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排序方式: 共有121条查询结果,搜索用时 78 毫秒
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Calvin J. Gordon Egor P. Tchesnokov Raymond F. Schinazi Matthias Gtte 《The Journal of biological chemistry》2021,297(1)
The RNA-dependent RNA polymerase of the severe acute respiratory syndrome coronavirus 2 is an important target in current drug development efforts for the treatment of coronavirus disease 2019. Molnupiravir is a broad-spectrum antiviral that is an orally bioavailable prodrug of the nucleoside analogue β-D-N4-hydroxycytidine (NHC). Molnupiravir or NHC can increase G to A and C to U transition mutations in replicating coronaviruses. These increases in mutation frequencies can be linked to increases in antiviral effects; however, biochemical data of molnupiravir-induced mutagenesis have not been reported. Here we studied the effects of the active compound NHC 5’-triphosphate (NHC-TP) against the purified severe acute respiratory syndrome coronavirus 2 RNA-dependent RNA polymerase complex. The efficiency of incorporation of natural nucleotides over the efficiency of incorporation of NHC-TP into model RNA substrates followed the order GTP (12,841) > ATP (424) > UTP (171) > CTP (30), indicating that NHC-TP competes predominantly with CTP for incorporation. No significant inhibition of RNA synthesis was noted as a result of the incorporated monophosphate in the RNA primer strand. When embedded in the template strand, NHC-monophosphate supported the formation of both NHC:G and NHC:A base pairs with similar efficiencies. The extension of the NHC:G product was modestly inhibited, but higher nucleotide concentrations could overcome this blockage. In contrast, the NHC:A base pair led to the observed G to A (G:NHC:A) or C to U (C:G:NHC:A:U) mutations. Together, these biochemical data support a mechanism of action of molnupiravir that is primarily based on RNA mutagenesis mediated via the template strand. 相似文献
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Myoglobin causes oxidative stress,increase of NO production and dysfunction of kidney's mitochondria
Egor Y. Plotnikov Anastasia A. Chupyrkina Irina B. Pevzner Nickolaj K. Isaev Dmitry B. Zorov 《生物化学与生物物理学报:疾病的分子基础》2009,1792(8):796-803
Rhabdomyolysis or crush syndrome is a pathology caused by muscle injury resulting in acute renal failure. The latest data give strong evidence that this syndrome caused by accumulation of muscle breakdown products in the blood stream is associated with oxidative stress with primary role of mitochondria. In order to evaluate the significance of oxidative stress under rhabdomyolysis we explored the direct effect of myoglobin on renal tubules and isolated kidney mitochondria while measuring mitochondrial respiratory control, production of reactive oxygen and nitrogen species and lipid peroxidation. In parallel, we evaluated mitochondrial damage under myoglobinurea in vivo. An increase of lipid peroxidation products in kidney mitochondria and release of cytochrome c was detected on the first day of myoglobinuria. In mitochondria incubated with myoglobin we detected respiratory control drop, uncoupling of oxidative phosphorylation, an increase of lipid peroxidation products and stimulated NO synthesis. Mitochondrial pore inhibitor, cyclosporine A, mitochondria-targeted antioxidant (SkQ1) and deferoxamine (Fe-chelator and ferryl-myoglobin reducer) abrogated these events. Similar effects (oxidative stress and mitochondrial dysfunction) were revealed when myoglobin was added to isolated renal tubules. Thus, rhabdomyolysis can be considered as oxidative stress-mediated pathology with mitochondria to be the primary target and possibly the source of reactive oxygen and nitrogen species. We speculate that rhabdomyolysis-induced kidney damage involves direct interaction of myoglobin with mitochondria possibly resulting in iron ions release from myoglobin's heme, which promotes the peroxidation of mitochondrial membranes. Usage of mitochondrial permeability transition blockers, Fe-chelators or mitochondria-targeted antioxidants, may bring salvage from this pathology. 相似文献
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Katkov II 《Cryobiology》2000,40(1):64-83
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Nina A. Osipova Kate A. Filimonenko Anna V. Talovskaya Egor G. Yazikov 《人类与生态风险评估》2015,21(6):1664-1685
Human health risks due to exposure of heavy metals in the atmospheric air of Tomsk, Russia, were studied. The concentrations of 22 metals in the ambient air were calculated on the basis of the ICP–MS experimental determination of their contents in the insoluble fraction of snow cover. Non-carcinogenic hazards were estimated for the areas of power plant (“Zone PP”), brickworks location (“Zone BF”), zone influenced by concrete product plants (“Zone CP”), and petrochemical plant suburbs (“Zone PCP”). Manganese, Al, Cu, and Ba make the largest contribution to the integral non-cancer hazard caused by chronic inhalation intake in all areas. Zinc is added to the above listed elements in the “Zone PP” and V, Co, Cr, and Ni in the “Zone BF” are also added. Densely populated residential areas “Zone BF” and “Zone PP” were characterized by the higher levels of diseases risks associated with human inhalation intake of metals in comparison with other areas. The dust load should be primarily decreased in the zones subjected to harmful effects of brick factories and other construction materials. As to the power station, the portion of natural gas in consumption should increase from year to year for decreasing heavy metal emissions from burning of coal. 相似文献
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Matthias Fellner Eleni Siakkou Abayomi S. Faponle Egor P. Tchesnokov Sam P. de Visser Sigurd M. Wilbanks Guy N. L. Jameson 《Journal of biological inorganic chemistry》2016,21(4):501-510
Cysteine dioxygenase is a non-heme mononuclear iron enzyme with unique structural features, namely an intramolecular thioether cross-link between cysteine 93 and tyrosine 157, and a disulfide bond between substrate l-cysteine and cysteine 164 in the entrance channel to the active site. We investigated how these posttranslational modifications affect catalysis through a kinetic, crystallographic and computational study. The enzyme kinetics of a C164S variant are identical to WT, indicating that disulfide formation at C164 does not significantly impair access to the active site at physiological pH. However, at high pH, the cysteine–tyrosine cross-link formation is enhanced in C164S. This supports the view that disulfide formation at position 164 can limit access to the active site. The C164S variant yielded crystal structures of unusual clarity in both resting state and with cysteine bound. Both show that the iron in the cysteine-bound complex is a mixture of penta- and hexa-coordinate with a water molecule taking up the final site (60 % occupancy), which is where dioxygen is believed to coordinate during turnover. The serine also displays stronger hydrogen bond interactions to a water bound to the amine of the substrate cysteine. However, the interactions between cysteine and iron appear unchanged. DFT calculations support this and show that WT and C164S have similar binding energies for the water molecule in the final site. This variant therefore provides evidence that WT also exists in an equilibrium between penta- and hexa-coordinate forms and the presence of the sixth ligand does not strongly affect dioxygen binding. 相似文献