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The relationships among the living apes and modern humans have effectively been resolved, but it is much more difficult to locate fossil apes on the tree of life because shared skeletal morphology does not always mean shared recent evolutionary history. Sorting fossil taxa into those that belong on the branch of the tree of life that leads to modern humans from those that belong on other closely related branches is a considerable challenge. 相似文献
3.
Earthquakes have long been recognized as being the result of stick-slip frictional instabilities. Over the past few decades, laboratory studies of rock friction have elucidated many aspects of tectonic fault zone processes and earthquake phenomena. Typically, the static friction of rocks grows logarithmically with time when they are held in stationary contact, but the mechanism responsible for this strengthening is not understood. This time-dependent increase of frictional strength, or frictional ageing, is one manifestation of the 'evolution effect' in rate and state friction theory. A prevailing view is that the time dependence of rock friction results from increases in contact area caused by creep of contacting asperities. Here we present the results of atomic force microscopy experiments that instead show that frictional ageing arises from the formation of interfacial chemical bonds, and the large magnitude of ageing at the nanometre scale is quantitatively consistent with what is required to explain observations in macroscopic rock friction experiments. The relative magnitude of the evolution effect compared with that of the 'direct effect'--the dependence of friction on instantaneous changes in slip velocity--determine whether unstable slip, leading to earthquakes, is possible. Understanding the mechanism underlying the evolution effect would enable us to formulate physically based frictional constitutive laws, rather than the current empirically based 'laws', allowing more confident extrapolation to natural faults. 相似文献
4.
The knockout mouse project 总被引:1,自引:0,他引:1
Austin CP Battey JF Bradley A Bucan M Capecchi M Collins FS Dove WF Duyk G Dymecki S Eppig JT Grieder FB Heintz N Hicks G Insel TR Joyner A Koller BH Lloyd KC Magnuson T Moore MW Nagy A Pollock JD Roses AD Sands AT Seed B Skarnes WC Snoddy J Soriano P Stewart DJ Stewart F Stillman B Varmus H Varticovski L Verma IM Vogt TF von Melchner H Witkowski J Woychik RP Wurst W Yancopoulos GD Young SG Zambrowicz B 《Nature genetics》2004,36(9):921-924
Mouse knockout technology provides a powerful means of elucidating gene function in vivo, and a publicly available genome-wide collection of mouse knockouts would be significantly enabling for biomedical discovery. To date, published knockouts exist for only about 10% of mouse genes. Furthermore, many of these are limited in utility because they have not been made or phenotyped in standardized ways, and many are not freely available to researchers. It is time to harness new technologies and efficiencies of production to mount a high-throughput international effort to produce and phenotype knockouts for all mouse genes, and place these resources into the public domain. 相似文献
5.
Shape skeletonization (i.e., medial axis extraction) is powerful in many visual computing applications, such as pattern recognition, object segmentation, registration, and animation. In this paper, the authors expand the use of diffusion equations combined with distance field information to approximate medial axes of arbitrary 3D differential properties. It offers an alternative solids represented by polygonal meshes based on their but natural way for medial axis extraction for commonly used 3D polygonal models. By solving the PDE along time axis, this system can not only quickly extract diffusion-based medial axes of input meshes, but also allow users to visualize the extraction process at each time step. In addition, the proposed model provides users a set of manipulation toolkits to sculpt extracted medial axes, then use diffusion-based techniques to recover corresponding deformed shapes according to the original input datasets. This skeleton-based shape manipulation offers a fast and easy way for animation and deformation of complicated mesh objects. 相似文献
6.
R. J. Terry 《Cellular and molecular life sciences : CMLS》1991,47(2):115-118
The Editors wish to thank Prof. Thomas Seebeck for coordinating this multi-author review 相似文献
7.
Otto Meyerhof 《Cellular and molecular life sciences : CMLS》1948,4(5):169-176
Résumé Le schéma des étapes du dédoublement des glucosides dans la glycolyse des tissus animaux est exposé ici conformément aux résultats obtenus de 1932 à 1939. Toutes les substances intermédiaires sont phosphorylées. La transphosphorylation s'accomplit selon le système adénylique (acides adénosinetri-, di- et monophosphoriques). La grande énergie libre de ce groupe phosphorique n'est pas perdue, mais transmise aux intermédiaires de la glycolyse et s'accumule dans la phosphocréatine. Un autre type de phosphorylation est représenté par la phosphorolyse réversible du glycogène, avec formation du glucose-1-phosphate. Ce type est en réalité une «transglucosidation» comme on peut le démontrer dans la formation semblable du disaccharide à partir du glucose-1-phosphate et de la lévulose. En l'absence de la lévulose, le glucose-1-phosphate réagit avec l'enzyme en proportion stoechiométrique, et conserve l'énergie du groupe phosphorique dans la combinaison du glucose avec l'enzyme.L'article traite des nombreuses réactions enzymatiques des enzymes purifiées et cristallisées et discute plus en détail la fonction des trois enzymes, soit: la transformation de l'acide 2-phosphoglycérique en phosphoénolpyruvique par l'énolase, la phosphorylation de la glucose par l'adénosinetriphosphate en présence de l'hexokinase, et le dédoublement de l'acide pyruvique par la carboxylase. Le rôle des vitamines comme groupes essentiels des coenzymes, et celui des hormones comme activateurs et inhibiteurs des enzymes sont mis en évidence dans les réactions métaboliques des glucosides. 相似文献
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9.
Doc. Dr. Otto Jírovec 《Cellular and molecular life sciences : CMLS》1947,3(4):168-168
Ohne Zusammenfassung 相似文献
10.
DNA methylation profiling of human chromosomes 6, 20 and 22 总被引:24,自引:0,他引:24