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701.
702.
Peter A. Hambäck Karl‐Olof Bergman Riccardo Bommarco Jochen Krauss Mikko Kuussaari Juha Pöyry Erik Öckinger 《Ecography》2010,33(6):1149-1156
Species are differentially affected by habitat fragmentation as a consequence of differences in mobility, area requirements, use of the matrix, and responses to edges. A quantitative understanding of these differences is essential not only for conservation biology but also for basic ecological theory. Here, we examine density responses by butterflies to patch size and use a quantitative theory on the scaling of population density with patch size to interpret results. Theory suggests that the density distribution of mobile species along a patch size gradient should depend on the scaling of net migration rates, whereas the density distribution of less mobile species should depend more on local growth. Using data from 11 localities in three European countries, we calculated the slope in the relationship between patch size and population density. These slopes were evaluated in relation to butterfly traits and matrix composition. As estimates of butterfly mobility we used both wing span and expert mobility rankings. The slope of the density–area relationship changed as predicted with wing span and the association of species to grasslands. Large and highly mobile species had a negative slope, similarly for grassland specialists and generalist species, and the slope matched quantitative predictions based on the scaling of net migration rates. Small and less mobile grassland specialists had a slope that was less negative than the slope of large and mobile grassland specialists, whereas the slope did not change with size for generalist species. These analyses suggest that the variability in response among butterfly species to patch size could be explained by accounting for body size/mobility and habitat associations among species. A caveat is that edge effects are not explicitly included in the model analysis, and future research should aim to combine area and edge effects in a common theoretical framework. 相似文献
703.
Mikko Uusi-Oukari 《Journal of neurochemistry》1992,59(2):560-567
The effects of treatment of brain membranes with diethyl pyrocarbonate (DEP), a histidine-modifying reagent, on the binding of 3H-labeled Ro 15-4513 (ethyl-8-azido-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a]- [1,4]benzodiazepine-3-carboxylate) and [3H]diazepam were compared. DEP pretreatment produced a dose-dependent decrease in [3H]diazepam binding, whereas low DEP concentrations enhanced the binding of [3H]Ro 15-4513. These effects were reversed by incubation with hydroxylamine after the treatment. The enhancement of [3H]Ro 15-4513 binding was due to an increase in the affinity of the binding sites (KD), without any effect on binding capacity (Bmax). The enhancement was perceived in cerebral cortical, cerebellar, and hippocampal membranes. DEP treatment decreased the displacement of [3H]Ro 15-4513 binding by diazepam and FG 7142 (N-methyl-beta-carboline-3-carboxamide) but not by Ro 15-4513 and Ro 19-4603 (tert-butyl-5,6-dihydro-5-methyl-6-oxo-4H-imidazol[1,5- a]thieno[2,3-f][1,4]diazepine-3-carboxylate). Although the stimulating effect of gamma-aminobutyric acid (GABA) on [3H]-diazepam binding was not affected by DEP treatment, such treatment reduced the inhibitory effect of GABA on [3H]Ro 15-4513 binding. The enhancement of [3H]Ro 15-4513 binding was observed in membranes pretreated with DEP in the presence of flunitrazepam, whereas such pretreatment reduced significantly the inhibitory effect of DEP on [3H]-diazepam binding.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
704.
Antti Soivio Mikko Nikinmaa Kai Westman 《Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology》1980,136(1):83-87
Summary The blood oxygen binding properties of rainbow trout responded to environmental hypoxia (the oxygen saturation of water 30% at 11°C) in three ways. The quickest response was a moderate acidosis, leading to slightly lowered blood oxygen loading due to the Bohr effect. The second response, an increase of blood oxygen carrying capacity, was completed with 6 h from the onset of hypoxia. The speed of the response suggests that the formation of new haemoglobin played no practical role, the increase being caused either by a decrease of plasma volume or the liberation of erythrocytes from a storage organ. The slowest response, a 25% increase of the blood oxygen affinity within a week of hypoxia, was probably caused by the concurrent decrease of the erythrocyte ATP concentration from 4.45 to 2.51 mol/ml erythrocytes. 相似文献
705.
Hannula-Jouppi K Kaminen-Ahola N Taipale M Eklund R Nopola-Hemmi J Kääriäinen H Kere J 《PLoS genetics》2005,1(4):e50
Dyslexia, or specific reading disability, is the most common learning disorder with a complex, partially genetic basis, but its biochemical mechanisms remain poorly understood. A locus on Chromosome 3, DYX5, has been linked to dyslexia in one large family and speech-sound disorder in a subset of small families. We found that the axon guidance receptor gene ROBO1, orthologous to the Drosophila roundabout gene, is disrupted by a chromosome translocation in a dyslexic individual. In a large pedigree with 21 dyslexic individuals genetically linked to a specific haplotype of ROBO1 (not found in any other chromosomes in our samples), the expression of ROBO1 from this haplotype was absent or attenuated in affected individuals. Sequencing of ROBO1 in apes revealed multiple coding differences, and the selection pressure was significantly different between the human, chimpanzee, and gorilla branch as compared to orangutan. We also identified novel exons and splice variants of ROBO1 that may explain the apparent phenotypic differences between human and mouse in heterozygous loss of ROBO1. We conclude that dyslexia may be caused by partial haplo-insufficiency for ROBO1 in rare families. Thus, our data suggest that a slight disturbance in neuronal axon crossing across the midline between brain hemispheres, dendrite guidance, or another function of ROBO1 may manifest as a specific reading disability in humans. 相似文献
706.
