Le informazioni sugli articoli di fonte ISI sono coperte da copyright

Per ulteriori informazioni selezionare i riferimenti di interesse.

1. Damas, JK; Gullestad, L; Aass, H; Simonsen, S; Fjeld, JG; Wikeby, L; Ueland, T; Eiken, HG; Froland, SS; Aukrust, P
   Enhanced gene expression of chemokines and their corresponding receptors in mononuclear blood cells in chronic heart failure - Modulatory effect of intravenous immunoglobulin
   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
   
   J.K. Damas et al., "Enhanced gene expression of chemokines and their corresponding receptors in mononuclear blood cells in chronic heart failure - Modulatory effect of intravenous immunoglobulin", J AM COL C, 38(1), 2001, pp. 187-193
2. Damas, JK; Aukrust, P; Ueland, T; Odegaard, A; Eiken, HG; Gullestad, L; Sejersted, OM; Christensen, G
   Monocyte chemoattractant protein-1 enhances and interleukin-10 suppresses the production of inflammatory cytokines in adult rat cardiomyocytes
   BASIC RESEARCH IN CARDIOLOGY
   
   J.K. Damas et al., "Monocyte chemoattractant protein-1 enhances and interleukin-10 suppresses the production of inflammatory cytokines in adult rat cardiomyocytes", BAS R CARD, 96(4), 2001, pp. 345-352
3. Eiken, HG; Oie, E; Damas, JK; Yndestad, A; Bjerkeli, V; Aass, H; Simonsen, S; Geiran, OR; Tonnessen, T; Christensen, G; Froland, SS; Gullestad, L; Attramadal, H; Aukrust, P
   Myocardial gene expression of leukaemia inhibitory factor, interleukin-6 and glycoprotein 130 in end-stage human heart failure
   EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
   
   H.G. Eiken et al., "Myocardial gene expression of leukaemia inhibitory factor, interleukin-6 and glycoprotein 130 in end-stage human heart failure", EUR J CL IN, 31(5), 2001, pp. 389-397
4. Jugessur, A; Frost, P; Andersen, TI; Steine, S; Lindblom, A; Borresen-Dale, AL; Eiken, HG
   Enhanced detection of mutations in BRCA1 exon 11 using restriction endonuclease fingerprinting-single-strand conformation polymorphism
   JOURNAL OF MOLECULAR MEDICINE-JMM
   
   A. Jugessur et al., "Enhanced detection of mutations in BRCA1 exon 11 using restriction endonuclease fingerprinting-single-strand conformation polymorphism", J MOL MED-J, 78(10), 2000, pp. 580-587
5. Damas, JK; Eiken, HG; Oie, E; Bjerkeli, V; Yndestad, A; Ueland, T; Tonnessen, T; Geiran, OR; Aass, H; Simonsen, S; Christensen, G; Froland, SS; Attramadal, H; Gullestad, L; Aukrust, P
   Myocardial expression of CC- and CXC-chemokines and their receptors in human end-stage heart failure
   CARDIOVASCULAR RESEARCH
   
   J.K. Damas et al., "Myocardial expression of CC- and CXC-chemokines and their receptors in human end-stage heart failure", CARDIO RES, 47(4), 2000, pp. 778-787
6. Ellingsen, S; Knappskog, PM; Apold, J; Eiken, HG
   Diverse PAH transcripts in lymphocytes of PKU patients with putative nonsense (G272X, Y356X) and missense (P281L, R408Q) mutations
   FEBS LETTERS
   
   S. Ellingsen et al., "Diverse PAH transcripts in lymphocytes of PKU patients with putative nonsense (G272X, Y356X) and missense (P281L, R408Q) mutations", FEBS LETTER, 457(3), 1999, pp. 505-508
7. ANDERSEN TI; EIKEN HG; COUCH F; KAADA G; SKREDE M; JOHNSEN H; ALOYSIUS TA; TVEIT KM; TRANEBJAERG L; DORUM A; MOLLER P; WEBER BL; BORRESENDALE AL
   CONSTANT DENATURANT GEL-ELECTROPHORESIS (CDGE) IN BRCA1 MUTATION SCREENING
   Human mutation
   
