Bruin T - Search Results

1

Ser447stop mutation in lipoprotein lipase is associated with elevated HDL cholesterol levels in normolipidemic males.

Kuivenhoven JA, Groenemeyer BE, Boer JM, Reymer PW, Berghuis R, Bruin T, Jansen H, Seidell JC, Kastelein JJ. Kuivenhoven JA, et al. Among authors: bruin t. Arterioscler Thromb Vasc Biol. 1997 Mar;17(3):595-9. doi: 10.1161/01.atv.17.3.595. Arterioscler Thromb Vasc Biol. 1997. PMID: 9102182

2

A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia.

Reymer PW, Groenemeyer BE, Gagné E, Miao L, Appelman EE, Seidel JC, Kromhout D, Bijvoet SM, van de Oever K, Bruin T, et al. Reymer PW, et al. Among authors: bruin t. Hum Mol Genet. 1995 Sep;4(9):1543-9. doi: 10.1093/hmg/4.9.1543. Hum Mol Genet. 1995. PMID: 8541837

3

Compound heterozygosity for a known and a novel defect in the lipoprotein lipase gene (Asp250-->Asn; Ser251-->Cys) resulting in lipoprotein lipase (LPL) deficiency.

Bijvoet SM, Wiebusch H, Ma Y, Reymer PW, Bruin T, Bakker HD, Funke H, Assmann G, Hayden MR, Kastelein JJ. Bijvoet SM, et al. Among authors: bruin t. Neth J Med. 1996 Nov;49(5):189-95. doi: 10.1016/0300-2977(96)00043-5. Neth J Med. 1996. PMID: 8973094

4

Genetic variant showing a positive interaction with beta-blocking agents with a beneficial influence on lipoprotein lipase activity, HDL cholesterol, and triglyceride levels in coronary artery disease patients. The Ser447-stop substitution in the lipoprotein lipase gene. REGRESS Study Group.

Groenemeijer BE, Hallman MD, Reymer PW, Gagné E, Kuivenhoven JA, Bruin T, Jansen H, Lie KI, Bruschke AV, Boerwinkle E, Hayden MR, Kastelein JJ. Groenemeijer BE, et al. Among authors: bruin t. Circulation. 1997 Jun 17;95(12):2628-35. doi: 10.1161/01.cir.95.12.2628. Circulation. 1997. PMID: 9193431 Clinical Trial.

5

[Lipoprotein lipase].

Kastelein JJ, Bruin T, ten Cate JW. Kastelein JJ, et al. Among authors: bruin t. Ned Tijdschr Geneeskd. 1992 Apr 11;136(15):727-30. Ned Tijdschr Geneeskd. 1992. PMID: 1560865 Review. Dutch. No abstract available.

6

Apolipoprotein CII-Padova (Tyr37-->stop) as a cause of chylomicronaemia in an Italian kindred from Siculiana.

Tuzgöl S, Bijvoet SM, Bruin T, Kastelein JJ, Hayden MR. Tuzgöl S, et al. Among authors: bruin t. J Med Genet. 1994 Aug;31(8):622-6. doi: 10.1136/jmg.31.8.622. J Med Genet. 1994. PMID: 7815420 Free PMC article.

7

A compound heterozygote for lipoprotein lipase deficiency, Val69-->Leu and Gly188-->Glu: correlation between in vitro LPL activity and clinical expression.

Bruin T, Tuzgöl S, Mulder WJ, van den Ende AE, Jansen H, Hayden MR, Kastelein JJ. Bruin T, et al. J Lipid Res. 1994 Mar;35(3):438-45. J Lipid Res. 1994. PMID: 7912254 Free article.

8

Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descent.

Bijvoet SM, Bruin T, Tuzgöl S, Bakker HD, Hayden MR, Kastelein JJ. Bijvoet SM, et al. Among authors: bruin t. Hum Genet. 1994 Mar;93(3):339-43. doi: 10.1007/BF00212035. Hum Genet. 1994. PMID: 8125488

9

The C-terminus of lipoprotein lipase is essential for biological function but contains no domain for glycosylphosphatidylinositol anchoring.

Bruin T, Groot NB, Jansen J, Kastelein JJ. Bruin T, et al. Eur J Biochem. 1994 May 1;221(3):1019-25. doi: 10.1111/j.1432-1033.1994.tb18819.x. Eur J Biochem. 1994. PMID: 8181457 Free article.

10

The familial hyperchylomicronaemia syndrome.

Bijvoet SM, Bruin T, Kastelein JJ. Bijvoet SM, et al. Among authors: bruin t. Neth J Med. 1993 Feb;42(1-2):36-44. Neth J Med. 1993. PMID: 8446222 Review.

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