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La ricerca find articoli where authors phrase all words ' Eiken, HG' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 27 riferimenti
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    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
    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
    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
    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
    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
    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
    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
    8. ELLINGSEN S; KNAPPSKOG PM; EIKEN HG
      PHENYLKETONURIA SPLICE MUTATION (EXON6NT-96A-]G) MASQUERADING AS MISSENSE MUTATION (Y204C)

      Human mutation
    9. LOVLIE R; EIKEN HG
      INCREASED P-32 SSCP SENSITIVITY BY COMBINING RE DIGESTION AND EXTENDED X-RAY-FILM EXPOSURES

      BioTechniques
    10. ZSCHOCKE J; MALLORY JP; EIKEN HG; NEVIN NC
      PHENYLKETONURIA AND THE PEOPLES OF NORTHERN-IRELAND

      Human genetics
    11. AARSKOG D; EIKEN HG; BJERKNES R; MYKING OL
      PITUITARY DWARFISM IN THE R271W PIT-1 GENE MUTATION

      European journal of pediatrics
    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
    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
    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
    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
    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
    17. LOVLIE R; EIKEN HG; SORHEIM JI; BOMAN H
      THE CA2-SENSING RECEPTOR GENE (PCAR1) MUTATION T151M IN ISOLATED AUTOSOMAL-DOMINANT HYPOPARATHYROIDISM()

      Human genetics
    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
    19. EIKEN HG; KNAPPSKOG PM; MOTZFELDT K; BOMAN H; APOLD J
      PHENYLKETONURIA GENOTYPES CORRELATED TO METABOLIC PHENOTYPE GROUPS INNORWAY

      European journal of pediatrics
    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
    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
    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
    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
    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
    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
    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
    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


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/01/21 alle ore 12:22:33