Rozen R - Search Results

1

Assignment of the gene for the core protein II (UQCRC2) subunit of the mitochondrial cytochrome bc1 complex to human chromosome 16p12.

Duncan AM, Ozawa T, Suzuki H, Rozen R. Duncan AM, et al. Among authors: rozen r. Genomics. 1993 Nov;18(2):455-6. doi: 10.1006/geno.1993.1500. Genomics. 1993. PMID: 8288258 No abstract available.

2

Assignment of the gene for the cytochrome c1 subunit of the mitochondrial cytochrome bc1 complex (CYC1) to human chromosome 8q24.3.

Duncan AM, Ozawa T, Suzuki H, Rozen R. Duncan AM, et al. Among authors: rozen r. Genomics. 1994 Jan 15;19(2):400-1. doi: 10.1006/geno.1994.1084. Genomics. 1994. PMID: 8188279 No abstract available.

3

Assignment of the gene (UQCRFS1) for the Rieske iron-sulfur protein subunit of the mitochondrial cytochrome bc1 complex to the 22q13 and 19q12-q13.1 regions of the human genome.

Duncan AM, Anderson L, Duff C, Ozawa T, Suzuki H, Worton R, Rozen R. Duncan AM, et al. Among authors: rozen r. Genomics. 1994 May 1;21(1):281-3. doi: 10.1006/geno.1994.1260. Genomics. 1994. PMID: 8088805 No abstract available.

4

Localization of short/branched chain acyl-CoA dehydrogenase (ACADSB) to human chromosome 10.

Arden KC, Viars CS, Fu K, Rozen R. Arden KC, et al. Among authors: rozen r. Genomics. 1995 Feb 10;25(3):743-5. doi: 10.1016/0888-7543(95)80023-f. Genomics. 1995. PMID: 7759115

5

Isolation and expression of a cDNA encoding the precursor for a novel member (ACADSB) of the acyl-CoA dehydrogenase gene family.

Rozen R, Vockley J, Zhou L, Milos R, Willard J, Fu K, Vicanek C, Low-Nang L, Torban E, Fournier B. Rozen R, et al. Genomics. 1994 Nov 15;24(2):280-7. doi: 10.1006/geno.1994.1617. Genomics. 1994. PMID: 7698750

6

Assignment of the gene for cystinuria (SLC3A1) to human chromosome 2p21 by fluorescence in situ hybridization.

Zhang XX, Rozen R, Hediger MA, Goodyer P, Eydoux P. Zhang XX, et al. Among authors: rozen r. Genomics. 1994 Nov 15;24(2):413-4. doi: 10.1006/geno.1994.1644. Genomics. 1994. PMID: 7698775 No abstract available.

7

Chromosomal localization of the gene for the human trifunctional enzyme, methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase.

Rozen R, Barton D, Du J, Hum DW, MacKenzie RE, Francke U. Rozen R, et al. Am J Hum Genet. 1989 Jun;44(6):781-6. Am J Hum Genet. 1989. PMID: 2786332 Free PMC article.

8

A pseudogene on the X chromosome for the human trifunctional enzyme MTHFD (methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase).

Italiano C, John SW, Hum DW, MacKenzie RE, Rozen R. Italiano C, et al. Among authors: rozen r. Genomics. 1991 Aug;10(4):1073-4. doi: 10.1016/0888-7543(91)90201-o. Genomics. 1991. PMID: 1916813

9

Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease.

Slipetz DM, Aprille JR, Goodyer PR, Rozen R. Slipetz DM, et al. Among authors: rozen r. Am J Hum Genet. 1991 Mar;48(3):502-10. Am J Hum Genet. 1991. PMID: 1847791 Free PMC article.

10

Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene.

Leclerc D, Odièvre M, Wu Q, Wilson A, Huizenga JJ, Rozen R, Scherer SW, Gravel RA. Leclerc D, et al. Among authors: rozen r. Gene. 1999 Nov 15;240(1):75-88. doi: 10.1016/s0378-1119(99)00431-x. Gene. 1999. PMID: 10564814

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