Mitchell GA - Search Results

1

Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution.

Boukaftane Y, Duncan A, Wang S, Labuda D, Robert MF, Sarrazin J, Schappert K, Mitchell GA. Boukaftane Y, et al. Among authors: mitchell ga. Genomics. 1994 Oct;23(3):552-9. doi: 10.1006/geno.1994.1542. Genomics. 1994. PMID: 7851882

2

Hormone-sensitive lipase maps to proximal chromosome 7 in mice and is genetically distinct from the Ad and Tub loci.

Wang S, Lapierre P, Robert MF, Nadeau JH, Mitchell GA. Wang S, et al. Among authors: mitchell ga. Genomics. 1994 Nov 15;24(2):416-7. doi: 10.1006/geno.1994.1646. Genomics. 1994. PMID: 7698777 No abstract available.

3

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL). Cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency.

Mitchell GA, Robert MF, Hruz PW, Wang S, Fontaine G, Behnke CE, Mende-Mueller LM, Schappert K, Lee C, Gibson KM, Miziorko HM, et al. Mitchell GA, et al. J Biol Chem. 1993 Feb 25;268(6):4376-81. J Biol Chem. 1993. PMID: 8440722 Free article.

4

3-Hydroxy-3-methylglutaryl CoA lyase (HL): mouse and human HL gene (HMGCL) cloning and detection of large gene deletions in two unrelated HL-deficient patients.

Wang SP, Robert MF, Gibson KM, Wanders RJ, Mitchell GA. Wang SP, et al. Among authors: mitchell ga. Genomics. 1996 Apr 1;33(1):99-104. doi: 10.1006/geno.1996.0164. Genomics. 1996. PMID: 8617516

5

Cloning and characterization of the human mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase gene.

Boukaftane Y, Mitchell GA. Boukaftane Y, et al. Among authors: mitchell ga. Gene. 1997 Aug 22;195(2):121-6. doi: 10.1016/s0378-1119(97)00067-x. Gene. 1997. PMID: 9305755

6

Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients.

Bouchard L, Robert MF, Vinarov D, Stanley CA, Thompson GN, Morris A, Leonard JV, Quant P, Hsu BY, Boneh A, Boukaftane Y, Ashmarina L, Wang S, Miziorko H, Mitchell GA. Bouchard L, et al. Among authors: mitchell ga. Pediatr Res. 2001 Mar;49(3):326-31. doi: 10.1203/00006450-200103000-00005. Pediatr Res. 2001. PMID: 11228257

7

Medical aspects of ketone body metabolism.

Mitchell GA, Kassovska-Bratinova S, Boukaftane Y, Robert MF, Wang SP, Ashmarina L, Lambert M, Lapierre P, Potier E. Mitchell GA, et al. Clin Invest Med. 1995 Jun;18(3):193-216. Clin Invest Med. 1995. PMID: 7554586 Review.

8

Alu sequences in the coding regions of mRNA: a source of protein variability.

Makałowski W, Mitchell GA, Labuda D. Makałowski W, et al. Among authors: mitchell ga. Trends Genet. 1994 Jun;10(6):188-93. doi: 10.1016/0168-9525(94)90254-2. Trends Genet. 1994. PMID: 8073532

9

Characterization of the hydroxymethylglutaryl-CoA lyase precursor, a protein targeted to peroxisomes and mitochondria.

Ashmarina LI, Robert MF, Elsliger MA, Mitchell GA. Ashmarina LI, et al. Among authors: mitchell ga. Biochem J. 1996 Apr 1;315 ( Pt 1)(Pt 1):71-5. doi: 10.1042/bj3150071. Biochem J. 1996. PMID: 8670134 Free PMC article.

10

Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient.

Kassovska-Bratinova S, Fukao T, Song XQ, Duncan AM, Chen HS, Robert MF, Pérez-Cerdá C, Ugarte M, Chartrand C, Vobecky S, Kondo N, Mitchell GA. Kassovska-Bratinova S, et al. Among authors: mitchell ga. Am J Hum Genet. 1996 Sep;59(3):519-28. Am J Hum Genet. 1996. PMID: 8751852 Free PMC article.

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