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H. Llaneza Coalla J.M. Blanco FernándezM.A. Morís Morán M.R. López Bobo 《Bioresource technology》2009,100(17):3843-3847
In view of the pressing problem that appears in our region (Asturias, north of Spain) with the residues from the cider production, it was decided to test this kind of material as a co-substrate joint with slaughterhouse waste in a laboratory unit. 相似文献
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Sherwood JL Amici M Dargan SL Culley GR Fitzjohn SM Jane DE Collingridge GL Lodge D Bortolotto ZA 《Neurochemistry international》2012,61(4):482-489
Long-term potentiation (LTP) is a well-established experimental model used to investigate the synaptic basis of learning and memory. LTP at mossy fibre - CA3 synapses in the hippocampus is unusual because it is normally N-methyl-d-aspartate (NMDA) receptor-independent. Instead it seems that the trigger for mossy fibre LTP involves kainate receptors (KARs). Although it is generally accepted that pre-synaptic KARs play an essential role in frequency facilitation and LTP, their subunit composition remains a matter of significant controversy. We have reported previously that both frequency facilitation and LTP can be blocked by selective antagonism of GluK1 (formerly GluR5/Glu(K5))-containing KARs, but other groups have failed to reproduce this effect. Moreover, data from receptor knockout and mRNA expression studies argue against a major role of GluK1, supporting a more central role for GluK2 (formerly GluR6/Glu(K6)). A potential reason underlying the controversy in the pharmacological experiments may reside in differences in the preparations used. Here we show differences in pharmacological sensitivity of synaptic plasticity at mossy fibre - CA3 synapses depend critically on slice orientation. In transverse slices, LTP of fEPSPs was invariably resistant to GluK1-selective antagonists whereas in parasagittal slices LTP was consistently blocked by GluK1-selective antagonists. In addition, there were pronounced differences in the magnitude of frequency facilitation and the sensitivity to the mGlu2/3 receptor agonist DCG-IV. Using anterograde labelling of granule cells we show that slices of both orientations possess intact mossy fibres and both large and small presynaptic boutons. Transverse slices have denser fibre tracts but a smaller proportion of giant mossy fibre boutons. These results further demonstrate a considerable heterogeneity in the functional properties of the mossy fibre projection. 相似文献
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昼间亚高温下番茄叶中糖含量与蔗糖代谢相关酶的活性日变化 总被引:3,自引:0,他引:3
研究番茄品种‘辽园多丽’幼苗在昼间35℃亚高温条件下叶中糖含量及蔗糖代谢相关酶活性日变化的结果表明,昼间亚高温处理后的幼苗叶中果糖、葡萄糖和淀粉含量下降,蔗糖含量升高。与蔗糖代谢相关的酶活性有明显的昼夜节律性变化,转化酶、蔗糖合成酶呈现昼间活性低、夜间活性高的节律性,而蔗糖磷酸合成酶活性在进入夜间时立刻升高。35℃昼间亚高温处理后的幼苗叶中,转化酶活性下降,蔗糖合成酶活性明显升高,蔗糖磷酸合成酶活性则略有升高。 相似文献
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在3间人工气候室精密受控环境中,保持日平均温度为22 ℃,设置昼夜温差分别为6 ℃(25 ℃/19 ℃)、8 ℃(26 ℃/18 ℃)、10 ℃(27 ℃/17 ℃),研究昼夜温差对番茄生长的影响.结果表明: 番茄不同品种、不同生长时期适宜的昼夜温差条件不同.番茄开花前,与6 ℃温差相比,8 ℃温差可显著加快野生种醋栗番茄LA1781生长发育,使幼苗株高增加23.1%,出叶加快1~2片,开花提前7 d;10 ℃温差对LA1781苗期的促进作用与8 ℃温差相似.对栽培种普通番茄LA2397和LA0490来说,6 ℃温差使幼苗生长良好,8 ℃温差对幼苗无显著促进作用;与6 ℃温差相比,10 ℃温差对苗期生长及开花有抑制作用,使株高降低12.0%~18.3%,出叶慢2~3片,开花推迟2~4 d.10 ℃温差使3个品种番茄地上部分干质量增加25.2%~44.2%.番茄开花后,与6 ℃温差相比,10 ℃温差可显著提高LA1781的产量和果实品质,使果实数增加34.7%,单株产量增加92.1%,平均单果质量增加40.0%,果实可溶性糖含量增加16.3%,番茄红素含量增加95.6%.与6 ℃温差相比,LA2397和LA0490在8 ℃温差下产量和果实品质提高,番茄红素含量增加超过2倍;在10 ℃温差下产量略有降低(5.0%),果实含糖量降低,但果实尺寸和番茄红素含量增加.表明番茄苗期生长温差不宜过大,花果期适当增大昼夜温差可提高产量和果实品质,但温差过大易造成生长不良和减产. 相似文献
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Vigilance and parallel occurrence of epileptic activity after administration of the 5-HT1A agonist 8-OH-DPAT and the NMDA receptor antagonist MK-801 were studied in the genetic absence epilepsy model WAG/Rij rats. Spike-wave discharges (SWD) were present predominantly in passive awake and light slow wave sleep (SWS1) either in control animals or after treatments. Injection of 8-OH-DPAT (20.0 μg/rat i.c.v.) caused marked increase and MK-801 (10.0 μg/rat i.c.v.) decrease in SWD densities, thus the ratios of SWD in passive awake and in SWS1. SWD densities of MK-801 plus 8-OH-DPAT in combination were similar to those of CSF+CSF treated control rats. Both 8-OH-DPAT and MK-801 transiently increased the duration of active awake, increased latency and decreased duration of rapid eye movement (REM) sleep. 8-OH-DPAT increased the amount of SWD despite the decrease in the duration of SWS1. MK-801 decreased the amount of SWD despite the lack of significant change in duration of passive awake or SWS1. Pre-treatment with MK-801 reversed 8-OH-DPAT- induced increase in duration of SWD without any effect on 8-OH-DPAT-induced changes in sleep parameters. Our studies provide evidence that 8-OH-DPAT-induced epileptic activity is independent of its effect on sleep, and that interaction of serotonergic and glutamatergic systems plays a role in the generation of SWD, but not in the regulation of vigilance and sleep. 相似文献
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