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91.
We have investigated the conformation of gramicidin A reconstituted in different phospholipid environments, small unilamellar vesicles, extensive bilayers, and micelles, by exploiting a recently proposed experimental approach based on high-performance liquid chromatography [Ba?ó et al. (1988) J. Chromatogr. 458, 105; Ba?ó et al. (1989) FEBS Lett. 250, 67]. The method allows the separation of conformational species of the peptide, namely, antiparallel double-stranded (APDS) dimers and beta 6.3-helical monomers, and quantitation of their proportions in the lipid environment. Various experimental parameters (e.g., nature of organic solvent, time of incubation in organic solvent, lipid-to-peptide mole ratio, time of sonication, and temperature) commonly involved in sample preparation protocols have been analyzed independently. The results show how the peptide conformation in model membranes is exquisitely dictated by the particular nature of the reconstitution protocol. In addition, we have elucidated the nature of the slow conformational transition of gramicidin toward the channel configuration that takes place upon incubation of the model membranes. This transition has been characterized as a temperature-dependent conversion from APDS dimeric to beta 6.3-helical monomeric forms. Analysis of kinetic data permits an accurate calculation of the rate constant for this process at different temperatures in phospholipid vesicles and micelles. Finally, an explanation is proposed for the laboratory-to-laboratory variation in the observed spectral patterns of inserted gramicidin.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
92.
Volume 62, no. 5, p. 1811, column 2, line 2: Reference "(16)" should read "(15)." Page 1812, column 1, line 17: "Willcocks and Carter (15)" should read "Willcocks et al. (14)." [This corrects the article on p. 1811 in vol. 62.]. 相似文献
93.
Albino Maggio Matilde Paino D'Urzo Laura R. Abad Satomi Takeda Paul M. Hasegawa Ray A. Bressan 《Plant Molecular Biology Reporter》1996,14(3):249-260
A procedure for the extraction of large quantities of PR-5 proteins that have been recalcitrant to microbial-based expression
systems is described. Targeting of the recombinant proteins to the extracellular matrix allowed efficient protein extraction
by a vacuum infiltration/centrifugation system. Approximately 1 kg of fresh leaves from transgenic tobacco plants overexpressing
either truncated osmotin (Liu et al., 1996) or A9 fromAtriplex nummularia L. (Casas et al., 1991) yielded between 3 and 5 mg of purified proteins that fully retained their antifungal activity. The
entire system of overexpression, extraction, and purification could be easily scaled up for the production of several grams
of protein. 相似文献
94.
Francesc Muñoz‐Muñoz Valeria Paula Carreira Neus Martínez‐Abadías Victoria Ortiz Rolando González‐José Ignacio M. Soto 《Evolution; international journal of organic evolution》2016,70(7):1530-1541
To predict the response of complex morphological structures to selection it is necessary to know how the covariation among its different parts is organized. Two key features of covariation are modularity and integration. The Drosophila wing is currently considered a fully integrated structure. Here, we study the patterns of integration of the Drosophila wing and test the hypothesis of the wing being divided into two modules along the proximo‐distal axis, as suggested by developmental, biomechanical, and evolutionary evidence. To achieve these goals we perform a multilevel analysis of covariation combining the techniques of geometric morphometrics and quantitative genetics. Our results indicate that the Drosophila wing is indeed organized into two main modules, the wing base and the wing blade. The patterns of integration and modularity were highly concordant at the phenotypic, genetic, environmental, and developmental levels. Besides, we found that modularity at the developmental level was considerably higher than modularity at other levels, suggesting that in the Drosophila wing direct developmental interactions are major contributors to total phenotypic shape variation. We propose that the precise time at which covariance‐generating developmental processes occur and/or the magnitude of variation that they produce favor proximo‐distal, rather than anterior‐posterior, modularity in the Drosophila wing. 相似文献
95.
96.
Evolutionarily distant pathogens require the Arabidopsis phytosulfokine signalling pathway to establish disease
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97.
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99.
R. V. Molina F. Nuez J. Cuartero M. L. Goméz-Guillamón J. Abadía 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1989,78(3):411-416
Summary Six fruit characters have been measured in 23 cultivars of Cucumis melo, representing a wide geographical range. Plants were grown both in the greenhouse and in the field. When the 23 cultivars were analyzed together, the largest component of variance was found between cultivars under both growth conditions, suggesting the existence of large genetic diversity for all the characters studied. Generally, variance between plants within cultivars was less than or equal to variance between fruits within plant. This indicates that environmental variation is the most important part of the variation within cultivars. Correlations between pairs of characters at cultivar, plant and fruit levels were calculated from the variance-covariance components. In the majority of paired traits, the correlation values indicated that genetic and environmental factors may act in the same direction. 相似文献
100.
A semi-empirical approach for the simulation of circular dichroism spectra of gramicidin A in a model membrane.
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In an extension of our previous work (Bañó, M. C., Braco, L., and Abad, C. 1991. Biochemistry. 30:886-94), the kinetics of dissociation of gramicidin A double-stranded dimers into beta 6.3-helical monomers in small unilamellar vesicles prepared following different protocols, were investigated using in combination circular dichroism (CD) and high-performance liquid chromatography (HPLC). The analysis of the data from both techniques according to a two-component model strongly supports that any given CD pattern of gramicidin incorporated in the phospholipid bilayer can be deconvoluted essentially as a linear combination of the reference subspectra calculated for the double-stranded dimer and the helical monomer. An HPLC-based, semi-empirical approach is proposed for the simulation of gramicidin CD curves in the model membrane used, and it is shown that the congruence between theoretical and experimental spectra is very satisfactory. 相似文献