707.
Local habitat patch pattern of the Siberian flying squirrel in a managed boreal forest landscape 总被引:2,自引:0,他引:2
Eija Hurme Pasi Reunanen Mikko Mönkkönen Ari Nikula Vesa Nivala Jari Oksanen 《Ecography》2007,30(2):277-287
We examined how the structure of a boreal forest landscape is related to the occurrence of the Siberian flying squirrel Pteromys volans in northern Finland. The flying squirrel inhabits mature spruce-dominated ( Picea abies ) mixed forests and is categorised as vulnerable species due to habitat loss and change. We classified a landscape of 374.5 km2 into potential habitat patches, potential dispersal areas, and areas incapable of being inhabited using national forest inventory data, and surveyed all 136 potential habitat patches for the presence of the species. Different landscape variables were defined, and also connections by the shortest distances to neighbouring habitat patches along both straight lines and least-cost distances based on specific movement costs were measured. Occupied patches were larger in size, contained more deciduous trees for food and nesting cavities, and were in closer proximity to the nearest occupied patches. Occupied patches were mainly located below 300 m a.s.l. The occurrence of flying squirrels was correctly predicted for 88% of the habitat patches using landscape variables. This modelling result proved to be rather general. In addition, the configuration of occupied patches was mainly clustered across the landscape, and distant occupied patches seemed to be linked to other patches via forested connections. We suggest that maintaining a clustered arrangement of good quality habitat patches and regenerating new potential habitat as well as dispersal areas between the habitat patches seem to be appropriate goals for long-term forest management planning to sustain populations of the flying squirrel in the landscape. 相似文献
708.
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture 总被引:7,自引:0,他引:7 下载免费PDF全文
Enattah NS Jensen TG Nielsen M Lewinski R Kuokkanen M Rasinpera H El-Shanti H Seo JK Alifrangis M Khalil IF Natah A Ali A Natah S Comas D Mehdi SQ Groop L Vestergaard EM Imtiaz F Rashed MS Meyer B Troelsen J Peltonen L 《American journal of human genetics》2008,82(1):57-72
The T−13910 variant located in the enhancer element of the lactase (LCT) gene correlates perfectly with lactase persistence (LP) in Eurasian populations whereas the variant is almost nonexistent among Sub-Saharan African populations, showing high prevalence of LP. Here, we report identification of two new mutations among Saudis, also known for the high prevalence of LP. We confirmed the absence of the European T−13910 and established two new mutations found as a compound allele: T/G−13915 within the −13910 enhancer region and a synonymous SNP in the exon 17 of the MCM6 gene T/C−3712, −3712 bp from the LCT gene. The compound allele is driven to a high prevalence among Middle East population(s). Our functional analyses in vitro showed that both SNPs of the compound allele, located 10 kb apart, are required for the enhancer effect, most probably mediated through the binding of the hepatic nuclear factor 1 α (HNF1α). High selection coefficient (s) ~0.04 for LP phenotype was found for both T−13910 and the compound allele. The European T−13910 and the earlier identified East African G−13907 LP allele share the same ancestral background and most likely the same history, probably related to the same cattle domestication event. In contrast, the compound Arab allele shows a different, highly divergent ancestral haplotype, suggesting that these two major global LP alleles have arisen independently, the latter perhaps in response to camel milk consumption. These results support the convergent evolution of the LP in diverse populations, most probably reflecting different histories of adaptation to milk culture. 相似文献
709.
Lorenzo Marini Erik Öckinger Karl‐Olof Bergman Birgit Jauker Jochen Krauss Mikko Kuussaari Juha Pöyry Henrik G. Smith Ingolf Steffan‐Dewenter Riccardo Bommarco 《Ecography》2014,37(6):544-551
Losses of both habitat area and connectivity have been identified as important drivers of species richness declines, but little theoretical and empirical work exists that addresses the effect of fragmentation on relative commonness of highly mobile species such as pollinating insects. With a large dataset of wild bee and butterfly abundances collected across Europe, we first tested the effect of habitat area and connectivity on evenness in pollinator communities using a large array of indexes that give different weight to dominance and rarity. Second, we tested if traits related to mobility and diet breadth could explain the observed evenness patterns. We found a clear negative effect of area and a weaker, but positive effect of connectivity on evenness. Communities in small habitat fragments were mainly composed of mobile and generalist species. The higher evenness in small fragments could thereby be generated by highly mobile species that maintain local populations with frequent inter‐fragment movements. Trait analysis suggested an increasing importance of dispersal over local recruitment, as we move from large to small fragments and from less to more connected fragments. Species richness and evenness were negatively correlated indicating that the two variables responded differently to habitat area and connectivity, although the mechanisms underlying the observed patterns are difficult to isolate. Even though habitat area and connectivity often decrease simultaneously due to habitat fragmentation, an interesting practical implication of the contrasting effect of the two variables is that the resulting community composition will depend on the relative strength of these two processes. 相似文献
710.
Quantitative analysis of hsp90-client interactions reveals principles of substrate recognition 总被引:1,自引:0,他引:1
M Taipale I Krykbaeva M Koeva C Kayatekin KD Westover GI Karras S Lindquist 《Cell》2012,150(5):987-1001