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81.
Invertebrate colonization of woody debris in coastal plain streams   总被引:4,自引:4,他引:0  
We studied colonization dynamics and habitat preferences of macroinvertebrates associated with submerged woody debris in Louisiana coastal plain streams. In an in situ experiment, Branches of magnolia Magnolia grandiflora and water oak Quercus nigra were anchored over sand and gravel substrate at two sites in the Bogue Falaya River, St. Tammany Parish, Louisiana, U.S.A. Branches were removed from the units weekly for 4 weeks and biweekly for 1 month to assess colonization. Invertebrate numbers were highest at weeks three and six on magnolia over gravel habitat, although numbers of the most dominant taxa (Baetidae, Hydropsyche sp., Cernotina sp., Oecetis sp. and Hydroptilia sp.) peaked at different times during the study. Abundances of Hydropsyche sp. and Cernotina sp. were greatest on magnolia branches secured over gravel substrate, whereas Oecetis sp. abundances were greatest on oak branches secured over sand substrate.We also surveyed six streams in southeast Louisiana to examine the relative importance of wood, gravel and sand as substrate for lotic macroinvertebrates. In fall 1997 and spring 1998, we took water samples and measured in situ water quality characteristics at one site on each stream, and then collected submerged wood (surface area about 3051 cm2) and sand and gravel substrate (Surber samples totaling 2800 cm2 for each substrate) to determine the density and taxonomic composition of resident macroinvertebrates. Highest numbers of invertebrates were collected in fall and spring from gravel substrate (P=0.0001). Macronychus sp. were more abundant on wood than gravel or sand (P<0.0003) and Hydropsyche sp. was more abundant on fall wood samples (P=0.0001). Analyses of water quality parameters revealed associations between Hydropsyche sp. abundance and potassium (P=0.0070) and specific conductance (P=0.0080), although both parameters exhibited interactions with substrate type (P<0.0144).  相似文献   
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83.
Amide- and ester-linked kinase inhibitor-cytotoxin conjugates were rationally designed and synthesised as prototype hypoxia-activated anticancer mutual prodrugs. Chemical reduction of an aryl nitro trigger moiety was shown to initiate a spontaneous cyclisation/fragmentation reaction that simultaneously released the kinase inhibitor semaxanib (SU5416) and the amine- or alcohol-linked cytotoxin from the prodrugs. Preliminary cell testing and reduction potential measurements support optimisation of the compounds towards tumour-selective mutual prodrugs.  相似文献   
84.

Background  

Current efforts within the biomedical ontology community focus on achieving interoperability between various biomedical ontologies that cover a range of diverse domains. Achieving this interoperability will contribute to the creation of a rich knowledge base that can be used for querying, as well as generating and testing novel hypotheses. The OBO Foundry principles, as applied to a number of biomedical ontologies, are designed to facilitate this interoperability. However, semantic extensions are required to meet the OBO Foundry interoperability goals. Inconsistencies may arise when ontologies of properties – mostly phenotype ontologies – are combined with ontologies taking a canonical view of a domain – such as many anatomical ontologies. Currently, there is no support for a correct and consistent integration of such ontologies.  相似文献   
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86.

Background  

The mosquito A. aegypti is vector of dengue and other viruses. New methods of vector control are needed and can be achieved by a better understanding of the life cycle of this insect. Embryogenesis is a part of A. aegypty life cycle that is poorly understood. In insects in general and in mosquitoes in particular energetic metabolism is well studied during oogenesis, when the oocyte exhibits fast growth, accumulating carbohydrates, lipids and proteins that will meet the regulatory and metabolic needs of the developing embryo. On the other hand, events related with energetic metabolism during A. aegypti embryogenesis are unknown.  相似文献   
87.
目的 制备一种新型的心肌急性缺血再灌注损伤模型,以探讨一种更符合临床实际需求的实验方法.方法 将20只雌性SD(Sprague-Dawley)大鼠随机分成2组(对照组、实验组),采用结扎主动脉根部引起心肌缺血5min再灌注30 min建立心肌急性缺血再灌注模型;通过应用透射电镜观察心肌细胞超微结构的改变,同时检测心肌组织匀浆丙二醛(Maleic Dialdehyde,MDA)含量、超氧化物歧化酶(Superoxide Dismutase,SOD)活力.结果 透射电镜下超微结构显示实验组较对照组明显加重了心肌组织结构和线粒体的损害;实验组心肌组织MDA明显高于对照组(P<0.01),而SOD明显低于对照组(P<0.01).结论 本实验成功建立了方法简便、易于操作、取材范围广泛的心肌缺血再灌注损伤模型,为心肌缺血再灌注损伤研究提供了一种更为可行的模型.  相似文献   
88.
Allele-specific transcript isoforms in human   总被引:2,自引:0,他引:2  
  相似文献   
89.
The hypothesis that endothelin (ET) receptor mechanisms are altered during development and progression of left ventricular hypertrophy (LVH) in vivo was tested using spontaneously hypertensive rats (SHRs). Ventricular cardiomyocytes were isolated from SHRs before onset (8 and 12 wk) and during progression (16, 20, and 24 wk) of LVH and compared with age-matched normotensive Wistar-Kyoto (WKY) rats. PreproET-1 mRNA expression was elevated in SHR (P < 0.05) relative to WKY cardiomyocytes at 20-24 wk. ET binding-site density was twofold greater in SHR than WKY cells at 12 wk (P < 0.05) but normalized at 20 wk. ET(B) receptors were detected on SHR cardiomyocytes as early as 8 wk and their affinity increased progressively with age (P < 0.05), whereas ET(B) receptors were not detected on WKY cells until 20 wk. ET-1 stimulated protein synthesis with similar maximum responses between strains (21-30%), in contrast with sarafotoxin 6c, which stimulated protein synthesis in SHR (13-20%) but not WKY cells at 12-20 wk. In SHR but not WKY cells, the ET(B) receptor-selective ligand A-192621 increased protein synthesis progressively with the development of LVH (15% maximum effect). In conclusion, the presence of ET(B) receptors (8-12 wk) coupled with functional responsiveness of SHR cells but not WKY cells to sarafotoxin 6c at 12 wk supports the involvement of ET(B) receptors before the onset of cardiomyocyte hypertrophy, whereas altered ET(B) receptor characteristics during active hypertrophy (16-24 wk) indicate that ET(B) receptor mechanisms may also contribute to disease progression.  相似文献   
90.
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