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1

Comparative susceptibility of turbot, halibut, and cod yolk-sac larvae to challenge with Vibrio spp.

Sandlund, N, Rødseth, OM, Knappskog, DH, Uglenes Fiksdal, I, Bergh, Ø

Journal:

Diseases of Aquatic Organisms

Year:

2010

Language:

english

File:

PDF, 1.00 MB

english, 2010

2

Performance comparison of three BRAF V600E detection methods in malignant melanoma and colorectal cancer specimens

Løes, Inger Marie, Immervoll, Heike, Angelsen, Jon-Helge, Horn, Arild, Geisler, Jürgen, Busch, Christian, Lønning, Per Eystein, Knappskog, Stian

Journal:

Year:

2015

Language:

english

File:

PDF, 1.09 MB

english, 2015

3

Friedreich ataxia in Norway – an epidemiological, molecular and clinical study

Wedding, Iselin Marie, Kroken, Mette, Henriksen, Sandra Pilar, Selmer, Kaja Kristine, Fiskerstrand, Torunn, Knappskog, Per Morten, Berge, Tone, Tallaksen, Chantal ME

Journal:

Orphanet Journal of Rare Diseases

Year:

2015

Language:

english

File:

PDF, 1.24 MB

english, 2015

4

Unusual Stüve-Wiedemann syndrome with complete maternal chromosome 5 isodisomy

Melone, Mariarosa A. B., Pellegrino, Michael J., Nolano, Maria, Habecker, Beth A., Johansson, Stefan, Nathanson, Neil M., Knappskog, Per M., Hahn, Angelika F., Boman, Helge

Journal:

Annals of Clinical and Translational Neurology

Year:

2014

Language:

english

File:

PDF, 845 KB

english, 2014

5

Rare genetic variation in mitochondrial pathways influences the risk for parkinson's disease

Gaare, Johannes J., Nido, Gonzalo S., Sztromwasser, Paweł, Knappskog, Per M., Dahl, Olav, Lund-Johansen, Morten, Maple-Grødem, Jodi, Alves, Guido, Tysnes, Ole-Bjørn, Johansson, Stefan, Haugarvoll, Kri

Journal:

Movement Disorders

Year:

2018

Language:

english

File:

PDF, 557 KB

english, 2018

6

BRCA1 methylation in newborns: genetic disposition, maternal transfer, environmental influence, or by chance only?

Lønning, Per Eystein, Knappskog, Stian

Journal:

Clinical Epigenetics

Year:

2018

Language:

english

File:

PDF, 666 KB

english, 2018

7

PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzyme

Hans Geir Eiken, Per M. Knappskog, Jaran Apold, Torgeir Flatmark

Journal:

Year:

1996

Language:

english

File:

PDF, 946 KB

english, 1996

8

DGGE analysis as supplement to SSCP analysis of the phenylalanine hydroxylase gene: Detection of eight (one de novo, seven inherited) of nine remaining Norwegian PKU mutations

Hans Geir Eiken, Per M. Knappskog, Per Guldberg, Jaran Apold

Journal:

Year:

1996

Language:

english

File:

PDF, 404 KB

english, 1996

9

PKU mutation (D143G) associated with an apparent high residual enzyme activity: Expression of a kinetic variant form of phenylalanine hydroxylase in three different systems

Per M. Knappskog, Hans Geir Eiken, Aurora Martínez, Ove Bruland, Jaran Apold, Torgeir Flatmark

Journal:

Year:

1996

Language:

english

File:

PDF, 1.24 MB

english, 1996

10

Phenylketonuria splice mutation (EXON6nt-96Ag) masquerading as missense mutation (Y204C)

Ståle Ellingsen, Per M. Knappskog, Hans Geir Eiken

Journal:

Year:

1997

Language:

english

File:

PDF, 117 KB

english, 1997

11

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

S. Johansson, H. Halleland, A. Halmøy, K.K. Jacobsen, E.T. Landaas, M. Dramsdahl, O.B. Fasmer, P. Bergsholm, A.J. Lundervold, C. Gillberg, K. Hugdahl, P.M. Knappskog, J. Haavik

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2008

Language:

english

File:

PDF, 81 KB

english, 2008

12

Meta-analysis of brain-derived neurotrophic factor p.Val66Met in adult ADHD in four European populations

C. Sánchez-Mora, M. Ribasés, J.A. Ramos-Quiroga, M. Casas, R. Bosch, A. Boreatti-Hümmer, M. Heine, C.P. Jacob, K-P. Lesch, O.B. Fasmer, P.M. Knappskog, J.J. Sandra Kooij, C. Kan, J.K. Buitelaar, E. Mi

