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La ricerca find articoli where authors phrase all words ' KUIVENHOVEN JA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 21 riferimenti
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    1. Boer, JMA; Feskens, EJM; Kuivenhoven, JA; Schouten, EG; Havekes, LM; Kastelein, JJP; Seidell, JC; Kromhout, D
      Parental history of myocardial infarction: lipid traits, gene polymorphisms and lifestyle

      ATHEROSCLEROSIS
    2. Evans, V; Hatzopoulos, A; Aird, WC; Rayburn, HB; Rosenberg, RD; Kuivenhoven, JA
      Targeting the Hprt locus in mice reveals differential regulation of Tie2 gene expression in the endothelium

      PHYSIOLOGICAL GENOMICS
    3. Guillot, PV; Liu, LX; Kuivenhoven, JA; Guan, J; Rosenberg, RD; Aird, WC
      Targeting of human eNOS promoter to the Hprt locus of mice leads to tissue-restricted transgene expression

      PHYSIOLOGICAL GENOMICS
    4. Guillot, PV; Guan, J; Liu, LX; Kuivenhoven, JA; Rosenberg, RD; Sessa, WC; Aird, WC
      A vascular bed-specific pathway regulates cardiac expression of endothelial nitric oxide synthase

      JOURNAL OF CLINICAL INVESTIGATION
    5. Boer, JMA; Kuivenhoven, JA; Feskens, EJM; Schouten, EG; Havekes, LM; Seidell, JC; Kastelein, JJP; Kromhout, D
      Physical activity modulates the effect of a lipoprotein lipase mutation (D9N) on plasma lipids and lipoproteins

      CLINICAL GENETICS
    6. KUIVENHOVEN JA; KASTELEIN JJP
      POLYMORPHISM OF THE CHOLESTERYL ESTER TRANSFER PROTEIN GENE - REPLY

      The New England journal of medicine
    7. KUIVENHOVEN JA; JUKEMA JW; ZWINDERMAN AH; DEKNIJFF P; MCPHERSON R; BRUSCHKE VG; LIE KI; KASTELEIN JJP
      THE ROLE OF A COMMON VARIANT OF THE CHOLESTEROL ESTER TRANSFER PROTEIN GENE IN THE PROGRESSION OF CORONARY ATHEROSCLEROSIS

      The New England journal of medicine
    8. VONECKARDSTEIN A; HUANG YD; KASTELEIN JJP; GEISEL J; REAL JT; KUIVENHOVEN JA; MICCOLI R; NOSEDA G; ASSMANN G
      LIPID-FREE APOLIPOPROTEIN (APO) A-I IS CONVERTED INTO ALPHA-MIGRATINGHIGH-DENSITY-LIPOPROTEINS BY LIPOPROTEIN-DEPLETED PLASMA OF NORMOLIPIDEMIC DONORS AND APO A-I-DEFICIENT PATIENTS BUT NOT OF TANGIER-DISEASEPATIENTS

      Atherosclerosis
    9. LI M; KUIVENHOVEN JA; AYYOBI AF; PRITCHARD PH
      T-]G OR T-]A MUTATION INTRODUCED IN THE BRANCHPOINT CONSENSUS SEQUENCE OF INTRON-4 OF LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE - INTRON RETENTION CAUSING LCAT DEFICIENCY

      Biochimica et biophysica acta, L. Lipids and lipid metabolism
    10. KUIVENHOVEN JA; DEKNIJFF P; BOER JMA; SMALHEER HA; BOTMA GJ; SEIDELL JC; KASTELEIN JJP; PRITCHARD PH
      HETEROGENEITY AT THE CETP GENE LOCUS - INFLUENCE ON PLASMA CETP CONCENTRATIONS AND HDL CHOLESTEROL LEVELS

      Arteriosclerosis, thrombosis, and vascular biology
    11. KUIVENHOVEN JA; GROENEMEYER BE; BOER JMA; REYMER PWA; BERGHUIS R; BRUIN T; JANSEN H; SEIDELL JC; KASTELEIN JJP
      SER(447STOP) MUTATION IN LIPOPROTEIN-LIPASE IS ASSOCIATED WITH ELEVATED HDL CHOLESTEROL LEVELS IN NORMOLIPIDEMIC MALES

