Smit M - Search Results

1

Apolipoprotein E polymorphism in The Netherlands and its effect on plasma lipid and apolipoprotein levels.

Smit M, de Knijff P, Rosseneu M, Bury J, Klasen E, Frants R, Havekes L. Smit M, et al. Hum Genet. 1988 Nov;80(3):287-92. doi: 10.1007/BF01790099. Hum Genet. 1988. PMID: 3192216

2

A common restriction fragment length polymorphism of the human apolipoprotein E gene and its relationship to type III hyperlipidaemia.

Klasen EC, Talmud PJ, Havekes L, de Wit E, van der Kooij-Meijs E, Smit M, Hansson G, Humphries SE. Klasen EC, et al. Among authors: smit m. Hum Genet. 1987 Mar;75(3):244-7. doi: 10.1007/BF00281067. Hum Genet. 1987. PMID: 2881878

3

Apolipoprotein gene cluster on chromosome 19. Definite localization of the APOC2 gene and the polymorphic Hpa I site associated with type III hyperlipoproteinemia.

Smit M, van der Kooij-Meijs E, Frants RR, Havekes L, Klasen EC. Smit M, et al. Hum Genet. 1988 Jan;78(1):90-3. doi: 10.1007/BF00291243. Hum Genet. 1988. PMID: 2892779

4

Rare apolipoprotein E variant cosegregating with a unique APOE-C1-C2 haplotype in a normolipidemic family.

Smit M, de Knijff P, Sijts A, Klasen EC, Frants RR, Havekes LM. Smit M, et al. Hum Hered. 1988;38(5):277-82. doi: 10.1159/000153799. Hum Hered. 1988. PMID: 2906903

5

The effect of apolipoprotein E allele substitutions on plasma lipid and apolipoprotein levels.

Havekes LM, de Knijff P, Smit M, Frants RR. Havekes LM, et al. Among authors: smit m. Adv Exp Med Biol. 1988;243:87-93. doi: 10.1007/978-1-4613-0733-4_12. Adv Exp Med Biol. 1988. PMID: 3066188 Review. No abstract available.

6

Apolipoprotein E phenotype and gene distribution in The Netherlands.

Klasen EC, Smit M, de Kniff P, Gevers Leuven J, Kempen-Voogd R, Havekes L. Klasen EC, et al. Among authors: smit m. Hum Hered. 1987;37(6):340-4. doi: 10.1159/000153731. Hum Hered. 1987. PMID: 3679233

7

Familial dysbetalipoproteinemic subjects with the E3/E2 phenotype exhibit an E2 isoform with only one cysteine residue.

Smit M, de Knijff P, Frants RR, Klasen EC, Havekes LM. Smit M, et al. Clin Genet. 1987 Nov;32(5):335-41. doi: 10.1111/j.1399-0004.1987.tb03298.x. Clin Genet. 1987. PMID: 3690877

8

Genetic heterogeneity in familial dysbetalipoproteinemia. The E2(lys146----gln) variant results in a dominant mode of inheritance.

Smit M, de Knijff P, van der Kooij-Meijs E, Groenendijk C, van den Maagdenberg AM, Gevers Leuven JA, Stalenhoef AF, Stuyt PM, Frants RR, Havekes LM. Smit M, et al. J Lipid Res. 1990 Jan;31(1):45-53. J Lipid Res. 1990. PMID: 2313204 Free article.

9

Exact localization of the familial dysbetalipoproteinemia associated HpaI restriction site in the promoter region of the APOC1 gene.

Smit M, van der Kooij-Meijs E, Woudt LP, Havekes LM, Frants RR. Smit M, et al. Biochem Biophys Res Commun. 1988 May 16;152(3):1282-8. doi: 10.1016/s0006-291x(88)80424-8. Biochem Biophys Res Commun. 1988. PMID: 2897845

10

A rapid micromethod for apolipoprotein E phenotyping directly in serum.

Havekes LM, de Knijff P, Beisiegel U, Havinga J, Smit M, Klasen E. Havekes LM, et al. Among authors: smit m. J Lipid Res. 1987 Apr;28(4):455-63. J Lipid Res. 1987. PMID: 3585179 Free article.

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