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221.
The pma1 and pma2 H(+)-ATPases from Schizosaccharomyces pombe are functionally interchangeable. 总被引:1,自引:0,他引:1
The pma2 gene of Schizosaccharomyces pombe codes for a polypeptide having a predicted Mr of 110,126 and which is 79% identical to the plasma membrane H(+)-ATPase encoded by the pma1 gene. The pma2 gene, unlike pma1, is weakly expressed and not essential to mitotic growth. By constructing yeast strains in which the chromosomal pma2 gene is under control of the adh promoter, it has been possible to identify the overproduced ATPase in plasma membrane via formation of a phosphoenzyme. In a pma1-1 mutant strain whose ATPase activity is insensitive to vanadate, the overexpressed pma2 gene restores vanadate sensitivity. It also rescues a pma1 null mutant from lethality. These results demonstrate that the two H(+)-ATPases are functionally interchangeable in vivo but differently expressed. 相似文献
222.
223.
The pleiotropic drug resistance protein, Pdr5p, is an ATP-binding cassette transporter of the plasma membrane of Saccharomyces cerevisiae. Overexpression of Pdr5p results in increased cell resistance to a variety of cytotoxic compounds, a phenotype reminiscent of the multiple drug resistance seen in tumor cells. Pdr5p and two other yeast ATP-binding cassette transporters, Snq2p and Yor1p, were found to be phosphorylated on serine residues in vitro. Mutations in the plasma membrane-bound casein kinase I isoforms, Yck1p and Yck2p, abolished Pdr5p phosphorylation and modified the multiple drug resistance profile. We showed Pdr5p to be ubiquitylated when overexpressed. However, instability of Pdr5p was only seen in Yck1p- and Yck2p-deficient strains, in which it was degraded in the vacuole via a Pep4p-dependent mechanism. Our results suggest that casein kinase I activity is required for membrane trafficking of Pdr5p to the cell surface. In the absence of functional Yck1p and Yck2p, Pdr5p is transported to the vacuole for degradation. 相似文献
224.
Carlos Canchaya Caroline Proux Ghislain Fournous Anne Bruttin Harald Brüssow 《Microbiology and molecular biology reviews》2003,67(2):238-76, table of contents
The majority of the bacterial genome sequences deposited in the National Center for Biotechnology Information database contain prophage sequences. Analysis of the prophages suggested that after being integrated into bacterial genomes, they undergo a complex decay process consisting of inactivating point mutations, genome rearrangements, modular exchanges, invasion by further mobile DNA elements, and massive DNA deletion. We review the technical difficulties in defining such altered prophage sequences in bacterial genomes and discuss theoretical frameworks for the phage-bacterium interaction at the genomic level. The published genome sequences from three groups of eubacteria (low- and high-G+C gram-positive bacteria and gamma-proteobacteria) were screened for prophage sequences. The prophages from Streptococcus pyogenes served as test case for theoretical predictions of the role of prophages in the evolution of pathogenic bacteria. The genomes from further human, animal, and plant pathogens, as well as commensal and free-living bacteria, were included in the analysis to see whether the same principles of prophage genomics apply for bacteria living in different ecological niches and coming from distinct phylogenetical affinities. The effect of selection pressure on the host bacterium is apparently an important force shaping the prophage genomes in low-G+C gram-positive bacteria and gamma-proteobacteria. 相似文献
225.
