Wang SP - Search Results

1

Hereditary diseases of coenzyme A thioester metabolism.

Yang H, Zhao C, Wang Y, Wang SP, Mitchell GA. Yang H, et al. Among authors: wang sp, wang y. Biochem Soc Trans. 2019 Feb 28;47(1):149-155. doi: 10.1042/BST20180423. Epub 2019 Jan 9. Biochem Soc Trans. 2019. PMID: 30626707 Review.

2

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. Among authors: wang sp. Clin Invest Med. 1995 Jun;18(3):193-216. Clin Invest Med. 1995. PMID: 7554586 Review.

3

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. Genomics. 1994 Nov 15;24(2):416-7. doi: 10.1006/geno.1994.1646. Genomics. 1994. PMID: 7698777 No abstract available.

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. 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. 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: wang sp. Mamm Genome. 1997 Feb;8(2):86-9. doi: 10.1007/s003359900363. Mamm Genome. 1997. PMID: 9060404

8

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.

9

Inborn errors of ketogenesis.

Mitchell GA, Wang SP, Ashmarina L, Robert MF, Bouchard G, Laurin N, Kassovska-Bratinova S, Boukaftane Y. Mitchell GA, et al. Among authors: wang sp. Biochem Soc Trans. 1998 May;26(2):136-40. doi: 10.1042/bst0260136. Biochem Soc Trans. 1998. PMID: 9649735 Review. No abstract available.

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. 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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