; Sipila I; Kaiser-Kupfer M; Valle D
J Biol Chem; 1992 Feb; 267(5):3302-7. PubMed ID: 1737786
[TBL] [Abstract][Full Text] [Related]
12. Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy.
Inana G; Chambers C; Hotta Y; Inouye L; Filpula D; Pulford S; Shiono T
J Biol Chem; 1989 Oct; 264(29):17432-6. PubMed ID: 2793865
[TBL] [Abstract][Full Text] [Related]
13. [Hyperornithinemia and gyrate atrophy: ornithine aminotransferase gene error causing a Finnish disease].
Sipilä I; Valle D; Mitchell GA; Brody LC
Duodecim; 1994; 110(7):681-6. PubMed ID: 8542823
[No Abstract] [Full Text] [Related]
14. Gyrate atrophy of the choroid and retina diagnosed by ornithine-δ-aminotransferase gene analysis: a case report.
Kim SJ; Lim DH; Kim JH; Kang SW
Korean J Ophthalmol; 2013 Oct; 27(5):388-91. PubMed ID: 24082780
[TBL] [Abstract][Full Text] [Related]
15. A deletion in the ornithine aminotransferase gene in gyrate atrophy.
Akaki Y; Hotta Y; Mashima Y; Murakami A; Kennaway NG; Weleber RG; Inana G
J Biol Chem; 1992 Jun; 267(18):12950-4. PubMed ID: 1618792
[TBL] [Abstract][Full Text] [Related]
16. Hyperornithinemia associated with gyrate atrophy of the choroid and retina in a child with myopia.
Shenoi A; L N; Christopher R
Indian Pediatr; 2001 Aug; 38(8):914-8. PubMed ID: 11521006
[No Abstract] [Full Text] [Related]
17. Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2.
Barrett DJ; Bateman JB; Sparkes RS; Mohandas T; Klisak I; Inana G
Invest Ophthalmol Vis Sci; 1987 Jul; 28(7):1037-42. PubMed ID: 3596985
[TBL] [Abstract][Full Text] [Related]
18. Retrovirus-mediated gene transfer of ornithine-delta-aminotransferase into keratinocytes from gyrate atrophy patients.
Jensen TG; Sullivan DM; Morgan RA; Taichman LB; Nussenblatt RB; Blaese RM; Csaky KG
Hum Gene Ther; 1997 Nov; 8(17):2125-32. PubMed ID: 9414260
[TBL] [Abstract][Full Text] [Related]
19. [Gyrate atrophy and craniopharyngioma: a case report].
Angioï-Duprez K; Maalouf T; George JL
J Fr Ophtalmol; 2001 May; 24(5):513-6. PubMed ID: 11397989
[TBL] [Abstract][Full Text] [Related]
20. Rapid and efficient molecular analysis of gyrate atrophy using denaturing gradient gel electrophoresis.
Mashima Y; Shiono T; Inana G
Invest Ophthalmol Vis Sci; 1994 Mar; 35(3):1065-70. PubMed ID: 8125717
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
