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La ricerca find articoli where authors phrase all words ' Cao, HN' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 20 riferimenti
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    1. Cao, HN; Hegele, RA
      Single nucleotide polymorphisms of the resistin (RSTN) gene

      JOURNAL OF HUMAN GENETICS
    2. Hegele, RA; Cao, HN
      Single nucleotide polymorphisms of RXRA encoding retinoid X receptor alpha

      JOURNAL OF HUMAN GENETICS
    3. Hegele, RA; Ramdath, DD; Ban, MR; Carruthers, MN; Carrington, CV; Cao, HN
      Polymorphisms in PNLIP, encoding pancreatic lipase, and associations with metabolic traits

      JOURNAL OF HUMAN GENETICS
    4. Hegele, RA; Yuen, J; Cao, HN
      Single-nucleotide polymorphisms of the nuclear lamina proteome

      JOURNAL OF HUMAN GENETICS
    5. Cao, HN; Hegele, RA
      Human aryl hydrocarbon receptor nuclear translocator gene (ARNT) D/N511 polymorphism

      JOURNAL OF HUMAN GENETICS
    6. Cao, HN; Hegele, RA
      Human cathepsin S gene (CTSS) promoter-25G/A polymorphism

      JOURNAL OF HUMAN GENETICS
    7. Cao, HN; Hegele, RA
      Human hepatocyte nuclear factor-1 beta (HNF1B) 1968A/G polymorphism

      JOURNAL OF HUMAN GENETICS
    8. Cao, HN; Hegele, RA
      Human C-reactive protein (CRP) 1059G/C polymorphism

      JOURNAL OF HUMAN GENETICS
    9. Hegele, RA; Cao, HN; Harris, SB; Zinman, B; Hanley, AJ; Anderson, CM
      Genetic variation in LMNA modulates plasma leptin and indices of obesity in aboriginal Canadians

      PHYSIOLOGICAL GENOMICS
    10. Hegele, RA; Anderson, CM; Wang, J; Jones, DC; Cao, HN
      Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes

      GENOME RESEARCH
    11. Hegele, RA; Cao, HN; Harris, SB; Hanley, AJG; Zinman, B; Connelly, PW
      The private hepatocyte nuclear factor-1 alpha G319S variant is associated with plasma lipoprotein variation in Canadian Oji-Cree

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    12. Hegele, RA; Anderson, CM; Cao, HN
      Lamin A/C mutation in a woman and her two daughters with Dunnigan-type partial lipodystrophy and insulin resistance

      DIABETES CARE
    13. Hegele, RA; Cao, HN; Huff, MW; Anderson, CM
      LMNA R482Q mutation in partial lipodystrophy associated with reduced plasma leptin concentration

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    14. Hegele, RA; Cao, HN; Anderson, CM; Hramiak, IM
      Heterogeneity of nuclear lamin A mutations in Dunnigan-type familial partial lipodystrophy

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    15. Fehlner-Gardiner, CC; Cao, HN; Jackson-Boeters, L; Nakamura, T; Elliott, BE; Uniyal, S; Chan, BMC
      Characterization of a functional relationship between hepatocyte growth factor and mouse bone marrow-derived mast cells

      DIFFERENTIATION
    16. Hegele, RA; Busch, CP; Young, TK; Connelly, PW; Cao, HN
      Mannose-binding lectin gene variation and cardiovascular disease in Canadian inuit

      CLINICAL CHEMISTRY
    17. LUCAS A; GUAN HY; DAI E; LIU LY; IVANOVA D; CAO HN; NASH P
      VIRAL SERPIN REDUCED ATHEROSCLEROSIS IS ASSOCIATED WITH UP-REGULATIONOF THE UPA RECEPTOR AND PAI-1

      European cytokine network
    18. HEGELE RA; HARRIS SB; HANLEY AJG; CAO HN; ZINMAN B
      G-PROTEIN BETA-3 SUBUNIT GENE VARIANT AND BLOOD-PRESSURE VARIATION INCANADIAN OJI-CREE

      Hypertension
    19. HEGELE RA; HARRIS SB; ZINMAN B; WANG J; CAO HN; HANLEY AJG; TSUI LC; SCHERER SW
      VARIATION IN THE AU(AT)-RICH ELEMENT WITHIN THE 3'-UNTRANSLATED REGION OF PPP1R3 IS ASSOCIATED WITH VARIATION IN PLASMA-GLUCOSE IN ABORIGINAL CANADIANS

      The Journal of clinical endocrinology and metabolism
    20. XI ZD; MA BL; YANG LM; CAO HN; WANG M
      ACTIVE-SITE OF TRICHOSANTHIN ACTING AS A RIBOSOME-INACTIVATING PROTEIN

      Zhongguo yaoli xuebao


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 22/10/20 alle ore 00:15:56