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101.
Identification and Localization of a Rickettsia sp. in Bemisia tabaci (Homoptera: Aleyrodidae) 总被引:1,自引:0,他引:1
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Yuval Gottlieb Murad Ghanim Elad Chiel Dan Gerling Vitaly Portnoy Shimon Steinberg Galil Tzuri A. Rami Horowitz Eduard Belausov Neta Mozes-Daube Svetlana Kontsedalov Moshe Gershon Shunit Gal Nurit Katzir Einat Zchori-Fein 《Applied microbiology》2006,72(5):3646-3652
Whiteflies (Homoptera: Aleyrodidae) are sap-sucking insects that harbor “Candidatus Portiera aleyrodidarum,” an obligatory symbiotic bacterium which is housed in a special organ called the bacteriome. These insects are also home for a diverse facultative microbial community which may include Hamiltonella, Arsenophonus, Fritchea, Wolbachia, and Cardinium spp. In this study, the bacteria associated with a B biotype of the sweet potato whitefly Bemisia tabaci were characterized using molecular fingerprinting techniques, and a Rickettsia sp. was detected for the first time in this insect family. Rickettsia sp. distribution, transmission and localization were studied using PCR and fluorescence in situ hybridizations (FISH). Rickettsia was found in all 20 Israeli B. tabaci populations screened but not in all individuals within each population. A FISH analysis of B. tabaci eggs, nymphs, and adults revealed a unique concentration of Rickettsia around the gut and follicle cells, as well as a random distribution in the hemolymph. We postulate that the Rickettsia enters the oocyte together with the bacteriocytes, leaves these symbiont-housing cells when the egg is laid, multiplies and spreads throughout the egg during embryogenesis and, subsequently, disperses throughout the body of the hatching nymph, excluding the bacteriomes. Although the role Rickettsia plays in the biology of the whitefly is currently unknown, the vertical transmission on the one hand and the partial within-population infection on the other suggest a phenotype that is advantageous under certain conditions but may be deleterious enough to prevent fixation under others. 相似文献
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M Kinoshita H Kayama T Kusu T Yamaguchi J Kunisawa H Kiyono S Sakaguchi K Takeda 《Journal of immunology (Baltimore, Md. : 1950)》2012,189(6):2869-2878
Dietary compounds as well as commensal microbiota contribute to the generation of a unique gut environment. In this study, we report that dietary folic acid (FA) is required for the maintenance of Foxp3(+) regulatory T cells (Tregs) in the colon. Deficiency of FA in the diet resulted in marked reduction of Foxp3(+) Tregs selectively in the colon. Blockade of folate receptor 4 and treatment with methotrexate, which inhibits folate metabolic pathways, decreased colonic Foxp3(+) Tregs. Compared with splenic Tregs, colonic Tregs were more activated to proliferate vigorously and were highly sensitive to apoptosis. In colonic Tregs derived from mice fed with a FA-deficient diet, expression of anti-apoptotic molecules Bcl-2 and Bcl-xL was severely decreased. A general reduction of peripheral Tregs was induced by a neutralizing Ab against IL-2, but a further decrease by additional FA deficiency was observed exclusively in the colon. Mice fed with an FA-deficient diet exhibited higher susceptibility to intestinal inflammation. These findings reveal the previously unappreciated role of dietary FA in promotion of survival of Foxp3(+) Tregs that are in a highly activated state in the colon. 相似文献
105.
Spiegel R Pines O Ta-Shma A Burak E Shaag A Halvardson J Edvardson S Mahajna M Zenvirt S Saada A Shalev S Feuk L Elpeleg O 《American journal of human genetics》2012,90(3):518-523
Degeneration of the cerebrum, cerebellum, and retina in infancy is part of the clinical spectrum of lysosomal storage disorders, mitochondrial respiratory chain defects, carbohydrate glycosylation defects, and infantile neuroaxonal dystrophy. We studied eight individuals from two unrelated families who presented at 2-6 months of age with truncal hypotonia and athetosis, seizure disorder, and ophthalmologic abnormalities. Their course was characterized by failure to acquire developmental milestones and culminated in profound psychomotor retardation and progressive visual loss, including optic nerve and retinal atrophy. Despite their debilitating state, the disease was compatible with survival of up to 18 years. Laboratory investigations were normal, but the oxidation of glutamate by muscle mitochondria was slightly reduced. Serial brain MRI displayed progressive, prominent cerebellar atrophy accompanied by thinning of the corpus callosum, dysmyelination, and frontal and temporal cortical atrophy. Homozygosity mapping followed by whole-exome sequencing disclosed a Ser112Arg mutation in ACO2, encoding mitochondrial aconitase, a component of the Krebs cycle. Specific aconitase activity in the individuals' lymphoblasts was severely reduced. Under restrictive conditions, the mutant human ACO2 failed to complement a yeast ACO1 deletion strain, whereas the wild-type human ACO2 succeeded, indicating that this mutation is pathogenic. Thus, a defect in mitochondrial aconitase is associated with an infantile neurodegenerative disorder affecting mainly the cerebellum and retina. In the absence of noninvasive biomarkers, determination of the ACO2 sequence or of aconitase activity in lymphoblasts are warranted in similarly affected individuals, based on clinical and neuroradiologic grounds. 相似文献
106.