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2010

Language:

english

File:

PDF, 200 KB

english, 2010

13

Clinical effect of temozolomide-based chemotherapy in poorly differentiated endocrine carcinoma after progression on first-line chemotherapy

Staffan Welin, Halfdan Sorbye, Sigrunn Sebjornsen, Stian Knappskog, Christian Busch, Kjell Öberg

Journal:

Year:

2011

Language:

english

File:

PDF, 186 KB

english, 2011

14

A novel type of deletion in the CDKN2A gene identified in a melanoma-prone family

Stian Knappskog, Jürgen Geisler, Thomas Arnesen, Johan R. Lillehaug, Per E. Lønning

Journal:

Genes, Chromosomes and Cancer

Year:

2006

Language:

english

File:

PDF, 297 KB

english, 2006

15

A de novo phenylketonuria mutation: ATG (met) to ATA (ile) in the start codon of the phenylalanine hydroxylase gene

Hans Geir Eiken, Per M. Knappskog, Jaran Apold, Leif Skjelkvåle, Helge Boman

Journal:

Year:

1992

Language:

english

File:

PDF, 314 KB

english, 1992

16

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

Irma Dianzani, Per M. Knappskog, Luisa de Sanctis, Sergio Giannattasio, Enrica Riva, Alberto Ponzone, Jaran Apold, Clara Camaschella

Journal:

Year:

1995

Language:

english

File:

PDF, 273 KB

english, 1995

17

Functional properties of missense variants of human tryptophan hydroxylase 2

Jeffrey A. McKinney, Banu Turel, Ingeborg Winge, Per M. Knappskog, Jan Haavik

Journal:

Year:

2009

Language:

english

File:

PDF, 231 KB

english, 2009

18

P21/WAF1 mutation and drug resistance to paclitaxel in locally advanced breast cancer

Ranjan Chrisanthar, Stian Knappskog, Vidar Staalesen, Johan Richard Lillehaug, Per Eystein Lønning

Journal:

International Journal of Cancer

Year:

2007

Language:

english

File:

PDF, 40 KB

english, 2007

19

Mutations and polymorphisms of the p21B transcript in breast cancer

Stian Knappskog, Ranjan Chrisanthar, Vidar Staalesen, Anne-Lise Børresen-Dale, Inger Torhild Gram, Johan Richard Lillehaug, Per Eystein Lønning

Journal:

International Journal of Cancer

Year:

2007

Language:

english

File:

PDF, 70 KB

english, 2007

20

Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standard

Ove Bruland, Elisabeth W Almqvist, Y Paul Goldberg, Helge Boman, Michael R Hayden, Per M Knappskog

Journal:

Clinical Genetics

Year:

1999

Language:

english

File:

PDF, 1.30 MB

english, 1999

21

Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease

Ingeborg Brønstad, Anette SB Wolff, Kristian Løvås, Per M Knappskog, Eystein S Husebye

Journal:

BMC Medical Genetics

Year:

2011

Language:

english

File:

PDF, 228 KB

english, 2011

22

The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzyme

Per M. Knappskog, Hans Geir Eiken, Aurora Martinez, Torgeir Flatmark, Jaran Apold

Journal:

Year:

1995

Language:

english

File:

PDF, 346 KB

english, 1995

23

Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway

H. G. Eiken, P. M. Knappskog, K. Motzfeldt, H. Boman, J. Apold

Journal:

European Journal of Pediatrics

Year:

1996

Language:

english

File:

PDF, 722 KB

english, 1996

24

PKU mutations R408Q and F299C in Norway: Haplotype associations, geographic distributions and phenotype characteristics

Hans Geir Eiken, Karin Stangeland, Leif Skjelkvålez, Per M. Knappskog, Helge Boman, Jaran Apold

Journal:

Year:

1992

Language:

english

File:

PDF, 684 KB

english, 1992

25

New species in the genusFrancisella(Gammaproteobacteria; Francisellaceae);Francisella piscicidasp. nov. isolated from cod (Gadus morhua)

Karl F. Ottem, Are Nylund, Egil Karlsbakk, Alice Friis-Møller, Bjørn Krossøy, Dag Knappskog

Journal:

Archives of Microbiology

Year:

2007

Language:

english

File:

PDF, 244 KB

english, 2007

26

Chronic mucocutaneous candidiasis and primary hypothyroidism in two families

Anne Grethe Myhre, Asbjørg Stray-Pedersen, Steinar Spangen, Eigill Eide, Dag Veimo, Per Morten Knappskog, Tore G. Abrahamsen, Eystein S. Husebye

Journal:

European Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 232 KB

english, 2004

27

Gene expression profiling of meningiomas: current status after a decade of microarray-based transcriptomic studies

