Haavik J - Search Results

1

An international multicenter association study of the serotonin transporter gene in persistent ADHD.

Landaas ET, Johansson S, Jacobsen KK, Ribasés M, Bosch R, Sánchez-Mora C, Jacob CP, Boreatti-Hümmer A, Kreiker S, Lesch KP, Kiemeney LA, Kooij JJ, Kan C, Buitelaar JK, Faraone SV, Halmøy A, Ramos-Quiroga JA, Cormand B, Reif A, Franke B, Mick E, Knappskog PM, Haavik J. Landaas ET, et al. Among authors: haavik j. Genes Brain Behav. 2010 Jul;9(5):449-58. doi: 10.1111/j.1601-183X.2010.00567.x. Epub 2010 Jan 25. Genes Brain Behav. 2010. PMID: 20113357 Free article.

2

Tryptophan fluorescence of human phenylalanine hydroxylase produced in Escherichia coli.

Knappskog PM, Haavik J. Knappskog PM, et al. Among authors: haavik j. 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. Among authors: haavik j. 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: haavik j. 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: haavik j. 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: haavik j. 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: haavik j. 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: haavik j. 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: haavik j. 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: haavik j. 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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