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La ricerca find articoli where soggetti phrase all words 'AMINO-ACID EXCHANGE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 23 riferimenti
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    1. Timmerman, M; Teng, C; Wilkening, RB; Chung, M; Battaglia, FC
      Net amino acid flux across the fetal liver and placenta during spontaneousovine parturition

      BIOLOGY OF THE NEONATE
    2. Gallwitz, B; Ropeter, T; Morys-Wortmann, C; Mentlein, R; Siegel, EG; Schmidt, WE
      GLP-1-analogues resistant to degradation by dipeptidyl-peptidase IV in vitro

      REGULATORY PEPTIDES
    3. Breitkreutz, R; Babylon, A; Hack, V; Schuster, K; Tokus, M; Bohles, H; Hagmuller, E; Edler, L; Holm, E; Droge, W
      Effect of carnitine on muscular glutamate uptake and intramuscular glutathione in malignant diseases

      BRITISH JOURNAL OF CANCER
    4. ARGYROPOULOS G; JENKINS A; KLEIN RL; LYONS T; WAGENHORST B; STARMAND J; MARCOVINA SM; ALBERS JJ; PRITCHARD PH; GARVEY WT
      TRANSMISSION OF 2 NOVEL MUTATIONS IN A PEDIGREE WITH FAMILIAL LECITHIN-CHOLESTEROL ACYLTRANSFERASE DEFICIENCY - STRUCTURE-FUNCTION-RELATIONSHIPS AND STUDIES IN A COMPOUND HETEROZYGOUS PROBAND

      Journal of lipid research
    5. 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
    6. BLANCOVACA F; QU SJ; FIOL C; FAN HZ; PAO Q; MARZALCASACUBERTA A; ALBERS JJ; HURTADO I; GRACIA V; PINTO X; MARTI T; POWNALL HJ
      MOLECULAR-BASIS OF FISH-EYE DISEASE IN A PATIENT FROM SPAIN - CHARACTERIZATION OF A NOVEL MUTATION IN THE LCAT GENE AND LIPID ANALYSIS OF THE CORNEA

      Arteriosclerosis, thrombosis, and vascular biology
    7. BOREL MJ; WILLIAMS PE; JABBOUR K; HIBBARD JC; FLAKOLL PJ
      MAINTAINING MUSCLE PROTEIN ANABOLISM AFTER A METABOLIC STRESS - ROLE OF DEXTROSE VS AMINO-ACID AVAILABILITY

      American journal of physiology: endocrinology and metabolism
    8. ELKHALIL L; MAJD Z; BAKIR R; PEREZMENDEZ O; CASTRO G; POULAIN P; LACROIX B; DUHAL N; FRUCHART JC; LUC G
      FISH-EYE DISEASE - STRUCTURAL AND IN-VIVO METABOLIC ABNORMALITIES OF HIGH-DENSITY-LIPOPROTEINS

      Metabolism, clinical and experimental
    9. FERRUZZA S; RANALDI G; DIGIROLAMO M; SAMBUY Y
      THE EFFLUX OF LYSINE FROM THE BASOLATERAL MEMBRANE OF HUMAN CULTURED INTESTINAL-CELLS (CACO-2) OCCURS BY DIFFERENT MECHANISMS DEPENDING ON THE EXTRACELLULAR AVAILABILITY OF AMINO-ACIDS

      The Journal of nutrition
    10. YANG XP; INAZU A; HONJO A; KOIZUMI I; KAJINAMI K; KOIZUMI J; MARCOVINA SM; ALBERS JJ; MABUCHI H
      CATALYTICALLY INACTIVE LECITHIN - CHOLESTEROL ACYLTRANSFERASE (LCAT) CAUSED BY A GLY-30 TO SER MUTATION IN A FAMILY WITH LCAT DEFICIENCY

      Journal of lipid research
    11. 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
    12. CULLEN P; VONECKARDSTEIN A; ASSMANN G
      GENETIC AND ACQUIRED ABNORMALITIES OF LIPOPROTEIN METABOLISM

      Cardiovascular risk factors
    13. 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
    14. CONTACOS C; SULLIVAN DR; RYE KA; FUNKE H; ASSMANN G
      A NEW MOLECULAR DEFECT IN THE LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE ASSOCIATED WITH FISH EYE DISEASE

      Journal of lipid research
    15. 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
    16. VONECKARDSTEIN A; HUANG YD; WU SL; FUNKE H; NOSEDA G; ASSMANN G
      REVERSE CHOLESTEROL TRANSPORT IN PLASMA OF PATIENTS WITH DIFFERENT FORMS OF FAMILIAL HDL DEFICIENCY

      Arteriosclerosis, thrombosis, and vascular biology
    17. MIETTINEN H; GYLLING H; MIETTINEN TA; KONTULA K
      2 DIFFERENT ALLELIC MUTATIONS IN A FINNISH FAMILY WITH LECITHIN, CHOLESTEROL ACYLTRANSFERASE DEFICIENCY

      Arteriosclerosis, thrombosis, and vascular biology
    18. QU SJ; FAN HZ; BLANCOVACA F; POWNALL HJ
      IN-VITRO EXPRESSION OF NATURAL MUTANTS OF HUMAN LECITHIN-CHOLESTEROL ACYLTRANSFERASE

      Journal of lipid research
    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. KLEIN HG; DUVERGER N; ALBERS JJ; MARCOVINA S; BREWER HB; SANTAMARINAFOJO S
      IN-VITRO EXPRESSION OF STRUCTURAL DEFECTS IN THE LECITHIN-CHOLESTEROLACYLTRANSFERASE GENE

      The Journal of biological chemistry
    21. MEHLUM A; STAELS B; DUVERGER N; TAILLEUX A; CASTRO G; FIEVET C; LUC G; FRUCHART JC; OLIVECRONA G; SKRETTING G; AUWERX J; PRYDZ H
      TISSUE-SPECIFIC EXPRESSION OF THE HUMAN GENE FOR LECITHIN-CHOLESTEROLACYLTRANSFERASE IN TRANSGENIC MICE ALTERS BLOOD-LIPIDS, LIPOPROTEINS AND LIPASES TOWARDS A LESS ATHEROGENIC PROFILE

      European journal of biochemistry
    22. RADER DJ; IKEWAKI K; DUVERGER N; SCHMIDT H; PRITCHARD H; FROHLICH J; CLERC M; DUMON MF; FAIRWELL T; ZECH L; SANTAMARINAFOJO S; BREWER HB
      MARKEDLY ACCELERATED CATABOLISM OF APOLIPOPROTEIN A-II (APOA-II) AND HIGH-DENSITY-LIPOPROTEINS CONTAINING APOA-II IN CLASSIC LECITHIN - CHOLESTEROL ACYLTRANSFERASE DEFICIENCY AND FISH-EYE DISEASE

      The Journal of clinical investigation
    23. SCHMIDT HHJ; DIEKSTALL FF; BOJANOVSKI D; MANNS MP
      FISH EYE DISEASE

      Deutsche Medizinische Wochenschrift


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 16/01/21 alle ore 13:27:29