Genetic testing for familial Mediterranean fever in Austria by means of reverse-hybridization teststrips.

نویسندگان

  • Christian Oberkanins
  • Andreas Weinhäusel
  • Gernot Kriegshäuser
  • Anne Moritz
  • Fritz Kury
  • Oskar A Haas
چکیده

poproteins in mouse peritoneal macrophages. J Mol Med 2000;78:217–27. 3. Wenham PR, Sedky A, Spooner RJ. Apolipoprotein E phenotyping: a word of caution. Ann Clin Biochem 1991;28:599–605. 4. Hixson JE, Vernier DT. Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI. J Lipid Res 1990;31:545–8. 5. Somsen GW, Welten HT, Mulder FP, Swart CW, Kema IP, de Jong GJ. Capillary electrophoresis with laser-induced fluorescence detection for fast and reliable apolipoprotein E genotyping. J Chromatogr B Anal Technol Biomed Life Sci 2002;775:17–26. 6. Wenham PR, Newton CR, Price WH. Analysis of apolipoprotein E genotypes by the Amplification Refractory Mutation System. Clin Chem 1991;37: 241–4. 7. Donohoe GG, Salomaki A, Lehtimaki T, Pulkki K, Kairisto V. Rapid identification of apolipoprotein E genotypes by multiplex amplification refractory mutation system PCR and capillary gel electrophoresis. Clin Chem 1999; 45:143–6. 8. Ballerini S, Bellincampi L, Bernardini S, Casciani S, Motti C, Cortese C, et al. Apolipoprotein E genotyping: a comparative study between restriction endonuclease mapping and allelic discrimination with the LightCycler. Clin Chim Acta 2002;317:71–6. 9. Koch W, Ehrenhaft A, Griesser K, Pfeufer A, Muller J, Schomig A, at al. TaqMan systems for genotyping of disease-related polymorphisms present in the gene encoding apolipoprotein E. Clin Chem Lab Med 2002;40:1123– 31. 10. Pantelidis P, Jones MG, Welsh KI, Taylor AN, du Bois RM. Identification of four novel interleukin-13 gene polymorphisms. Genes Immun 2000;1: 341–5.

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عنوان ژورنال:
  • Clinical chemistry

دوره 49 11  شماره 

صفحات  -

تاریخ انتشار 2003