      Arteriosclerosis, thrombosis, and vascular biology
    12. KUIVENHOVEN JA; PRITCHARD H; HILL J; FROHLICH J; ASSMANN G; KASTELEIN J
      THE MOLECULAR PATHOLOGY OF LECITHIN - CHOLESTEROL ACYLTRANSFERASE (LCAT) DEFICIENCY SYNDROMES

      Journal of lipid research
    13. SHAMBUREK RD; TALLEY GD; KINDT MR; KUIVENHOVEN JA; KASTELEIN JJP; STALENHOEF AFH; BREWER HB
      LECITHIN-CHOLESTEROL ACYLTRANSFERASE DEFICIENCY - HUMAN IN-VIVO KINETICS OF LDL, APOA-I AND APOA-II IN PARTIAL LCAT DEFICIENCY (FISH EYE DISEASE) WITH AND WITHOUT CAD

      Circulation
    14. GROENEMEIJER BE; HALLMAN MD; REYMER PWA; GAGNE E; KUIVENHOVEN JA; BRUIN T; JANSEN H; LIE KI; BRUSCHKE AVG; BOERWINKLE E; HAYDEN MR; KASTELEIN JJP
      GENETIC VARIANT SHOWING A POSITIVE INTERACTION WITH BETA-BLOCKING-AGENTS WITH A BENEFICIAL INFLUENCE ON LIPOPROTEIN-LIPASE ACTIVITY, HDL CHOLESTEROL, AND TRIGLYCERIDE LEVELS IN CORONARY-ARTERY DISEASE PATIENTS- THE SER(447)-STOP SUBSTITUTION IN THE LIPOPROTEIN-LIPASE GENE

      Circulation
    15. KUIVENHOVEN JA; STALENHOEF AFH; HILL JS; DEMACKER PNM; ERRAMI A; KASTELEIN JJP; PRITCHARD PH
      2 NOVEL MOLECULAR DEFECTS IN THE LCAT GENE ARE ASSOCIATED WITH FISH EYE DISEASE

      Arteriosclerosis, thrombosis, and vascular biology
    16. KUIVENHOVEN JA; WIEBUSCH H; PRITCHARD PH; FUNKE H; BENNE R; ASSMANN G; KASTELEIN JJP
      AN INTRONIC MUTATION IN A LARIAT BRANCHPOINT SEQUENCE IS A DIRECT CAUSE OF AN INHERITED HUMAN DISORDER (FISH-EYE DISEASE) (VOL 98, PG 358, 1996)

      The Journal of clinical investigation
    17. KUIVENHOVEN JA; WEIBUSCH H; PRITCHARD PH; FUNKE H; BENNE R; ASSMANN G; KASTELEIN JJP
      AN INTRONIC MUTATION IN A LARIAT BRANCHPOINT SEQUENCE IS A DIRECT CAUSE OF AN INHERITED HUMAN DISORDER (FISH-EYE DISEASE)

      The Journal of clinical investigation
    18. KUIVENHOVEN JA; DEMACKER PNM; STALENHOEF AFH; PAJKRT D; VANDEVENTER SJH; DORAN JE; PRITCHARD H; KASTELEIN JPP
      INFUSION OF RECONSTITUTED HDL - REVERSE CHOLESTEROL TRANSPORT IN HEREDITARY HDL DEFICIENCIES

      Circulation
    19. KUIVENHOVEN JA; VOORST EJGMVT; WIEBUSCH H; MARCOVINA SM; FUNKE H; ASSMANN G; PRITCHARD PH; KASTELEIN JJP; HILL J; ADLER L; ERRRAMI A
      A UNIQUE GENETIC AND BIOCHEMICAL PRESENTATION OF FISH-EYE DISEASE

      The Journal of clinical investigation
    20. KUIVENHOVEN JA; WIEBUSH H; VANTOL A; SENZ J; PRITCHARD H; FUNKE H; ASSMANN G; KASTELEIN JP
      A NON-SPLICE SITE INTRONIC POINT MUTATION INTERFERES WITH CORRECT MESSENGER-RNA PROCESSING - A GENETIC-BASIS FOR FISH-EYE DISEASE (FED)

      Circulation
    21. LOOMAN AC; KUIVENHOVEN JA
      INFLUENCE OF THE 3 NUCLEOTIDES UPSTREAM OF THE INITIATION CODON ON EXPRESSION OF THE ESCHERICHIA-COLI LACZ GENE IN SACCHAROMYCES-CEREVISIAE

      Nucleic acids research


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 16/01/21 alle ore 13:41:35