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81.
Differential cytokine modulation and T cell activation by two distinct classes of thalidomide analogues that are potent inhibitors of TNF-alpha. 总被引:19,自引:0,他引:19
L G Corral P A Haslett G W Muller R Chen L M Wong C J Ocampo R T Patterson D I Stirling G Kaplan 《Journal of immunology (Baltimore, Md. : 1950)》1999,163(1):380-386
TNF-alpha mediates both protective and detrimental manifestations of the host immune response. Our previous work has shown thalidomide to be a relatively selective inhibitor of TNF-alpha production in vivo and in vitro. Additionally, we have recently reported that thalidomide exerts a costimulatory effect on T cell responses. To develop thalidomide analogues with increased anti-TNF-alpha activity and reduced or absent toxicities, novel TNF-alpha inhibitors were designed and synthesized. When a selected group of these compounds was examined for their immunomodulatory activities, different patterns of cytokine modulation were revealed. The tested compounds segregated into two distinct classes: one class of compounds, shown to be potent phosphodiesterase 4 inhibitors, inhibited TNF-alpha production, increased IL-10 production by LPS-induced PBMC, and had little effect on T cell activation; the other class of compounds, similar to thalidomide, were not phosphodiesterase 4 inhibitors and markedly stimulated T cell proliferation and IL-2 and IFN-gamma production. These compounds inhibited TNF-alpha, IL-1beta, and IL-6 and greatly increased IL-10 production by LPS-induced PBMC. Similar to thalidomide, the effect of these agents on IL-12 production was dichotomous; IL-12 was inhibited when PBMC were stimulated with LPS but increased when cells were stimulated by cross-linking the TCR. The latter effect was associated with increased T cell CD40 ligand expression. The distinct immunomodulatory activities of these classes of thalidomide analogues may potentially allow them to be used in the clinic for the treatment of different immunopathological disorders. 相似文献
82.
Historically in the European Union, all Leptospira vaccines were released using the European Pharmacopoeia (Ph. Eur.) hamster potency assay. Recently, there has been a shift toward alternatives that offer either refinement of testing or replacement of animals for product release. This is being driven by animal welfare concerns but also by a drive to have more consistent, cheaper, and faster batch release tests. This publication discusses one such example of a multicomponent canine vaccine that includes three Leptospira serovars and has recently been registered in the European Union. The potency release test is a refinement because it uses rabbit serology rather than hamster challenge. This publication covers the principles of the test method, challenges faced during its development and registration, and discussion about benefits and limitations of this method. It concludes with a view of how the use of serology testing could fit into an overall strategy to move to fully in vitro testing by adopting a consistency approach. 相似文献
83.
J W Stirling 《The journal of histochemistry and cytochemistry》1989,37(5):709-714
The distribution of lysozyme (muramidase) within eosinophil leukocytes situated in the lamina propria of human colon was studied by immunoelectron microscopy using a range of standard techniques. Tissue processed in a variety of glutaraldehyde- or paraformaldehyde-based fixatives was partially dehydrated and embedded in the acrylic resin LR White. Tissue thus treated showed lysozyme in pale cytoplasmic granules and the matrix of specific granules, but not in their crystalloids. Trypsinization of sections had little effect on this result, and tissues fixed in glutaraldehyde and embedded in Araldite showed a low level of reactivity with a similar distribution. After etching LR or Araldite sections with sodium metaperiodate, the pale granules and specific granule matrices became negative for lysozyme and the crystalloids became positive. Because crystalloids also were labeled with normal rabbit immunoglobulin after etching, this apparent redistribution of label could be due to nonspecific binding rather than exposure of masked epitope. 相似文献
84.
Human N-acetyl-beta-hexosaminidases As and P are probably sialylated since they are susceptible to neuraminidase attack. twhen infused into the circulation of a rat they are removed more slowly than the non-sialylated forms of the enzyme from tissue and urine. 相似文献
85.
Terence P. Dawson Mark D. A. Rounsevell Tatiana Kluvánková-Oravská Veronika Chobotová Andrew Stirling 《Biodiversity and Conservation》2010,19(10):2843-2853
Predicting environmental change and its impacts on ecosystem goods and services at local to global scales remains a significant
challenge for the international scientific community. This is due largely to the fact that the Earth is made up of open, coupled,
complex, interactive and non-linear dynamic systems that are inherently unpredictable. Uncertainties over interactions and
feedbacks between natural and human drivers of environmental change (operating at different spatial and temporal scales) can
compound intrinsic intractable difficulties faced by plural societies aiming at sustainable management of ecosystems. Social-Ecological
Systems (SES) theory addresses these strongly coupled and complex characteristics of social and ecological systems. It can
provide a useful framework for articulating contrasting drivers and pressures on ecosystems and associated service provision,
spanning different temporalities and provenances. Here, system vulnerabilities (defined as exposure to threats affecting ability
of an SES to cope in delivering relevant functions), can arise from both endogenous and exogenous factors across multiple
time-scales. Vulnerabilities may also take contrasting forms, ranging from transient shocks or disruptions, through to chronic
or enduring pressures. Recognising these diverse conditions, four distinct dynamic properties emerge (resilience, stability, durability and robustness), under which it is possible to maintain system function and, hence, achieve sustainability. 相似文献
86.
