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排序方式: 共有263条查询结果,搜索用时 46 毫秒
61.
Anna Małolepszy Terry Mun Niels Sandal Vikas Gupta Manu Dubin Dorian Urbański Niraj Shah Asger Bachmann Eigo Fukai Hideki Hirakawa Satoshi Tabata Marcin Nadzieja Katharina Markmann Junyi Su Yosuke Umehara Takashi Soyano Akira Miyahara Shusei Sato Makoto Hayashi Jens Stougaard Stig U. Andersen 《The Plant journal : for cell and molecular biology》2016,88(2):306-317
Long terminal repeat (LTR) retrotransposons are closely related to retroviruses, and their activities shape eukaryotic genomes. Here, we present a complete Lotus japonicus insertion mutant collection generated by identification of 640 653 new insertion events following de novo activation of the LTR element Lotus retrotransposon 1 (LORE1) ( http://lotus.au.dk ). Insertion preferences are critical for effective gene targeting, and we exploit our large dataset to analyse LTR element characteristics in this context. We infer the mechanism that generates the consensus palindromes typical of retroviral and LTR retrotransposon insertion sites, identify a short relaxed insertion site motif, and demonstrate selective integration into CHG‐hypomethylated genes. These characteristics result in a steep increase in deleterious mutation rate following activation, and allow LORE1 active gene targeting to approach saturation within a population of 134 682 L. japonicus lines. We suggest that saturation mutagenesis using endogenous LTR retrotransposons with germinal activity can be used as a general and cost‐efficient strategy for generation of non‐transgenic mutant collections for unrestricted use in plant research. 相似文献
62.
M Aoyagi N Fukai H Sakamoto T Shinkai Y Matsushima M Yamamoto K Yamamoto 《Journal of cellular physiology》1991,147(2):191-198
Progressive stenosis or occlusion of bilateral internal carotid arteries by fibrocellular intimal thickening results in cerebral ischemia in moyamoya disease. The etiology is unknown. We examined cultured arterial smooth muscle cells (SMC) from scalp arteries of five patients with moyamoya disease. In this study we investigated the responsiveness of the cells in culture to serum mitogens including platelet-derived growth factor (PDGF), a major mitogen of SMC, and compared the response to that of cells derived from age-matched control patients. SMC from patients with moyamoya disease proliferated less rapidly in a medium with 15% serum than did control SMC and responded poorly to the addition of PDGF to 5% serum. PDGF alone did not stimulate SMC in a quiescent state to initiate DNA synthesis in moyamoya disease, without serum factors other than bovine serum albumin, though it significantly stimulated the controls. Simultaneous additions of epidermal growth factor, insulin-like growth factor-I, and PDGF stimulated initiation of DNA synthesis in cells from moyamoya disease, but not as much as PDGF alone did in the controls. Although direct correlations with the pathogenesis of the disease remain to be clarified, the results indicate altered interrelations between serum factors and the cellular responses in vessels of moyamoya disease. 相似文献
63.
F Fukai T Kase T Shidotani T Nagai T Katayama 《Biochemical and biophysical research communications》1987,147(3):899-903
Intracellular transport and storage of retinoids were shown to be conducted by fatty acid-binding protein (FABP). When rat liver cytosol was gel filtrated, retinyl palmitate-binding activity was mainly eluted in the fraction with a Mr. of around 14,000, in which both FABP and cellular retinol-binding protein (CRBP) co-existed. From the binding analysis of purified FABP and CRBP to retinyl palmitate, FABP was found to have a relatively high affinity (Kd = 1.4 X 10(-6) M) to retinyl palmitate, while binding of retinyl palmitate to CRBP was scarcely detectable. By using anti-FABP serum, it was shown that FABP was distributed in organs relating to absorption and storage of retinoids, such as jejunum, ileum, and liver. In liver, the protein was localized in the parenchymal cells and with particularly high concentration in the perisinusoidal cells, probably fat-storing cells. 相似文献
64.
