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961.
Hashimoto T Tashiro T Sasaki M Takikawa H 《Bioscience, biotechnology, and biochemistry》2007,71(8):2046-2051
A new and concise synthesis of (+/-)-sundiversifolide (1), an allelopathic bisnor-sesquiterpene lactone isolated from germinating sunflower (Helianthus annuus L.) seeds, was achieved by employing Lewis acid-mediated Claisen rearrangement as the key step. 相似文献
962.
963.
Mimitsuka T Sawai H Hatsu M Yamada K 《Bioscience, biotechnology, and biochemistry》2007,71(9):2130-2135
Cadaverine, the expected raw material of polyamides, is produced by decarboxylation of L-lysine. If we could produce cadaverine from the cheapest sugar, and as a renewable resource, it would be an effective solution against global warming, but there has been no attempt to produce cadaverine from glucose by fermentation. We focused on Corynebacterium glutamicum, whose L-lysine fermentation ability is superior, and constructed a metabolically engineered C. glutamicum in which the L-homoserine dehydrogenase gene (hom) was replaced by the L-lysine decarboxylase gene (cadA) of Escherichia coli. In this recombinant strain, cadaverine was produced at a concentration of 2.6 g/l, equivalent to up to 9.1% (molecular yield) of the glucose transformed into cadaverine in neutralizing cultivation. This is the first report of cadaverine fermentation by C. glutamicum. 相似文献
964.
965.
A cell line designated "HEPFT" was established from a human fallopian tubal hepatoid carcinoma. This line grew well without interruption for 13 months and was subcultivated over 35 times. The cells were spherical and polygonal in shape and showed neoplastic and pleomorphic features such as a bizarre aggregation of chromatin granules, an irregular thickening membrane and multiple large nucleoli. The cells formed epithelial colonies with a jigsaw puzzle-like arrangement and multilayering without contact inhibition. The cells contained moderate to abundant amounts of eosinophilic cytoplasm and were immunohistochemically positive for alpha-fetoprotein. The cells proliferated rapidly, and the population doubling time was about 45 h. The chromosome number showed a wide distribution of aneuploidy. The modal chromosome number was stable in the hyper triploid range and many marker chromosomes were observed. The culture cells produced bile and a large amount of lentil lectin-reactive alpha-fetoprotein. The recently developed bacterial artificial chromosome array comparative genomic hybridization facilitated detailed analysis with high resolution and sensitivity. Different profiles of genomic copy-number abnormalities were demonstrated in various chromosomal regions in HEPFT cells. 相似文献
966.
The Evolutionarily Significant Unit (ESU) was conceptualized in 1986 as a conservation unit below the species level, theoretically
applicable to a wide range of taxa. The concept has gained support, and various definitions or criteria, some of which are
inconsistent with each other, have since been proposed. Recent critiques of the ESU have pointed out the dominance of definitions
biased to the identification of long-term isolation or neutral genetic variation, which has largely ignored the adaptive components.
We present here the validity of such claims and show how the ESU definitions have actually been applied in research. We surveyed
scientific journals for original papers supporting ESU designations and determined who among the proponents of ESU definitions
have gained wider support. Our results indicate that indeed there are inconsistencies with the original concept and with the
existing definitions. Although the original concept recommended both ecological and genetic data as the basis for identification
of ESUs, which reflect true evolutionary variation, recent definitions have become biased to either neutral genetic variation
or adaptive variation. The definition which uses genetic data to assess neutral genetic variation (long-term isolation) has
gained major support, and therefore validates the earlier claims. To bridge the gap between the original concept and the practical
application, we propose the use of partial ESU and full ESU designations. The application of full ESU should be limited solely
to when both information about neutral genetic variation and adaptive variation are available. In other cases, in which only
a part of the variation is examined, we should use the term partial ESU (e.g., molecular-based ESU) and continue to investigate
focal populations from other aspects of variations to designate full ESU. 相似文献
967.
Tamura T Tomimatsu K Katakura Y Yamashita M Matsumoto SE Aiba Y Jung YS Abe Y Fujiki T Teruya K Shirahata S 《Bioscience, biotechnology, and biochemistry》2007,71(12):2871-2875
Human monoclonal antibodies have great potential for use in the treatment of various diseases. We have established an in vitro immunization protocol for inducing antigen-specific antibody production from human peripheral blood mononuclear cells (PBMCs). In the in vitro immunization protocol, PBMCs are pretreated with L-leucyl-L-leucine methyl ester (LLME) to remove suppressive cells, and are sensitized and cultured with a soluble antigen in the presence of IL-2, IL-4 and muramyl dipeptide for 8 d, and then an antigen-specific antibody is produced. In this study, we examined the novel possibility of an in vitro immunization protocol, specifically, whether LLME-treated PBMCs can be sensitized with a peptide antigen to produce an anti-peptide antibody. The results indicate that antigen-specific immune responses were elicited by a peptide antigen derived from rice allergen, a cholera toxin B subunit, and TNF-alpha as a sensitizing antigen in in vitro immunization. These results suggest that the in vitro immunization protocol is applicable in the generation of an anti-peptide antibody against various antigens, including food allergens, foreign antigens, and self-antigens. 相似文献
968.
The cytotoxicity of aged PrP(106-126) was examined using an immortalized prion protein (PrP) gene-deficient neuronal cell line. The N-terminal half of the hydrophobic region (HR) but not the octapeptide repeat (OR) of PrP was required for aged PrP(106-126) neurotoxicity, suggesting that neurotoxic signals of aged PrP(106-126) are mediated by this region. 相似文献
969.
970.