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41.
The reaction of ribose with horseradish peroxidase in the presence of H2O2 is accompanied by light emission. The detection of horseradish peroxidase Compound II (FeO2+) indicates that the enzyme participates in a normal peroxidatic cycle. Hydrogen peroxide converts horseradish peroxidase into Compound I (FeO3+) which in turn is converted into Compound II by abstracting a hydrogen atom from ribose forming a ribosyl radical. In aerated solutions oxygen rapidly adds to the ribosyl radical. Based on the spectral characteristics and the enhancement of the chemiluminescence by chlorophyll-a, xanthene dyes, D2O and DABCO, it is suggested that the excited species, apparently triplet carbonyls and 1O2, are formed from the bimolecular decay of the peroxyl radicals via the Russell mechanism. 相似文献
42.
Volume-dependent regulation of ion transport and membrane phosphorylation in human and rat erythrocytes 总被引:2,自引:0,他引:2
Sergei N. Orlov Nikolai I. Pokudin Yuri V. Kotelevtsev Pavel V. Gulak 《The Journal of membrane biology》1989,107(2):105-117
Summary Osmotic swelling of human and rat erythrocytes does not induce regulatory volume decrease. Regulatory volume increase was observed in shrunken erythrocytes of rats only. This reaction was blocked by the inhibitors of Na+/H+ exchange. Cytoplasmic acidification in erythrocytes of both species increases the amiloride-inhibited component of22Na influx by five- to eight-fold. Both the osmotic and isosmotic shrinkage of rat erythrocytes results in the 10- to 30-fold increase of amiloride-inhibited22Na influx and a two-fold increase of furosemide-inhibited86Rb influx. We failed to indicate any significant changes of these ion transport systems in shrunken human erythrocytes. The shrinking of quin 2-loaded human and rat erythrocytes results in the two- to threefold increase of the rate of45Ca influx, which is completely blocked by amiloride. The dependence of volume-induced22Na influx in rat erythrocytes and45Ca influx in human erythrocytes on amiloride concentration does not differ. The rate of45Ca influx in resealed ghosts was reduced by one order of magnitude when intravesicular potassium and sodium were replaced by choline. It is assumed that the erythrocyte shrinkage increases the rate of a nonselective Ca
o
2+
(Na
i
+
, K
i
+
) exchange. Erythrocyte shrinking does not induce significant phosphorylation of membrane protein but increases the32P incorporation in diphosphoinositides. The effect of shrinkage on the32P labeling of phosphoinositides is diminished after addition of amiloride. It is assumed that volume-induced phosphoinositide response plays an essential role in the mechanism of the activation of transmembrane ion movements. 相似文献
43.
Most carcinogens, including polycyclic aromatic hydrocarbons (PAH), require metabolic activation to produce the ultimate electrophilic species that bind covalently with cellular macromolecules to trigger the cancer process. Metabolic activation of PAH can be understood in terms of two main pathways: one-electron oxidation to yield reactive intermediate radical cations and monooxygenation to produce bay-region diol epoxides. The reason we have postulated that one-electron oxidation plays an important role in the activation of PAH derives from certain common characteristics of the radical cation chemistry of the most potent carcinogenic PAH. Two main features common to these PAH are: 1) a relatively low ionization potential, which allows easy metabolic removal of one electron, and 2) charge localization in the PAH radical cation that renders this intermediate specifically and efficiently reactive toward nucleophiles. Equally important, cytochrome P-450 and mammalian peroxidases catalyze one-electron oxidation. This mechanism plays a role in the binding of PAH to DNA. Chemical, biochemical and biological evidence will be presented supporting the important role of one-electron oxidation in the activation of PAH leading to initiation of cancer. 相似文献
44.
How to Characterize a Biological Antioxidant 总被引:15,自引:0,他引:15
Barry Halliwell 《Free radical research》1990,9(1):1-32
An antioxidant is a substance that, when present at low concentrations compared to those of an oxidizable substrate, significantly delays or prevents oxidation of that substrate. Many substances have been suggested to act as antioxidants in vivo, but few have been proved to do so. The present review addresses the criteria necessary to evaluate a proposed antioxidant activity. Simple methods for assessing the possibility of physiologically-feasible scavenging of important biological oxidants (superoxide, hydrogen peroxide, hydroxyl radical, hypochlorous acid, haem-associated ferryl species, radicals derived from activated phagocytes, and peroxyl radicals, both lipid-soluble and water-soluble) are presented, and the appropriate control experiments are described. Methods that may be used to gain evidence that a compound actually does function as an antioxidant in vivo are discussed. A review of the pro-oxidant and anti-oxidant properties of ascorbic acid that have been reported in the literature leads to the conclusion that this compound acts as an antioxidant in vivo under most circumstances. 相似文献
45.
