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421.
Cecile Albenne Herve Canut Georges Boudart Yu Zhang Helene San Clemente Rafael Pont-Lezica Elisabeth Jamet 《植物生理学报》2009,(5):977-989
Proteomics allows the large-scale study of protein expression either in whole organisms or in purified organelles. In particular, mass spectrometry (MS) analysis of gel-separated proteins produces data not only for protein identification, but for protein structure, location, and processing as well. An in-depth analysis was performed on MS data from etiolated hypocotyl cell wall proteomics ofArabidopsis thaliana. These analyses show that highly homologous members of multigene families can be differentiated. Two lectins presenting 93% amino acid identity were identified using peptide mass fingerprinting. Although the identification of structural proteins such as extensins or hydroxyproline/proline-rich proteins (H/PRPs) is arduous, different types of MS spectra were exploited to identify and characterize an H/PRP. Maturation events in a couple of cell wall proteins (CWPs) were analyzed using site mapping. N-glycosylation of CWPs as well as the hydroxylation or oxidation of amino acids were also explored, adding information to improve our understanding of CWP structure/function relationships. A bioinformatic tool was developed to locate by means of MS the N-terminus of mature secreted proteins and N-glycosylation. 相似文献
422.
Evaluation of a Medium for the Rapid Recovery of Escherichia coli from Shellfish 总被引:2,自引:1,他引:1
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A medium (A-1) which shortens the time necessary to identify and enumerate Escherichia coli found in estuarine water was evaluated for use for recovery of E. coli found in shellfish. Productivity of E. coli by this medium was comparable to that of the lengthier American Public Health Association method, and the occurrence of false positives was substantially reduced. 相似文献
423.
Characterization of Peroxidase Secretion and Subcellular Organization of Phanerochaete chrysosporium INA-12 in the Presence of Various Soybean Phospholipid Fractions 总被引:4,自引:3,他引:1
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Cecile Capdevila Serge Moukha Miklos Ghyczy Jacques Theilleux Brigitte Gelie Michel Delattre Georges Corrieu Marcel Asther 《Applied microbiology》1990,56(12):3811-3816
Stimulation of lignin peroxidase production by exogenous phospholipids depends on the composition of the phospholipid fraction prepared by using the Nattermann process. The fraction composed mainly of negatively charged phospholipids (NAT 89) was the most efficient source for exoprotein secretion by Phanerochaete chrysosporium INA-12. The results of biochemical marker assays and ultrastructural morphology determination by electron microscopy were correlated. Activities of succinate dehydrogenase, a mitochondrial marker, and cytochrome c oxidoreductase, an endoplasmic reticulum (ER) marker, were increased 1.3- and 2.2-fold, respectively, in the presence of NAT 89. Electron microscopy observations suggested that the amount of mitochondria and ER in culture containing phospholipids was increased at the optimum day of lignin peroxidase production. Therefore, phospholipids enhanced energetic metabolism of strain INA-12 and markedly modified fungus physiology. Since ER is involved in enzyme synthesis, we suggest that its increased amount in mycelium cultured with NAT 89 is directly associated with the higher production of lignin peroxidase. 相似文献
424.
Effects of Proteinase Inhibitor Ingestion on Survival,Learning Abilities and Digestive Proteinases of the Honeybee 总被引:2,自引:0,他引:2
Girard Cecile Picard-Nizou Anne-Lorraine Grallien Etienne Zaccomer Bruno Jouanin Lise Pham-Delegue Minh-Ha 《Transgenic research》1998,7(4):239-246
The impact on beneficial insects of proteinase inhibitors expressed in pest-resistant transgenic crops needs to be assessed before the release of these plants into the environment. Three proteinase inhibitors, suitable for incorporation into oilseed rape, were tested on worker bees: the chicken egg white cystatin, oryzacystatin I (OCI) and Bowman-Birk soyabean inhibitor (BBI). Ingestion of low doses of the inhibitors did not cause short-term mortality, and a conditioned proboscis extension assay showed that olfactory learning performances were unchanged when the inhibitors were added to the reward. Long-term ingestion of BBI or OCI did not disrupt total digestive proteolytic activity, but ingestion of BBI induced a new proteinase form, suggesting the existence of a mechanism of control of proteinase synthesis in the honeybee. 相似文献
425.
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427.
