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91.
Destro T Prasad D Martignago D Bernet IL Trentin AR Renu IK Ferretti M Masi A 《Journal of experimental botany》2011,62(2):805-814
γ-Glutamyl transferases (GGT; EC 2.3.2.2) are glutathione-degrading enzymes that are represented in Arabidopsis thaliana by a small gene family of four members. Two isoforms, GGT1 and GGT2, are apoplastic, sharing broad similarities in their amino acid sequences, but they are differently expressed in the tissues: GGT1 is expressed in roots, leaves, and siliques, while GGT2 was thought to be expressed only in siliques. It is demonstrated here that GGT2 is also expressed in wild-type roots, albeit in very small amounts. GGT2 expression is enhanced in ggt1 knockout mutants, suggesting a compensatory effect to restore GGT activity in the root apoplast. Supplementation with 100 μM glutathione (GSH) resulted in the up-regulation of GGT2 gene expression in wild-type and ggt1 knockout roots, and of GGT1 gene expression in wild-type roots. Glutathione recovery was hampered by the GGT inhibitor serine/borate, suggesting a major role for apoplastic GGTs in this process. These findings can explain the ability of ggt1 knockout mutants to retrieve exogenously added glutathione from the growth medium. 相似文献
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93.
Neurotransmitter stimulation of plasma membrane receptors stimulates salivary gland fluid secretion via a complex process that is determined by coordinated temporal and spatial regulation of several Ca2+ signaling processes as well as ion flux systems. Studies over the past four decades have demonstrated that Ca2+ is a critical factor in the control of salivary gland function. Importantly, critical components of this process have now been identified, including plasma membrane receptors, calcium channels, and regulatory proteins. The key event in activation of fluid secretion is an increase in intracellular [Ca2+] ([Ca2+]i) triggered by IP3-induced release of Ca2+ from ER via the IP3R. This increase regulates the ion fluxes required to drive vectorial fluid secretion. IP3Rs determine the site of initiation and the pattern of [Ca2+]i signal in the cell. However, Ca2+ entry into the cell is required to sustain the elevation of [Ca2+]i and fluid secretion. This Ca2+ influx pathway, store-operated calcium influx pathway (SOCE), has been studied in great detail and the regulatory mechanisms as well as key molecular components have now been identified. Orai1, TRPC1, and STIM1 are critical components of SOCE and among these, Ca2+ entry via TRPC1 is a major determinant of fluid secretion. The receptor-evoked Ca2+ signal in salivary gland acinar cells is unique in that it starts at the apical pole and then rapidly increases across the cell. The basis for the polarized Ca2+ signal can be ascribed to the polarized arrangement of the Ca2+ channels, transporters, and signaling proteins. Distinct localization of these proteins in the cell suggests compartmentalization of Ca2+ signals during regulation of fluid secretion. This chapter will discuss new concepts and findings regarding the polarization and control of Ca2+ signals in the regulation of fluid secretion. 相似文献
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95.
Gunjan Tyagi Shrikant Pradhan Tapasya Srivastava Ranjana Mehrotra 《Biochimica et Biophysica Acta (BBA)/General Subjects》2014
Background
Allicin has received much attention due to its anti-proliferative activity and not-well elucidated underlying mechanism of action. This work focuses towards determining the cellular toxicity of allicin and understanding its interaction with nucleic acid at molecular level.Methods
MTT assay was used to assess the cell viability of A549 lung cancer cells against allicin. Fourier transform infrared (FTIR) and UV-visible spectroscopy were used to study the binding parameters of nucleic acid-allicin interaction.Results
Allicin inhibits the proliferation of cancer cells in a concentration dependent manner. FTIR spectroscopy exhibited that allicin binds preferentially to minor groove of DNA via thymine base. Analysis of tRNA allicin complex has also revealed that allicin binds primarily through nitrogenous bases. Some amount of external binding with phosphate backbone was also observed for both DNA and RNA. UV visible spectra of both DNA allicin and RNA allicin complexes showed hypochromic shift with an estimated binding constant of 1.2 × 104 M- 1 for DNA and 1.06 × 103 M− 1for RNA binding. No major transition from the B-form of DNA and A-form of RNA is observed after their interaction with allicin.Conclusions
The results demonstrated that allicin treatment inhibited the proliferation of A549 cells in a dose-dependent manner. Biophysical outcomes are suggestive of base binding and helix contraction of nucleic acid structure upon binding with allicin.General significance
The results describe cytotoxic potential of allicin and its binding properties with cellular nucleic acid, which could be helpful in deciphering the complete mechanism of cell death exerted by allicin. 相似文献96.
97.
Parul Mehrotra Shilpa V. Jamwal Najmuddin Saquib Neeraj Sinha Zaved Siddiqui Venkatasamy Manivel Samrat Chatterjee Kanury V. S. Rao 《PLoS pathogens》2014,10(7)
The success of Mycobacterium tuberculosis as a pathogen derives from its facile adaptation to the intracellular milieu of human macrophages. To explore this process, we asked whether adaptation also required interference with the metabolic machinery of the host cell. Temporal profiling of the metabolic flux, in cells infected with differently virulent mycobacterial strains, confirmed that this was indeed the case. Subsequent analysis identified the core subset of host reactions that were targeted. It also elucidated that the goal of regulation was to integrate pathways facilitating macrophage survival, with those promoting mycobacterial sustenance. Intriguingly, this synthesis then provided an axis where both host- and pathogen-derived factors converged to define determinants of pathogenicity. Consequently, whereas the requirement for macrophage survival sensitized TB susceptibility to the glycemic status of the individual, mediation by pathogen ensured that the virulence properties of the infecting strain also contributed towards the resulting pathology. 相似文献
98.
In this paper, an autonomic performance management approach is introduced that can be applied to a general class of web services deployed in large scale distributed environment. The proposed approach utilizes traditional large scale control-based algorithms by using interaction balance approach in web service environment for managing the response time and the system level power consumption. This approach is developed in a generic fashion that makes it suitable for web service deployments, where web service performance can be adjusted by using a finite set of control inputs. This approach maintains the service level agreements, maximizes the revenue, and minimizes the infrastructure operating cost. Additionally, the proposed approach is fault-tolerant with respect to the failures of the computing nodes inside the distributed deployment. Moreover, the computational overhead of the proposed approach can also be managed by using appropriate value of configuration parameters during its deployment. 相似文献
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100.
Bernadette Thomas Maurits van Pelt Rajnish Mehrotra Cassianne Robinson-Cohen James LoGerfo 《PloS one》2014,9(1)