   T.I. Andersen et al., "CONSTANT DENATURANT GEL-ELECTROPHORESIS (CDGE) IN BRCA1 MUTATION SCREENING", Human mutation, 11(2), 1998, pp. 166-174
8. ELLINGSEN S; KNAPPSKOG PM; EIKEN HG
   PHENYLKETONURIA SPLICE MUTATION (EXON6NT-96A-]G) MASQUERADING AS MISSENSE MUTATION (Y204C)
   Human mutation
   
   S. Ellingsen et al., "PHENYLKETONURIA SPLICE MUTATION (EXON6NT-96A-]G) MASQUERADING AS MISSENSE MUTATION (Y204C)", Human mutation, 9(1), 1997, pp. 88-90
9. LOVLIE R; EIKEN HG
   INCREASED P-32 SSCP SENSITIVITY BY COMBINING RE DIGESTION AND EXTENDED X-RAY-FILM EXPOSURES
   BioTechniques
   
   R. Lovlie e H.G. Eiken, "INCREASED P-32 SSCP SENSITIVITY BY COMBINING RE DIGESTION AND EXTENDED X-RAY-FILM EXPOSURES", BioTechniques, 22(4), 1997, pp. 598
10. ZSCHOCKE J; MALLORY JP; EIKEN HG; NEVIN NC
    PHENYLKETONURIA AND THE PEOPLES OF NORTHERN-IRELAND
    Human genetics
    
    J. Zschocke et al., "PHENYLKETONURIA AND THE PEOPLES OF NORTHERN-IRELAND", Human genetics, 100(2), 1997, pp. 189-194
11. AARSKOG D; EIKEN HG; BJERKNES R; MYKING OL
    PITUITARY DWARFISM IN THE R271W PIT-1 GENE MUTATION
    European journal of pediatrics
    
    D. Aarskog et al., "PITUITARY DWARFISM IN THE R271W PIT-1 GENE MUTATION", European journal of pediatrics, 156(11), 1997, pp. 829-834
12. KNAPPSKOG PM; EIKEN HG; MARTINEZ A; BRULAND O; APOLD J; FLATMARK T
    PKU MUTATION (D143G) ASSOCIATED WITH AN APPARENT HIGH RESIDUAL ENZYME-ACTIVITY - EXPRESSION OF A KINETIC VARIANT FORM OF PHENYLALANINE-HYDROXYLASE IN 3 DIFFERENT SYSTEMS
    Human mutation
    
    P.M. Knappskog et al., "PKU MUTATION (D143G) ASSOCIATED WITH AN APPARENT HIGH RESIDUAL ENZYME-ACTIVITY - EXPRESSION OF A KINETIC VARIANT FORM OF PHENYLALANINE-HYDROXYLASE IN 3 DIFFERENT SYSTEMS", Human mutation, 8(3), 1996, pp. 236-246
13. EIKEN HG; KNAPPSKOG PM; GULDBERG P; APOLD J
    DGGE ANALYSIS AS SUPPLEMENT TO SSCP ANALYSIS OF THE PHENYLALANINE-HYDROXYLASE GENE - DETECTION OF 8 (ONE DE-NOVO, 7 INHERITED) OF 9 REMAINING NORWEGIAN PKU MUTATIONS
    Human mutation
    
    H.G. Eiken et al., "DGGE ANALYSIS AS SUPPLEMENT TO SSCP ANALYSIS OF THE PHENYLALANINE-HYDROXYLASE GENE - DETECTION OF 8 (ONE DE-NOVO, 7 INHERITED) OF 9 REMAINING NORWEGIAN PKU MUTATIONS", Human mutation, 8(1), 1996, pp. 19-22
14. EIKEN HG; KNAPPSKOG PM; APOLD J; FLATMARK T
    PKU MUTATION G46S IS ASSOCIATED WITH INCREASED AGGREGATION AND DEGRADATION OF THE PHENYLALANINE-HYDROXYLASE ENZYME
    Human mutation
    
