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131.
Kamei K Wu X Xu X Minami K Huy NT Takano R Kato H Hara S 《Analytical biochemistry》2001,295(2):203-213
Evanescent wave biosensor has been recently employed as a powerful tool for analyses of macromolecular interactions. In the present study, evanescent wave biosensor analysis was developed to analyze the heparin-protein interaction using as ligands a series of heparin derivatives regioselectively desulfated by chemical methods, particularly to evaluate the effect of each sulfate group of heparin. The method for immobilizing heparin on the cuvette of the evanescent wave biosensor equipment was optimized to obtain the high response required for accurate measurement. The best result was achieved when the amino group introduced at the reducing end of heparin was coupled with carboxymethyl dextran on the surface of the cuvette using glycolchitosan as a multivalent linker. The established system appeared to describe well the interactions of heparin with such proteins as acidic and basic fibroblast growth factors and tissue factor pathway inhibitor. 相似文献
132.
Immune response induced by airway sensitization after influenza A virus infection depends on timing of antigen exposure in mice 总被引:2,自引:0,他引:2
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Yamamoto N Suzuki S Suzuki Y Shirai A Nakazawa M Suzuki M Takamasu T Nagashima Y Minami M Ishigatsubo Y 《Journal of virology》2001,75(1):499-505
To study which phase of viral infection promotes antigen sensitization via the airway and which type of antigen-presenting cells contributes to antigen sensitization, BALB/c mice were sensitized by inhalation of ovalbumin (OA) during the acute phase or the recovery phase of influenza A virus infection, and then 3 weeks later animals were challenged with OA. The numbers of eosinophils and lymphocytes, the amounts of interleukin-4 (IL-4) and IL-5 in the bronchoalveolar lavage fluid, and the serum levels of OA-specific immunoglobulin G1 (IgG1) and IgE increased in mice sensitized during the acute phase (acute phase group), while a high level of gamma interferon production was detected in those sensitized during the recovery phase (recovery phase group). In the acute phase group, both major histocompatibility complex class II molecules and CD11c were strongly stained on the bronchial epithelium; in the recovery phase group, however, neither molecule was detected. OA-capturing dendritic cells (DCs) migrated to the regional lymph nodes, and a small number of OA-capturing macrophages were also observed in the lymph nodes of the acute phase group. In the recovery group, however, no OA-capturing DCs were detected in either the lungs or the lymph nodes, while OA-capturing macrophages were observed in the lymph nodes. These results indicate that the timing of antigen sensitization after viral infection determines the type of immune response. 相似文献
133.
Nakamura T Houchi H Minami A Sakamoto S Tsuchiya K Niwa Y Minakuchi K Nakaya Y 《Life sciences》2001,69(15):1709-1715
The relaxation effect of cilostazol, a phosphodiesterase III inhibitor, on the thoracic aorta was investigated. Cilostazol induced the relaxation of the thoracic aorta precontracted by phenylephrine in a concentration-dependent manner. The concentration-dependent relaxation was shifted to the right in the endothelium denuded aorta compared with that of intact endothelium, suggesting that this relaxation was partly dependent on endothelium. Cilostazol-induced relaxation of thoracic aorta tone was reversed by treatment with N(G)-nitro L-arginine (L-NNA), a competitive inhibitor of nitric oxide (NO) synthase. Cilostazol also significantly increased the NO level in the porcine thoracic aorta. In rats treated with cilostazol, the urinary excretion of nitrites, a stable metabolite of NO, and basal production of NO of the aortic ring were significantly greater than in those without treatment. These findings indicate that cilostazol-induced vasodilation of the rat thoracic aorta was dependent on the endothelium, which released NO from aortic endothelial cells. 相似文献
134.
Triterpene and flavanone glycoside from Rhododendron simsii 总被引:2,自引:0,他引:2
Antioxidative substances were isolated from the leaves of Rhododendron simsii. These were a triterpene and flavanone glycoside, together with the known matteucinol and two known benzoic acid derivatives. Their structures were characterized as 19,24-dihydroxyurs-12-en-3-one-28-oic acid and 7-O-beta-D-apiofuranosyl-(1-->6)-beta-D-glucopyranosylmatteucinol by spectroscopic analysis. 相似文献
135.
Makino R Matsuda H Obayashi E Shiro Y Iizuka T Hori H 《The Journal of biological chemistry》1999,274(12):7714-7723
The nature of the metal-proximal base bond of soluble guanylate cyclase from bovine lung was examined by EPR spectroscopy. When the ferrous enzyme was mixed with NO, a new species was transiently produced and rapidly converted to a five-coordinate ferrous NO complex. The new species exhibited the EPR signal of six-coordinate ferrous NO complex with a feature of histidine-ligated heme. The histidine ligation was further examined by using the cobalt protoporphyrin IX-substituted enzyme. The Co2+-substituted enzyme exhibited EPR signals of a broad g perpendicular;1 component and a g;1 component with a poorly resolved triplet of 14N superhyperfine splittings, which was indicative of the histidine ligation. These EPR features were analogous to those of alpha-subunits of Co2+-hemoglobin in tense state, showing a tension on the iron-histidine bond of the enzyme. The binding of NO to the Co2+-enzyme markedly stimulated the cGMP production by forming the five-coordinate NO complex. We found that N3- elicited the activation of the ferric enzyme by yielding five-coordinate high spin N3- heme. These results indicated that the activation of the enzymes was initiated by NO binding to the metals and proceeded via breaking of the metal-histidine bonds, and suggested that the iron-histidine bond in the ferric enzyme heme was broken by N3- binding. 相似文献
136.
