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71.
2048 subjects in North Thailand were examined for AB0 blood groups. A control group representative of the population of the provinces of Chiengmai and Lampun was formed of 382 examinees and 3403 blood donors.The distribution of AB0 groups in this population is similar to that of Central Thailand. Some ethnic groups show significant deviations: The Miao tribe, originating in South China, has a much higher frequency of B. There was a significant reduction in gene A and B in the younger generation of this tribe. The Thai Yong, people who migrated to North Thailand from Yunnan in the 19th century, show an AB0 distribution similar to Chinese in Yunnan. They differ significantly from the Northern Thai. There is also a difference in the distribution of -thalassaemia and hemoglobin E between these two groups.Male leprosy patients showed an excess of group A which was not present in female patients. The percentage of severely ill patients was much higher in the males. Differentiation into lepromatous and tuberculid forms is not available. Among 108 people who had suffered from smallpox approximately 20 years ago there was an excess of groups 0 an B in comparison to the control group.
Mit Unterstützung durch die Deutsche Forschungsgemeinschaft. 相似文献
Mit Unterstützung durch die Deutsche Forschungsgemeinschaft. 相似文献
72.
Adrian S. Dobs Christiane Broussolle M. Daniel Lane 《In vitro cellular & developmental biology. Plant》1989,25(2):112-114
Summary The insulin-producing cell line RINm5F, has been used in short-term experiments to evaluate insulin secretion. We sought to
maintain the responsiveness of these cells to stimuli for up to 2 days. We examined the course of new insulin synthesis over
this period by measuring at intervals immunoreactive insulin (IRI) in two parts: IRI in the medium (M) and IRI extracted from
the cells (C). Control cells were incubated in RPMI 1640/2.8 mM glucose/10% fetal bovine serum/200 μg/ml bacitracin (to prevent
insulin degradation). The addition of dibutyryl cAMP 10 mM to the experimental dishes significantly increased total (M+C)
IRI at 48 hr to 37% above the insulin content of the control dishes (p<0.01). Theophylline 10 mM increased total (M+C) IRI
by 24% over control (p<0.05) after 24 hrs. Glucose, glyceraldehyde, leucine, arginine, glucagon and tolbutamide, other stimulants
of insulin production, had no effect. Under the experimental conditions reported here, including the use of bacitracin, IRI
synthesis can be studied for up to 48 hr.
Portions of this study have been published in abstract form for the 47th Annual Meeting of the American Diabetes Association,
Indianapolis, Indiana, 1987.
Supported in part by the American Diabetic Association, Maryland Affiliate. 相似文献
73.
Ch. O. Coleman 《Polar Biology》1989,10(1):43-48
Summary Species of the amphipod genus Paraceradocus found near the Antarctic Peninsula were observed in aquaria. The animals live under stones in burrows in sediment which they excavate with their gnathopods. During burrowing the animal regularly turns backwards in a somersault-like movement. Paraceradocus feeds on detritus, which is manipulated by the gnathopods and the antennes. The gnathopods are also used for grooming. A dense brush of setae at the medial surface of the carpi of the gnathopods I is used to clean off fine particles from the antennes. These particles are transferred to the maxillipeds and are ingested. The rear appendages are mainly cleaned by the gnathopods II. Young animals sitting between the gnathopods of the adult participate in feeding. 相似文献
74.
75.
Christiane Gulat-Marnay rée Lafitte Jean-Michel Arrang Jean-Charles Schwartz 《Journal of neurochemistry》1990,55(1):47-53
The opioid modulation of histamine release was studied in rat brain slices labeled with L-[3H]histidine. The K(+)-induced [3H]histamine release from cortical slices was progressively inhibited by the preferential kappa-agonists ketocyclazocine, dynorphin A (1-13), Cambridge 20, spiradoline, U50,488H, and U69,593 in increasing concentrations. In contrast, the mu-agonists morphine, morphiceptin, and Tyr-D-Ala-Gly-(NMe)Phe-Gly-ol (DAGO) were ineffective as were the preferential delta-agonists [D-Ala2,D-Leu5]enkephalin (DA-DLE) and [D-Pen2,D-Pen5]enkephalin (DPDPE). Nor-binaltorphimine (nor-BNI) and MR 2266, two preferential kappa-antagonists, reversed the inhibitory effect of the various kappa-agonists more potently than did naloxone, with mean Ki values of 4 nM and 25 nM, respectively. The effects of ketocyclazocine and naloxone also were seen in slices of rat striatum, another brain region known to contain histaminergic nerve endings. We conclude that kappa-opioid receptors, presumably located on histaminergic axons, control histamine release in the brain. However, nor-BNI and naloxone failed, when added alone, to enhance significantly [3H]histamine release from cerebral cortex or striatum, and bestatin, an aminopeptidase inhibitor, failed to decrease K(+)-evoked [3H]histamine release. These two findings suggest that under basal conditions these kappa-opioid receptors are not tonically activated by endogenous dynorphin peptides. The inhibition of cerebral histamine release by kappa-agonists may mediate the sedative actions of these agents in vivo. 相似文献
76.