    H.G. Eiken et al., "PKU MUTATION G46S IS ASSOCIATED WITH INCREASED AGGREGATION AND DEGRADATION OF THE PHENYLALANINE-HYDROXYLASE ENZYME", Human mutation, 7(3), 1996, pp. 228-238
15. EIKEN HG; KNAPPSKOG PM; BOMAN H; THUNE KS; KAADA G; MOTZFELDT K; APOLD J
    RELATIVE FREQUENCY, HETEROGENEITY AND GEOGRAPHIC CLUSTERING OF PKU MUTATIONS IN NORWAY
    European journal of human genetics
    
    H.G. Eiken et al., "RELATIVE FREQUENCY, HETEROGENEITY AND GEOGRAPHIC CLUSTERING OF PKU MUTATIONS IN NORWAY", European journal of human genetics, 4(4), 1996, pp. 205-213
16. STEEN VM; GULBRANDSEN AK; EIKEN HG; BERLE JO
    LACK OF GENETIC-VARIATION IN THE CODING REGION OF THE MYOINOSITOL MONOPHOSPHATASE GENE IN LITHIUM-TREATED PATIENTS WITH MANIC-DEPRESSIVE ILLNESS
    Pharmacogenetics
    
    V.M. Steen et al., "LACK OF GENETIC-VARIATION IN THE CODING REGION OF THE MYOINOSITOL MONOPHOSPHATASE GENE IN LITHIUM-TREATED PATIENTS WITH MANIC-DEPRESSIVE ILLNESS", Pharmacogenetics, 6(1), 1996, pp. 113-116
17. LOVLIE R; EIKEN HG; SORHEIM JI; BOMAN H
    THE CA2-SENSING RECEPTOR GENE (PCAR1) MUTATION T151M IN ISOLATED AUTOSOMAL-DOMINANT HYPOPARATHYROIDISM()
    Human genetics
    
    R. Lovlie et al., "THE CA2-SENSING RECEPTOR GENE (PCAR1) MUTATION T151M IN ISOLATED AUTOSOMAL-DOMINANT HYPOPARATHYROIDISM()", Human genetics, 98(2), 1996, pp. 129-133
18. OLSEN TC; EIKEN HG; KNAPPSKOG PM; KASE BF; MANSSON JE; BOMAN H; APOLD J
    MUTATIONS IN THE IDURONATE-2-SULFATASE GENE IN 5 NORWEGIANS WITH HUNTER SYNDROME
    Human genetics
    
    T.C. Olsen et al., "MUTATIONS IN THE IDURONATE-2-SULFATASE GENE IN 5 NORWEGIANS WITH HUNTER SYNDROME", Human genetics, 97(2), 1996, pp. 198-203
19. EIKEN HG; KNAPPSKOG PM; MOTZFELDT K; BOMAN H; APOLD J
    PHENYLKETONURIA GENOTYPES CORRELATED TO METABOLIC PHENOTYPE GROUPS INNORWAY
    European journal of pediatrics
    
    H.G. Eiken et al., "PHENYLKETONURIA GENOTYPES CORRELATED TO METABOLIC PHENOTYPE GROUPS INNORWAY", European journal of pediatrics, 155(7), 1996, pp. 554-560
20. KNAPPSKOG PM; EIKEN HG; MARTINEZ A; FLATMARK T; APOLD J
    THE PKU MUTATION S349P CAUSES COMPLETE LOSS OF CATALYTIC ACTIVITY IN THE RECOMBINANT PHENYLALANINE-HYDROXYLASE ENZYME
    Human genetics
    
    P.M. Knappskog et al., "THE PKU MUTATION S349P CAUSES COMPLETE LOSS OF CATALYTIC ACTIVITY IN THE RECOMBINANT PHENYLALANINE-HYDROXYLASE ENZYME", Human genetics, 95(2), 1995, pp. 171-173
21. MARTINEZ A; KNAPPSKOG PM; OLAFSDOTTIR S; DOSKELAND AP; EIKEN HG; SVEBAK RM; BOZZINI M; APOLD J; FLATMARK T
    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
    Biochemical journal
    