S Shteingart R Hadar I Cohen T Ravid B Tirosh 《The Journal of biological chemistry》2012,287(37):31223-31232
Endoplasmic reticulum (ER) stress develops when the ER is overloaded with too many proteins to fold. This elicits a signaling pathway called the unfolded protein response. The unfolded protein response is physiologically required for the terminal development of B cells into antibody-secreting plasma cells. Ring Box Protein 1 (RBX1) is a 14-kDa protein necessary for ubiquitin ligation activity of the multimeric cullin ring ubiquitin ligases (CRLs). As RBX1 is shared by a large number of CRLs, alterations in its activity may lead to global changes in protein stability. We discovered that RBX1 is cleaved in the course of LPS-induced plasma cell differentiation and in multiple myeloma cell lines upon induction of pharmacological ER stress. The cleavage is executed by several caspase proteases that cleave RBX1 eight amino acids from the N terminus. To address the possible implication of RBX1 cleavage for CRL activity, we replaced the endogenous RBX1 homolog of the yeast Saccharomyces cerevisiae, Roc1, with the wild type or the N-terminal Δ8 mutant human RBX1. We show that yeast expressing the cleaved RBX1 are hypersensitive to ER stress and are impaired in CRL-mediated ubiquitination and degradation. We propose a model by which N-terminal cleavage of RBX1 impairs its activity and promotes susceptibility to ER stress induction. 相似文献
107.
Elad Chiel Dan Gerling Shimon Steinberg Johannette Klapwijk Karel Bolckmans 《Biocontrol Science and Technology》2012,22(1):61-66
The parasitoid wasp Eretmocerus mundus (Hymenoptera: Aphelinidae) is used commercially to control the sweet potato whitefly Bemisia tabaci (Homoptera: Aleyrodidae). Recently, a rapid deterioration of E. mundus populations has been documented under mass-rearing conditions. We found that deteriorating cultures consist of increasing proportions of sterile individuals, up to 90% within 6 months. Microscopic examination revealed that the gonads of wasps from both sexes are severely underdeveloped. Preliminary screening for potential pathogen candidates by means of polymerase chain reaction and denaturating-gradient gel electrophoresis did not provide any indication of possible causative agents. 相似文献
108.
Annual variation in soil respiration and its component parts in two structurally contrasting woody savannas in Central Brazil 总被引:1,自引:0,他引:1
Andre Butler Patrick Meir Gustavo Saiz Leandro Maracahipes Beatriz Schwantes Marimon John Grace 《Plant and Soil》2012,352(1-2):129-142
Background and aims
Due to the high spatial and temporal variation in soil CO2 efflux, terrestrial carbon budgets rely on a detailed understanding of the drivers of soil respiration from a diverse range of ecosystems and climate zones. In this study we aim to evaluate the independent influence of vegetation structure and climate on soil CO2 efflux within cerrado ecosystems.Methods
We examine the seasonal and diel variation of soil CO2 efflux, including its autotrophic and heterotrophic components, within two adjacent and structurally contrasting woody savannas in central Brazil.Principle results
We found no significant difference in the annual soil CO2 efflux between the two stands (p?=?0.53) despite a clear disparity in both LAI (p?<?0.01) and leaf litterfall (p?<?0.01). The mean annual loss of carbon from the soil was 17.32(±1.48) Mg C?ha?1 of which approximately 63% was accounted for by autotrophic respiration. The relative contribution of autotrophic respiration varied seasonally between 55% in the wet season to 79% of the total soil CO2 efflux in the dry season. Furthermore, seasonal fluctuations of all the soil respiration components were strongly correlated with soil moisture (R 2?=?0.79–0.90, p?<?0.01).Conclusions
Across these two structurally distinct cerrado stands, seasonal variations in rainfall, was the main driver of soil CO2 efflux and its components. Consequently, soil respiration within these ecosystems is likely to be highly sensitive to any changes in seasonal precipitation patterns. 相似文献109.
Wei Wang Lin Ao Elizabeth R. Rayburn Hongxia Xu Xiangrong Zhang Xu Zhang Subhasree Ashok Nag Xuming Wu Ming-Hai Wang Hui Wang Erwin G. Van Meir Ruiwen Zhang 《PloS one》2012,7(9)
The purpose of the present study was to determine the in vitro and in vivo anti-cancer activity and pharmacological properties of 3,4-dimethoxy-N-[(2,2-dimethyl-2H-chromen-6-yl)methyl]-N-phenylbenzenesulfonamide, KCN1. In the present study, we investigated the in vitro activity of KCN1 on cell proliferation and cell cycle distribution of pancreatic cancer cells, using the MTT and BrdUrd assays, and flow cytometry. The in vivo anti-cancer effects of KCN1 were evaluated in two distinct xenograft models of pancreatic cancer. We also developed an HPLC method for the quantitation of the compound, and examined its stability in mouse plasma, plasma protein binding, and degradation by mouse S9 microsomal enzymes. Furthermore, we examined the pharmacokinetics of KCN1 following intravenous or intraperitoneal injection in mice. Results showed that, in a dose-dependent manner, KCN1 inhibited cell growth and induced cell cycle arrest in human pancreatic cancer cells in vitro, and showed in vivo anticancer efficacy in mice bearing Panc-1 or Mia Paca-2 tumor xenografts. The HPLC method provided linear detection of KCN1 in all of the matrices in the range from 0.1 to 100 µM, and had a lower limit of detection of 0.085 µM in mouse plasma. KCN1 was very stable in mouse plasma, extensively plasma bound, and metabolized by S9 microsomal enzymes. The pharmacokinetic studies indicated that KCN1 could be detected in all of the tissues examined, most for at least 24 h. In conclusion, our preclinical data indicate that KCN1 is a potential therapeutic agent for pancreatic cancer, providing a basis for its future development. 相似文献
110.