Philippe E Van Den Steen Anja Wuyts Steven J Husson Paul Proost Jo Van Damme Ghislain Opdenakker 《European journal of biochemistry》2003,270(18):3739-3749
On chemokine stimulation, leucocytes produce and secrete proteolytic enzymes for innate immune defence mechanisms. Some of these proteases modify the biological activity of the chemokines. For instance, neutrophils secrete gelatinase B (matrix metalloproteinase-9, MMP-9) and neutrophil collagenase (MMP-8) after stimulation with interleukin-8/CXCL8 (IL-8). Gelatinase B cleaves and potentiates IL-8, generating a positive feedback. Here, we extend these findings and compare the processing of the CXC chemokines human and mouse granulocyte chemotactic protein-2/CXCL6 (GCP-2) and the closely related human epithelial-cell derived neutrophil activating peptide-78/CXCL5 (ENA-78) with that of human IL-8. Human GCP-2 and ENA-78 are cleaved by gelatinase B at similar rates to IL-8. In addition, GCP-2 is cleaved by neutrophil collagenase, but at a lower rate. The cleavage of GCP-2 is exclusively N-terminal and does not result in any change in biological activity. In contrast, ENA-78 is cleaved by gelatinase B at eight positions at various rates, finally generating inactive fragments. Physiologically, sequential cleavage of ENA-78 may result in early potentiation and later in inactivation of the chemokine. Remarkably, in the mouse, which lacks IL-8 which is replaced by GCP-2/LIX as the most potent neutrophil activating chemokine, N-terminal clipping and twofold potentiation by gelatinase B was also observed. In addition to the similarities in the potentiation of IL-8 in humans and GCP-2 in mice, the conversion of mouse GCP-2/LIX by mouse gelatinase B is the fastest for any combination of chemokines and MMPs so far reported. This rapid conversion was also performed by crude neutrophil granule secretion under physiological conditions, extending the relevance of this proteolytic cleavage to the in vivo situation. 相似文献
226.
Oxalis tuberosa is an important crop cultivated in the highest Andean zones. A germplasm collection is maintained ex situ by CIP, which has
developed a morphological markers system to classify the accessions into morphotypes, i.e. groups of morphologically identical
accessions. However, their genetic uniformity is currently unknown. The ISSR technique was used in two experiments to determine
the relationships between both morphological and molecular markers systems. The intra-morphotype genetic diversity, the spatial
structures of the diversity and the congruence between both markers systems were determined. In the first experience, 44 accessions
representing five morphotypes, clearly distinct from each other, were analyzed. At the molecular level, the accessions exactly
clustered according to their morphotypes. However, a genetic variability was observed inside each morphotype. In the second
experiment, 34 accessions gradually differing from each other on morphological base were analyzed. The morphological clustering
showed no geographical structure. On the opposite, the molecular analysis showed that the genetic structure was slightly related
to the collection site. The correlation between both markers systems was weak but significant. The lack of perfect congruence
between morphological and molecular data suggests that the morphological system may be useful for the morphotypes management
but is not appropriate to study the genetic structure of the oca. The spatial structure of the genetic diversity can be related
to the evolution of the species and the discordance between the morphological and molecular structures may result from similar
selection pressures at different places leading to similar forms with a different genetic background. 相似文献
227.
Evariste Tshibangu-Kabamba Bui Hoang Phuc Vo Phuoc Tuan Kartika Afrida Fauzia Augustin Kabongo-Tshibaka Nadine Kalenda Kayiba Angel Rosas-Aguirre Brecht Devleesschauwer Alain Cimuanga-Mukanya Patrick de Jsus Ngoma Kisoko Takashi Matsumoto Junko Akada Ghislain Tumba Disashi Dieudonn Mumba Ngoyi Yasutoshi Kido Niko Speybroeck Yoshio Yamaoka 《PLoS neglected tropical diseases》2021,15(9)
