Liu MS - Search Results

1

High frequency of mutations in the human lipoprotein lipase gene in pregnancy-induced chylomicronemia: possible association with apolipoprotein E2 isoform.

Ma Y, Ooi TC, Liu MS, Zhang H, McPherson R, Edwards AL, Forsythe IJ, Frohlich J, Brunzell JD, Hayden MR. Ma Y, et al. Among authors: liu ms. J Lipid Res. 1994 Jun;35(6):1066-75. J Lipid Res. 1994. PMID: 8077845 Free article.

2

Mapping of the epitope on lipoprotein lipase recognized by a monoclonal antibody (5D2) which inhibits lipase activity.

Liu MS, Ma Y, Hayden MR, Brunzell JD. Liu MS, et al. Biochim Biophys Acta. 1992 Sep 22;1128(1):113-5. doi: 10.1016/0005-2760(92)90264-v. Biochim Biophys Acta. 1992. PMID: 1382603

3

Two naturally occurring mutations at the first and second bases of codon aspartic acid 156 in the proposed catalytic triad of human lipoprotein lipase. In vivo evidence that aspartic acid 156 is essential for catalysis.

Ma YH, Bruin T, Tuzgol S, Wilson BI, Roederer G, Liu MS, Davignon J, Kastelein JJ, Brunzell JD, Hayden MR. Ma YH, et al. Among authors: liu ms. J Biol Chem. 1992 Jan 25;267(3):1918-23. J Biol Chem. 1992. PMID: 1730727 Free article.

4

Mutagenesis in four candidate heparin binding regions (residues 279-282, 291-304, 390-393, and 439-448) and identification of residues affecting heparin binding of human lipoprotein lipase.

Ma Y, Henderson HE, Liu MS, Zhang H, Forsythe IJ, Clarke-Lewis I, Hayden MR, Brunzell JD. Ma Y, et al. Among authors: liu ms. J Lipid Res. 1994 Nov;35(11):2049-59. J Lipid Res. 1994. PMID: 7868983 Free article.

5

Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries.

Ma Y, Liu MS, Chitayat D, Bruin T, Beisiegel U, Benlian P, Foubert L, De Gennes JL, Funke H, Forsythe I, et al. Ma Y, et al. Among authors: liu ms. Hum Mutat. 1994;3(1):52-8. doi: 10.1002/humu.1380030109. Hum Mutat. 1994. PMID: 7906986

6

Gene environment interaction and plasma triglyceride levels: the crucial role of lipoprotein lipase.

Hayden MR, Liu MS, Ma Y. Hayden MR, et al. Among authors: liu ms. Clin Genet. 1994 Jul;46(1 Spec No):15-8. doi: 10.1111/j.1399-0004.1994.tb04197.x. Clin Genet. 1994. PMID: 7988072 Review. No abstract available.

7

Structure-function relationships of lipoprotein lipase: mutation analysis and mutagenesis of the loop region.

Henderson HE, Ma Y, Liu MS, Clark-Lewis I, Maeder DL, Kastelein JJ, Brunzell JD, Hayden MR. Henderson HE, et al. Among authors: liu ms. J Lipid Res. 1993 Sep;34(9):1593-602. J Lipid Res. 1993. PMID: 8228642 Free article.

8

A 4 basepair deletion in exon 4 of the human lipoprotein lipase gene results in type I hyperlipoproteinemia.

Ma Y, Liu MS, Zhang H, Forsythe IJ, Brunzell JD, Hayden MR. Ma Y, et al. Among authors: liu ms. Hum Mol Genet. 1993 Jul;2(7):1049-50. doi: 10.1093/hmg/2.7.1049. Hum Mol Genet. 1993. PMID: 8364543 No abstract available.

9

Gene-environment interaction in the conversion of a mild-to-severe phenotype in a patient homozygous for a Ser172-->Cys mutation in the lipoprotein lipase gene.

Ma Y, Liu MS, Ginzinger D, Frohlich J, Brunzell JD, Hayden MR. Ma Y, et al. Among authors: liu ms. J Clin Invest. 1993 May;91(5):1953-8. doi: 10.1172/JCI116414. J Clin Invest. 1993. PMID: 8486765 Free PMC article.

10

Patients with apoE3 deficiency (E2/2, E3/2, and E4/2) who manifest with hyperlipidemia have increased frequency of an Asn 291-->Ser mutation in the human LPL gene.

Zhang H, Reymer PW, Liu MS, Forsythe IJ, Groenemeyer BE, Frohlich J, Brunzell JD, Kastelein JJ, Hayden MR, Ma Y. Zhang H, et al. Among authors: liu ms. Arterioscler Thromb Vasc Biol. 1995 Oct;15(10):1695-703. doi: 10.1161/01.atv.15.10.1695. Arterioscler Thromb Vasc Biol. 1995. PMID: 7583546

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