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201.
Activation of NADPH oxidase of human neutrophils. Potentiation of chemotactic peptide by a diacylglycerol 总被引:3,自引:0,他引:3
B Dewald T G Payne M Baggiolini 《Biochemical and biophysical research communications》1984,125(1):367-373
Formyl-methionyl-leucyl-phenylalanine (fMLP) and 1-oleoyl-2-acetyl-glycerol (OAG) are synergistic stimuli of the respiratory burst of neutrophils. Simultaneous exposure to both agents greatly enhanced superoxide production, both in rate and extent. OAG potentiated the response to fMLP also in Ca++ -free medium. Pretreatment of the neutrophils with fMLP drastically shortened the lag of superoxide production in response to OAG. Our findings lead to the following conclusions: (i) Protein kinase C is likely to be involved in the activation of the NADPH oxidase by fMLP; (ii) OAG appears to be utilized as an intermediate in the activation process; (iii) prestimulation of the cells with fMLP facilitates the response to OAG. 相似文献
202.
Hans A. Braun Mathias Dewald Klaus Schäfer Karlheinz Voigt Xing Pei Kevin Dolan Frank Moss 《Journal of computational neuroscience》1999,7(1):17-32
We report the results of a search for evidence of unstable periodic orbits in the sensory afferents of the facial cold receptors of the rat. Cold receptors are unique in that they exhibit a diversity of action potential firing patterns as well as pronounced transients in firing rate following rapid temperature changes. These characteristics are the result of an internal oscillator operating at the level of the membrane potential. If such oscillators have three or more degree of freedom, and at least one of which also exhibits a nonlinearity, they are potentially capable of complex activity. By detecting the existence of unstable periodic orbits, we demonstrate low-dimensional dynamical behavior whose characteristics depend on the temperature range, impulse pattern, and temperature transients. 相似文献
203.
JP Reyes A Huanosta-Gutiérrez A López-Rodríguez A Martínez-Torres 《Channels (Austin, Tex.)》2015,9(2):88-95
We studied the effects of mutations of positively charged amino acid residues in the pore of X. tropicalis TMEM16A calcium-activated chloride channels: K613E, K628E, K630E; R646E and R761E. The activation and deactivation kinetics were not affected, and only K613E showed a lower current density. K628E and R761E affect anion selectivity without affecting Na+ permeation, whereas K613E, R646E and the double mutant K613E + R646E affect anion selectivity and permeability to Na+. Furthermore, altered blockade by the chloride channel blockers anthracene-9-carboxylic acid (A-9-C), 4, 4''-Diisothiocyano-2,2''-stilbenedisulfonic acid (DIDS) and T16inh-A01 was observed. These results suggest the existence of 2 binding sites for anions within the pore at electrical distances of 0.3 and 0.5. These sites are also relevant for anion permeation and blockade. 相似文献
204.
Jennifer McQueen Dewald van Dyk Barry Young Chris Loewen Vivien Measday 《Cell cycle (Georgetown, Tex.)》2012,11(18):3421-3432
The glycogen synthase kinase-3 homolog, Mck1, has been implicated in many cellular functions, from sporulation to calcium stress response in budding yeast. Here, we report a novel function for Mck1 in the inhibition of Clb2-Cdk1 activity post nuclear division. Clb2-Cdk1, the major mitotic cyclin-Cdk complex in yeast, accumulates before anaphase and must be inhibited in telophase for cells to exit mitosis and enter into the next cell cycle. We show that the mck1Δ mutant is highly sensitive to increased Clb2-Cdk1 activity caused either by overexpression of Clb2 or the Cdk1-activating phosphatase Mih1. Deletion of the Cdk1 inhibitory kinase, SWE1, in combination with a mck1Δ mutant results in a synthetic growth defect, suggesting that Mck1 and Swe1 function in parallel pathways to inhibit Clb2-Cdk1. We find that mck1Δ strains have a delay in mitotic exit as well as elevated levels of Clb2-Cdk1 activity post-nuclear division. Using a co-immunoprecipitation assay, we identify a physical interaction between Mck1 and both Clb2 and Mih1. Finally, we demonstrate that phosphorylation of purified Clb2 by Cdk1 is inhibited by catalytically active Mck1 but not catalytically inactive Mck1 in vitro. We propose that Mck1 inhibits the activity of Clb2-Cdk1 via interaction with Clb2. The mammalian glycogen synthase kinase-3 homolog has been implicated in cyclin inhibition, suggesting a conserved cell cycle function for both yeast and mammalian glycogen synthase kinases. 相似文献