M. Jonathan Fray Paul V. Fish Gillian A. Allan Gerwyn Bish Nick Clarke Rachel Eccles Anthony C. Harrison Jean-Loic Le Net Stephen C. Phillips Nicola Regan Cecile Sobry Alan Stobie Florian Wakenhut Dominique Westbrook Simon L. Westbrook Gavin A. Whitlock 《Bioorganic & medicinal chemistry letters》2010,20(12):3788-3792
New N-(1,2-diphenylethyl)piperazines 6 are disclosed as dual serotonin and noradrenaline reuptake inhibitors (SNRI) which may have potential in treating stress urinary incontinence (SUI). In this Letter, we present new data for SNRI PF-526014 (4) including performance in a canine in vivo model of SUI, cardiovascular assessment, pharmacokinetics in dog and determination of the primary routes of metabolism in vitro. Starting from 4, detailed structure activity relationships established that potent dual SNRIs could be achieved by appropriate substitution of the phenyl rings (6: R; R1) combined with a preferred stereochemistry. From this set of compounds, piperazine (?)-6a was identified as a potent and selective dual SNRI with improved metabolic stability and reduced ion channel activity when compared to 4. Based on this profile, (?)-6a was selected for further evaluation in a preclinical model of SUI. 相似文献
428.
Keryer-Bibens C Barreau C Osborne HB 《Biology of the cell / under the auspices of the European Cell Biology Organization》2008,100(2):125-138
Many steps in the control of gene expression are dependent on RNA-binding proteins, most of which are bi-functional, in as much as they both bind to RNA and interact with other protein partners in a functional complex. A powerful approach to study the functional properties of these proteins in vivo, independently of their RNA-binding ability, is to attach or tether them to specifically engineered reporter mRNAs whose fate can be easily followed. Two tethering systems have been mainly used in eukaryotic cells, namely the MS2 coat protein system and the lambda N-B box system. In this review, we firstly describe several studies in which these tethering systems have been used and provide an overview of these applications. We next describe the major features of these two systems, and, finally, we highlight a number of points that should be considered when designing experiments using this approach. 相似文献
429.
Meagher C Tang Q Fife BT Bour-Jordan H Wu J Pardoux C Bi M Melli K Bluestone JA 《Journal of immunology (Baltimore, Md. : 1950)》2008,180(12):7793-7803
Autoimmune pancreatitis (AIP) is a heterogeneous autoimmune disease in humans characterized by a progressive lymphocytic and plasmacytic infiltrate in the exocrine pancreas. In this study, we report that regulatory T cell-deficient NOD.CD28KO mice spontaneously develop AIP that closely resembles the human disease. NOD mouse AIP was associated with severe periductal and parenchymal inflammation of the exocrine pancreas by CD4(+) T cells, CD8(+) T cells, and B cells. Spleen CD4(+) T cells were found to be both necessary and sufficient for the development of AIP. Autoantibodies and autoreactive T cells from affected mice recognized a approximately 50-kDa protein identified as pancreatic amylase. Importantly, administration of tolerogenic amylase-coupled fixed spleen cells significantly ameliorated disease severity, suggesting that this protein functions as a key autoantigen. The establishment and characterization of this spontaneous pancreatic amylase-specific AIP in regulatory T cell-deficient NOD.CD28KO mice provides an excellent model for the study of disease pathogenesis and development of new therapies for human autoimmune pancreatitis. 相似文献
430.
Ackerman ME Chalouni C Schmidt MM Raman VV Ritter G Old LJ Mellman I Wittrup KD 《Cancer immunology, immunotherapy : CII》2008,57(7):1017-1027
The A33 antigen is a cell surface glycoprotein of the small intestine and colonic epithelium with homology to tight junction-associated
proteins of the immunoglobulin superfamily, including CAR and JAM. Its restricted tissue localization and high level of expression
have led to its use as a target in colon cancer immunotherapy. Although the antigen is also present in normal intestine, radiolabeled
antibodies against A33 are selectively retained by tumors in the gut as well as in metastatic lesions for as long as 6 weeks.
Accordingly, we have studied the trafficking and kinetic properties of the antigen to determine its promise in two-step, pretargeted
therapies. The localization, mobility, and persistence of the antigen were investigated, and this work has demonstrated that
the antigen is both highly immobile and extremely persistent—retaining its surface localization for a turnover halflife of
greater than 2 days. In order to explain these unusual properties, we explored the possibility that A33 is a component of
the tight junction. The simple property of surface persistence, described here, may contribute to the prolonged retention
of the clinically administered antibodies, and their uncommon ability to penetrate solid tumors. 相似文献