Mads Aarhus, Morten Lund-Johansen, Per Morten Knappskog

Journal:

Acta Neurochirurgica

Year:

2011

Language:

english

File:

PDF, 451 KB

english, 2011

28

Iron coordination geometry in full-length, truncated, and dehydrated forms of human tyrosine hydroxylase studied by Mössbauer and X-ray absorption spectroscopy

Volker Schünemann, Christian Meier, Wolfram Meyer-Klaucke, Heiner Winkler, Alfred X. Trautwein, Per M. Knappskog, Karen Toska, J. Haavik

Journal:

JBIC Journal of Biological Inorganic Chemistry

Year:

1999

Language:

english

File:

PDF, 145 KB

english, 1999

29

Alterations of the retinoblastoma gene in metastatic breast cancer

Elisabet Ognedal Berge, Stian Knappskog, Johan Richard Lillehaug, Per Eystein Lønning

Journal:

Clinical and Experimental Metastasis

Year:

2011

Language:

english

File:

PDF, 241 KB

english, 2011

30

Microarray analysis reveals down-regulation of the tumour suppressor gene WWOX and up-regulation of the oncogene TYMS in intracranial sporadic meningiomas

Mads Aarhus, Ove Bruland, Geir Bredholt, Helle Lybæk, Eystein S. Husebye, Bård K. Krossnes, Christian Vedeler, Knut Wester, Morten Lund-Johansen, Per M. Knappskog

Journal:

Journal of Neuro-Oncology

Year:

2008

Language:

english

File:

PDF, 506 KB

english, 2008

31

Proteomic profiles differ between bone invasive and noninvasive benign meningiomas of fibrous and meningothelial subtype

Carl Wibom, Lina Mörén, Mads Aarhus, Per Morten Knappskog, Morten Lund-Johansen, Henrik Antti, A Tommy Bergenheim

Journal:

Journal of Neuro-Oncology

Year:

2009

Language:

english

File:

PDF, 424 KB

english, 2009

32

Infliximab Treatment of Rheumatoid Arthritis Patients Simultaneously Increases TNF-α Protein Levels and Reduces mRNA Expression in the Blood

T. O. Hjelmevik, A. G. Kvalvik, P. M. Knappskog, L. Lefsaker, A. S. Kleiven, S. Dyvik, J. G. Brun, H. Østergaard, H. G. Eiken

Journal:

Scandinavian Journal of Immunology

Year:

2004

Language:

english

File:

PDF, 259 KB

english, 2004

33

Immunochemical analyses of Vibrio anguillarum strains isolated from cod, Gadus morhua L., suffering from vibriosis

D. H. KNAPPSKOG, O. M. RØDSETH, E. SLINDE, C. ENDRESEN

Journal:

Journal of Fish Diseases

Year:

1993

Language:

english

File:

PDF, 7.13 MB

english, 1993

34

Detection of Autoantibodies to the BTB-kelch Protein KLHL7 in Cancer Sera

G. Bredholt, A. Storstein, M. Haugen, B. K. Krossnes, E. Husebye, P. Knappskog, C. A. Vedeler

Journal:

Scandinavian Journal of Immunology

Year:

2006

Language:

english

File:

PDF, 1.27 MB

english, 2006

35

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

Jeffrey McKinney, Per M. Knappskog, Jan Haavik

Journal:

Journal of Neurochemistry

Year:

2005

Language:

english

File:

PDF, 191 KB

english, 2005

36

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

Ingeborg Winge, Jeffrey A. McKinney, Per M. Knappskog, Jan Haavik

Journal:

Journal of Neurochemistry

Year:

2007

Language:

english

File:

PDF, 731 KB

english, 2007

37

Pyridoxal phosphatase is a novel cancer autoantigen in the central nervous system

Bøe, A S, Bredholt, G, Knappskog, P M, Storstein, A, Vedeler, C A, Husebye, E S

Journal:

British Journal of Cancer

Year:

2004

Language:

english

File:

PDF, 178 KB

english, 2004

38

AIRE variations in Addison's disease and autoimmune polyendocrine syndromes (APS): partial gene deletions contribute to APS I

Bøe Wolff, A S, Oftedal, B, Johansson, S, Bruland, O, Løvås, K, Meager, A, Pedersen, C, Husebye, E S, Knappskog, P M

Journal:

Genes and Immunity

Year:

2008

Language:

english

File:

PDF, 203 KB

english, 2008

39

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, P M, Haavik, J

Journal:

Molecular Psychiatry

Year:

2008

Language:

english

File:

