Ramesh V - Search Results

1

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. Ramesh V, et al. Hum Genet. 1987 Jun;76(2):121-6. doi: 10.1007/BF00284906. Hum Genet. 1987. PMID: 2886418

2

Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3.

Ramesh V, Cheng SV, Kozak CA, Herron BJ, Shih VE, Taylor BA, Gusella JF. Ramesh V, et al. Mamm Genome. 1992;3(1):17-22. doi: 10.1007/BF00355836. Mamm Genome. 1992. PMID: 1349842

3

Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophy.

McClatchey AI, Kaufman DL, Berson EL, Tobin AJ, Shih VE, Gusella JF, Ramesh V. McClatchey AI, et al. Among authors: ramesh v. Am J Hum Genet. 1990 Nov;47(5):790-4. Am J Hum Genet. 1990. PMID: 2220818 Free PMC article.

4

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. Ramesh V, et al. Am J Hum Genet. 1988 Feb;42(2):365-72. Am J Hum Genet. 1988. PMID: 2893548 Free PMC article.

5

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. Park JK, et al. Among authors: ramesh v. Hum Mutat. 1992;1(4):293-7. doi: 10.1002/humu.1380010405. Hum Mutat. 1992. PMID: 1301936

6

Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency.

Ramesh V, Gusella JF, Shih VE. Ramesh V, et al. Mol Biol Med. 1991 Feb;8(1):81-93. Mol Biol Med. 1991. PMID: 1682785 Review.

7

The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10.

Wu J, Ramesh V, Kidd JR, Castiglione CM, Myers S, Carson N, Anderson L, Gusella JF, Simpson NE, Kidd KK. Wu J, et al. Among authors: ramesh v. Cytogenet Cell Genet. 1988;48(2):126-7. doi: 10.1159/000132606. Cytogenet Cell Genet. 1988. PMID: 3197452 No abstract available.

8

Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy.

Ramesh V, McClatchey AI, Ramesh N, Benoit LA, Berson EL, Shih VE, Gusella JF. Ramesh V, et al. Among authors: ramesh n. Proc Natl Acad Sci U S A. 1988 Jun;85(11):3777-80. doi: 10.1073/pnas.85.11.3777. Proc Natl Acad Sci U S A. 1988. PMID: 3375240 Free PMC article.

9

Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase.

Ramesh V, Shaffer MM, Allaire JM, Shih VE, Gusella JF. Ramesh V, et al. DNA. 1986 Dec;5(6):493-501. doi: 10.1089/dna.1.1986.5.493. DNA. 1986. PMID: 3816496

10

Chromosomal localization of the gene for human B-cell antigen CD40.

Ramesh N, Ramesh V, Gusella JF, Geha R. Ramesh N, et al. Among authors: ramesh v. Somat Cell Mol Genet. 1993 May;19(3):295-8. doi: 10.1007/BF01233077. Somat Cell Mol Genet. 1993. PMID: 7687385

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