    A. Martinez et al., "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", Biochemical journal, 306, 1995, pp. 589-597
22. EISENSMITH RC; GOLTSOV AA; ONEILL C; TYFIELD LA; SCHWARTZ EI; KUZMIN AI; BARANOVSKAYA SS; TSUKERMAN GL; TREACY E; SCRIVER CR; GUTTLER F; GULDBERG P; EIKEN HG; APOLD J; SVENSSON E; NAUGHTEN E; CAHALANE SF; CROKE DT; COCKBURN F; WOO SLC
    RECURRENCE OF THE R408W MUTATION IN THE PHENYLALANINE-HYDROXYLASE LOCUS IN EUROPEANS
    American journal of human genetics
    
    R.C. Eisensmith et al., "RECURRENCE OF THE R408W MUTATION IN THE PHENYLALANINE-HYDROXYLASE LOCUS IN EUROPEANS", American journal of human genetics, 56(1), 1995, pp. 278-286
23. STEEN VM; GULBRANDSEN AK; EIKEN HG; BERLE JO
    MUTATION ANALYSIS BY SSCP OF MYOINOSITOL MONOPHOSPHATASE-CODING CDNA FROM LITHIUM-TREATED PATIENTS WITH BIPOLAR MANIC-DEPRESSIVE ILLNESS
    Psychopharmacology
    
    V.M. Steen et al., "MUTATION ANALYSIS BY SSCP OF MYOINOSITOL MONOPHOSPHATASE-CODING CDNA FROM LITHIUM-TREATED PATIENTS WITH BIPOLAR MANIC-DEPRESSIVE ILLNESS", Psychopharmacology, 118(2), 1995, pp. 8-8
24. SCHWARTZ M; ANVRET M; CLAUSTRES M; EIKEN HG; EIKLID K; SCHAEDEL C; STOLPE L; TRANEBJAERG L
    394DELTT - A NORDIC CYSTIC-FIBROSIS MUTATION
    Human genetics
    
    M. Schwartz et al., "394DELTT - A NORDIC CYSTIC-FIBROSIS MUTATION", Human genetics, 93(2), 1994, pp. 157-161
25. APOLD J; EIKEN HG; SVENSSON E; KUNERT E; KOZAK L; CECHAK P; GUTTLER F; GILTAY J; LICHTERKONECKI U; MELLE D; JARUZELSKA JM
    THE PHENYLKETONURIA G272X HAPLOTYPE-7 MUTATION IN EUROPEAN POPULATIONS
    Human genetics
    
    J. Apold et al., "THE PHENYLKETONURIA G272X HAPLOTYPE-7 MUTATION IN EUROPEAN POPULATIONS", Human genetics, 92(2), 1993, pp. 107-109
26. EIKLID K; TRANEBJAERG L; EIKEN HG; PEDERSEN JC; MICHALSEN H; FLUGE G; SCHWARTZ M; NILSEN BR; BOLLE R; SKYBERG D; BOMAN H; BERG K
    FREQUENCY OF THE DELTA-F508-MUTATIONS AND EXON-11-MUTATIONS IN NORWEGIAN CYSTIC-FIBROSIS PATIENTS
    Clinical genetics
    
    K. Eiklid et al., "FREQUENCY OF THE DELTA-F508-MUTATIONS AND EXON-11-MUTATIONS IN NORWEGIAN CYSTIC-FIBROSIS PATIENTS", Clinical genetics, 44(1), 1993, pp. 12-14
27. EIKEN HG; STANGELAND K; SKJELKVALE L; KNAPPSKOG PM; BOMAN H; APOLD J
    PKU MUTATION-R408Q AND MUTATION-F299C IN NORWAY - HAPLOTYPE ASSOCIATIONS, GEOGRAPHIC DISTRIBUTIONS AND PHENOTYPE CHARACTERISTICS
    Human genetics
    
    H.G. Eiken et al., "PKU MUTATION-R408Q AND MUTATION-F299C IN NORWAY - HAPLOTYPE ASSOCIATIONS, GEOGRAPHIC DISTRIBUTIONS AND PHENOTYPE CHARACTERISTICS", Human genetics, 88(6), 1992, pp. 608-612