Mitchell GA - Search Results

1

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.

2

Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: two pathogenic mutations, V133E and C456F, in Japanese siblings.

Song XQ, Fukao T, Watanabe H, Shintaku H, Hirayama K, Kassovska-Bratinova S, Kondo N, Mitchell GA. Song XQ, et al. Among authors: mitchell ga. Hum Mutat. 1998;12(2):83-8. doi: 10.1002/(SICI)1098-1004(1998)12:2<83::AID-HUMU2>3.0.CO;2-P. Hum Mutat. 1998. PMID: 9671268

3

Liver-specific silencing of the human gene encoding succinyl-CoA: 3-ketoacid CoA transferase.

Orii KE, Fukao T, Song XQ, Mitchell GA, Kondo N. Orii KE, et al. Among authors: mitchell ga. Tohoku J Exp Med. 2008 Jul;215(3):227-36. doi: 10.1620/tjem.215.227. Tohoku J Exp Med. 2008. PMID: 18648183 Free article.

4

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

5

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.

6

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

7

Hormone-sensitive lipase (Lipe): sequence analysis of the 129Sv mouse Lipe gene.

Sztrolovics R, Wang SP, Lapierre P, Chen HS, Robert MF, Mitchell GA. Sztrolovics R, et al. Among authors: mitchell ga. Mamm Genome. 1997 Feb;8(2):86-9. doi: 10.1007/s003359900363. Mamm Genome. 1997. PMID: 9060404

8

Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency.

Song XQ, Fukao T, Mitchell GA, Kassovska-Bratinova S, Ugarte M, Wanders RJ, Hirayama K, Shintaku H, Churchill P, Watanabe H, Orii T, Kondo N. Song XQ, et al. Among authors: mitchell ga. Biochim Biophys Acta. 1997 Apr 12;1360(2):151-6. doi: 10.1016/s0925-4439(96)00074-9. Biochim Biophys Acta. 1997. PMID: 9128180 Free article.

9

HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q.

Mitchell GA, Ozand PT, Robert MF, Ashmarina L, Roberts J, Gibson KM, Wanders RJ, Wang S, Chevalier I, Plöchl E, Miziorko H. Mitchell GA, et al. Am J Hum Genet. 1998 Feb;62(2):295-300. doi: 10.1086/301730. Am J Hum Genet. 1998. PMID: 9463337 Free PMC article.

10

3-Hydroxy-3-methylglutaryl-CoA lyase (HL): gene targeting causes prenatal lethality in HL-deficient mice.

Wang SP, Marth JD, Oligny LL, Vachon M, Robert MF, Ashmarina L, Mitchell GA. Wang SP, et al. Among authors: mitchell ga. Hum Mol Genet. 1998 Dec;7(13):2057-62. doi: 10.1093/hmg/7.13.2057. Hum Mol Genet. 1998. PMID: 9817922

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