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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 278 (1973), S. 435-440 
    ISSN: 1432-1912
    Keywords: Diphosphanates ; Vitamin D Metabolism ; 25-Hydroxycholecalciferol ; 1,25-Dihydroxycholecalciferol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The application of disodium dichloromethylene diphosphonate (Cl2MDP), a diphosphonate which is known to inhibit bone formation and bone destruction leads to changes in the metabolism of 25-Hydroxycholecalciferol. The concentration of the tissue active form of vitamin D, i.e. 1,25-Dihydroxycholecalciferol, was found to be markedly diminished in blood serum, kidney and intestine. It is discussed whether this finding is due to a direct effect of Cl2MDP on 25-Hydroxycholecalciferol-1-hydroxylase in the kidney or indirectly caused by a disturbance of the regulation of 1,25-Dihydroxycholecalciferol production.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-4726
    Keywords: Mononuclear cells ; Adhesion molecules ; Cellular distribution ; Squamous cell carcinoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The expressions and cellular distributions of two pairs of adhesion molecules CD2/LFA-3 (leukocyte function-associated antigen-3) and LFA-1/ICAM-1 (intercellular adhesion molecule-1) were examined in inflammatory cellular infiltrates of advanced squamous cell carcinomas of the head and neck by immunohistochemical techniques including double-staining methods. Thirteen patients were investigated using the following monoclonal antibodies (mAbs): CD2, LFA-3 (CD58), ICAM-1 (CD54), LFA-1 (CD11a), the alpha/beta and gamma/delta T-cell receptor, pan T cells and broadly distributed monocyte/macrophage (m/mø) [Fc gamma RII (CD32), 25F9, RM3/1]. LFA-3 staining was observed on a high number of cells (968 ± 112 cells/mm2), correlating to the number of Fe gamma RII (CD32; P 〈 0.01), 25F9 (P 〈 0.05) and RM3/1 (P 〈 0.05) positive m/mø. Its ligand CD2 was found on 365 ± 126 cells/mm2, representing about 50% of CD3+ cells (730 ± 286 cells/mm2). CD2 positivity correlated to CD3 and CD8 (P 〈 0.01) but not to CD4+ T cells. LFA-1 and ICAM-1 were expressed on lymphocytes as well as on m/mø. ICAM-1+ cells (902 ± 205 cells/mm2) correlated to CD3+, CD8+ and RM3/1+ cells (P 〈 0.01). LFA-1 positivity (803 ± 255 cells/mm2) showed correlations to nearly all investigated antigens, as well as to CD4+ T cells (P 〈 0.05). These results show that different m/mø subsets display distinct patterns of adhesion molecule expressions suggesting different pathways of regulation. The CD3+ lymphocyte population revealed a lack of CD2 expression that was more pronounced in the CD4+ subset and indicated impaired lmyphocyte function.
    Type of Medium: Electronic Resource
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