We used whole-cell patch-clamp recording techniques to investigate G protein-activated currents in cultured rat retinal pigment
epithelial (RPE) cells. Using 140 mm KCl intracellular and 130 mm NaCl extracellular solutions, rat RPE cells possessed both inward and outward K+ currents. Upon addition of the nonhydrolyzable guanine triphosphate analogue, guanosine-5′-O-(3-thiophosphate) (GTPγS, 0.1
mm), to the recording electrode, a nonspecific cation (NSC) current was elicited. The NSC current had a mean reversal potential
of +5.7 mV in 130 mm extracellular NaCl with Cs+-aspartate in the pipette, and was not affected by alterations in the extracellular Ca2+ or Cl− concentration. The GTPγS-activated current was found to be permeable to several monovalent cations (K+, Na+, choline, TRIS, and NMDG). Addition of fluoroaluminate, an activator of large molecular weight heterotrimeric GTP-binding
proteins (G proteins), to the intracellular recording solution activated the NSC current. The G protein involved was pertussis
toxin (PTX)-sensitive, since GTPγS failed to activate the NSC current in cells pretreated with PTX. Further investigation
of second messenger molecules suggested that activation of the NSC current was not affected by alterations in intracellular
Ca2+ or ATP. From these results, we conclude that a G protein-regulated NSC current is present in rat RPE cells. Activation of
the NSC current may sufficiently depolarize RPE cells to activate outward K+ currents. This would provide a mechanism by which these cells could rid themselves of accumulated K+.
Received: 25 January 1996/Revised: 24 April 1996 相似文献
46.
The prokaryotic endosymbionts that became plastids and mitochondria contained genes destined for one of three fates. Genes
required for free-living existence were lost. Most genes useful to the symbiosis were transferred to the nucleus of the host.
Some genes, a small minority, were retained within the organelle. Here we suggest that a selective advantage of movement of
genes to the nucleus is decreased mutation: plastids and mitochondria have high volume-specific rates of redox reactions,
producing oxygen free radicals that chemically modify DNA. These mutations lead to synthesis of modified electron carriers
that in turn generate more mutagenic free radicals—the “vicious circle” theory of aging. Transfer of genes to the nucleus
is also advantageous in facilitating sexual recombination and DNA repair. For genes encoding certain key components of photosynthesis
and respiration, direct control of gene expression by redox state of electron carriers may be required to minimize free radical
production, providing a selective advantage of organelle location which outweighs that of location in the nucleus. A previous
proposal for transfer of genes to the nucleus is an economy of resources in having a single genome and a single apparatus
for gene expression, but this argument fails if any organellar gene is retained. A previous proposal for the retention of
genes within organelles is that certain proteins are organelle-encoded because they cannot be imported, but there is now evidence
against this view. Decreased free radical mutagenesis and increased sexual recombination upon transfer to the nucleus together
with redox control of gene expression in organelles may now account for the slightly different gene distributions among nuclei,
plastids, and mitochondria found in major eukaryote taxa. This analysis suggests a novel reason for uniparental inheritance
of organelles and the evolution of anisogametic sex, and may also account for the occurrence of nitrogen fixation in symbionts
rather than in nitrogen-fixing organelles.
Correspondence to: J.F. Allen 相似文献
47.
