148 related articles for article (PubMed ID: 3170546)
1. Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene.
Mitchell GA; Looney JE; Brody LC; Steel G; Suchanek M; Engelhardt JF; Willard HF; Valle D
J Biol Chem; 1988 Oct; 263(28):14288-95. PubMed ID: 3170546
[TBL] [Abstract][Full Text] [Related]
2. Analysis of the human ornithine aminotransferase gene family.
Zintz CB; Inana G
Exp Eye Res; 1990 Jun; 50(6):759-70. PubMed ID: 2373169
[TBL] [Abstract][Full Text] [Related]
3. Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7.
O'Donnell JJ; Vannas-Sulonen K; Shows TB; Cox DR
Am J Hum Genet; 1988 Dec; 43(6):922-8. PubMed ID: 3195589
[TBL] [Abstract][Full Text] [Related]
4. Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase.
Ramesh V; Shaffer MM; Allaire JM; Shih VE; Gusella JF
DNA; 1986 Dec; 5(6):493-501. PubMed ID: 3816496
[TBL] [Abstract][Full Text] [Related]
5. Molecular cloning and nucleotide sequence analysis of mRNA for human kidney ornithine aminotransferase. An examination of ornithine aminotransferase isozymes between liver and kidney.
Kobayashi T; Nishii M; Takagi Y; Titani K; Matsuzawa T
FEBS Lett; 1989 Sep; 255(2):300-4. PubMed ID: 2507357
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.
Mitchell GA; Brody LC; Sipila I; Looney JE; Wong C; Engelhardt JF; Patel AS; Steel G; Obie C; Kaiser-Kupfer M
Proc Natl Acad Sci U S A; 1989 Jan; 86(1):197-201. PubMed ID: 2492100
[TBL] [Abstract][Full Text] [Related]
8. The ornithine aminotransferase-encoding gene family of rat: cloning, characterization, and evolutionary relationships between a single expressed gene and three pseudogenes.
Shull JD; Pennington KL; George SM; Kilibarda KA
Gene; 1991 Aug; 104(2):203-9. PubMed ID: 1916291
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy.
Ramesh V; Benoit LA; Crawford P; Harvey PT; Shows TB; Shih VE; Gusella JF
Am J Hum Genet; 1988 Feb; 42(2):365-72. PubMed ID: 2893548
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.
Mitchell GA; Brody LC; Looney J; Steel G; Suchanek M; Dowling C; Der Kaloustian V; Kaiser-Kupfer M; Valle D
J Clin Invest; 1988 Feb; 81(2):630-3. PubMed ID: 3339136
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Regulation of ornithine aminotransferase in retinoblastomas.
Fagan RJ; Sheffield WP; Rozen R
J Biol Chem; 1989 Dec; 264(34):20513-7. PubMed ID: 2584228
[TBL] [Abstract][Full Text] [Related]
15. Isolation and characterization of an ornithine aminotransferase-related sequence (OATL3) mapping to 10q26.
Geraghty MT; Kearns WG; Pearson PL; Valle D
Genomics; 1993 Aug; 17(2):510-3. PubMed ID: 8406505
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Inheritance of ornithine aminotransferase gene, mRNA, and enzyme defect in a family with gyrate atrophy of the choroid and retina.
Hotta Y; Kennaway NG; Weleber RG; Inana G
Am J Hum Genet; 1989 Mar; 44(3):353-7. PubMed ID: 2916581
[TBL] [Abstract][Full Text] [Related]
19. Promoter region of the rat gene encoding ornithine aminotransferase: transcriptional activity, sequence, and DNase-I-hypersensitive sites.
Shull JD; Pennington KL; Rader AE
Gene; 1993 Mar; 125(2):169-75. PubMed ID: 8462871
[TBL] [Abstract][Full Text] [Related]
20. Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes.
Ramesh V; Eddy R; Bruns GA; Shih VE; Shows TB; Gusella JF
Hum Genet; 1987 Jun; 76(2):121-6. PubMed ID: 2886418
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
