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Results: 1-8 |
Results: 8

Authors: Gjetting, T Romstad, A Haavik, J Knappskog, PM Acosta, AX Silva, WA Zago, MA Guldberg, P Guttler, F
Citation: T. Gjetting et al., A phenylalanine hydroxylase amino acid polymorphism with implications for molecular diagnostics, MOL GEN MET, 73(3), 2001, pp. 280-284

Authors: Martinez, A Knappskog, PM Haavik, J
Citation: A. Martinez et al., A structural approach into human tryptophan hydroxylase and its implications for the regulation of serotonin biosynthesis, CURR MED CH, 8(9), 2001, pp. 1077-1091

Authors: Krossoy, B Devold, M Sanders, L Knappskog, PM Aspehaug, V Falk, K Nylund, A Koumans, S Endresen, C Biering, E
Citation: B. Krossoy et al., Cloning and identification of the infectious salmon anaemia virus haemagglutinin, J GEN VIROL, 82, 2001, pp. 1757-1765

Authors: Schunemann, V Meier, C Meyer-Klaucke, W Winkler, H Trautwein, AX Knappskog, PM Toska, K Haavik, J
Citation: V. Schunemann et al., Iron coordination geometry in full-length, truncated, and dehydrated formsof human tyrosine hydroxylase studied by Mossbauer and X-ray absorption spectroscopy, J BIOL I CH, 4(2), 1999, pp. 223-231

Authors: Kleppe, R Uhlemann, K Knappskog, PM Haavik, J
Citation: R. Kleppe et al., Urea-induced denaturation of human phenylalanine hydroxylase, J BIOL CHEM, 274(47), 1999, pp. 33251-33258

Authors: Ellingsen, S Knappskog, PM Apold, J Eiken, HG
Citation: S. Ellingsen et al., Diverse PAH transcripts in lymphocytes of PKU patients with putative nonsense (G272X, Y356X) and missense (P281L, R408Q) mutations, FEBS LETTER, 457(3), 1999, pp. 505-508

Authors: Flatmark, T Almas, B Knappskog, PM Berge, SV Svebak, RM Chehin, R Muga, A Martinez, A
Citation: T. Flatmark et al., Tyrosine hydroxylase binds tetrahydrobiopterin cofactor with negative cooperativity, as shown by kinetic analyses and surface plasmon resonance detection, EUR J BIOCH, 262(3), 1999, pp. 840-849

Authors: Bruland, O Almqvist, EW Goldberg, YP Boman, H Hayden, MR Knappskog, PM
Citation: O. Bruland et al., Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standard, CLIN GENET, 55(3), 1999, pp. 198-202
Risultati: 1-8 |