Hayden M - Search Results

1

A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry.

Foubert L, Bruin T, De Gennes JL, Ehrenborg E, Furioli J, Kastelein J, Benlian P, Hayden M. Foubert L, et al. Among authors: hayden m. Hum Mutat. 1997;10(3):179-85. doi: 10.1002/(SICI)1098-1004(1997)10:3<179::AID-HUMU1>3.0.CO;2-E. Hum Mutat. 1997. PMID: 9298816

2

Support for founder effect for two lipoprotein lipase (LPL) gene mutations in French Canadians by analysis of GT microsatellites flanking the LPL gene.

Wood S, Schertzer M, Hayden M, Ma Y. Wood S, et al. Among authors: hayden m. Hum Genet. 1993 May;91(4):312-6. doi: 10.1007/BF00217348. Hum Genet. 1993. PMID: 8099055

3

Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency.

Benlian P, Foubert L, Gagné E, Bernard L, De Gennes JL, Langlois S, Robinson W, Hayden M. Benlian P, et al. Among authors: hayden m. Am J Hum Genet. 1996 Aug;59(2):431-6. Am J Hum Genet. 1996. PMID: 8755931 Free PMC article.

4

Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase gene.

Benlian P, De Gennes JL, Foubert L, Zhang H, Gagné SE, Hayden M. Benlian P, et al. Among authors: hayden m. N Engl J Med. 1996 Sep 19;335(12):848-54. doi: 10.1056/NEJM199609193351203. N Engl J Med. 1996. PMID: 8778602 Free article.

5

Lack of association of the apolipoprotein A-I-C-III-A-IV gene XmnI and SstI polymorphisms and of the lipoprotein lipase gene mutations in familial combined hyperlipoproteinemia in French Canadian subjects.

Marcil M, Boucher B, Gagné E, Davignon J, Hayden M, Genest J Jr. Marcil M, et al. Among authors: hayden m. J Lipid Res. 1996 Feb;37(2):309-19. J Lipid Res. 1996. PMID: 9026529 Free article.

6

Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol.

Wellington CL, Yang YZ, Zhou S, Clee SM, Tan B, Hirano K, Zwarts K, Kwok A, Gelfer A, Marcil M, Newman S, Roomp K, Singaraja R, Collins J, Zhang LH, Groen AK, Hovingh K, Brownlie A, Tafuri S, Genest J Jr, Kastelein JJ, Hayden MR. Wellington CL, et al. Among authors: hayden mr. J Lipid Res. 2002 Nov;43(11):1939-49. doi: 10.1194/jlr.m200277-jlr200. J Lipid Res. 2002. PMID: 12401893 Free article.

7

Efflux and atherosclerosis: the clinical and biochemical impact of variations in the ABCA1 gene.

Singaraja RR, Brunham LR, Visscher H, Kastelein JJ, Hayden MR. Singaraja RR, et al. Arterioscler Thromb Vasc Biol. 2003 Aug 1;23(8):1322-32. doi: 10.1161/01.ATV.0000078520.89539.77. Epub 2003 May 22. Arterioscler Thromb Vasc Biol. 2003. PMID: 12763760 Review.

8

Long-term correction of murine lipoprotein lipase deficiency with AAV1-mediated gene transfer of the naturally occurring LPL(S447X) beneficial mutation.

Ross CJ, Twisk J, Meulenberg JM, Liu G, van den Oever K, Moraal E, Hermens WT, Rip J, Kastelein JJ, Kuivenhoven JA, Hayden MR. Ross CJ, et al. Among authors: hayden mr. Hum Gene Ther. 2004 Sep;15(9):906-19. doi: 10.1089/hum.2004.15.906. Hum Gene Ther. 2004. PMID: 15353045

9

Complete rescue of lipoprotein lipase-deficient mice by somatic gene transfer of the naturally occurring LPLS447X beneficial mutation.

Ross CJ, Liu G, Kuivenhoven JA, Twisk J, Rip J, van Dop W, Excoffon KJ, Lewis SM, Kastelein JJ, Hayden MR. Ross CJ, et al. Among authors: hayden mr. Arterioscler Thromb Vasc Biol. 2005 Oct;25(10):2143-50. doi: 10.1161/01.ATV.0000176971.27302.b0. Epub 2005 Jul 7. Arterioscler Thromb Vasc Biol. 2005. PMID: 16002740

10

Gene therapy for lipoprotein lipase deficiency: working toward clinical application.

Rip J, Nierman MC, Sierts JA, Petersen W, Van den Oever K, Van Raalte D, Ross CJ, Hayden MR, Bakker AC, Dijkhuizen P, Hermens WT, Twisk J, Stroes E, Kastelein JJ, Kuivenhoven JA, Meulenberg JM. Rip J, et al. Among authors: hayden mr. Hum Gene Ther. 2005 Nov;16(11):1276-86. doi: 10.1089/hum.2005.16.1276. Hum Gene Ther. 2005. PMID: 16259561

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