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61.
In vitro influence of zinc and magnesium on the deformability of red blood cells artificially hardened by heating 总被引:2,自引:0,他引:2
Collette Dupuy-Fons Jean-Frédéric Brun Claire Mallart Joseph Carvajal Michèle Fussellier Lucette Bardet André Orsetti 《Biological trace element research》1995,47(1-3):247-255
Trace elements have been shown to improve red blood cell (RBC) deformability: zinc in sickle cell disease and magnesium in
an in vitro model of chemically rigidified erythrocytes. In this study, we investigated the effect and the influence of incubation
time of zinc or magnesium on an in vitro model of rigidified RBCs by heating. Erythrocyte rigidity was determined by viscosimetry
at high shear rate by a falling ball viscosimeter MT 90.
In the first part of the study, six normal volunteers participated. Viscosimetry was performed on native blood before and
after heating the sample for 10 min at 50°C. Therefore, increasing concentrations of zinc gluconate (final concentration:
0.5–4 g/L) or isotonic NaCl as control medium were added to the sample. Heating induced a twofold increase in all indices
of RBC rigidity (p<0.05). At all these concentrations of zinc, a highly significant, dose-related fluidifying effect was observed (40–70%):
this effect was immediately obtained and did not change over 60 min. Even at the highest concentration, recovery was not complete.
In the second part of the study, we studied magnesium’s effects on blood. In a first protocol, whole blood was rigidified
by heating at 56°C for 10 min, and the correcting effect of 5 min of incubation at 37°C of RBCs in 150 mmol/L NaCl, MgSO4, magnesium acetate, and magnesium gluconate was investigated. In a second protocol, the same incubation with NaCl and magnesium
salts was made on blood that had not been previously heated. In a third protocol, the correcting effect of magnesium gluconate
on heated red blood cells was tested at four concentrations (75, 150, 225, and 300 mmol/L) over 1 h, for evaluating the effects
of both concentration and time. Erythrocyte rigidity by heating is corrected by the three salts employed in protocol 1 (compared
to sodium). In protocol 2, the deformability of normal (nonheated) red cells is not modified by magnesium. In protocol 3,
no marked modification over 1 h is observed. The correcting effect is not complete for 75 mmol/L Mg, but remains the same
at the three other concentrations.
This study shows that zinc and magnesium at supraphysiological concentration are able to reverse RBC’s rigidification induced
by heating, but that magnesium does not modify the flexibility of normal RBCs. This article suggests that zinc and magnesium
may be studied in vivo as potential pharmacologic tools for improving hemorheologic disturbances. 相似文献
62.
The present study was conducted to investigate the effect of zinc deficiency on fatty acid desaturation in rats fed two different
types of dietary fat, a mixture of coconut oil and safflower oil (7∶1, w/w, “coconut oil diet”) or linseed oil (“linseed oil
diet”). In order to ensure an adequate food intake, all rats were force-fed by gastric tube. Zinc deficiency caused statistical
significant reducion of Δ9-desaturase activity in liver microsomes of rats fed coconut oil diet and tendencial reduction (p<0.15) in rats fed linseed oil diet compared with control rats fed diets with the same type of fat. In agreement with this
effect, zinc deficiency in the rats fed both types of dietary fat increased the ratio between total saturated and total monounsaturated
fatty in liver phospholipids and liver microsomes. Zinc deficient rats on the coconut oil diet had unchanged Δ6-desaturase
activity with linoleic acid as substrate and lowered activity with α-linolenic acid as substrate. In contrast, zinc deficient
rats on the linseed oil diet had increased Δ6-desaturase activity with linoleic acid as substrate and unchanged activity with
α-linolenic acid. Because linoleic acid is the main substrate for Δ6-desaturase in the rats fed coconut oil diet, and α-linolenic
acid is the main substrate in the rats fed linseed oil diet, it is concluded that in vivo Δ6-desaturation was not changed
by zinc deficiency in the rats fed both types of dietary fat. Activity of Δ5-desaturase was also not changed by zinc deficiency
in the rats fed both dietary fats. Levels of fatty acids in liver phospholipids and microsomes derived by Δ4-, Δ5-, and Δ6-desaturation
were not consistently changed by zinc deficiency in the rats fed both types of dietary fat. Thus, the enzyme studies and also
fatty acid composition data of liver phospholipids and microsomes indicate that zinc deficiency does not considerably disturb
desaturation of linoleic and α-linolenic acid. Therefore, it is suggested that similarities between deficiencies of zinc and
essential fatty acids described in literature are not due to disturbed desaturation of linoleic acid in zinc deficiency. The
present study also indicates that zinc deficiency enhances incorporation of eicosapentaenoic acid into phosphatidylcholine
of rats fed diets with large amounts ofn-3 polyunsaturated fatty acids. 相似文献
63.
