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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 3 |
1994 | 1 |
1996 | 1 |
1999 | 1 |
2024 | 0 |
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6 results
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Page 1
Rapid and efficient molecular analysis of gyrate atrophy using denaturing gradient gel electrophoresis.
Invest Ophthalmol Vis Sci. 1994 Mar;35(3):1065-70.
Invest Ophthalmol Vis Sci. 1994.
PMID: 8125717
A deletion in the ornithine aminotransferase gene in gyrate atrophy.
Akaki Y, Hotta Y, Mashima Y, Murakami A, Kennaway NG, Weleber RG, Inana G.
Akaki Y, et al.
J Biol Chem. 1992 Jun 25;267(18):12950-4.
J Biol Chem. 1992.
PMID: 1618792
Free article.
Item in Clipboard
Genotype-phenotype correlation of a pyridoxine-responsive form of gyrate atrophy.
Mashima YG, Weleber RG, Kennaway NG, Inana G.
Mashima YG, et al.
Ophthalmic Genet. 1999 Dec;20(4):219-24. doi: 10.1076/opge.20.4.219.2271.
Ophthalmic Genet. 1999.
PMID: 10617919
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Heterogeneity and uniqueness of ornithine aminotransferase mutations found in Japanese gyrate atrophy patients.
Mashima Y, Shiono T, Tamai M, Inana G.
Mashima Y, et al.
Curr Eye Res. 1996 Jul;15(7):792-6. doi: 10.3109/02713689609003464.
Curr Eye Res. 1996.
PMID: 8670789
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A single-base change at a splice acceptor site in the ornithine aminotransferase gene causes abnormal RNA splicing in gyrate atrophy.
Mashima Y, Weleber RG, Kennaway NG, Inana G.
Mashima Y, et al.
Hum Genet. 1992 Nov;90(3):305-7. doi: 10.1007/BF00220086.
Hum Genet. 1992.
PMID: 1487247
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Nonsense-codon mutations of the ornithine aminotransferase gene with decreased levels of mutant mRNA in gyrate atrophy.
Mashima Y, Murakami A, Weleber RG, Kennaway NG, Clarke L, Shiono T, Inana G.
Mashima Y, et al.
Am J Hum Genet. 1992 Jul;51(1):81-91.
Am J Hum Genet. 1992.
PMID: 1609808
Free PMC article.
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