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101.
E Rewald M M Francischetti L Barberis 《Cellular and molecular biology, including cyto-enzymology》2002,48(3):265-269
Here we consider certain therapeutic effects that intravenous administration of pooled high dose immunoglobulin and anti-D IgG share. Despite million-fold difference in doses such an effect occurs at least in idiopathic thrombocytopenic purpura (ITP). We postulate that spontaneous bleeding events may remit even when platelet numbers show refractoriness. We also mention the possible sparing of anti-D antibody-coated red blood cell (RBC) destruction and, finally, an acceleration of fibrotic involution. Fc receptors (FcRs) play a central role; beyond the well-established interactions with the immunoglobulin Fc fragment, FcRs are supposed to display special cognitive properties that enable them to pick out the therapeutic molecules from the recipient's IgG pool. Such subtle selection suggests some disarray in the host. On the other hand it may explain why the often-encouraging outcome of IVIG therapy remains unpredictable. 相似文献
102.
Silvio Zaina Alcide Bertani Luciano Lombardi Sergio Mapelli Giuseppe Torti 《Planta》1989,179(2):222-227
As described previously, the sensitivity of rice (Oryza sativa L.) coleoptiles to auxin is modulated by oxygen. Under anoxia, coleoptile elongation is insensitive to exogenously applied indole-3-acetic acid (IAA), whereas its sensitivity increases in air in the presence of the exogenous stimulus. Here we report the presence of two independent classes of membrane-bound IAA-binding sites in air-grown coleoptiles. Their binding activity is strictly correlated with the system's sensitivity to IAA. We designate them as site A (high affinity) and site B (low affinity). Site A shows a relatively fast response to anoxia, and is highly specific for auxins. Regulation of site-A binding activity through ATP, whose availability decreases under anoxia, is postulated. A role as auxin carrier is suggested for site B.Abbreviations ABS(s)
auxin-binding site(s)
- IAA
indole-3-acctic acid
- NAA
2-naphthaleneacetic acid
- ION3
valinomycin, nigericin, carbonylcyanide p-trifluoromethoxyphenyl hydrazone
Dedicated to the memory of Professor G. Torti, who passed away on 2 May, 1988 相似文献
103.
J Elands C Barberis S Jard B Lammek M Manning W H Sawyer E R de Kloet 《FEBS letters》1988,229(2):251-255
A radioiodinated vasopressin antagonist, d(CH2)5[Tyr(NH2)9]AVP has been prepared. Iodination was carried out at the phenyl moiety of the tyrosylamide residue at position 9, followed by HPLC purification. Non-radiolabelled monoiodinated antagonist was used as a reference for identification. 125I-d(CH2)5[Tyr(Me)2, Tyr(NH2)9]AVP binding appeared to take place with a dissociation constant of 0.28 +/- 0.09 nM (Kd +/- SD) to V1 vasopressin receptors on rat liver membranes. 相似文献
104.
Summary Three organic fertilizers: a farmyard manure (FYM), humified poplar barks (PBF) and spruce barks (SBF) were investigated by means of chemical analysis and by the study of humic substances extracted by 0.1M sodium pyrophosphate (pH=10.0). The organic carbon content and the C/N ratio were higher in SBF, probably as a consequence of the short fermentation period (5 months). Yields of organic substances removed by three consecutive extractions with Na4P2O7 solution were in the order: PBF>FYM>SBF. Nominal molecular weight distribution of total extracts was studied using Sephadex G type gels; TRIS buffer (pH=9.0) was the eluant, since the use of water produced complex gel-solute interactions. It was shown that SBF had a higher content of small size particles than the other two products which exhibited quite similar elution curves. Slopes of log A(absorbance)vs log plots and ratio of absorbances at 465 and 665 nm (E4/E6) of fractions containing particle of lower size were the steepest and the highest, respectively. 相似文献
105.
A Guerrasio G Saglio C Camaschella P G Pich E Barberis D Del Ponte P Izzo 《Bollettino della Società italiana di biologia sperimentale》1979,55(10):967-973
The Authors report the data concerning a family coming from Ficarolo (Rovigo). The father and one son were found hematologically healthy, but resulted carriers of Hb G-Ferrara. This is an unstable rare pigment with a replacement in the beta 57 (E-1) helicoidal position. The type and site of the mutation explain the "in vitro" molecular instability; on the other hand, this latter doesn't seem to cause any hematological disorder, even if an increased met-Hb production was found when affected blood was incubated at 37 degrees C for two hours in sterile conditions. 相似文献
106.
