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  • 1α,25-Dihydroxyvitamin D3  (1)
  • Alcoholics  (1)
  • Association  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Clinica Chimica Acta 215 (1993), S. 1-7 
    ISSN: 0009-8981
    Schlagwort(e): Alcohol ; Alcoholics ; Erythrocyte membranes ; Stimulatory GTP-binding regulatory protein
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Medizin
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1432-069X
    Schlagwort(e): 1α,25-Dihydroxyvitamin D3 ; Vitamin D3 ; Contact hypersensitivity
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Recent evidence indicates that the biologically active metabolite of vitamin D3, 1α,25-dihydroxy-vitamin D3 [1α,25(OH)2D3], has an effect on the regulation of the immune response. We investigated whether topical treatment of mice with 1α,25(OH)2D3 influences the contact hypersensitivity (CHS) response to trinitrochlorobenzene (TNCB). 1α,25(OH)2D3 was applied to the dorsal trunk of A/J mice on days 0–3, and on day 4 topical application of 5% TNCB on the 1α,25(OH)2D3-treated site was performed. The mice were tested for CHS on day 10 by applying 1% TNCB to the ears. No effect on induction of CHS response to TNCB was observed in 1α,25(OH)2D3-treated mice compared with 24,25-dihydroxyvitamin D3[24,25-(OH)2D3]-treated mice as control. In a second experiment, the dorsal trunk of A/J mice was treated with 5% TNCB on day 0. The topical application of 1α,25(OH)2D3 on the ears was performed from days 2 to 5. On day 6, the mice were tested for CHS by applying 1% TNCB to the 1α,25(OH)2D3-treated ears. When 1α,25(OH)2D3 increased their response to TNCB by 40% compared with 24,25(OH)2D3-treated mice as 1α,25(OH)2D3 increased their response to TNCB by 40% compared with 24,25(OH)2D3-treated mice as control (P〈0.01). There were no findings suggesting that the pretreatment of the challenge site with 1α,25(OH)2D3 induced an irritant dermatitis that was superimposed on a subsequent CHS reaction. The 1α,25(OH)2D3 modulation of CHS response to TNCB in mice suggests that the hormone may play a role in the regulation of the immune response in vivo.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Journal of human genetics 45 (2000), S. 24-30 
    ISSN: 1435-232X
    Schlagwort(e): Key words Activator protein 2 ; Association ; Polymorphism ; Schizophrenics ; Linkage disequilibrium ; Episodic course
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract The transcription factor activator protein 2 (AP-2) gene is a possible candidate gene for schizophrenia, since it maps near D6S470, a marker on chromosome 6p24 that provided evidence of linkage to schizophrenia. In the present study we analyzed the promoter region and the whole coding region of the human AP-2 gene in order to identify genetic variations that may lead to the modification of AP-2 expression or the alteration of protein function, contributing to schizophrenia or particular schizophrenic phenotypes. Genomic DNA was isolated from the whole blood samples of 87 unrelated schizophrenics and 100 healthy controls. Polymerase chain reaction (PCR) was performed, using 15 primer sets that spanned the promoter region and the whole coding region, and amplified products were screened by single-strand conformational polymorphism (SSCP) analysis. Aberrant SSCP patterns were analyzed by direct sequencing. Three novel polymorphisms were found in the promoter region; two relatively common (−90G→C, −803G→T) and one rare (−1769G→A). Polymorphic status at both loci suggested strong linkage disequilibrium between the −90G and −803G alleles, and between the −90C and −803T alleles. Although no significant differences in genotypic and allelic frequencies at the −90 and −803 loci were found between patients and controls, significant differences in the distribution of genotypes at the −90 (P = 0.008) and −803 (P = 0.037) loci were observed in patients with an episodic course compared with controls. However, the difference for the −803 locus was not significant after Bonferroni correction for multiple comparisons. Our data provided no direct evidence of an association between schizophrenia and the polymorphisms of the AP-2 gene, although the positive result at the −90 locus in schizophrenics with an episodic course is potentially interesting.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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