KASSO DAÏNOU JEAN‐PHILIPPE BIZOUX JEAN‐LOUIS DOUCET GRÉGORY MAHY OLIVIER J. HARDY MYRIAM HEUERTZ 《Molecular ecology》2010,19(20):4462-4477
The impact of the Pleistocene climate oscillations on the structure of biodiversity in tropical regions remains poorly understood. In this study, the forest refuge theory is examined at the molecular level in Milicia excelsa, a dioecious tree with a continuous range throughout tropical Africa. Eight nuclear microsatellites (nSSRs) and two sequences and one microsatellite from chloroplast DNA (cpDNA) showed a deep divide between samples from Benin and those from Lower Guinea. This suggests that these populations were isolated in separate geographical regions, probably for several glacial cycles of the Pleistocene, and that the nuclear gene pools were not homogenized despite M. excelsa’s wind‐pollination syndrome. The divide could also be related to seed dispersal patterns, which should be largely determined by the migration behaviour of M. excelsa’s main seed disperser, the frugivorous bat Eidolon helvum. Within Lower Guinea, a north–south divide, observed with both marker types despite weak genetic structure (nSSRs: FST = 0.035, cpDNA: GST = 0.506), suggested the existence of separate Pleistocene refugia in Cameroon and the Gabon/Congo region. We inferred a pollen‐to‐seed dispersal distance ratio of c. 1.8, consistent with wide‐ranging gene dispersal by both wind and bats. Simulations in an Approximate Bayesian Computation framework suggested low nSSR and cpDNA mutation rates, but imprecise estimates of other demographic parameters, probably due to a substantial gene flow between the Lower Guinean gene pools. The decline of genetic diversity detected in some Gabonese populations could be a consequence of the relatively recent establishment of a closed canopy forest, which could negatively affect M. excelsa’s reproductive system. 相似文献
87.
Timothy R. Sexton Robert J. Henry Luke J. McManus Stirling Bowen Mervyn Shepherd 《Molecular breeding : new strategies in plant improvement》2010,25(3):471-480
Mis-priming associated with uncharacterised single nucleotide polymorphisms (SNPs) may lead to failure of PCR for genotyping.
This is particularly troublesome in high-throughput SNP genotyping applications relying on multiplex PCR (2–40-plex) generating
many short amplicons (80–120 bp) of similar size, an approach best suited for whole genome scans. However, if the target SNPs
are clustered within a few target genes one option to ameliorate this is to increase the amplicon length, effectively reducing
the potential for primer/template interactions and mis-priming. We tested this approach in a diverse population of 372 Eucalyptus pilularis individuals (π = 8.11 × 10−3, H
e = 0.75) using a modified Sequenom iPLEX gold assay. Four candidate genes (MYB1, MYB2, CAD and CCR) were amplified in a single
long range multiplex capture PCR generating 6 long amplicons ranging in size from 907 to 2,225 bp. This contrasts with the
standard approach which would have required the amplification of 98 short amplicons in 4 multiplex reactions. These 6 long
amplicons provided the assay template for 98 assays (87 SNP and 11 InDel) within the 4 candidate genes. Reaction results indicated
that longer amplicons could provide a suitable template for genotyping assays, with 90.8% of assays functional and 84.3% of
assays suitable for downstream analysis. Additional advantages of this approach were the capacity for troubleshooting using
gel electrophoresis and savings of 94% in capture primer synthesis costs. This approach will have the greatest relevance for
candidate gene approaches for association testing in uncharacterised populations of organisms with high sequence diversity. 相似文献
88.
Type III secretion is a widespread method whereby Gram-negative bacteria introduce toxins into eukaryotic cells. These toxins mimic or subvert a normal cellular process by interacting with a specific target, although how toxins reach their site of action is unclear. We set out to investigate the intracellular localization of a type III toxin of Pseudomonas aeruginosa called ExoU, which has phospholipase activity and requires a eukaryotic factor for activity. We found that ExoU is localized to the plasma membrane and undergoes modification within the cell by addition of two ubiquitin molecules at lysine-178. A region of five amino acids at position 679-683 near the C-terminus of the ExoU protein controls both membrane localization and ubiquitinylation. Site-directed mutagenesis identified a tryptophan at position 681 as crucial for these effects. We found that the same region at position 679-683 was also required for cell toxicity produced by ExoU as well as in vitro phospholipase activity. Localization of the phospholipase ExoU to the plasma membrane is thus required for activation and allows efficient utilization of adjacent substrate phospholipids. 相似文献
89.
90.