Haavik J - Search Results

1

Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD.

Franke B, Vasquez AA, Johansson S, Hoogman M, Romanos J, Boreatti-Hümmer A, Heine M, Jacob CP, Lesch KP, Casas M, Ribasés M, Bosch R, Sánchez-Mora C, Gómez-Barros N, Fernàndez-Castillo N, Bayés M, Halmøy A, Halleland H, Landaas ET, Fasmer OB, Knappskog PM, Heister AJ, Kiemeney LA, Kooij JJ, Boonstra AM, Kan CC, Asherson P, Faraone SV, Buitelaar JK, Haavik J, Cormand B, Ramos-Quiroga JA, Reif A. Franke B, et al. Among authors: haavik j. Neuropsychopharmacology. 2010 Feb;35(3):656-64. doi: 10.1038/npp.2009.170. Epub 2009 Nov 4. Neuropsychopharmacology. 2010. PMID: 19890261 Free PMC 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

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.

4

[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.

5

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.

6

Characterization of wild-type and mutant forms of human tryptophan hydroxylase 2.

Winge I, McKinney JA, Knappskog PM, Haavik J. Winge I, et al. Among authors: haavik j. J Neurochem. 2007 Mar;100(6):1648-57. doi: 10.1111/j.1471-4159.2006.04290.x. Epub 2006 Dec 23. J Neurochem. 2007. PMID: 17181551 Free article.

7

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: haavik j. 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

8

A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder.

McKinney J, Johansson S, Halmøy A, Dramsdahl M, Winge I, Knappskog PM, Haavik J. McKinney J, et al. Among authors: haavik j. Mol Psychiatry. 2008 Apr;13(4):365-7. doi: 10.1038/sj.mp.4002152. Mol Psychiatry. 2008. PMID: 18347598 No abstract available.

9

Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults.

Halleland H, Lundervold AJ, Halmøy A, Haavik J, Johansson S. Halleland H, et al. Among authors: haavik j. Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):403-10. doi: 10.1002/ajmg.b.30831. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18802928

10

Functional properties of missense variants of human tryptophan hydroxylase 2.

McKinney JA, Turel B, Winge I, Knappskog PM, Haavik J. McKinney JA, et al. Among authors: haavik j. Hum Mutat. 2009 May;30(5):787-94. doi: 10.1002/humu.20956. Hum Mutat. 2009. PMID: 19319927

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