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91.
Tomá? ?pringer Hana ?ípová Hana Vaisocherová Josef ?těpánek Ji?í Homola 《Nucleic acids research》2010,38(20):7343-7351
Solid-phase hybridization, i.e. the process of recognition between DNA probes immobilized on a solid surface and complementary targets in a solution is a central process in DNA microarray and biosensor technologies. In this work, we investigate the simultaneous effect of monovalent and divalent cations on the hybridization of fully complementary or partly mismatched DNA targets to DNA probes immobilized on the surface of a surface plasmon resonance sensor. Our results demonstrate that the hybridization process is substantially influenced by the cation shielding effect and that this effect differs substantially for solid-phase hybridization, due to the high surface density of negatively charged probes, and hybridization in a solution. In our study divalent magnesium is found to be much more efficient in duplex stabilization than monovalent sodium (15 mM Mg2+ in buffer led to significantly higher hybridization than even 1 M Na+). This trend is opposite to that established for oligonucleotides in a solution. It is also shown that solid-phase duplex destabilization substantially increases with the length of the involved oligonucleotides. Moreover, it is demonstrated that the use of a buffer with the appropriate cation composition can improve the discrimination of complementary and point mismatched DNA targets. 相似文献
92.
Béatris Mastelic Sohail Ahmed William M. Egan Giuseppe Del Giudice Hana Golding Ian Gust Pieter Neels Steven G. Reed Rebecca L. Sheets Claire-Anne Siegrist Paul-Henri Lambert 《Biologicals》2010,38(5):594-601
For decades, the search for new vaccine adjuvants has been largely empirical. A series of new adjuvants and related formulations are now emerging that are acting through identified immunological mechanisms. Understanding adjuvant mechanism of action is crucial for vaccine design, since this allows for directing immune responses towards efficacious disease-specific effector mechanisms and appropriate memory. It is also of great importance to build new paradigms for assessing adjuvant safety at development stages and at regulatory level. This report reflects the conclusions of a group of scientists from academia, regulatory agencies and industry who attended a conference, organized by the International Association for Biologicals (IABS), on the mode of action of adjuvants on 29–30 April 2010 in Bethesda, Maryland, USA, particularly focusing on how understanding adjuvants mode of action can impact on the assessment of vaccine safety and help to develop target-specific vaccines. More information on the conference output can be found on the IABS website, http://www.iabs.org/. 相似文献
93.
Martin Flajšhans David Gela Martin Kocour Hana Buchtová Marek Rodina Martin Pšenička Vojtěch Kašpar Veronika Piačková Eliška Sudová Otomar Linhart 《Reviews in Fish Biology and Fisheries》2010,20(3):317-329
Performance and physiological traits and health of spontaneous and induced triploid tench are reviewed. Triploidy is best
induced with cold shock; with triploids exhibiting 13.5–51.5% better weight gain, 2.69–3.94% higher slaughtering value, 20–60%
lower gonadosomatic index, 0.9–4.5% higher dry matter in flesh and up to 107% more flesh fat than diploids, if farmed untill
post sexual maturity. Triploids exhibit more abdominal fat and less polyunsaturated fatty acids of the n-3 and n-6 groups
in the flesh. Triploid females are sterile, while triploid males may produce aneuploid spermatozoa with varying DNA content
(1–1.9n) which may initiate development of embryos. Triploids have milder seasonal dynamics in their erythrocyte profile than
the diploids. Thinner diffusion distance in gills of triploids than in diploids is interpreted as adaptation to lower aerobic
capacity. Triploids show neither stronger tendencies to anatomic malformations, nor have bigger affinity to parasitic diseases
than the diploids. Production of triploid tench could be an economically interesting method of farming to higher marketable
weight, bringing a relatively high product quality. 相似文献
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95.
Hana Nůsková Marek Vrbacký Zdeněk Drahota Josef Houštěk 《Journal of bioenergetics and biomembranes》2010,42(5):395-403
The mechanism of cyanide’s inhibitory effect on the mitochondrial cytochrome c oxidase (COX) as well as the conditions for its recovery have not yet been fully explained. We investigated three parameters
of COX function, namely electron transport (oxygen consumption), proton transport (mitochondrial membrane potential Δψ
m) and the enzyme affinity to oxygen (p
50
value) with regard to the inhibition by KCN and its reversal by pyruvate. 250 μM KCN completely inhibited both the electron
and proton transport function of COX. The inhibition was reversible as demonstrated by washing of mitochondria. The addition
of 60 mM pyruvate induced the maximal recovery of both parameters to 60–80% of the original values. When using low KCN concentrations
of up to 5 μM, we observed a profound, 30-fold decrease of COX affinity for oxygen. Again, this decrease was completely reversed
by washing mitochondria while pyruvate induced only a partial, yet significant recovery of oxygen affinity. Our results demonstrate
that the inhibition of COX by cyanide is reversible and that the potential of pyruvate as a cyanide poisoning antidote is
limited. Importantly, we also showed that the COX affinity for oxygen is the most sensitive indicator of cyanide toxic effects. 相似文献
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97.
David Pincus Michael W. Chevalier Tomás Aragón Eelco van Anken Simon E. Vidal Hana El-Samad Peter Walter 《PLoS biology》2010,8(7)
The unfolded protein response (UPR) is an intracellular signaling pathway that counteracts variable stresses that impair protein folding in the endoplasmic reticulum (ER). As such, the UPR is thought to be a homeostat that finely tunes ER protein folding capacity and ER abundance according to need. The mechanism by which the ER stress sensor Ire1 is activated by unfolded proteins and the role that the ER chaperone protein BiP plays in Ire1 regulation have remained unclear. Here we show that the UPR matches its output to the magnitude of the stress by regulating the duration of Ire1 signaling. BiP binding to Ire1 serves to desensitize Ire1 to low levels of stress and promotes its deactivation when favorable folding conditions are restored to the ER. We propose that, mechanistically, BiP achieves these functions by sequestering inactive Ire1 molecules, thereby providing a barrier to oligomerization and activation, and a stabilizing interaction that facilitates de-oligomerization and deactivation. Thus BiP binding to or release from Ire1 is not instrumental for switching the UPR on and off as previously posed. By contrast, BiP provides a buffer for inactive Ire1 molecules that ensures an appropriate response to restore protein folding homeostasis to the ER by modulating the sensitivity and dynamics of Ire1 activity. 相似文献
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