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991.
Hydroxymethylglutaryl--CoA reductase inhibitor inhibits induction of nitric oxide synthase in 3T3--L1 preadipocytes 总被引:1,自引:0,他引:1
Preadipocytes are considered to play a role in adipose tissue inflammation in obesity. The purpose of this study was to determine whether hydroxymethylglutaryl-CoA reductase inhibitor (statin) modulates the nitric oxide (NO) production via inducible NO synthase (iNOS) in preadipocytes. Undifferentiated 3T3-L1 cells, a model of preadipocytes, significantly produced NO by the treatment with the combination of lipopolysaccharide (L), tumor necrosis factor-alpha (T) and interferon-gamma (I). Pre-incubation with simvastatin, a lipophilic statin, or pravastatin, a hydrophilic one, dose-dependently inhibited the NO production in the LTI-treated cells. The effect of simvastatin was offset by mevalonate or geranylgeranyl pyrophosphate (GGPP) but not by squalene. The mRNA level for iNOS paralleled the NO production. The nuclear factor-kappaB (NF-kappaB) was activated by the LTI-treatment, and was inhibited by addition of simvastatin or pravastatin. Mevalonate or GGPP completely offset the effect of simvastatin. Simvastatin or pravastatin also decreased the LTI-stimulated interleukin-6 (IL-6) secretion. These effects of pravastatin were relatively weak compared with those of simvastatin. Y27632, an inhibitor of Rho kinase, also inhibited the LTI-induced NF-kappaB activation and iNOS expression, and decreased the production of NO and IL-6 in 3T3-L1 preadipocytes. These results suggest that statins, especially lipophilic types, inhibit induction of iNOS by inhibiting the small GTP-binding protein signal in preadipocytes. 相似文献
992.
993.
The leiognathid genus Nuchequula can be defined by the following combination of characters: mouth protruding downward; a narrow band of small, slender, villiform
teeth in both jaws; teeth on upper jaw strongly recurved; the lateral line almost complete; a dark blotch on the nape. Although
the genus was first established as a subgenus of Eubleekeria, it is here raised to generic level on the basis of the aforementioned morphological characters and recent molecular biological
evidence. The genus comprises six valid species: N. blochii (Valenciennes 1835), distributed in India and Thailand; N. flavaxilla sp. nov., occurring only at Panay I., Philippines; N. gerreoides (Bleeker 1851), widely distributed in the Indo-West Pacific, from the Persian Gulf to Cape York, Australia, and north to
Taiwan; N. glenysae sp. nov., from northern Australia and Ambon, Indonesia; N. longicornis sp. nov., from the Gulf of Thailand and Indonesia; and N. nuchalis (Temminck and Schlegel 1845), occurring in southern China including Taiwan, and southern Japan. Diagnostic characters of
the species belonging to the genus are as follows: N. blochii—breast scaled, cheek naked, and a conspicuous black blotch distally on spinous dorsal fin; N. flavaxilla sp. nov.—breast naked, dorsolateral body surface fully scaled, preorbital spine bicuspid and not expanded distally, and second
dorsal and anal fin spines conspicuously elongated; N. gerreoides—breast naked, anterior part of dorsolateral surface of body almost completely scaled, and second dorsal and anal fin spines
not conspicuously elongated; N. glenysae sp. nov.—breast completely scaled, cheek scaled, and unique complicated sensory canals present on the suborbital area, extending
to the nape; N. longicornis sp. nov.—breast naked, dorsolateral body surface fully scaled, preorbital spine bicuspid or tricuspid and extended distally,
and second dorsal fin spines only conspicuously elongated; N. nuchalis—breast naked, anterior part of dorsolateral surface of body widely naked, and a conspicuous dark blotch distally on spinous
dorsal fin. 相似文献
994.
995.
996.
