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Earlier age of onset of Alzheimer's disease in patients with both the transferrin C2 and apolipoprotein E-epsilon 4 alleles.
van Rensburg SJ, Potocnik FC, De Villiers JN, Kotze MJ, Taljaard JJ. van Rensburg SJ, et al. Among authors: kotze mj. Ann N Y Acad Sci. 2000 Apr;903:200-3. doi: 10.1111/j.1749-6632.2000.tb06369.x. Ann N Y Acad Sci. 2000. PMID: 10818508
Exome Sequencing in a Family with Luminal-Type Breast Cancer Underpinned by Variation in the Methylation Pathway.
van der Merwe N, Peeters AV, Pienaar FM, Bezuidenhout J, van Rensburg SJ, Kotze MJ. van der Merwe N, et al. Among authors: kotze mj. Int J Mol Sci. 2017 Feb 22;18(2):467. doi: 10.3390/ijms18020467. Int J Mol Sci. 2017. PMID: 28241424 Free PMC article.
Clinical relevance of apolipoprotein E genotyping based on a family history of Alzheimer's disease.
Luckhoff HK, Brand T, van Velden DP, Kidd M, Fisher LR, van Rensburg SJ, Kotze MJ. Luckhoff HK, et al. Among authors: kotze mj. Curr Alzheimer Res. 2015;12(3):210-7. doi: 10.2174/1567205012666150302154354. Curr Alzheimer Res. 2015. PMID: 25731628
Simultaneous detection of multiple familial hypercholesterolemia mutations facilitates an improved diagnostic service in South african patients at high risk of cardiovascular disease.
Kotze MJ, Kriegshäuser G, Thiart R, de Villiers NJ, Scholtz CL, Kury F, Moritz A, Oberkanins C. Kotze MJ, et al. Mol Diagn. 2003;7(3-4):169-74. doi: 10.1007/BF03260034. Mol Diagn. 2003. PMID: 15068387
Pathology supported genetic testing and treatment of cardiovascular disease in middle age for prevention of Alzheimer's disease.
Kotze MJ, van Rensburg SJ. Kotze MJ, et al. Metab Brain Dis. 2012 Sep;27(3):255-66. doi: 10.1007/s11011-012-9296-8. Epub 2012 Apr 19. Metab Brain Dis. 2012. PMID: 22552896 Free PMC article. Review.
Expression of the SLC11A1 (NRAMP1) 5'-(GT)n repeat: opposite effect in the presence of -237C-->T.
Zaahl MG, Robson KJ, Warnich L, Kotze MJ. Zaahl MG, et al. Among authors: kotze mj. Blood Cells Mol Dis. 2004 Jul-Aug;33(1):45-50. doi: 10.1016/j.bcmd.2004.04.003. Blood Cells Mol Dis. 2004. PMID: 15223010
Prenatal diagnosis of familial hypercholesterolemia: importance of DNA analysis in the high-risk South African population.
Vergotine J, Thiart R, Langenhoven E, Hillermann R, De Jong G, Kotze MJ. Vergotine J, et al. Among authors: kotze mj. Genet Couns. 2001;12(2):121-7. Genet Couns. 2001. PMID: 11491306
Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics.
Kotze MJ, Peeters AV, Langenhoven E, Wauters JG, Van Gaal LF. Kotze MJ, et al. Atherosclerosis. 1994 Dec;111(2):217-25. doi: 10.1016/0021-9150(94)90096-5. Atherosclerosis. 1994. PMID: 7718024
Allelic variation in the promoter region of the LDL receptor gene: analysis of an African-specific variant in the FP2 cis-acting regulatory element.
Hoogendijk CF, Scholtz CL, Pimstone SM, Ehrenborg E, Kastelein JJ, Defesche JC, Thiart R, du Plessis L, de Villiers JN, Zaahl MG, Delport R, Rubinsztein DC, Raffel LJ, Grim CE, Mediene-Benchekor S, Amouyel P, Brousseau T, Steyn K, Lombard CJ, Hayden MR, Kotze MJ. Hoogendijk CF, et al. Among authors: kotze mj. Mol Cell Probes. 2003 Aug;17(4):175-81. doi: 10.1016/s0890-8508(03)00050-1. Mol Cell Probes. 2003. PMID: 12944120
Mutational and genetic origin of LDL receptor gene mutations detected in both Belgian and Dutch familial hypercholesterolemics.
Peeters AV, Van Gaal LF, du Plessis L, Lombardi MP, Havekes LM, Kotze MJ. Peeters AV, et al. Among authors: kotze mj. Hum Genet. 1997 Aug;100(2):266-70. doi: 10.1007/s004390050503. Hum Genet. 1997. PMID: 9254862
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