F Fukai S Yatomi T Morita S Nishizawa T Nagai T Katayama 《Journal of biochemistry》1989,105(6):968-973
Inhibition of the enzyme activity of glutathione S-transferase (GST) by a physiological concentration of bilirubin was studied using various substrates. When rat liver cytosol was used as an unfractionated GST, its GSH-conjugation activity toward 1-chloro-2,4-dinitrobenzene was decreased to one-half by bilirubin, while the activity toward 1,2-dichloro-4-nitrobenzene, p-nitrobenzyl chloride, or 1,2-epoxy-(p-nitrophenoxy)propane and also the non-selenium dependent GSH-peroxidase activity toward cumene hydroperoxide (CHPx activity) were hardly affected under the same conditions. In contrast, bilirubin inhibited each of the purified GST isozymes and no remarkable difference in bilirubin inhibition was observed with any of the substrates tested. From the chromatographic analysis of the cytosol incubated with [3H]bilirubin, it was found that a major part of the added bilirubin binds to subunit 1 (Ya) of GST isozyme, leaving not only the conjugation activity derived from 3-4 type GST but also the CHPx activity of subunit 2 (Yc) quantitatively intact. The bilirubin inhibition of both the conjugation activity of GST 3-4 and the CHPx activity of GST 2-2 was prevented almost completely by addition of a 3-fold molar excess of GST 1-1. From these results, it was assumed that the enzyme activities of both 3-4 type GSTs and subunit 2 (Yc) were protected from the inhibitory action of bilirubin by the scavenger effect of subunit 1 (Ya). 相似文献
65.
Tail-anchored (TA) proteins are integral membrane proteins that possess a single transmembrane domain near their carboxy terminus. TA proteins play critical roles in many important cellular processes such as membrane trafficking, protein translocation, and apoptosis. The GET complex mediates posttranslational insertion of newly synthesized TA proteins to the endoplasmic reticulum membrane. The GET complex is composed of the homodimeric Get3 ATPase and its heterooligomeric receptor, Get1/2. During insertion, the Get3 dimer shuttles between open and closed conformational states, coupled with ATP hydrolysis and the binding/release of TA proteins. We report crystal structures of ADP-bound Get3 in complex with the cytoplasmic domain of Get1 (Get1CD) in open and semi-open conformations at 3.0‐ and 4.5‐Å resolutions, respectively. Our structures and biochemical data suggest that Get1 uses two interfaces to stabilize the open dimer conformation of Get3. We propose that one interface is sufficient for binding of Get1 by Get3, while the second interface stabilizes the open dimer conformation of Get3. 相似文献
66.
Fukai E Soyano T Umehara Y Nakayama S Hirakawa H Tabata S Sato S Hayashi M 《The Plant journal : for cell and molecular biology》2012,69(4):720-730
We established a gene tagging population of the model legume Lotus japonicus using an endogenous long terminal repeat (LTR) retrotransposon Lotus Retrotransposon 1 (LORE1). The population was composed of 2450 plant lines, from which a total of 4532 flanking sequence tags of LORE1 were recovered by pyrosequencing. The two-dimensional arrangement of the plant population, together with the use of multiple identifier sequences in the primers used to amplify the flanking regions, made it possible to trace insertions back to the original plant lines. The large-scale detection of new LORE1 insertion sites revealed a preference for genic regions, especially in exons of protein-coding genes, which is an interesting feature to consider in the interaction between host genomes and chromoviruses, to which LORE1 belongs, a class of retrotransposon widely distributed among plants. Forward screening of the symbiotic mutants from the population succeeded to identify five symbiotic mutants of known genes. These data suggest that LORE1 is robust as a genetic tool. 相似文献
67.
Patrick R. Maloney Pasha Khan Michael Hedrick Palak Gosalia Monika Milewski Linda Li Gregory P. Roth Eduard Sergienko Eigo Suyama Eliot Sugarman Kevin Nguyen Alka Mehta Stefan Vasile Ying Su Derek Stonich Hung Nguyen Fu-Yue Zeng Arianna Mangravita Novo Michael Vicchiarelli Jena Diwan Anthony B. Pinkerton 《Bioorganic & medicinal chemistry letters》2012,22(21):6656-6660
The recently discovered apelin/APJ system has emerged as a critical mediator of cardiovascular homeostasis and is associated with the pathogenesis of cardiovascular disease. A role for apelin/APJ in energy metabolism and gastrointestinal function has also recently emerged. We disclose the discovery and characterization of 4-oxo-6-((pyrimidin-2-ylthio)methyl)-4H-pyran-3-yl 4-nitrobenzoate (ML221), a potent APJ functional antagonist in cell-based assays that is >37-fold selective over the closely related angiotensin II type 1 (AT1) receptor. ML221 was derived from an HTS of the ~330,600 compound MLSMR collection. This antagonist showed no significant binding activity against 29 other GPCRs, except to the κ-opioid and benzodiazepinone receptors (<50/<70%I at 10 μM). The synthetic methodology, development of structure–activity relationship (SAR), and initial in vitro pharmacologic characterization are also presented. 相似文献
68.
