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101.
An improved method for the collection of large numbers of inseminated eggs ofDrosophila melanogaster
F. E. Würgler H. Ulrich H. W. Spring 《Cellular and molecular life sciences : CMLS》1968,24(10):1082-1083
Zusammenfassung Es wird eine verbesserte Methode beschrieben, mit der innerhalb einer Sammelperiode von 3 min etwa 50-100 frisch besamte Eier vonDrosophila melanogaster gewonnen werden können. Verglichen mit den bisher üblichen Sammelperioden von 10, 30 oder mehr min erhält man wesentlich stadienhomogenere Gelege. Eine weitere Verkürzung der Sammelperiode unter 3 min ist wegen der stark abnehmenden Anzahl Eier je Gelege nicht möglich. Vorausgesetzt, dass alle Störungen der Fliegen durch Erschütterungen, Licht, Temperaturschwankungen usw ausgeschaltet werden, können z.B. für strahlenbiologische Experimente zahlreiche 3-min-Gelege im Laufe von 6 oder mehr Stunden gewonnen werden.
Work supported by Schweizerischer Nationalfonds zur Förderung der wissenschaftlichen Forschung and Jubiläumsfond 1930 der ETH. 相似文献
Work supported by Schweizerischer Nationalfonds zur Förderung der wissenschaftlichen Forschung and Jubiläumsfond 1930 der ETH. 相似文献
102.
103.
1A6/DRIM has been identified as UTP20, a small subunit processome component, functioning in 18S rRNA processing. In the present study, the maturation of 28S rRNA and 5.8S rRNA was inhibited when 1A6/DRIM was silenced in HeLa cells; and coin-cidently, an accumulation of 32S rRNA precursor was observed. Immunoprecipitation was performed with the anti-1A6/DRIM antibody, followed by Northern blot with the ITS2 probe. The results showed that 1A6/DRIM was associated with both 32S and 12S rRNA precursors in vivo. The expression profile of 1A6/DRIM during rRNA processing was investigated by sucrose density gradient fractionation in combination with Western blot analysis. The results demonstrated that 1A6/DRIM was involved in the pre-60S particles in addition to the pre-40S particles and co-sediment with the 32S and 12S rRNA precursors in the nucleolus. Furthermore, the interaction of U8 snoRNA with 1A6/DRIM was revealed by immunoprecipitation. These results demonstrated that 1A6/DRIM interacted with both 32S rRNA and U8 snoRNA, being involved in 28S rRNA and 5.8S rRNA processing. 相似文献
104.
Ahel I Rass U El-Khamisy SF Katyal S Clements PM McKinnon PJ Caldecott KW West SC 《Nature》2006,443(7112):713-716
Ataxia oculomotor apraxia-1 (AOA1) is a neurological disorder caused by mutations in the gene (APTX) encoding aprataxin. Aprataxin is a member of the histidine triad (HIT) family of nucleotide hydrolases and transferases, and inactivating mutations are largely confined to this HIT domain. Aprataxin associates with the DNA repair proteins XRCC1 and XRCC4, which are partners of DNA ligase III and ligase IV, respectively, suggestive of a role in DNA repair. Consistent with this, APTX-defective cell lines are sensitive to agents that cause single-strand breaks and exhibit an increased incidence of induced chromosomal aberrations. It is not, however, known whether aprataxin has a direct or indirect role in DNA repair, or what the physiological substrate of aprataxin might be. Here we show, using purified aprataxin protein and extracts derived from either APTX-defective chicken DT40 cells or Aptx-/- mouse primary neural cells, that aprataxin resolves abortive DNA ligation intermediates. Specifically, aprataxin catalyses the nucleophilic release of adenylate groups covalently linked to 5'-phosphate termini at single-strand nicks and gaps, resulting in the production of 5'-phosphate termini that can be efficiently rejoined. These data indicate that neurological disorders associated with APTX mutations may be caused by the gradual accumulation of unrepaired DNA strand breaks resulting from abortive DNA ligation events. 相似文献
105.