Monica Mattana Immacolata Coraggio Ida Brambilla Alcide Bertani Remo Reggiani 《Planta》1996,199(1):74-78
Ferredoxin-dependent glutamate synthase (Fd-GOGAT; EC 1.4.7.1) is the last enzyme involved in the pathway of nitrate assimilation in higher plants. This paper describes the synthesis and expression of the enzyme in anaerobic coleoptiles of rice (Oryza sativa L.) and its regulation by exogenous nitrate. The activity of Fd-GOGAT was strongly inhibited by cycloheximide between 4 and 9 d of anaerobic germination. The addition of nitrate slightly increased, in the first 5 h, the specific activity of Fd-GOGAT as well as the amount of a 160-kDa protein specifically immunoprecipitated with anti-Fd-GOGAT serum. Northern blot analysis, performed with a specific riboprobe, showed the presence of mRNA of the expected size and the inductive effect of nitrate. The role of Fd-GOGAT is discussed in relation to the anaerobic assimilation of nitrate by rice coleoptiles.Abbreviations CHX
cycloheximide
- Fd
ferredoxin
- GOGAT
glutamate synthase
- GS
glutamine synthetase
- NiR
nitrite reductase
- NR
nitrate reductase
The authors wish to thank Dr. J. Turner (Rothamsted Experimental Station, Harpenden, UK) for providing Fd-GOGAT antibody and Dr. H. Sakakibara (Nagoya University, Nagoya, Japan) for Fd-GOGAT clone. This research was supported by the National Research Council of Italy, special project RAISA, sub-projekt N. 2, paper N. 2174. 相似文献
107.
Claude Barberis Neil Moorcroft James Pribish Elina Tserlin Alexandre Gross Mark Czekaj Matthieu Barrague Paul Erdman Tahir Majid Joseph Batchelor Mikhail Levit Andrew Hebert Liduo Shen Sandra Moreno-Mazza Anlai Wang 《Bioorganic & medicinal chemistry letters》2017,27(20):4735-4740
N-Substituted azaindoles have been discovered as pan-PIM kinase inhibitors. Initial SAR, early ADME and PK/PD data of a series of compounds is described and led to the identification of promising pan-PIM inhibitors which validated our interest in the 7-azaindole scaffold and led us to pursue the identification of a clinical candidate. 相似文献
108.
N Cotte M N Balestre A Aumelas E Mahé S Phalipou D Morin M Hibert M Manning T Durroux C Barberis B Mouillac 《European journal of biochemistry》2000,267(13):4253-4263
Despite their opposite effects on signal transduction, the nonapeptide hormone arginine-vasopressin (AVP) and its V1a receptor-selective cyclic peptide antagonist d(CH2)5[Tyr(Me)2]AVP display homologous primary structures, differing only at residues 1 and 2. These structural similarities led us to hypothesize that both ligands could interact with the same binding pocket in the V1a receptor. To determine receptor residues responsible for discriminating binding of agonist and antagonist ligands, we performed site-directed mutagenesis of conserved aromatic and hydrophilic residues as well as nonconserved residues, all located in the transmembrane binding pocket of the V1a receptor. Mutation of aromatic residues of transmembrane region VI (W304, F307, F308) reduced affinity for the d(CH2)5[Tyr(Me)2]AVP and markedly decreased affinity for the unrelated strongly hydrophobic V1a-selective nonpeptide antagonist SR 49059. Replacement of these aromatic residues had no effect on AVP binding, but increased AVP-induced coupling efficacy of the receptor for its G protein. Mutating hydrophilic residues Q108, K128 and Q185 in transmembrane regions II, III and IV, respectively, led to a decrease in affinity for both agonists and antagonists. Finally, the nonconserved residues T333 and A334 in transmembrane region VII, controlled the V1a/V2 binding selectivity for both nonpeptide and cyclic peptide antagonists. Thus, because conserved aromatic residues of the V1a receptor binding pocket seem essential for antagonists and do not contribute at all to the binding of agonists, we propose that these residues differentiate agonist vs. antagonist ligand binding. 相似文献
109.
110.