PDF, 72 KB

english, 2008

40

Field validation of experimental challenge models for IPN vaccines

A Ramstad, A B Romstad, D H Knappskog, P J Midtlyng

Journal:

Journal of Fish Diseases

Year:

2007

Language:

english

File:

PDF, 202 KB

english, 2007

41

The MDM2 Promoter SNP285C/309G Haplotype Diminishes Sp1 Transcription Factor Binding and Reduces Risk for Breast and Ovarian Cancer in Caucasians

Stian Knappskog, Merete Bjørnslett, Line M. Myklebust, Petra E.A. Huijts, Maaike P. Vreeswijk, Hege Edvardsen, Yongli Guo, Xuemei Zhang, Ming Yang, Sanna K. Ylisaukko-oja, Pia Alhopuro, Johanna Arola,

Journal:

Year:

2011

Language:

english

File:

PDF, 452 KB

english, 2011

42

Partial characterization and three-dimensional-structural localization of eight mutations in exon 7 of the human phenylalanine hydroxylase gene associated with phenylketonuria

Elisa Bjørgo, Per M. Knappskog, Aurora Martinez, Raymond C. Stevens, Torgeir Flatmark

Journal:

Year:

1998

Language:

english

File:

PDF, 587 KB

english, 1998

43

Tyrosine hydroxylase binds tetrahydrobiopterin cofactor with negative cooperativity, as shown by kinetic analyses and surface plasmon resonance detection

Torgeir Flatmark, Bjørg Almås, Per M. Knappskog, Sissel V. Berge, Randi M. Svebak, Rosana Chehin, Arturo Muga, Aurora Martínez

Journal:

Year:

1999

Language:

english

File:

PDF, 719 KB

english, 1999

44

Structure/Function Relationships in Human Phenylalanine Hydroxylase : Effect of Terminal Deletions on the Oligomerization, Activation and Cooperativity of Substrate Binding to the Enzyme

Per M. Knappskog, Torgeir Flatmark, Johanna M. Aarden, Jan Haavik, Aurora Martínez

Journal:

Year:

1996

Language:

english

File:

PDF, 1.08 MB

english, 1996

45

Synergistic induction of p53 mediated apoptosis by valproic acid and nutlin-3 in acute myeloid leukemia

McCormack, E, Haaland, I, Venås, G, Forthun, R B, Huseby, S, Gausdal, G, Knappskog, S, Micklem, D R, Lorens, J B, Bruserud, Ø

Journal:

Year:

2011

Language:

english

File:

PDF, 608 KB

english, 2011

46

Uptake and processing of a Vibrio anguillarum bacterin in Artemia franciscana measured by ELISA and immunohistochemistry

Øivind Bergh, Lisbeth Vikanes, Pavlos Makridis, Jorunn Skjermo, Dag Knappskog, Odd Magne Rødseth

Journal:

Fish & Shellfish Immunology

Year:

2001

Language:

english

File:

PDF, 1.69 MB

english, 2001

47

A Phenylalanine Hydroxylase Amino Acid Polymorphism with Implications for Molecular Diagnostics

Torben Gjetting, Anne Romstad, Jan Haavik, Per M. Knappskog, Angelina X. Acosta, W.Araújo Silva Jr., Marco A. Zago, Per Guldberg, Flemming Gttler

Journal:

Molecular Genetics and Metabolism

Year:

2001

Language:

english

File:

PDF, 87 KB

english, 2001

48

A Second Decorin Frame Shift Mutation in a Family With Congenital Stromal Corneal Dystrophy

Eyvind Rødahl, Rita Van Ginderdeuren, Per M. Knappskog, Cecilie Bredrup, Helge Boman

Journal:

American Journal of Ophthalmology

Year:

2006

Language:

english

File:

PDF, 104 KB

english, 2006

49

Epitope mapping of human aromatic l-amino acid decarboxylase

Eirik Bratland, Anette S. Bøe Wolff, Jan Haavik, Olle Kämpe, Filip Sköldberg, Jaakko Perheentupa, Geir Bredholt, Per M. Knappskog, Eystein S. Husebye

Journal:

Biochemical and Biophysical Research Communications

Year:

2007

Language:

english

File:

PDF, 577 KB

english, 2007

50

SNP285C modulates oestrogen receptor/Sp1 binding to the MDM2 promoter and reduces the risk of endometrial but not prostatic cancer

Stian Knappskog, Jone Trovik, Janusz Marcickiewicz, Solveig Tingulstad, Annetine C. Staff, Pål Romundstad, Kristian Hveem, Lars Vatten, Helga B. Salvesen, Per E. Lønning

Journal:

European Journal of Cancer

Year:

2012

Language:

english

File:

PDF, 388 KB

english, 2012