Beside diagnostic uncertainties due to the lack of a perfect gold standard test for Helicobacter pylori infection, the diagnosis and the prevalence estimation for this infection encounter particular challenges in Africa including limited diagnostic tools and specific genetic background. We developed and evaluated the accuracy of an enzyme-linked immunosorbent assay (ELISA) system tailored for H. pylori genetics in Africa (HpAfr-ELISA). Strains belonging to main genetic populations infecting Africans were exploited as sources for whole-cell antigens to establish in-house the ELISA system. A phase II unmatched case-control study explored the diagnostic accuracy of the HpAfr-ELISA using a training set of samples collected from dyspeptic patients from Kinshasa, the Democratic Republic of Congo (DRC) who had been tested with invasive standard tests (i.e., histology, culture, and rapid urease test) in 2017. Then the assay was cross-validated through a community-based survey assessing the prevalence of H. pylori and associated factors in 425 adults from Mbujimayi, DRC in 2018. Bayesian inferences were used to deal with statistical uncertainties of estimates (true prevalence, sensitivity, and specificity) in the study population. At its optimal cut-off-value 20.2 U/mL, the assay achieved an estimated sensitivity of 97.6% (95% credible interval [95%CrI]: 89.2; 99.9%) and specificity of 90.5% (95%CrI: 78.6; 98.5). Consistent outcomes obtained at repeated tests attested the robustness of the assay (negative and positive agreements always > 70%). The true prevalence of H. pylori was estimated 53.8% [95%CrI: 42.8; 62.7%]. Increasing age (adjusted odds ratio [aOR] > 1.0 [95% confidence interval (CI): > 1.0; 1.1]; p<0.001), overcrowding households (aOR = 3.2 [95%CI: 2.0; 5.1]; p<0.001), and non-optimal hand hygiene (aOR = 4.5 [95%CI: 2.0; 11.4]; p = 0.001) were independently associated with the H. pylori-seropositivity. The novel ELISA system has demonstrated good diagnostic accuracy and potential usefulness for management and mitigation strategies for H. pylori infection in African settings. 相似文献
228.
229.
Flor Rodríguez Marc Ghislain Andrea M. Clausen Shelley H. Jansky David M. Spooner 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》2010,121(6):1187-1198
Solanum section Petota is taxonomically difficult, partly because of interspecific hybridization at both the diploid and polyploid levels. The taxonomy
of cultivated potatoes is particularly controversial. Using DNA sequence data of the waxy gene, we here infer relationships among the four species of cultivated potatoes accepted in the latest taxonomic treatment
(S. ajanhuiri, S. curtilobum, S. juzepczukii and S. tuberosum, the latter divided into the Andigenum and Chilotanum Cultivar Groups). The data support prior ideas of hybrid origins of
S. ajanhuiri from the S. tuberosum Andigenum Group (2x = S. stenotomum) × S. megistacrolobum; S. juzepczukii from the S. tuberosum Andigenum Group (2x = S. stenotomum) × S. acaule; and S. curtilobum from the S. tuberosum Andigenum Group (4x = S. tuberosum subsp. andigenum) × S. juzepczukii. For the tetraploid cultivar-groups of S. tuberosum, hybrid origins are suggested entirely within much more closely related species, except for two of three examined accessions
of the S. tuberosum Chilotanum Group that appear to have hybridized with the wild species S. maglia. Hybrid origins of the crop/weed species S. sucrense are more difficult to support and S. vernei is not supported as a wild species progenitor of the S. tuberosum Andigenum Group. 相似文献
230.
Question: How to refine simulations based on a global vegetation model in order to apply it to regional scale? Location: Europe from 35° N to 71° N and 25° W to 70° E. Methods: Geographical ranges of European plants were georeferenced and used with monthly mean climatic data (diurnal temperature ranges, ground frost frequencies, precipitation, relative humidity, rain frequencies, amount of sunshine hours and temperature) and growing degree days to infer climatic boundaries for 320 taxa. We performed a discriminant analysis to define their potential geographic ranges. Hierarchical clustering was computed on potential ranges. Results: Clustering provided 25 Bioclimatic Affinity Groups (BAG) of plants consisting of 13 tree, seven shrub and five herb groups. These B AGs are characterized by different geographical ranges and climatic tolerances and requirements. Conclusion: The use of monthly data instead of annual values improved the prediction of potential distribution ranges and highlighted the importance of climate seasonality for defining the plant groups with accuracy. The B AGs are detailed enough to provide finer reconstructions and simulations of the vegetation at the regional scale. 相似文献