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91.
Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes   总被引:41,自引:0,他引:41  
Ashrafi K  Chang FY  Watts JL  Fraser AG  Kamath RS  Ahringer J  Ruvkun G 《Nature》2003,421(6920):268-272
Regulation of body fat storage involves signalling between centres that regulate feeding in the brain and sites of fat storage and use in the body. Here we describe an assay for analysing fat storage and mobilization in living Caenorhabditis elegans. By using RNA-mediated interference (RNAi) to disrupt the expression of each of the 16,757 worm genes, we have systematically screened the C. elegans genome for genes necessary for normal fat storage. We identify 305 gene inactivations that cause reduced body fat and 112 gene inactivations that cause increased fat storage. Analysis of the fat-reducing gene inactivations in insulin, serotonin and tubby signalling mutants of C. elegans, which have increased body fat, identifies a core set of fat regulatory genes as well as pathway-specific fat regulators. Many of the newly identified worm fat regulatory genes have mammalian homologues, some of which are known to function in fat regulation. Other C. elegans fat regulatory genes that are conserved across animal phylogeny, but have not previously been implicated in fat storage, may point to ancient and universal features of fat storage regulation, and identify targets for treating obesity and its associated diseases.  相似文献   
92.
Moore P  Clayton J 《Nature》2003,426(6967):725-731
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93.
94.
Mills MM  Ridame C  Davey M  La Roche J  Geider RJ 《Nature》2004,429(6989):292-294
The role of iron in enhancing phytoplankton productivity in high nutrient, low chlorophyll oceanic regions was demonstrated first through iron-addition bioassay experiments and subsequently confirmed by large-scale iron fertilization experiments. Iron supply has been hypothesized to limit nitrogen fixation and hence oceanic primary productivity on geological timescales, providing an alternative to phosphorus as the ultimate limiting nutrient. Oceanographic observations have been interpreted both to confirm and refute this hypothesis, but direct experimental evidence is lacking. We conducted experiments to test this hypothesis during the Meteor 55 cruise to the tropical North Atlantic. This region is rich in diazotrophs and strongly impacted by Saharan dust input. Here we show that community primary productivity was nitrogen-limited, and that nitrogen fixation was co-limited by iron and phosphorus. Saharan dust addition stimulated nitrogen fixation, presumably by supplying both iron and phosphorus. Our results support the hypothesis that aeolian mineral dust deposition promotes nitrogen fixation in the eastern tropical North Atlantic.  相似文献   
95.
Clayton J  Butler D 《Nature》2004,430(7002):937
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96.
97.
Atmospheric science: early peak in Antarctic oscillation index   总被引:1,自引:0,他引:1  
Jones JM  Widmann M 《Nature》2004,432(7015):290-291
The principal extratropical atmospheric circulation mode in the Southern Hemisphere, the Antarctic oscillation (or Southern Hemisphere annular mode), represents fluctuations in the strength of the circumpolar vortex and has shown a trend towards a positive index in austral summer in recent decades, which has been linked to stratospheric ozone depletion and to increased atmospheric greenhouse-gas concentrations. Here we reconstruct the austral summer (December-January) Antarctic oscillation index from sea-level pressure measurements over the twentieth century and find that large positive values, and positive trends of a similar magnitude to those of past decades, also occurred around 1960, and that strong negative trends occurred afterwards. This positive Antarctic oscillation index and large positive trend during a period before ozone-depleting chemicals were released into the atmosphere and before marked anthropogenic warming, together with the later negative trend, indicate that natural forcing factors or internal mechanisms in the climate system must also strongly influence the state of the Antarctic oscillation.  相似文献   
98.
Clayton J 《Nature》2004,430(6996):136-137
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99.
Pascual A  Huang KL  Neveu J  Préat T 《Nature》2004,427(6975):605-606
The asymmetrical positioning of neural structures on the left or right side of the brain in vertebrates and in invertebrates may be correlated with brain laterality, which is associated with cognitive skills. But until now this has not been illustrated experimentally. Here we describe an asymmetrically positioned brain structure in the fruitfly Drosophila and find that the small proportion of wild-type flies that have symmetrical brains with two such structures lack a normal long-term memory, although their short-term memory is intact. Our results indicate that brain asymmetry may be required for generating or retrieving long-term memory.  相似文献   
100.
Nugent FS  Penick EC  Kauer JA 《Nature》2007,446(7139):1086-1090
Excitatory brain synapses are strengthened or weakened in response to specific patterns of synaptic activation, and these changes in synaptic strength are thought to underlie persistent pathologies such as drug addiction, as well as learning. In contrast, there are few examples of synaptic plasticity of inhibitory GABA (gamma-aminobutyric acid)-releasing synapses. Here we report long-term potentiation of GABA(A)-mediated synaptic transmission (LTP(GABA)) onto dopamine neurons of the rat brain ventral tegmental area, a region required for the development of drug addiction. This novel form of LTP is heterosynaptic, requiring postsynaptic NMDA (N-methyl-d-aspartate) receptor activation at glutamate synapses, but resulting from increased GABA release at neighbouring inhibitory nerve terminals. NMDA receptor activation produces nitric oxide, a retrograde signal released from the postsynaptic dopamine neuron. Nitric oxide initiates LTP(GABA) by activating guanylate cyclase in GABA-releasing nerve terminals. Exposure to morphine both in vitro and in vivo prevents LTP(GABA). Whereas brief treatment with morphine in vitro blocks LTP(GABA) by inhibiting presynaptic glutamate release, in vivo exposure to morphine persistently interrupts signalling from nitric oxide to guanylate cyclase. These neuroadaptations to opioid drugs might contribute to early stages of addiction, and may potentially be exploited therapeutically using drugs targeting GABA(A) receptors.  相似文献   
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