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131.
Strathmann J Paal K Ittrich C Krause E Appel KE Glauert HP Buchmann A Schwarz M 《Proteomics》2007,7(18):3318-3331
Mouse liver tumors frequently harbor mutations in Ha-ras, B-raf, or Ctnnb1 (encoding beta-catenin). We conducted a proteome analysis with protein extracts from normal mouse liver and from liver tumors which were induced by a single injection of N-nitrosodiethylamine (DEN) as initiator followed by multiple injections of two different polychlorinated biphenyls (PCBs) as tumor promoters, or corn oil as a control. Liver tumors were stratified into two classes: they were either mutated in Ctnnb1 and positive for the marker glutamine synthetase (GS(+)), or they lacked Ctnnb1 mutations and were therefore GS-negative (GS(-)). Proteome analysis by 2-DE and MS revealed 98 significantly deregulated proteins, 44 in GS(+) and 54 in GS(-) tumors. Twelve of these proteins showed expression changes in both tumor types, but only seven of them were deregulated in the same direction. Several of the identified enzymes could be assigned to fundamental metabolic or other cellular pathways with characteristically different alterations in GS(+) and GS(-) tumors such as ammonia and amino acid turnover, cellular energy supply, and calcium homeostasis. Our data suggest that GS(+) and GS(-) tumor cells show a completely different biology and use divergent evolutionary strategies to gain a selective advantage over normal hepatocytes. 相似文献
132.
Evan C. Palmer-Young Ryan S. Schwarz Yanping Chen Jay D. Evans 《Environmental microbiology》2022,24(4):1805-1817
Gut parasites of plant-eating insects are exposed to antimicrobial phytochemicals that can reduce infection. Trypanosomatid gut parasites infect insects of diverse nutritional ecologies as well as mammals and plants, raising the question of how host diet-associated phytochemicals shape parasite evolution and host specificity. To test the hypothesis that phytochemical tolerance of trypanosomatids reflects the chemical ecology of their hosts, we compared related parasites from honey bees and mosquitoes – hosts that differ in phytochemical consumption – and contrasted our results with previous studies on phylogenetically related, human-parasitic Leishmania. We identified one bacterial and 10 plant-derived substances with known antileishmanial activity that also inhibited honey bee parasites associated with colony collapse. Bee parasites exhibited greater tolerance of chrysin – a flavonoid found in nectar, pollen and plant resin-derived propolis. In contrast, mosquito parasites were more tolerant of cinnamic acid – a product of lignin decomposition present in woody debris-rich larval habitats. Parasites from both hosts tolerated many compounds that inhibit Leishmania, hinting at possible trade-offs between phytochemical tolerance and mammalian infection. Our results implicate the phytochemistry of host diets as a potential driver of insect–trypanosomatid associations and identify compounds that could be incorporated into colony diets or floral landscapes to ameliorate infection in bees. 相似文献
133.
Katherine L. Helbig Robert J. Lauerer Jacqueline C. Bahr Ivana A. Souza Candace T. Myers Betül Uysal Niklas Schwarz Maria A. Gandini Sun Huang Boris Keren Cyril Mignot Alexandra Afenjar Thierry Billette de Villemeur Delphine Héron Caroline Nava Stéphanie Valence Julien Buratti Christina R. Fagerberg Heather C. Mefford 《American journal of human genetics》2019,104(3):562
134.
135.
Nucleotide sequence of the celC gene encoding endoglucanase C of Clostridium thermocellum 总被引:11,自引:0,他引:11
W H Schwarz S Schimming K P Rücknagel S Burgschwaiger G Kreil W L Staudenbauer 《Gene》1988,63(1):23-30
The nucleotide sequence of the cellulase gene celC, encoding endoglucanase C of Clostridium thermocellum, has been determined. The coding region of 1032 bp was identified by comparison with the N-terminal amino acid (aa) sequence of endoglucanase C purified from Escherichia coli. The ATG start codon is preceded by an AGGAGG sequence typical of ribosome-binding sites in Gram-positive bacteria. The derived amino acid sequence corresponds to a protein of Mr 40,439. Amino acid analysis and apparent Mr of endoglucanase C are consistent with the amino acid sequence as derived from the DNA sequencing data. A proposed N-terminal 21-aa residue leader (signal) sequence differs from other prokaryotic signal peptides and is non-functional in E. coli. Most of the protein bears no resemblance to the endoglucanases A, B, and D of the same organism. However, a short region of homology between endoglucanases A and C was identified, which is similar to the established active sites of lysozymes and to related sequences of fungal cellulases. 相似文献
136.
Athina Efthymiadis Jürgen Rettinger Wolfgang Schwarz 《Cell biology international》1993,17(12):1107-1116
In Na+- and K+-free solution, an inward-directed current can be detected in Xenopus oocytes, which is inhibited by cardic glycosides and activated by ATP. Therefore, it is assumed to be generated by the Na+, K+ pump. At negative membrane potentials, the pump current increases with more negative potentials and with increasing [H+] in the external medium. This current is not observed when Mg2+ instead of Ba2+ is the only divalent cation present in the bath medium, and it does not depend on whether Na+ or K+ is present internally. At 5 to 10 mM Na+ externally, maximum pump-generated current is obtained while no current can be detected in presence of physiological [Na+]. It is suggested that in low-Na+ and K+-free medium the Na+, K+ pump molecule can either form a conductive pathway that is permeable to Ba2+ or protons or operate in its conventional transport mode accepting Ba2+ as a K+ congener. A reversed pump mode or an electrogenic uncoupled Na+-efflux mode is excluded. 相似文献
137.
138.
