Knappskog PM - Search Results

1

Attention-deficit/hyperactivity disorder symptoms in offspring of mothers with impaired serotonin production.

Halmøy A, Johansson S, Winge I, McKinney JA, Knappskog PM, Haavik J. Halmøy A, et al. Among authors: knappskog pm. Arch Gen Psychiatry. 2010 Oct;67(10):1033-43. doi: 10.1001/archgenpsychiatry.2010.124. Arch Gen Psychiatry. 2010. PMID: 20921119

2

Comparative analysis of phenylalanine hydroxylase A104D mutant, associated with variant phenylketonuria, and wild-type enzyme.

Waters PI, Hewson AS, Scriver CR, Treacy EP, Martinez A, Knappskog PM, Parniak MA. Waters PI, et al. Among authors: knappskog pm. Biochem Soc Trans. 1997 May;25(2):362S. doi: 10.1042/bst025362s. Biochem Soc Trans. 1997. PMID: 9191407 No abstract available.

3

Domain structure and stability of human phenylalanine hydroxylase inferred from infrared spectroscopy.

Chehin R, Thorolfsson M, Knappskog PM, Martinez A, Flatmark T, Arrondo JL, Muga A. Chehin R, et al. Among authors: knappskog pm. FEBS Lett. 1998 Jan 30;422(2):225-30. doi: 10.1016/s0014-5793(97)01596-2. FEBS Lett. 1998. PMID: 9490012 Free article.

4

Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene.

Lüdecke B, Knappskog PM, Clayton PT, Surtees RA, Clelland JD, Heales SJ, Brand MP, Bartholomé K, Flatmark T. Lüdecke B, et al. Among authors: knappskog pm. Hum Mol Genet. 1996 Jul;5(7):1023-8. doi: 10.1093/hmg/5.7.1023. Hum Mol Genet. 1996. PMID: 8817341

5

Cold-induced sweating syndrome: a report of two cases and demonstration of genetic heterogeneity.

Hahn AF, Jones DL, Knappskog PM, Boman H, McLeod JG. Hahn AF, et al. Among authors: knappskog pm. J Neurol Sci. 2006 Dec 1;250(1-2):62-70. doi: 10.1016/j.jns.2006.07.001. Epub 2006 Sep 6. J Neurol Sci. 2006. PMID: 16952376

6

Novel missense mutation in the phenylalanine hydroxylase gene leading to complete loss of enzymatic activity.

Dianzani I, Knappskog PM, de Sanctis L, Giannattasio S, Riva E, Ponzone A, Apold J, Camaschella C. Dianzani I, et al. Among authors: knappskog pm. Hum Mutat. 1995;6(3):247-9. doi: 10.1002/humu.1380060308. Hum Mutat. 1995. PMID: 8535444 No abstract available.

7

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

8

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.

9

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.

10

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.

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