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Kleppe, Rune; Uhlemann, K; Knappskog, Per
et al. (1999). Urea-induced denaturation of human phenylalanine hydroxylase. (ekstern lenke)
-
Schünemann, V; Meier, C; Meyer-Klaucke, W
et al. (1999). Iron coordination geometry in full-length, truncated, and dehydrated forms of human tyrosine hydroxylase studied by Mossbauer and X-ray spectroscopy. (ekstern lenke)
-
Flatmark, Torgeir; Almås, Bjørg; Knappskog, Per
et al. (1999). Tyrosine hydroxylase binds tetrahydrobiopterin cofactor with negative cooperativity as shown by kinetic analysis and surface plasmon resonance detection. (ekstern lenke)
-
Chehin, R; Thorolfsson, Mathias; Knappskog, Per
et al. (1998). Domain structure and stability of human phenylalanin hydroxylase inferred from infrared spectroscopy. (ekstern lenke)
-
Bjørgo, Elisa; Knappskog, Per; Martínez, Aurora
et al. (1998). Expression, characterization and 3D-structural localization of eight phnylketonuria mutations in exon 7 of the human phenylalanine hydroxylase gene. (ekstern lenke)
-
Waters, P.J; Hewson, A.C; Scriver, C.R
et al. (1997). Comparative analysis of phenylalanine hydroxylase A104D mutant, associated with variant phenylketonuria, and wild-type enzyme. (ekstern lenke)
-
Knappskog, Per; Martinez, Aurora
(1997). Effect of mutations at cys 237 on the activation state and activity of human phenylalanine hydroxylase. (ekstern lenke)
-
Erlandsen, H.; Martinez, S.; Knappskog, Per
et al. (1997). Crystallization and preliminary crystallographic studies of a truncated recombinant form of human phenylalanine hydroxylase. (ekstern lenke)
-
Erlandsen, H; Martinez, Aurora; Knappskog, Per
et al. (1997). Crystallization and preliminary diffraction analysis of a truncated homodimer of human phenylalanine hydroxylase. (ekstern lenke)
-
Knappskog, Per; Martinez, Aurora
(1997). Effect of mutations at Cys 237 on the activation state and activity of human phenylalanine hydroxylase. (ekstern lenke)
-
Olsen, T.C.; Eiken, Hans Geir; Knappskog, Per
et al. (1996). Mutations in the iduronate-2-sulfatase gene in five Norwegians with Hunter syndrome. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, Per; Motzfeldt, K.
et al. (1996). Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway. (ekstern lenke)
-
Døskeland, Anne Paulus; Martinez, Aurora; Knappskog, Per
et al. (1996). Phosphorylation of recombinant human phenylalanine hydroxylase. Effect on catalytic activity, substrate activation and protection against non-spesific cleavage of the fusion protein by restriction protease. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, Per; Apold, Jaran
et al. (1996). PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzyme. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, Per; Guldberg, P.
et al. (1996). DGGE analysis as a supplement to SSCP analysis of the phenylalanine hydroxylase gene: detection of eight (one de novo, seven inherited) of nine remaining Norwegian PKU mutations. (ekstern lenke)
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Knappskog, Per; Flatmark, Torgeir; Aarden, J. M.
et al. (1996). Structure-function relationship in human phenylalanine hydroxylase . Effect of terminal deletions on the oligomerization, activation and cooperativity of substrate binding to the enzyme. (ekstern lenke)
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Lüdecke, B.; Knappskog, Per; Clayton, P. T.
et al. (1996). Recessively inherited L-DOPA-responsive Parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene. (ekstern lenke)
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Døskeland, Anne Paulus; Martinez, Aurora; Knappskog, Per
et al. (1996). Phosphorylation of recombinant human phenylalanine hydroxylase. Effect on catalytic activity, substrate activation and protection against non-spesific cleavage of the fusion protein by restriction protease. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, Per; Apold, Jaran
et al. (1996). PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzyme. (ekstern lenke)
-
Knappskog, Per; Eiken, Hans Geir; Martinez, Aurora
et al. (1996). PKU mutation (D143G) associated with an apparent high residual enzyme activity: Expression of a kinetic variant form of phenylalanine hydroxilase in three different systems. (ekstern lenke)
-
Lüdecke, B.; Knappskog, Per; Clayton, P.T.