Elektronenmikroskopische Untersuchungen an der Interzellularsubstanz des menschlichen Knochengewebes
Zusammenfassung Die Interzellularsubstanz des Knochengewebes wurde im Durchstrahlungsbild elektronenmikroskopisch untersucht. Die aus der Licht-mikroskopie bekannten Knochenfibrillen setzen sich aus nur elektronenmikroskopisch sichtbaren Elementarfibrillen (Knochenfibrillen) und einer amorphen Kittsubstanz zusammen. In diese Kittsubstanz ist der Kalk eingelagert.Die Knochenfibrillen zeigen die charakteristische Querstreifung der Fibrillen aller Binde- und Stützgewebe. Bei der Bindegewebsversilberung nach Gömöri stimmt der Versilberungsmodus der Fibrillen des erwachsenen Knochens mit dem der reifen Fibrillen des Sehnenkollagens überein. Eine Differenzierung der Knochenfibrillen während der Entwicklung und Alterung läßt sich mit dieser Versilberungsmethode ebenfalls nachweisen. Es wurden Dickenunterschiede der Fibrillen im embryonalen Osteoid, im Faserknochen des Embryos und frühen Kindesalters und im lamellären Knochen festgestellt und tabellarisch zusammengefaßt. Auch die Periodenlängen der Fibrillen nehmen mit dem Alter des Knochengewebes zu. Zur Darstellung der Fibrillen wurden verschiedene Mazerations- und Fermentmethoden benutzt. Auch wurden mehrere Entkalkungsflüssigkeiten angewendet. Alle diese Methoden führen zu einer mehr oder weniger starken Quellung der Fibrillen. Als beste Methode zur Isolierung der Knochenfibrillen hat sich die Kombination von Trypsin- oder Papainverdauuung und Entkalkung mit Salpetersäure erwiesen. Die Knochenkittsubstanz wird mit zunehmendem Alter dichter und enthält sehr wenig Polysaccharide. Der Kalk ist in Form von ovalären und spindelförmigen Partikeln in die Kittsubstanz eingelagert. Die Größe der Kalkteilchen schwankt zwischen 15 und 130 m. Ihre Längsachse ist der Längsachse der Fibrillen parallel gerichtet. Die kleinsten Elemente liegen den Fibrillen, und zwar deren D-Teil an. Die Fibrillen selbst sind kalkfrei.Durchgeführt mit Unterstützung der Deutschen Forschungsgemeinschaft. 相似文献
139.
Eugene J. DeRango Jonas F. L. Schwarz Paolo Piedrahita Diego PezRosas Daniel E. Crocker Oliver Krüger 《Ecology and evolution》2021,11(12):7579
- Hormones are extensively known to be physiological mediators of energy mobilization and allow animals to adjust behavioral performance in response to their environment, especially within a foraging context.
- Few studies, however, have narrowed focus toward the consistency of hormonal patterns and their impact on individual foraging behavior. Describing these relationships can further our understanding of how individuals cope with heterogeneous environments and exploit different ecological niches.
- To address this, we measured between‐ and within‐individual variation of basal cortisol (CORT), thyroid hormone T3, and testosterone (TEST) levels in wild adult female Galápagos sea lions (Zalophus wollebaeki) and analyzed how these hormones may be associated with foraging strategies. In this marine predator, females exhibit one of three spatially and temporally distinct foraging patterns (i.e., “benthic,” “pelagic,” and “night” divers) within diverse habitat types.
- Night divers differentiated from other strategies by having lower T3 levels. Considering metabolic costs, night divers may represent an energetically conservative strategy with shorter dive durations, depths, and descent rates to exploit prey which migrate up the water column based on vertical diel patterns.
- Intriguingly, CORT and TEST levels were highest in benthic divers, a strategy characterized by congregating around limited, shallow seafloors to specialize on confined yet reliable prey. This pattern may reflect hormone‐mediated behavioral responses to specific risks in these habitats, such as high competition with conspecifics, prey predictability, or greater risks of predation.
- Overall, our study highlights the collective effects of hormonal and ecological variation on marine foraging. In doing so, we provide insights into how mechanistic constraints and environmental pressures may facilitate individual specialization in adaptive behavior in wild populations.
140.
Schwarz K Walther M Anton M Gerth C Feussner I Kuhn H 《The Journal of biological chemistry》2001,276(1):773-779
Mammalian lipoxygenases constitute a heterogeneous family of lipid-peroxidizing enzymes, and the various isoforms are categorized with respect to their positional specificity of arachidonic acid oxygenation into 5-, 8-, 12-, and 15-lipoxygenases. Structural modeling suggested that the substrate binding pocket of the human 5-lipoxygenase is 20% bigger than that of the reticulocyte-type 15-lipoxygenase; thus, reduction of the active-site volume was suggested to convert a 5-lipoxygenase to a 15-lipoxygenating enzyme species. To test this "space-based" hypothesis of the positional specificity, the volume of the 5-lipoxygenase substrate binding pocket was reduced by introducing space-filling amino acids at critical positions, which have previously been identified as sequence determinants for the positional specificity of other lipoxygenase isoforms. We found that single point mutants of the recombinant human 5-lipoxygenase exhibited a similar specificity as the wild-type enzyme but double, triple, and quadruple mutations led to a gradual alteration of the positional specificity from 5S- via 8S- toward 15S-lipoxygenation. The quadruple mutant F359W/A424I/N425M/A603I exhibited a major 15S-lipoxygenase activity (85-95%), with (8S,5Z,9E,11Z,14Z)-8-hydroperoxyeicosa-5,9 ,11, 14-tetraenoic acid being a minor side product. These data indicate the principle possibility of interconverting 5- and 15-lipoxygenases by site-directed mutagenesis and appear to support the space-based hypothesis of positional specificity. 相似文献