María-Carmen Rodríguez-Yoldi José-Emilio Mesonero Maríaa-Jesús Rodríguez-Yoldi 《Biological trace element research》1995,50(1):1-11
Zinc is an essential trace element necessary to life. This metal may exert some of its physiological effects by acting directly
on cellular membranes, either by altering permeability or by modulating the activity of membrane-bound enzymes. On the other
hand, calcium is an essential element in a wide variety of cellular activities. The aim of the present work was to study a
possible interaction between zinc and calcium on intestinal transport ofd-galactose in jejunum of rabbit in vitro. In media with Ca2+, when ZnCl2 was present at 0.5 or 1 mM, zinc was found to reduce thed-galactose absorption significantly. In Ca2+-free media, where CaCl2 was omitted and replaced isotonically with choline chloride, the sugar transport was not modified by zinc. Verapamil at 10−6
M (blocking mainly Ca2+ transport) did not modify the inhibitory effect of zinc ond-galactose transport. When 10−6
M of A 23187 (Ca2+-specific ionophore) was added with/without Ca2+ to the media, ZnCl2 produced no change in sugar transport. These results could suggest a possible interaction of calcium and zinc for the same
chemical groups of membrane, which could affect the intestinal absorption of sugars. 相似文献
64.
65.
稀有鮈鲫──一种新的鱼类毒性试验材料 总被引:7,自引:0,他引:7
本文研究了稀有鲫(Gobiocyprisrarus)作为毒性试验材料的可行性。采用换水式试验,在硬度为200mg/L(以CaCO3计)、pH7.8±0.2、温度24-25℃条件下研究了铬、铜、锌和五氯酚(PCP)对稀有鲫的急性毒性。重铬酸钾对2日龄稀有鲫的24h和96h和LC50控制范围分别263.6-334.7和1153-178.5mg/L(n=8)。铬、铜、锌和五氯酚对2日龄稀有鲫的急性毒性值(96hLC50)范围,从铜的52.2μg/L到铬的52000μg/L,毒性大小的顺序是铜>五氯酚>锌>铬。研究结果表明,稀有鲫有可能发展成为一种较为理想的毒性试验材料。 相似文献
66.
Zfy1 is a mouse Y chromosomal gene encoding a zincfinger protein which is thought to have some function during spermatogenesis. Here we show that, when introduced into tissue culture cells, Zfy1 is targeted to the nucleus. Two independent signals are present within the protein for nuclear localization. This nuclear Zfy1 protein is able to bind strongly to DNA-cellulose and, using site-selection assays, we have identified specific Zfy1 DNA binding sites. Taken together these results suggest that Zfy1 is a nuclear-located sequence-specific DNA binding protein which functions during spermatogenesis. 相似文献
67.
Fabrice Cornille Loïc Martin Christine Lenoir Didier Cussac Bernard P. Roques Marie-Claude Fournié-Zaluski 《Letters in Peptide Science》1997,4(4-6):207-212
The light chain of tetanus neurotoxin (TeNT L chain)has been shown to be endowed with zinc endopeptidaseactivity, selectively directed towards theGln76–Phe77 bond of synaptobrevin, avesicle-associated membrane protein criticallyinvolved in neuroexocytosis. In previous reports,truncations at the NH2- and COOH-terminus ofsynaptobrevin have shown that the sequence 39–88 ofsynaptobrevin is the minimum substrate of TeNT,suggesting either the requirement of a well-definedthree-dimensional structure of synaptobrevin or a rolein the mechanism of substrate hydrolysis for residuesdistal from the cleavage site. In this study, theaddition of NH2- and COOH-terminal peptides ofsynaptobrevin, S 27–55 (S1) and S 82–93(S2), to the synaptobrevin fragment S 56–81allowed the cleavage of this latter peptide by TeNT tooccur. This appears to result from an activationprocess mediated by the simultaneous binding ofS1 and S2 with complementary sites presenton TeNT as shown by surface plasmon resonanceexperiments. All these results favor anexosite-controlled hydrolysis of synaptobrevin by TeNTprobably involving a conformational change of thetoxin. This could account for the high degree ofsubstrate specificity of TeNT and, probably, botulinumneurotoxins. 相似文献
68.