Nakanishi A Bae JG Fukai K Tokumoto N Kuroda K Ogawa J Nakatani M Shimizu S Ueda M 《Applied microbiology and biotechnology》2012,94(4):939-948
A gene encoding laccase I was identified and cloned from the white-rot fungus Trametes sp. Ha1. Laccase I contained 10 introns and an original secretion signal sequence. After laccase I without introns was prepared by overlapping polymerase chain reaction, it was inserted into expression vector pULD1 for yeast
cell surface display. The oxidation activity of a laccase-I-displaying yeast as a whole-cell biocatalyst was examined with
2,2′-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) (ABTS), and the constructed yeast showed a high oxidation activity.
After the pretreatment of hydrothermally processed rice straw (HPRS) with laccase-I-displaying yeast with ABTS, fermentation
was conducted with yeast codisplaying endoglucanase, cellobiohydrolase, and β-glucosidase with HPRS. Fermentation of HPRS
treated with laccase-I-displaying yeast was performed with 1.21-fold higher activities than those of HPRS treated with control
yeast. The results indicated that pretreatment with laccase-I-displaying yeast with ABTS was effective for direct fermentation
of cellulosic materials by yeast codisplaying endoglucanase, cellobiohydrolase, and β-glucosidase. 相似文献
69.
The activity patterns of the globus pallidus (GPe) and subthalamic nucleus (STN) are closely associated with motor function
and dysfunction in the basal ganglia. In the pathological state caused by dopamine depletion, the STN–GPe network exhibits
rhythmic synchronous activity accompanied by rebound bursts in the STN. Therefore, the mechanism of activity transition is
a key to understand basal ganglia functions. As synchronization in GPe neurons could induce pathological STN rebound bursts,
it is important to study how synchrony is generated in the GPe. To clarify this issue, we applied the phase-reduction technique
to a conductance-based GPe neuronal model in order to derive the phase response curve (PRC) and interaction function between
coupled GPe neurons. Using the PRC and interaction function, we studied how the steady-state activity of the GPe network depends
on intrinsic membrane properties, varying ionic conductances on the membrane. We noted that a change in persistent sodium
current, fast delayed rectifier Kv3 potassium current, M-type potassium current and small conductance calcium-dependent potassium
current influenced the PRC shape and the steady state. The effect of those currents on the PRC shape could be attributed to
extension of the firing period and reduction of the phase response immediately after an action potential. In particular, the
slow potassium current arising from the M-type potassium and the SK current was responsible for the reduction of the phase
response. These results suggest that the membrane property modulation controls synchronization/asynchronization in the GPe
and the pathological pattern of STN–GPe activity. 相似文献
70.
Comparison of the genome structure of the self-incompatibility (S) locus in interspecific pairs of S haplotypes 总被引:1,自引:0,他引:1
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The determinants of recognition specificity of self-incompatibility in Brassica are SRK in the stigma and SP11/SCR in the pollen, both of which are encoded in the S locus. The nucleotide sequence analyses of many SRK and SP11/SCR alleles have identified several interspecific pairs of S haplotypes having highly similar sequences between B. oleracea and B. rapa. These interspecific pairs of S haplotypes are considered to be derived from common ancestors and to have maintained the same recognition specificity after speciation. In this study, the genome structures of three interspecific pairs of S haplotypes were compared by sequencing SRK, SP11/SCR, and their flanking regions. Regions between SRK and SP11/SCR in B. oleracea were demonstrated to be much longer than those of B. rapa and several retrotransposon-like sequences were identified in the S locus in B. oleracea. Among the seven retrotransposon-like sequences, six sequences were found to belong to the ty3 gypsy group. The gag sequences of the retrotransposon-like sequences were phylogenetically different from each other. In Southern blot analysis using retrotransposon-like sequences as probes, the B. oleracea genome showed more signals than the B. rapa genome did. These findings suggest a role for the S locus and genome evolution in self-incompatible plant species. 相似文献