Tohno S Tohno Y Masuda M Minami T Moriwake Y Utsumi M Yamada M 《Biological trace element research》1999,70(3):233-241
It is known that a large quantity of magnesium contains bones, and the magnesium contents in spongy bones decrease gradually
with advancing age. To elucidate the relationships between a decrease of mineral contents in human bones and an accumulation
of minerals in the other human tissues, the content of magnesium was analyzed by inductively coupled plasma-atomic emission
spectrometry among human bones, arteries, veins, and cartilages in 27 subjects (17 men and 10 women). These were resected
from the subjects who died in the age range 40–98 yr. Calcanei were chosen for analysis of magnesium contents in contrast
with femoral, popliteal, and common carotid arteries, internal jugular and femoral veins, superior and inferior venae cavae,
and pubic symphyses.
The magnesium contents in the calcanei decreased gradually with aging, whereas they increased progressively in the arteries,
veins, and pubic symphyses with aging. It was found that as the magnesium contents decreased in the calcanei, they increased
in the arteries, such as the femoral, popliteal, and common carotid arteries, whereas they decreased inversely in the veins,
such as the internal jugular and femoral veins and superior and inferior venae cavae. Furthermore, as the magnesium contents
decreased in the calcanei, they hardly changed in the pubic symphyses. These suggest that magnesium released from bones is
accompanied by accumulation of magnesium in the arteries. 相似文献
137.
Utsumi M Tohno S Minami T Okazaki Y Moriwake Y Yamada M Tohno Y 《Biological trace element research》1999,67(2):165-171
On age relationships of mineral contents in human bones, the contents of the sixth rib and a piece of its compact bone were determined by inductively coupled plasma atomic emission spectrometry (ICPS). The ribs were resected from 21 subjects (14 men and 7 women) who died in age ranging from 65 to 93 yr. There were no age-dependent decreases in Ca and P contents of the ribs in the age range on ICPS. It was found that there were no age-dependent decreases in Ca and P in compact bones of ribs. 相似文献
138.
Koyama M Katayama S Kaji M Taniguchi Y Matsushita O Minami J Morita S Okabe A 《Microbiology and immunology》1999,43(10):947-957
The hem gene cluster, which consists of hemA, cysG(B), hemC, hemD, hemB, and hemL genes, and encodes enzymes involved in the biosynthetic pathway from glutamyl-tRNA to uroporphyrinogen III, has been identified by the cloning and sequencing of two overlapping DNA fragments from Clostridium perfringens NCTC8237. The deduced amino acid sequence of the N-terminal region of C. perfringens HemD is homologous to those reported for the C-terminal region of Salmonella typhimurium CysG and Clostridium josui HemD. C. perfringens CysG(B) is a predicted 220-residue protein which shows homology to the N-terminal region of S. typhimurium CysG. Disruption of the cysG(B) gene in C. perfringens strain 13 by homologous recombination reduced cobalamin (vitamin B12) levels by a factor of 200. When grown in vitamin B12-deficient medium, the mutant strain showed a four-fold increase in its doubling time compared with that of the wild-type strain, and this effect was counteracted by supplementing the medium with vitamin B12. These results suggest that C. perfringens CysG(B) is involved in the chelation of cobalt to precorrin II as suggested for the CysG(B) domain of S. typhimurium CysG, enabling the synthesis of cobalamin. 相似文献
139.
Nuki Y Uchinokura S Miyata S Fukushima T Hamasuna R Nakano S Wakisaka S Akiyama Y Itoh H Kataoka H 《Human cell》2004,17(3):145-150
A cell line designated NYGM was established from a human cerebral glioblastoma multiforme (GBM) obtained from a 75-year-old Japanese woman. The cell line has grown slowly without interruption and has been propagated continuously by serial passages (more than 80 passage) during the past 3 years. The cultured cells were fusiform or polyhedral in shape. The population doubling time was 24 hours. The chromosomal number varied between 77 and 88, with modal chromosomal number of 84. NYGM cells concomitantly expressed MET receptor tyrosine kinase (a product of c-met protooncogene) and its ligand HGF/SF (hepatocyte growth factor/scatter factor), as well as HGF activator and HGF activator inhibitors. The cells might be useful for the study of pericellular regulation of HGF/SF-MET signaling and HGF activation of GBM cells. 相似文献
140.