Inada A Kanamori H Arai H Akashi T Araki M Weir GC Fukatsu A 《Journal of cellular physiology》2008,215(2):383-391
We have previously found progressive diabetic nephropathy in inducible cAMP early repressor (ICER Igamma) transgenic (Tg) mice. The ICER Igamma Tg mouse is an interesting model of sustained hyperglycemia due to its low production of insulin and insulin-producing beta cells. Here in a longitudinal study we further analyzed diabetic nephropathy and structural and functional alterations in other organs, comparing our model with streptozotocin (STZ)-diabetic model mice. The high-dose STZ-diabetic model showed marked variation in blood glucose levels and severe toxicity of STZ in the liver and kidney. The low-dose STZ-diabetic model showed less toxicity, but the survival rate was very low. STZ-diabetic mice had much more variation of glomerular hypertrophy and sclerosis. Furthermore, non-specific toxicity of STZ or insulin injections to maintain optimal blood glucose levels might have another effect upon the diabetic renal changes. In contrast, ICER Igamma Tg mice exhibited a stable and progressive phenotype of diabetic kidney disease solely due to chronic hyperglycemia without other modulating factors. Thus, ICER Igamma Tg mouse has advantages for examining diabetic renal disease, and offers unique and very different perspectives compared to STZ model. 相似文献
997.
998.
Akihiko Wada Nobuyuki Yanagihara Futoshi Izumi Seishi Sakurai Hideyuki Kobayashi 《Journal of neurochemistry》1983,40(2):481-486
Abstract: In isolated adrenal medullary cells, carbamyl-choline and high K+ cause the calcium-dependent secretion of catecholamines with a simultaneous increase in the synthesis of 14 C-catecholamines from [14 C]tyrosine. In these cells, trifluoperazine, a selective antagonist of calmodulin, inhibited both the secretion and synthesis of catecholamines. The stimulatory effect of carbamyl-choline was inhibited to a greater extent than that of high K+ . The inhibitory effect of trifluoperazine on carbamylcholine-evoked secretion of catecholamines was not overcome by an increase in either carbamylcholine or calcium concentration, showing that inhibition by trifluoperazine occurs by a mechanism distinct from competitive antagonism at the cholinergic receptor and from direct inactivation of calcium channels. Doses of trifluoperazine that inhibited catecholamine secretion and synthesis also inhibited the uptake of radioactive calcium by the cells. These results suggest that trifluoperazine inhibits the secretion and synthesis of catecholamines mainly due to its inhibition of calcium uptake. Trifluoperazine seems to inhibit calcium uptake by uncoupling the linkage between cholinergic receptor stimulation and calcium channel activation. 相似文献
999.
Dissociated cells of neural retinas of 3.5-day-old chick embryos differentiated into “lentoid bodies” within about 10–12 days when cultured in vitro. Protein synthesis of these cultured cells was studied with the use of SDS-polyacrylamide gel electrophoresis, affinity chromatography, and autoradiography combined with immunological techniques. Incorporation of [14C]leucine into total proteins, α-crystallin, and δ-crystallin was estimated after increasing times of culture up to about 30 days. Isotope incorporation into δ-crystallin was detected at 9 days, and it increased sevenfold after another 17 days. α-Crystallin was also first detected at 9 days, but its relative content reached a maximum at 12 days and then decreased gradually. The ratio of δ-crystallin synthesis to total protein synthesis increased up to 40% at 26 days, while that of α-crystallin synthesis remained 3% throughout the culture period. These results show that lens differentiation from neural retinal cells is associated with the preferential synthesis of lens crystallins, particularly of δ-crystallin. 相似文献
1000.
Accurate determination of DNA content in single cell nuclei stained with Hoechst 33258 fluorochrome at high salt concentration 总被引:2,自引:0,他引:2
In an attempt to achieve accurate quantification of DNA levels in cell nuclei, we studied the influence of salt concentration on the fluorescence of cell nuclei complexed with Hoechst-33258 (Hoe) fluorochrome. The fluorescence of cell nuclei was compared with that of extracted DNA as well as that of nucleosome core. Conformational changes in these complexes were examined by measuring both fluorescence anisotropy and fluorescence lifetime in the nanosecond region. The results showed that the fluorescence of DNA-Hoe was quenched by the nucleosomal structure, there being an associated increase in anisotropy and a decrease in the fluorescence lifetime; however, the fluorescence was restored to the original level by the addition of a high concentration of NaCl, CsCl, or LiCl. The reduction in fluorescence may have been due to loss of fluorescence energy caused by collision of the fluorophore with histones in the nucleosome. The addition of 1 M NaCl to the medium used for staining with Hoe greatly stabilized the fluorescence of DNA in cell nuclei. The DNA content of individual cell nuclei was determined by comparing the fluorescence of these nuclei with that of a standard DNA solution. For lymphocytes and liver ploidy cells, reasonably accurate values were obtained by applying the present method. 相似文献