The governing factors for soil nitrogen dynamics were identified with a simulation model. In addition, the model was used to interpret measurements from a plot fertilisation experiment in southwest Sweden.Simulated moisture and temperature conditions were the driving variables for the simulation of soil nitrogen dynamics and leaching during a 6-year period. The results of the simulation were compared with monthly observations on two plots with grain crops, one with liquid manure and commercial fertilisers applied and one with commercial fertilisers only.Simulated temporal variations of the nitrate and ammonium storages generally agreed with observations. The dominant role of the crops as a determinant of soil nitrogen conditions was demonstrated. A higher leaching loss from the plot with application of commerical fertilisers only occurred both in simulations and measurements compared to the plot with application of both commercial fertilisers and manure. The main reason was the higher N-application in the former treatment.The effect of water flows in macropores was interpreted as a delay of simulated leaching compared to observed leaching on some occasions in summer and early autumn. No direct effect of the macropores on the yearly rates of leaching could be seen. 相似文献
77.
Fertilizers labelled with 32P were used to measure amounts of phosphorus, Ps and PF, taken up by Lolium perenne from available soil P and from P fertilizer respectively, when applied at a rate of 66 mg P·(kg soil–1) in greenhouse experiments. The quantity Ps of phosphorus taken up from soil in the presence of P fertilizer was compared to the quantity Po taken up from soil without P fertilizer. The quantity (Ps–Po) is positive for low Po values, i.e. in soils poor in available phosphorus, but is negative for high Po values indicating that an input of P fertilizer can induce a decrease in the utilization of available soil phosphorus. Moreover, for a given soil, the quantity (Ps–Po) depends on the chemical form of the fertilizer. The standard method of evaluation of P fertilizer efficiency is based on the assumption that Ps=Po, but Ps can differ from Po. This result can explain the contradictory data published from field experiments about the efficiency of the various P fertilizers. 相似文献
78.
Christiane Gulat-Marnay rée Lafitte Jean-Michel Arrang Jean-Charles Schwartz 《Journal of neurochemistry》1989,52(1):248-254
The cholinergic modulation of histamine release and synthesis was studied in rat brain slices or synaptosomes labeled with L-[3H]histidine. Carbachol in increasing concentrations progressively reduced the K+-induced [3H]histamine release from cortical slices. Pirenzepine, a preferential M1-receptor antagonist, reversed the carbachol effect in an apparently competitive manner and with Ki values of 1-6 X 10(-8) M. 11-[(2-[(Diethylamino)methyl]-1-piperidinyl)acetyl]-5,11-dihydro-6H- pyrido[2,3-b][1,4]benzodiazepine-6-one (AF-DX 116), considered a preferential M2-receptor antagonist, reversed the carbachol effect with a mean Ki of approximately 2 X 10(-7) M. Oxotremorine behaved as a partial agonist in the modulation of histamine release. Neostigmine, an acetylcholinesterase inhibitor, inhibited the K+-induced release of [3H]histamine from cortical slices, and the effect was largely reversed by pirenzepine, an observation suggesting a modulation by endogenous acetylcholine. The effects of carbachol and pirenzepine were observed with slices of other brain regions known to contain histaminergic nerve terminals or perikarya, as well as with cortical synaptosomes. The two drugs also modified, in opposite directions, [3H]histamine formation in depolarized cortical slices. In vivo oxotremorine inhibited [3H]histamine formation in cerebral cortex, and this effect was reversed by scopolamine. When administered alone, scopolamine failed to enhance significantly the 3H- labeled amine formation, a finding suggesting that muscarinic receptors are not activated by endogenous acetylcholine released under basal conditions. It is concluded that muscarinic heteroreceptors, directly located on histaminergic nerve terminals, control release and synthesis of histamine in the brain. These receptors apparently belong to the broad M1-receptor category and may correspond to a receptor subclass displaying a rather high affinity for AF-DX 116. 相似文献
79.
Resistance to arsenic salts in aPseudomonas aeruginosa clinical isolate was shown to be determined by a 100 kb transferable plasmid. The resistance pattern included arsenate, arsenite, and antimonate ions. Arsenate and arsenite resistances were inducible by previous exposure of cultures to subinhibitory amounts of either of the two ions. Phosphate ions protectedP. aeruginosa cells from the toxic effects of arsenate but did not alter arsenite toxicity. 相似文献
80.
Christiane Sommer Barbara Thonke Marianne Popp 《Plant biology (Stuttgart, Germany)》1990,103(3):270-273
Pinitol (1d -3-O-methyl-chiro-inositol) and 1d -1-O-methyl-muco-inositol, two cyclitols wide-spread in the plant kingdom, were isolated from plant sources in order to test their compatibility with malate dehydrogenase activity. Both compounds had no inhibitory effect on malate dehydrogenase from Rhizophora mangle in a range of 100 to 1000 mol . m?3. Their influence on malate dehydrogenase activity from different plant sources (Rh. mangle L., Mesembryanthemum crystallinum L., Cicer arietinum L. and Spinacia oleracea L.) was also small and similar to that observed for a number of well established compatible solutes (e.g. proline, glycine betaine). A possible role of cyclitols as cryoprotectants or radical scavengers is discussed. 相似文献