Hayden MR - Search Results

1

Partial gene duplication involving exon-Alu interchange results in lipoprotein lipase deficiency.

Devlin RH, Deeb S, Brunzell J, Hayden MR. Devlin RH, et al. Among authors: hayden mr. Am J Hum Genet. 1990 Jan;46(1):112-9. Am J Hum Genet. 1990. PMID: 2294743 Free PMC article.

2

Amino acid substitution (Ile194----Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric origin.

Henderson HE, Ma Y, Hassan MF, Monsalve MV, Marais AD, Winkler F, Gubernator K, Peterson J, Brunzell JD, Hayden MR. Henderson HE, et al. Among authors: hayden mr. J Clin Invest. 1991 Jun;87(6):2005-11. doi: 10.1172/JCI115229. J Clin Invest. 1991. PMID: 1674945 Free PMC article.

3

Frameshift mutation in exon 3 of the lipoprotein lipase gene causes a premature stop codon and lipoprotein lipase deficiency.

Henderson HE, Devlin R, Peterson J, Brunzell JD, Hayden MR. Henderson HE, et al. Among authors: hayden mr. Mol Biol Med. 1990 Dec;7(6):511-7. Mol Biol Med. 1990. PMID: 2077351

4

Characterization of a lipoprotein lipase class III type defect in hypertriglyceridemic cats.

Peritz LN, Brunzell JD, Harvey-Clarke C, Pritchard PH, Jones BR, Hayden MR. Peritz LN, et al. Among authors: hayden mr. Clin Invest Med. 1990 Oct;13(5):259-63. Clin Invest Med. 1990. PMID: 2276220

5

A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiency.

Langlois S, Deeb S, Brunzell JD, Kastelein JJ, Hayden MR. Langlois S, et al. Among authors: hayden mr. Proc Natl Acad Sci U S A. 1989 Feb;86(3):948-52. doi: 10.1073/pnas.86.3.948. Proc Natl Acad Sci U S A. 1989. PMID: 2536938 Free PMC article.

6

Retroviral-mediated gene transfer and expression of human lipoprotein lipase in somatic cells.

Lewis ME, Forsythe IJ, Marth JD, Brunzell JD, Hayden MR, Humphries RK. Lewis ME, et al. Among authors: hayden mr. Hum Gene Ther. 1995 Jul;6(7):853-63. doi: 10.1089/hum.1995.6.7-853. Hum Gene Ther. 1995. PMID: 7578404

7

Phenotypic variation of mutations in the human lipoprotein-lipase gene.

Hayden MR, Kastelein JJ, Funke H, Brunzell JD, Ma Y. Hayden MR, et al. Biochem Soc Trans. 1993 May;21(2):506-9. doi: 10.1042/bst0210506. Biochem Soc Trans. 1993. PMID: 8359520 Review.

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: hayden mr. 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: hayden mr. J Clin Invest. 1993 May;91(5):1953-8. doi: 10.1172/JCI116414. J Clin Invest. 1993. PMID: 8486765 Free PMC article.

10

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: hayden mr. J Biol Chem. 1992 Jan 25;267(3):1918-23. J Biol Chem. 1992. PMID: 1730727 Free article.

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