Knappskog PM - Search Results

1

Genetic analyses of dopamine related genes in adult ADHD patients suggest an association with the DRD5-microsatellite repeat, but not with DRD4 or SLC6A3 VNTRs.

Johansson S, Halleland H, Halmøy A, Jacobsen KK, Landaas ET, Dramsdahl M, Fasmer OB, Bergsholm P, Lundervold AJ, Gillberg C, Hugdahl K, Knappskog PM, Haavik J. Johansson S, et al. Among authors: knappskog pm. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1470-5. doi: 10.1002/ajmg.b.30662. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18081165

2

Tryptophan fluorescence of human phenylalanine hydroxylase produced in Escherichia coli.

Knappskog PM, Haavik J. Knappskog PM, et al. Biochemistry. 1995 Sep 19;34(37):11790-9. doi: 10.1021/bi00037a017. Biochemistry. 1995. PMID: 7547912

3

Structure/function relationships in human phenylalanine hydroxylase. Effect of terminal deletions on the oligomerization, activation and cooperativity of substrate binding to the enzyme.

Knappskog PM, Flatmark T, Aarden JM, Haavik J, Martínez A. Knappskog PM, et al. Eur J Biochem. 1996 Dec 15;242(3):813-21. doi: 10.1111/j.1432-1033.1996.0813r.x. Eur J Biochem. 1996. PMID: 9022714 Free article.

4

Crystallization and preliminary diffraction analysis of a truncated homodimer of human phenylalanine hydroxylase.

Erlandsen H, Martinez A, Knappskog PM, Haavik J, Hough E, Flatmark T. Erlandsen H, et al. Among authors: knappskog pm. FEBS Lett. 1997 Apr 7;406(1-2):171-4. doi: 10.1016/s0014-5793(97)00259-7. FEBS Lett. 1997. PMID: 9109411 Free article.

5

Urea-induced denaturation of human phenylalanine hydroxylase.

Kleppe R, Uhlemann K, Knappskog PM, Haavik J. Kleppe R, et al. Among authors: knappskog pm. J Biol Chem. 1999 Nov 19;274(47):33251-8. doi: 10.1074/jbc.274.47.33251. J Biol Chem. 1999. PMID: 10559199 Free article.

6

A structural approach into human tryptophan hydroxylase and its implications for the regulation of serotonin biosynthesis.

Martínez A, Knappskog PM, Haavik J. Martínez A, et al. Among authors: knappskog pm. Curr Med Chem. 2001 Jul;8(9):1077-91. doi: 10.2174/0929867013372616. Curr Med Chem. 2001. PMID: 11472242 Review.

7

[Why do mutations cause disease--a protein chemical perspective].

Kleppe R, Knappskog PM, Haavik J. Kleppe R, et al. Among authors: knappskog pm. Tidsskr Nor Laegeforen. 2001 Sep 30;121(23):2717-20. Tidsskr Nor Laegeforen. 2001. PMID: 11699380 Review. Norwegian.

8

Conformation of the substrate and pterin cofactor bound to human tryptophan hydroxylase. Important role of Phe313 in substrate specificity.

McKinney J, Teigen K, Frøystein NA, Salaün C, Knappskog PM, Haavik J, Martínez A. McKinney J, et al. Among authors: knappskog pm. Biochemistry. 2001 Dec 25;40(51):15591-601. doi: 10.1021/bi015722x. Biochemistry. 2001. PMID: 11747434

9

Expression and purification of human tryptophan hydroxylase from Escherichia coli and Pichia pastoris.

McKinney J, Knappskog PM, Pereira J, Ekern T, Toska K, Kuitert BB, Levine D, Gronenborn AM, Martinez A, Haavik J. McKinney J, et al. Among authors: knappskog pm. Protein Expr Purif. 2004 Feb;33(2):185-94. doi: 10.1016/j.pep.2003.09.014. Protein Expr Purif. 2004. PMID: 14711505

10

Different properties of the central and peripheral forms of human tryptophan hydroxylase.

McKinney J, Knappskog PM, Haavik J. McKinney J, et al. Among authors: knappskog pm. J Neurochem. 2005 Jan;92(2):311-20. doi: 10.1111/j.1471-4159.2004.02850.x. J Neurochem. 2005. PMID: 15663479 Free article.

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