全文获取类型
收费全文 | 75篇 |
免费 | 2篇 |
专业分类
化学 | 48篇 |
晶体学 | 1篇 |
力学 | 2篇 |
数学 | 6篇 |
物理学 | 20篇 |
出版年
2020年 | 1篇 |
2015年 | 2篇 |
2014年 | 1篇 |
2013年 | 2篇 |
2012年 | 5篇 |
2011年 | 6篇 |
2010年 | 4篇 |
2009年 | 1篇 |
2008年 | 7篇 |
2007年 | 1篇 |
2006年 | 5篇 |
2005年 | 6篇 |
2004年 | 6篇 |
2003年 | 4篇 |
2002年 | 6篇 |
2001年 | 1篇 |
2000年 | 2篇 |
1999年 | 4篇 |
1997年 | 1篇 |
1996年 | 1篇 |
1994年 | 2篇 |
1993年 | 1篇 |
1991年 | 1篇 |
1987年 | 1篇 |
1984年 | 1篇 |
1982年 | 1篇 |
1978年 | 1篇 |
1974年 | 1篇 |
1969年 | 1篇 |
1932年 | 1篇 |
排序方式: 共有77条查询结果,搜索用时 31 毫秒
1.
2.
Gareth AD Hardy Nesrina Imami Mark R Nelson Ann K Sullivan Ron Moss Marlén MI Aasa-Chapman Brian Gazzard Frances M Gotch 《Journal of immune based therapies and vaccines》2007,5(1):6-12
Background
Fully functional HIV-1-specific CD8 and CD4 effector T-cell responses are vital to the containment of viral activity and disease progression. These responses are lacking in HIV-1-infected patients with progressive disease. We attempted to augment fully functional HIV-1-specific CD8 and CD4 effector T-cell responses in patients with advanced chronic HIV-1 infection. 相似文献3.
4.
Nathan Hollingsworth Graeme A. Horley Muhammed Mazhar Mary F. Mahon Kieran C. Molloy Peter W. Haycock Christopher P. Myers Gary W. Critchlow 《应用有机金属化学》2006,20(10):687-695
Tin(II) methoxide reacts with N,N′‐dimethylaminoethanol (dmaeH) to yield Sn(dmae)2 ( 1 ) along with small amounts of the hydrolysis product Sn6(O)4(dmae)4 ( 2 ). The geometrically more regular iso‐structural cage Sn6(O)4(OEt)4 ( 3 ) was obtained as the only tractable product isolated from reaction of 2 and Sb(OEt)3, while 1 reacted with CdX2 (X = acac, I) to afford Sn(dmae)2Cd(acac)2 ( 4 ) and Sn(dmae)2CdI2 ( 5 ). The X‐ray structures of 2, 3 and 4 are reported. Decomposition of 4 under aerosol‐assisted chemical vapour deposition conditions leads to amorphous tin oxide films with no detectable cadmium (i.e. ca < 2% cadmium), rather than a stoichiometric Sn:Cd oxide. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
5.
Sullivan MT Zhao K Hollingsworth AD Austin RH Russel WB Chaikin PM 《Physical review letters》2006,96(1):015703
Particle concentration is a dominant control parameter for colloids and other soft matter systems. We demonstrate a simple technique, "dielectrophoretic equilibrium," implemented as an "electric bottle," a planar capacitor in a larger volume. The uniform field in the capacitor traps particles in this force-free region at a higher density than in the zero field regions outside. We show how the technique measures the equation of state and we initiate and grow colloidal crystals. "Dielectrophoretic equilibria" enable the study of a complete concentration-dependent phase diagram from a single microscopic sample, obviating the previous need for preparing a large number of samples. 相似文献
6.
Veenu Bala Yashpal S. Chhonker Richard L. Sleightholm Ayrianne J. Crawford Michael A. Hollingsworth Daryl J. Murry 《Biomedical chromatography : BMC》2020,34(8):e4859
A rapid, selective, and sensitive liquid chromatography coupled with tandem mass spectrometry (MS/MS) method was developed and validated for the quantitation of the novel CDK5 inhibitor ‘20–223' in mouse plasma. Separation of analytes was achieved by a reverse-phase ACE Excel C18 column (1.7 μm, 100 × 2.1 mm) with gradient elution using 0.1% formic acid (FA) in methanol and 0.1% FA as the mobile phase. Analytes were monitored by MS/MS with an electrospray ionization source in the positive multiple reaction monitoring mode. The MS/MS response was linear over the concentration range 0.2–500 ng/mL for 20–223. The within- and between-batch precision were within the acceptable limits as per Food and Drug Administration guidelines. The validated method was successfully applied to plasma protein binding and in vitro metabolism studies. Compound 20–223 was highly bound to mouse plasma proteins (>98% bound). Utilizing mouse S9 fractions, in vitro intrinsic clearance (CLint) was 24.68 ± 0.99 μL/min/mg protein. A total of 12 phase I and II metabolites were identified with hydroxylation found to be the major metabolic pathway. The validate method required a low sample volume, was linear from 0.2 to 500 ng/mL, and had acceptable accuracy and precision. 相似文献
7.
8.
9.
We report results from complementary electrokinetic measurements-dielectric relaxation and electrophoretic mobility-undertaken to test the applicability of the standard electrokinetic theory with a model system. Dielectric spectra were obtained at frequencies between 1 kHz and 40 MHz with a new, two-electrode cell design [Hollingsworth and Saville, J. Colloid Interface Sci. 257 (2003) 65-76]; mobility data were acquired with an electrophoretic light scattering instrument. Data from the two-electrode cell were collected at different electrode separations and interpreted with newly developed procedures to remove the influence of electrode polarization. Methodology A employs extrapolation to infinite electrode separation to compute the dielectric constant and conductivity as functions of frequency. The contributions from suspended particles are reported in terms of dielectric constant and conductivity increments. Methodology B uses a theoretical model of electrode polarization and the standard electrokinetic model in a nonlinear regression scheme. Results are presented in several forms: frequency-dependent dielectric constant and conductivity increments, frequency-dependent dielectric constants and conductivities, and the complex dipole coefficient. It is shown that the standard model provides a consistent methodology for interpreting particle behavior; zeta-potentials inferred from mobility and dielectric relaxation agree to within experimental error. Moreover, the cell design and interpretation are straightforward and provide relatively simple ways to obtain complementary measurements over a wide frequency range. The results unambiguously show that electrokinetic character of this dispersion follows the standard model. 相似文献
10.