Kastelein JJ - Search Results

1

HindIII-polymorphism in the LPL-gene detected by PCR.

Bruin T, Reymer PW, Groenemeyer BE, Talmud PJ, Kastelein JJ. Bruin T, et al. Among authors: kastelein jj. Nucleic Acids Res. 1991 Nov 25;19(22):6346. doi: 10.1093/nar/19.22.6346-a. Nucleic Acids Res. 1991. PMID: 1956806 Free PMC article.

2

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: kastelein jj. 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

3

Apolipoprotein E genotyping on agarose gels.

Reymer PW, Groenemeyer BE, van de Burg R, Kastelein JJ. Reymer PW, et al. Among authors: kastelein jj. Clin Chem. 1995 Jul;41(7):1046-7. Clin Chem. 1995. PMID: 7600689 No abstract available.

4

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. Among authors: kastelein jj. J Lipid Res. 1994 Mar;35(3):438-45. J Lipid Res. 1994. PMID: 7912254 Free article.

5

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: kastelein jj. Neth J Med. 1996 Nov;49(5):189-95. doi: 10.1016/0300-2977(96)00043-5. Neth J Med. 1996. PMID: 8973094

6

A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosis.

Reymer PW, Gagné E, Groenemeyer BE, Zhang H, Forsyth I, Jansen H, Seidell JC, Kromhout D, Lie KE, Kastelein J, et al. Reymer PW, et al. Nat Genet. 1995 May;10(1):28-34. doi: 10.1038/ng0595-28. Nat Genet. 1995. PMID: 7647785

7

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: kastelein jj. 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.

8

South African founder mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia in the Dutch population.

Defesche JC, van Diermen DE, Lansberg PJ, Lamping RJ, Reymer PW, Hayden MR, Kastelein JJ. Defesche JC, et al. Among authors: kastelein jj. Hum Genet. 1993 Dec;92(6):567-70. doi: 10.1007/BF00420940. Hum Genet. 1993. PMID: 7903269

9

The familial hyperchylomicronaemia syndrome.

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

10

Analysis of the Afrikaner mutation in exon 9 of the low-density lipoprotein receptor gene in a large Dutch kindred suffering from familial hypercholesterolaemia.

Defesche JC, Lansberg PJ, Reymer PW, Lamping RJ, Kastelein JJ. Defesche JC, et al. Among authors: kastelein jj. Neth J Med. 1993 Feb;42(1-2):53-60. Neth J Med. 1993. PMID: 8446226

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

905 results

Search Page

Filters