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1.
Aihara H Alston-Garnjost M Avery RE Barbaro-Galtieri A Barker AR Barnes AV Barnett BA Bauer DA Bengtsson H Bintinger DL Bobbink GJ Bolognese TS Bross AD Buchanan CD Buijs A Cain MP Caldwell DO Clark AR Cowan GD Crane DA Dahl OI Derby KA Eastman JJ Eberhard PH Eisner AM Enomoto R Erné FC Fujii T Gary JW Gorn W Hauptman JM Hofmann W Huth JE Hylen J Kamae T Kaye HS Kees KH Kenney RW Kerth LT Ko W Koda RI Kofler RR Kwong KK Lander RL Langeveld WG Layter JG Linde FL Lindsey CS Loken SC Lu A Lu X 《Physical review letters》1986,57(8):945-948
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F. FRÉZARD A. GARNIER-SUILLEROT C. DEMICHELI 《Journal of inclusion phenomena and macrocyclic chemistry》1997,28(1):51-62
The recent discovery that mithramycin(MTR) in aqueous solution forms a high affinity[Ca(MTR)4]2- complex led us to the idea thatCa2+-loaded liposomes might be able to accumulateMTR in their aqueous internal compartment. Wetherefore investigated the uptake of MTR into largeunilamellar vesicles (LUV) containing NaCl orCaCl2. Our data show that MTR was efficientlyaccumulated within LUV made fromdipalmitoylphosphatidylcholine and cholesterol, onlywhen the liposomes contained Ca2+ and wereresuspended in a Ca2+-free medium. A drugencapsulation efficiency as high as 60% was achieved,at a drug to lipid molar ratio of 1/18. The circulardichroism and fluorescence excitation spectra ofliposome-encapsulated MTR (LMTR) displayed strongsimilarities with those of the [Ca(MTR)4]2-complex. LMTR was found to be stable, when submittedto conditions that destabilized the[Ca(MTR)4]2- complex. Upon dilution andincubation for 24 h at 37 °C, MTR-containingliposomes did not release a significant amount of MTR.These properties were attributed to the formation ofa high affinity complex between MTR and Ca2+inthe aqueous compartment of liposomes. 相似文献
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Maxfield Leidner 《Graphs and Combinatorics》2014,30(2):377-388
The article shrinks the Δ = 6 hole that exists in the family of planar graphs which satisfy the total coloring conjecture. Let G be a planar graph. If ${v_n^k}$ represents the number of vertices of degree n which lie on k distinct 3-cycles, for ${n, k \in \mathbb{N}}$ , then the conjecture is true for planar graphs which satisfy ${v_5^4 +2(v_5^{5^+} +v_6^4) +3v_6^5 +4v_6^{6^+} < 24}$ . 相似文献
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Exact solutions of sine Gordon and multiple sine Gordon equations are constructed in terms of solutions of a linear base equation, the Klein Gordon equation and also in terms of nonlinear base equations where the nonlinearity is polynomial in the dependent variable. Further, exact solutions of nonlinear generalizations of the Schrodinger equation and of additional nonlinear generalizations of the Klein Gordon equation are constructed in terms of solutions of linear base equations. Finally, solutions with spherical symmetry, of nonlinear Klein Gordon equations are given. 相似文献
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Walczak W Pipalia NH Soni M Faruqi AF Ralph H Maxfield FR Webb BL 《Combinatorial chemistry & high throughput screening》2006,9(9):711-718
The conversion of the genomic information produced by the recent sequencing projects into a comprehensive understanding of the human proteome has yet to occur. A new technology that represents a potential bridge between genomics and proteomics is reverse transfection. Reverse transfection cell microarrays are produced by overlaying cDNA arrays with mammalian cells, generating localized clusters of transfected cells with each cluster overexpressing a unique protein. This miniaturized cell-based microarray format affords parallel functional analysis of thousands of cDNA constructs in a high throughput format. In this report we document the development of a co-transfection methodology for reverse transfection applications. The demonstrated high co-transfection efficiency with a "marker" plasmid encoding for GFP enables the identification of transfected cells and eliminates the need for epitope-tagged constructs in cell-based high throughput screening applications using reverse transfection. This co-transfection method was used to study in parallel the structure/function of multiple versions of the v-Src protein using automated fluorescence microscopy. The wild-type v-Src protein and four mutants having insertions or deletions in the SH2 or SH3 domains displayed high levels of tyrosine kinase activity in HEK293T cells. Three other mutated v-Src proteins, including a kinase-dead version, were shown to be defective for tyrosine kinase activity. This reverse co-transfection approach is applicable for high throughput screening of both cDNA libraries and positional scanning recombinant protein libraries. 相似文献
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Aihara H Alston-Garnjost M Avery RE Barker AR Bauer DA Bay A Belcinski R Bingham HH Bloom ED Buchanan CD Caldwell DO Chao HY Chun SB Clark AR Cowan GD Crane DA Dahl OI Daoudi M Derby KA Eastman JJ Eberhard PH Edberg TK Eisner AM Erné FC Fairfield KH Fridman A Godfrey G Hauptman JM Ho C Hofmann W Kamae T Kenney RW Khacheryan S Kofler RR Lambert DJ Langeveld WG Layter JG Lin WT Linde FL Loken SC Lu A Lynch GR Lys JE Madaras RJ Magnuson BD Marsiske H Masek GE Mathis LG Maxfield SJ Miller ES 《Physical review D: Particles and fields》1991,43(1):29-33