et al. (1996). Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a poin mutation (L205P) in the tyrosine hydroxylase gene. (ekstern lenke)
-
Knappskog, Per; Eiken, Hans Geir; Martinez, Aurora
et al. (1996). PKU mutation (D143G) associated with an apparent high residual enzyme activity: Expression of a kinetic variant form of phenylalanine hydroxilase in three different systems. (ekstern lenke)
-
Døskeland, Anne Paulus; Martinez, Aurora; Knappskog, Per
et al. (1996). Phosphorylation of recombinant human phenylalanine hydroxylase. Effect on catalytic activity, substrate activation and protection against non-specific cleavage of the fusion protein by restriction protease. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, Per; Guldberg, P.
et al. (1996). DGGE analysis as a supplement to SSCP analysis of the phenylalanine hydroxylase gene: detection of eight (one de novo, seven inherited) of nine remaining Norwegian PKU mutations. (ekstern lenke)
-
Dianzani, I.; Knappskog, Per; Desanctis, L.
et al. (1996). Novel missense mutation in the phenylalanine-hydroxylase gene leading to complete loss of enzymatic-activity. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, Per; Motzfeldt, K.
et al. (1996). Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, Per; Boman, H.
et al. (1996). Relative frequency, heterogeneity, and geographic clustering of PKU mutations in Norway. (ekstern lenke)
-
Olsen, T.C.; Eiken, Hans Geir; Knappskog, Per
et al. (1996). Mutations in the iduronate-2-sulfatase gene in five Norwegians with Hunter syndrome. (ekstern lenke)
-
Olsen, T.F.; Eiken, Hans Geir; Knappskog, P.M.
et al. (1996). Mutations in the Induronate 2-sulfatase gene in five Norwegians with Hunter syndrome. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, P.M.; Motzeldt, Kristina
et al. (1996). Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, P.M.; Boman, H.
et al. (1996). Relative frequency, heterogeneity and geographic clustering of PKU mutations in Norway. (ekstern lenke)
-
Knappskog, Per; Haavik, Jan
(1995). Tryptophan fluorescence of human phenylalanine hydroxylase expressed in Escherichia coli. (ekstern lenke)
-
Knappskog, Per; Eiken, Hans Geir; Martinez, Aurora
et al. (1995). The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzyme. (ekstern lenke)
-
Dianzani, I; Knappskog, Per; de Sanctis, L
et al. (1995). Novel missence mutation in the phenylalanine hydroxylase gene leading to complete loss of enzymatic activity. (ekstern lenke)
-
Knappskog, Per; Flatmark, Torgeir; Mallet, J
et al. (1995). Reccessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene. (ekstern lenke)
-
Martinez, Aurora; Knappskog, Per; Olafsdottir, S
et al. (1995). Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. (ekstern lenke)
-
Martinez, Aurora; Knappskog, Per; Olafsdottir, S
et al. (1995). Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characterization of the wild-type enzyme. (ekstern lenke)
-
Knappskog, Per; Haavik, Jan
(1995). Tryptophan fluorescence of human phenylalanine hydroxylase produced in Escherichia coli. (ekstern lenke)
-
Knappskog, Per; Flatmark, Torgeir; Mallet, J.
et al. (1995). Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene. (ekstern lenke)
-
Knappskog, Per; Eiken, Hans Geir; Martinez, Aurora
et al. (1994). The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzyme. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, Per; Apold, Jaran
(1993). Restriction enzyme based assays for complete genotyping of phenylketonuria patients. (ekstern lenke)
-
Eiken, Hans Geir; Stangeland, K.; Skjelkvåle, L.