Marc Mathieu Christian Lehmann Alain Razaname Gabriele Tuchscherer 《Letters in Peptide Science》1997,4(2):95-100
The assembly of helical and -sheet peptide blocks containing reactive chain ends results inhighly branched chain architectures (locked-in folds) mimicking native tertiary structures.This molecular kit strategy allows to bypass the protein folding problem in protein de novodesign and gives access to protein mimetics of high thermodynamic stability. The validity ofthis concept is exemplified for the design and synthesis of locked-in folds mimicking the zincfinger and MHC folding motifs. 相似文献
69.
Gerhard Schenk Roy Layfield Judith M. Candy Ronald G. Duggleby Peter F. Nixon 《Journal of molecular evolution》1997,44(5):552-572
Members of the transketolase group of thiamine-diphosphate-dependent enzymes from 17 different organisms including mammals,
yeast, bacteria, and plants have been used for phylogenetic reconstruction. Alignment of the amino acid and DNA sequences
for 21 transketolase enzymes and one putative transketolase reveals a number of highly conserved regions and invariant residues
that are of predicted importance for enzyme activity, based on the crystal structure of yeast transketolase. One particular
sequence of 36 residues has some similarities to the nucleotide-binding motif and we designate it as the transketolase motif.
We report further evidence that the recP protein from Streptococcus pneumoniae might be a transketolase and we list a number of invariant residues which might be involved in substrate binding. Phylogenies
derived from the nucleotide and the amino acid sequences by various methods show a conventional clustering for mammalian,
plant, and gram-negative bacterial transketolases. The branching order of the gram-positive bacteria could not be inferred
reliably. The formaldehyde transketolase (sometimes known as dihydroxyacetone synthase) of the yeast Hansenula polymorpha appears to be orthologous to the mammalian enzymes but paralogous to the other yeast transketolases. The occurrence of more
than one transketolase gene in some organisms is consistent with several gene duplications. The high degree of similarity
in functionally important residues and the fact that the same kinetic mechanism is applicable to all characterized transketolase
enzymes is consistent with the proposition that they are all derived from one common ancestral gene. Transketolase appears
to be an ancient enzyme that has evolved slowly and might serve as a model for a molecular clock, at least within the mammalian
clade.
Received: 13 September 1995 / Accepted: 14 November 1996 相似文献
70.
W. H. H. Krueger G. E. Gonye D. L. Madison K. E. Murray M. Kumar N. Spoerel S. E. Pfeiffer 《Journal of neurochemistry》1997,69(4):1343-1355
Abstract: Although the myelin membrane contains only a small set of major proteins, more sensitive assays indicate the presence of a plethora of uncharacterized proteins. We have used an antibody perturbation approach to reversibly block the differentiation of prooligodendroblasts into myelinating cells, and, in combination with a differential screening procedure, identified novel mRNAs that are activated during this period. One cDNA, TPO1, recognizes a 5.5-kb mRNA that is strongly up-regulated in oligodendrocytes after release of the differentiation block and that is expressed at high levels in brain tissue during active myelination. This cDNA represents at least two mRNAs differing from each other in their 5'-termini. The TPO1 cDNA contains an open reading frame of 1,380 bp, encoding a protein of 51.8 kDa with a predicted pl of 9.1 that contains two regions homologous to nonclassic zinc finger motifs. Subcellular localization studies suggest the enriched presence of TPO1 in spherical structures along the major cytoplasmic processes of oligodendrocytes. TPO1, along with homologues expressed in testis, placenta, and PC12 cells, form a novel family of proteins with multiple hydrophobic domains possibly serving as membrane spanning regions. We postulate that in oligodendrocytes, TPO1 encodes a protein factor involved in myelin biogenesis. 相似文献