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  • American Scientific Publishers  (4)
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  • American Scientific Publishers  (4)
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  • 1
    Online Resource
    Online Resource
    American Scientific Publishers ; 2015
    In:  Journal of Computational and Theoretical Nanoscience Vol. 12, No. 9 ( 2015-09-01), p. 2808-2811
    In: Journal of Computational and Theoretical Nanoscience, American Scientific Publishers, Vol. 12, No. 9 ( 2015-09-01), p. 2808-2811
    Type of Medium: Online Resource
    ISSN: 1546-1955
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2015
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  • 2
    Online Resource
    Online Resource
    American Scientific Publishers ; 2008
    In:  Journal of Nanoscience and Nanotechnology Vol. 8, No. 3 ( 2008-03-01), p. 1359-1363
    In: Journal of Nanoscience and Nanotechnology, American Scientific Publishers, Vol. 8, No. 3 ( 2008-03-01), p. 1359-1363
    Abstract: The supra-molecular assemblies and optical properties of the symmetrical neutral porphyrin chromophore, meso-tetra(4-pyridyl)porphine, bound to a modified α -zirconium phosphate framework have been studied. The interlayer distance of the cetyltrimethylammonium zirconium phosphate framework is 39.6 Å. After the addition of meso-tetra(4-pyridyl)porphine to the framework, the X-ray powder diffraction (XRPD) patterns show that the interlayer distance of the framework is 30.3 Å, demonstrating the formation of novel assemblies. In the framework, organic chromophores are assumed to align in a canted monolayer. The interaction of organic chromophores with the frame-work causes noticeable red shifts of the Soret absorption band from 416 to 427 nm. In contrast, the luminescence peak is blue shifted from 660 nm in aqueous media to 648 nm when mesotetra(4-pyridyl)porphine is bound to the framework. Furthermore, the emission yield of the organic chromophore in the framework is dramatically enhanced compared to that of organic aqueous solutions. The spectroscopic change of meso-tetra(4-pyridyl)porphine is ascribed to the unique microenvironments of the nano-lamellar framework. The juxtaposition of the porphyrin chromophores in the framework tunes their electronic interactions. In comparison, the organic chromophores also attempted to bind with another modified α -zirconium phosphate, n -butylammonium zirconium phosphate. However, the chromophores could not enter into n -butylammonium zirconium phosphate due to its smaller interlayer distance (18.8 Å).
    Type of Medium: Online Resource
    ISSN: 1533-4880
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2008
    SSG: 11
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  • 3
    Online Resource
    Online Resource
    American Scientific Publishers ; 2008
    In:  Journal of Nanoscience and Nanotechnology Vol. 8, No. 3 ( 2008-03-01), p. 1359-1363
    In: Journal of Nanoscience and Nanotechnology, American Scientific Publishers, Vol. 8, No. 3 ( 2008-03-01), p. 1359-1363
    Type of Medium: Online Resource
    ISSN: 1533-4880
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2008
    SSG: 11
    Location Call Number Limitation Availability
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  • 4
    Online Resource
    Online Resource
    American Scientific Publishers ; 2022
    In:  Journal of Biomaterials and Tissue Engineering Vol. 12, No. 7 ( 2022-07-01), p. 1417-1422
    In: Journal of Biomaterials and Tissue Engineering, American Scientific Publishers, Vol. 12, No. 7 ( 2022-07-01), p. 1417-1422
    Abstract: This study assesses lncRNA-CCAT2’s role in reducing the drug resistance of ovarian cancer cell lines. Cisplatin-resistant SKOV-3/DDP cells were established and assigned into CC group (transfected with lncRNA CCAT2 siRNA-NC) and CA group (transfected with lncRNA CCAT2 siRNA) followed by analysis of cell proliferation, apoptosis, expression of CCAT2, ERK1/2, Sp1 and relationship between CCAT2 and ERK1/2 and Sp1. CCAT2 expression in SKOV-3/DDP was higher than IOSE80 and SKOV-3 ( P 〈 0.001). ERK1/2 expression in SKOV-3 and SKOV-3/DDP was 0.67±0.09, 1.97±0.40 ( t = 14.18, P 〈 0.001). Sp1 level in SKOV-3 and SKOV-3/DDP was 0.49±0.05, 1.07±0.11 ( P = 21.47, P 〈 0.001). Transfection of CCAT2 reduced cell fluorescence activity of ERK1/2 and Sp1 ( P 〈 0.001). Cell proliferation in CC group and CA group had no difference at 0 h ( P 〉 0.001) and the inhibition of cell proliferation was found at 24 h ( P 〈 0.001). CC group (5.13±0.51) had lower cell apoptosis rate than CA group (20.52±2.24) ( t = 29.96, P 〈 0.001) but higher ERK1/2 and Sp1 protein level CC group than CA group ( P 〈 0.001). In conclusion, transfection of lncRNA-CCAT2 inhibits SKOV-3/DDP proliferation by targeting ERK1/2-Sp1 signaling pathway, promotes apoptosis and reduces drug resistance.
    Type of Medium: Online Resource
    ISSN: 2157-9083
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2022
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