et al. (1992). PKU mutations R408Q and F299C in Norway: haplotype associations, geographic distributions, and phenotype characteristics. (ekstern lenke)
-
Eiken, Hans Geir; Knappskog, Per; Apold, Jaran
et al. (1992). A de novo phenylketonuria mutation: ATG(Met) to ATA(Ile) in the start codon of the phenylalanine hydroxylase gene. (ekstern lenke)
Poster
-
Pakdaman, Yasaman; Denker, Elsa; Austad, Eirik
et al. (2020). Modeling neurodegeneration in zebrafish – mutation in spinocerebellar ataxia 16 associated gene stub1 affects Purkinje neuron morphology and leads to behavioral changes.. (ekstern lenke)
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Pakdaman, Yasaman; Denker, Elsa; Austad, Eirik
et al. (2020). Modeling Spinocerebellar Ataxia in zebrafish:U-box domain knockout of stub1 gene affects Purkinje neuron morphology and leads to behavioral changes.. (ekstern lenke)
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Pakdaman, Yasaman; Austad, Eirik; Denker, Elsa
et al. (2019). Characterization of STUB1in zebrafish-development of a new knock-out model to study neurodegeneration. (ekstern lenke)
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Lundstad, Anne Christine; Winge, Ingeborg; Mckinney, Jeffrey Alan
et al. (2005). Expression and molecular characterization of human tryptophan hydroxylases. (ekstern lenke)
-
Halleland, Helene; Knappskog, Per; Fasmer, Ole Bernt
et al. (2005). A Nation-wide Bio-bank of blood samples from adult ADHD patients in Norway. (ekstern lenke)
-
Halleland, Helene; Halmøy, Anne; Fasmer, Ole Bernt
et al. (2005). A Nation-wide Bio-bank of blood samples from adult ADHD patients in Norway. (ekstern lenke)
-
Haavik, Jan; Mckinney, Jeffrey Alan; Knappskog, Per
(2004). Molecular properties of the central and peripheral forms of human tryptophan hydroxylase (TPH1 and TPH2). (ekstern lenke)
Doktorgradsavhandling
Brev til redaktøren
Mastergradsoppgave
Short communication
Sammendrag/abstract
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Oftedal, Bergithe Eikeland; Erichsen, Martina Moter; Hellesen, Alexander
et al. (2013). Dominant Inheritance in Autoimmune Endocrine Syndrome Type 1. (ekstern lenke)
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Brønstad, Ingeborg; Skinningsrud, Beate; Wolff, Anette Susanne Bøe
et al. (2013). Characterisation of the CYP21A2 Gene in Patients with Autoimmune Addison's Disease. (ekstern lenke)
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Winge, Ingeborg; Mc Kinney, Jeffrey Alan; Halmøy, Anne
et al. (2010). FUNCTIONAL STUDIES OF DISEASE-RELATED VARIANTS IN HUMAN TRYPTOPHAN HYDROXYLASE 1 AND 2. (ekstern lenke)
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Bindoff, Laurence; Fiskerstrand, Torunn; H'mida-Ben Brahim, D
et al. (2010). Genetic characterisation of PHARC - a novel syndrome resembling Refsum's disease. (ekstern lenke)
-
Haavik, Jan; Johansson, Stefan; Knappskog, Per Morten
et al. (2009). From synthesis to uptake - serotonergic genes in adult ADHD. (ekstern lenke)
-
Bratland, Eirik; Wolff, Anette Susanne Bøe; Haavik, Jan
et al. (2007). Epitope mapping of human aromatic L-amino acid decarboxylase. (ekstern lenke)
-
Haavik, Jan; Winge, Ingeborg; Mckinney, Jeffrey Alan
et al. (2005). Biochemical characterization of mutant aromatic amino acid hydroxylases implicated in psychiatric disorders. (ekstern lenke)
-
Winge, Ingeborg; Mckinney, Jeffrey Alan; Knappskog, Per
et al. (2005). Effects of mutations in human tryptophan hydroxylases associated with altered monoaminergic neurotransmission. (ekstern lenke)
Vitenskapelig oversiktsartikkel/review
Vitenskapelig Kapittel/Artikkel/Konferanseartikkel
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Rødahl, Eyvind; Christensen, Anne Elisabeth; Fiskerstrand, Torunn
