Riin Tamm

Summary

Affiliation: University of Tartu
Country: Estonia

Publications

  1. doi request reprint Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population
    Riin Tamm
    Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia
    Clin Chem Lab Med 46:974-9. 2008
  2. ncbi request reprint Determination of thiopurine S-methyltransferase (TPMT) activity by comparing various normalization factors: reference values for Estonian population using HPLC-UV assay
    Kersti Oselin
    Department of Pharmacology, Tartu University, 51014 Tartu, Estonia
    J Chromatogr B Analyt Technol Biomed Life Sci 834:77-83. 2006
  3. pmc Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements
    Mark Braschinsky
    Department of Neurology, University of Tartu, Estonia
    BMC Neurol 10:17. 2010

Detail Information

Publications3

  1. doi request reprint Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population
    Riin Tamm
    Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia
    Clin Chem Lab Med 46:974-9. 2008
    ..To date, at least 25 single nucleotide polymorphisms have been reported in the TPMT gene, 23 of these are associated with reduced enzyme activity...
  2. ncbi request reprint Determination of thiopurine S-methyltransferase (TPMT) activity by comparing various normalization factors: reference values for Estonian population using HPLC-UV assay
    Kersti Oselin
    Department of Pharmacology, Tartu University, 51014 Tartu, Estonia
    J Chromatogr B Analyt Technol Biomed Life Sci 834:77-83. 2006
    ..001). This sensitive HPLC assay for quantitative determination of TPMT activity could easily be used in clinical settings. Under constant experimental conditions for haemolysate preparation no normalization is required...
  3. pmc Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements
    Mark Braschinsky
    Department of Neurology, University of Tartu, Estonia
    BMC Neurol 10:17. 2010
    ..The most common autosomal-dominant form of the disease derives from mutations in the SPAST gene...