106.
Genetic variation in DLG5 is associated with inflammatory bowel disease 总被引:22,自引:0,他引:22
Stoll M Corneliussen B Costello CM Waetzig GH Mellgard B Koch WA Rosenstiel P Albrecht M Croucher PJ Seegert D Nikolaus S Hampe J Lengauer T Pierrou S Foelsch UR Mathew CG Lagerstrom-Fermer M Schreiber S 《Nature genetics》2004,36(5):476-480
Crohn disease and ulcerative colitis are two subphenotypes of inflammatory bowel disease (IBD), a complex disorder resulting from gene-environment interaction. We refined our previously defined linkage region for IBD on chromosome 10q23 and used positional cloning to identify genetic variants in DLG5 associated with IBD. DLG5 encodes a scaffolding protein involved in the maintenance of epithelial integrity. We identified two distinct haplotypes with a replicable distortion in transmission (P = 0.000023 and P = 0.004 for association with IBD, P = 0.00012 and P = 0.04 for association with Crohn disease). One of the risk-associated DLG5 haplotypes is distinguished from the common haplotype by a nonsynonymous single-nucleotide polymorphism 113G-->A, resulting in the amino acid substitution R30Q in the DUF622 domain of DLG5. This mutation probably impedes scaffolding of DLG5. We stratified the study sample according to the presence of risk-associated CARD15 variants to study potential gene-gene interaction. We found a significant difference in association of the 113A DLG5 variant with Crohn disease in affected individuals carrying the risk-associated CARD15 alleles versus those carrying non-risk-associated CARD15 alleles. This is suggestive of a complex pattern of gene-gene interaction between DLG5 and CARD15, reflecting the complex nature of polygenic diseases. Further functional studies will evaluate the biological significance of DLG5 variants. 相似文献
107.
Söllner C Rauch GJ Siemens J Geisler R Schuster SC Müller U Nicolson T;Tübingen Screen Consortium 《Nature》2004,428(6986):955-959
Hair cells have highly organized bundles of apical projections, or stereocilia, that are deflected by sound and movement. Displacement of stereocilia stretches linkages at the tips of stereocilia that are thought to gate mechanosensory channels. To identify the molecular machinery that mediates mechanotransduction in hair cells, zebrafish mutants were identified with defects in balance and hearing. In sputnik mutants, stereociliary bundles are splayed to various degrees, with individuals displaying reduced or absent mechanotransduction. Here we show that the defects in sputnik mutants are caused by mutations in cadherin 23 (cdh23). Mutations in Cdh23 also cause deafness and vestibular defects in mice and humans, and the protein is present in hair bundles. We show that zebrafish Cdh23 protein is concentrated near the tips of hair bundles, and that tip links are absent in homozygous sputnik(tc317e) larvae. Moreover, tip links are absent in larvae carrying weak alleles of cdh23 that affect mechanotransduction but not hair bundle integrity. We conclude that Cdh23 is an essential tip link component required for hair-cell mechanotransduction. 相似文献
108.
Monoclonal antibodies show that neurofibrillary tangles and neurofilaments share antigenic determinants 总被引:49,自引:0,他引:49
B H Anderton D Breinburg M J Downes P J Green B E Tomlinson J Ulrich J N Wood J Kahn 《Nature》1982,298(5869):84-86
109.
110.
Conclusions The total proton load found in these ecosystems exceeds by far the known rates of buffering in soils by silicate weathering and release of basic cations (see above).Under the present proton load most forest soils will therefore acidify and besides losses of nutrients the occurrence of possible toxic ions in the soil unavoidable (Al-buffer range)20, 21.The proportion of the total proton load of the soil that is represented by the internal production emphasizes the importance of acid deposition as main cause of soil acidification and destabilization of forest ecosystems under Central European conditions. 相似文献