et al. (2012). ADAMTSL4-Related Eye Disorders Includes: Autosomal Recessive Isolated Ectopia Lentis, Ectopia Lentis et Pupillae. (ekstern lenke)
-
Aubi, Oscar; Knappskog, Per; Martinez, Aurora
(2012). Early Stage Discovery and Validation of Pharmacological Chaperones for the Correction of Protein Misfolding Diseases. (ekstern lenke)
-
Flatmark, Torgeir; Knappskog, Per
(1998). Mutations in the genes of the catecholamine biosynthetic enzymes and human diseases. (ekstern lenke)
-
Flatmark, Torgeir; Knappskog, Per
(1998). Mutations in the genes of the catecholamine biosynthetic enzymes and human diseases. (ekstern lenke)
-
Flatmark, Torgeir; Knappskog, Per; Bjørgo, Elisa
et al. (1997). Molecular characterization of disease related mutant forms of human phenylalanine hydroxylase and tyrosine hydroxylase. (ekstern lenke)
-
Flatmark, Torgeir; Knappskog, Per; Bjørgo, Elisa
et al. (1997). Molecular (-en 1) characterization of disease related mutant forms of human phenylalanine hydroxylase and tyrosine hydroxylase. (ekstern lenke)
-
Knappskog, Per; Eiken, Hans Geir; Martinez, Aurora
et al. (1993). Expression of wild type and mutant forms of human phenylalanine hydroxylase in E.Coli. (ekstern lenke)
-
Knappskog, Per; Eiken, Hans Geir; Martinez, Aurora
et al. (1993). Expression of recombinant wild type and mutant forms of human phenylalanine hydroxylase in E. coli. (ekstern lenke)
Leserinnlegg
Leder
Rapport
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Bjervamoen, Siv Grete; Eiken, Hans Geir; Smith, Martin
et al. (2008). Populasjonsovervåkning av brunbjørn 2005-2008 : rapport for Sør-Norge, 2007. (ekstern lenke)
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Eiken, Hans Geir; Bjervamoen, Siv Grete; Smith, Martin
et al. (2007). Populasjonsovervåkning av brunbjørn 2005-2008: Rapport for Sør-Trøndelag, Nord-Trøndelag, Nordland, Troms og Finnmark 2006. (ekstern lenke)
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Eiken, Hans Geir; Wikan, Steinar; Smith, Martin
et al. (2006). Populasjonsovervåkning av brunbjørn 2005-2008 : Rapport for Sør-Varanger, Finnmark for 2004 og 2005. (ekstern lenke)
Vitenskapelig foredrag
-
Hammenfors, D; Løvås, Kristian; Bredholt, G
et al. (2005). Variable expression of FKBP51 in Addison's Disease - a parameter of glucocorticoid sensitivity ?. (ekstern lenke)
-
Bratland, E; Bredholt, G; Knappskog, Per
et al. (2005). Cellular immunity to 21-hydroxylase in patients with autoimmune Addison's disease. (ekstern lenke)
-
Ekern, Trude; Toska, Karen; Knappskog, Per
et al. (1998). Strategies for the expression, purification and immunological characterization of aromatic amino acid hydroxylases. (ekstern lenke)
-
Toska, Karen; Haavik, Jan; Knappskog, Per
(1998). Expression and purification strategies for aromatic amino acid hydroxylases. (ekstern lenke)
-
Boman, Helge; Løvlie, Roger; Knappskog, Per
(1998). Three new FHH mutations and eight genetic variants in the calcium sensing receptor (CASR) gene. (ekstern lenke)
-
Kleppe, Rune; Knappskog, Per; Haavik, Jan
(1998). Thermodynamic stability of human phenylalanine hydroxylase. (ekstern lenke)
-
Waters, P.J.; Hewson, A.S.; Scriver, C.R.
et al. (1996). Comparative analysis of phenylalanine hydroxylase (PAH) A104D mutant, associated with variant phenylketonuria (PKU) and wild-type enzyme. (ekstern lenke)
-
Døskeland, Anne Paulus; Knappskog, Per; Martinez, Aurora
et al. (1995). Phosphorylation of recombinant human phenylalanine hydroxylase expressed in E.coli. (ekstern lenke)
-
Flatmark, Torgeir; Knappskog, Per; Martinez, Aurora
et al. (1995). Characterization of the wild-type and mutant forms of recombinant human phenylalanine hydroxylase. (ekstern lenke)
Hovedfagsoppgave
Se en full oversikt over publikasjoner i Cristin