ATP-Activated Nonselective Cation Current in NG108-15 Cells 总被引:5,自引:0,他引:5
Hiromi Kaiho Junko Kimura Isao Matsuoka Tadanori Kumasaka Hironori Nakanishi 《Journal of neurochemistry》1996,67(1):398-406
Abstract: ATP (1 mM) induced a biphasic increase in intracellular Ca2+ concentration ([Ca2+]i), i.e., an initial transient increase decayed to a level of sustained increase, in NG108-15 cells. The transient increase was inhibited by a phospholipase C inhibitor, 1-[6-[[17β-3-methoxyestra-1,3,5(10)-trien-17-yl]amino]hexyl]-1H-pyrrole-2,5-dione (U73122), whereas the sustained increase was abolished by removal of external Ca2+. We examined the mechanism of the ATP-elicited sustained [Ca2+]i increase using the fura-2 fluorescent method and the whole-cell patch clamp technique. ATP (1 mM) induced a membrane current with the reversal potential of 12.5 ± 0.8 mV (n = 10) in Tyrode external solution. The EC50 of ATP was ~0.75 mM. The permeability ratio of various cations carrying this current was Na+ (defined as 1) > Li+ (0.92 ± 0.01; n = 5) > K+ (0.89 ± 0.03; n = 6) > Rb+ (0.55 ± 0.02; n = 6) > Cs+ (0.51 ± 0.01; n = 5) > Ca2+ (0.22 ± 0.03; n = 3) > N-methyl-d -glucamine (0.13 ± 0.01; n = 5), suggesting that ATP activated a nonselective cation current. The ATP-induced current was larger at lower concentrations of external Mg2+. ATP analogues that induced the current were 2-methylthio-ATP (2MeSATP), benzoylbenzoic-ATP, adenosine 5′-thiotriphosphate (ATPγS), and adenosine 5′-O-(2-thiodiphosphate), but not adenosine, ADP, α,β-methylene-ATP (AMPCPP), β,γ-methylene-ATP (AMPPCP), or UTP. Concomitant with the current data, 2MeSATP and ATPγS, but not AMPCPP or AMPPCP, increased the sustained [Ca2+]i increase. We conclude that ATP activates a class of Ca2+-permeable nonselective cation channels via the P2z receptor in NG108-15 cells. 相似文献
48.
In many German forest soils low base saturation of CEC in deeper soil layers was reported and acidic deposition is seen as
the major cause of these findings. To test this hypothesis we sampled 5 New Zealand forest soils from pristine beech (Nothofagus fusca, N. menziesii, N. solandri) sites under climatic and geological conditions comparable to higher elevations in Germany. The soils developed from granite
and greywacke. Soil samples were analyzed for pH and the exchangeable cations were extracted with 1M NH4Cl. The base saturation of all soil profiles was very low, even in deeper layers and was thus similar to the patterns found
in many German forest soils. The pH was generally higher in the New Zealand soils as compared to Germany. The reason for the
depletion of base cations in deeper soil layers of New Zealand forest soils is most likely the leaching of base cations with
HCO3
- resulting from the dissociation of carbonic acid in connection with high amounts of seepage. Thus, under high rainfall conditions,
the low base saturation found in deeper layers of forest soils cannot exclusively be attributed to the effects of acidic depositions
and land use. ei]Section editor: R F Huettl 相似文献
49.
Caesium accumulation by microorganisms: uptake mechanisms,cation competition,compartmentalization and toxicity 总被引:4,自引:0,他引:4
Simon V. Avery 《Journal of industrial microbiology & biotechnology》1995,14(2):76-84
Summary The continued release of caesium radioisotopes into the environment has led to a resurgence of interest in microbe-Cs interactions. Caesium exists almost exclusively as the monovalent cation Cs+ in the natural environment. Although Cs+ is a weak Lewis acid that exhibits a low tendency to form complexes with ligands, its chemical similarity to the biologically essential alkali cation K+ facilitates high levels of metabolism-dependent intracellular accumulation. Microbial Cs+ (K+) uptake is generally mediated by monovalent cation transport systems located on the plasma membrane. These differe widely in specificity for alkali cations and consequently microorganisms display large differences in their ability to accumulate Cs+; Cs+ appears to have an equal or greater affinity than K+ for transport in certain microorganisms. Microbial Cs+ accumulation is markedly influenced by the presence of external cations, e.g. K+, Na+, NH4
+ and H+, and is generally accompanied by an approximate stoichiometric exchange for intracellular K+. However, stimulation of growth of K+-starved microbial cultures by Cs+ is limited and its has been proposed that it is not the presence of Cs+ in cells that is growth inhibitory but rather the resulting loss of K+. Increased microbial tolerance to Cs+ may result from sequestration of Cs+ in vacuoles or changes in the activity and/or specificity of transport systems mediating Cs+ uptake. The precise intracellular target(s) for Cs+-induced toxicity has yet to be clearly defined, although certain internal structures, e.g. ribosomes, become unstable in the presence of Cs+ and Cs+ is known to substitute poorly for K+ in the activation of many K+-requiring enzymes. 相似文献
50.
用不同自由基源处理的胆红素与鼠肝细胞相互作用,结果表明:胆红素自由基可引起鼠肝细胞脂质过氧化,使总谷胱甘肽及GSSG水平明显下降,细胞损伤后,乳酸脱氢酶外漏,上述结果与自由基浓度正相关,而与其种类无关,牛血清白蛋白有明显的抑制作用。差示光谱表明:胆红素可能与细胞色素P-450快速形成络合物。根据以上结果,重点讨论了胆红素自由基对肝细胞损伤的化学本质及其与胆结石形成的关系。 相似文献