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11.
E. Wada R. Imaizumi Y. Kabaya T. Yasuda T. Kanamori G. Saito A. Nishimune 《Plant and Soil》1986,93(2):269-286
Summary Plants from agricultural and natural upland ecosystem were investigated for15N content to evaluate the role of symbiotic N2-fixation in the nitrogen nutrition of soybean. Increased yields and lower δ15N values of nodulating soybeansvs, non-nodulating isolines gave semi-quantitative estimates of N2 fixation. A fairly large discrepancy was found between estimations by δ15N and by N yield at 0 kg N/ha of fertilizer. More precise estimates were made by following changes in plant δ15N when fertilizer δ15N was varied near15N natural abundance level. Clearcut linear relationships between δ15N values of whole plants and of fertilizer were obtained at 30 kg N/ha of fertilizer for three kinds of soils. In experimental
field plots, nodulating soybeans obtained 13±1% of their nitrogen from fertilizer, 66±8% from N2 fixation and 21±10% from soil nitrogen in Andosol brown soil; 30%, 16% and 54% in Andosol black soil; 7%, 77% and 16% in
Alluvial soil, respectively. These values for N2 fixation coincided with each corresponding estimation by N yield method.
Other results include: 1)15N content in upland soils and plants was variable, and may reflect differences in the mode of mineralization of soil organics,
and 2) nitrogen isotopic discrimination during fertilizer uptake (δ15N of plant minus fertilizer) ranged from −2.2 to +4.9‰ at 0–30 kg N/ha of fertilizer, depending on soil type and plant species.
The proposed method can accurately and relatively simply establish the importance of symbiotic nitrogen fixation for soybeans
growing in agricultural settings. 相似文献
12.
In an effort to obtain orange mutants ofBlastocladiella emersonii
Cantino &Hyatt, wild type zoospores were treated with mitomycin. From the variants produced, we obtained a stable, albino mutant (Ma-1) that differs significantly from another, previously described (Shaw &Cantino, 1969) UV-induced, albino variant. This report concerns the origin of Ma-1, its distinguishing features, and its apparent similarity to the few LC (late colorless) plants that normally appear in wild type populations. A preliminary note regarding mitomycin-induced variants ofB. emersonii has been published (Matsumae &Cantino, 1970). 相似文献
13.
Control of IL-2 receptor-alpha expression by IL-1, tumor necrosis factor, and IL-2. Complex regulation via elements in the 5' flanking region 总被引:2,自引:0,他引:2
G Plaetinck M C Combe P Corthésy P Sperisen H Kanamori T Honjo M Nabholz 《Journal of immunology (Baltimore, Md. : 1950)》1990,145(10):3340-3347
14.
Ammonia assimilation pathways in nitrogen-fixing Clostridium kluyverii and Clostridium butyricum. 总被引:2,自引:1,他引:1
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Pathways of ammonia assimilation into glutamic acid were investigated in ammonia-grown and N2-fixing Clostridium kluyverii and Clostridium butyricum by measuring the specific activities of glutamate dehydrogenase, glutamine synthetase, and glutamate synthase. C. kluyverii had NADPH-glutamate dehydrogenase with a Km of 12.0 mM for NH4+. The glutamate dehydrogenase pathway played an important role in ammonia assimilation in ammonia-grown cells but was found to play a minor role relative to that of the glutamine synthetase/NADPH-glutamate synthase pathway in nitrogen-fixing cells when the intracellular NH4+ concentration and the low affinity of the enzyme for NH4+ were taken into account. In C. butyricum grown on glucose-salt medium with ammonia or N2 as the nitrogen source, glutamate dehydrogenase activity was undetectable, and the glutamine synthetase/NADH-glutamate synthase pathway was the predominant pathway of ammonia assimilation. Under these growth conditions, C. butyricum also lacked the activity of glucose-6-phosphate dehydrogenase, which catalyzes the regeneration of NADPH from NADP+. However, high activities of glucose-6-phosphate dehydrogenase as well as of NADPH-glutamate dehydrogenase with a Km of 2.8 mM for NH4+ were present in C. butyricum after growth on complex nitrogen and carbon sources. The ammonia-assimilating pathway of N2-fixing C. butyricum, which differs from that of the previously studied Bacillus polymyxa and Bacillus macerans, is discussed in relation to possible effects of the availability of ATP and of NADPH on ammonia-assimilating pathways. 相似文献
15.
Akihiro Ohira Eugene de Juan Jr Yasuo Tano Charles A. Wilson 《The Histochemical journal》1996,28(9):607-611
Summary It has been proposed that basic fibroblast growth factor (basic FGF) mediates the neovascular response in a variety of conditions,
including diabetic retinopathy and branch retinal vein occlusion. To test the hypothesis that basic FGF was released from
retinal stores as a result of retinal ischaemia, transient retinal ischaemia was induced, followed by 48 h of reperfusion,
in the rat by combined central retinal vasculature and optic nerve ligation. The immunolocalization of basic FGF was studied
in the retina. We found that basic FGF in the normal retina is present around the deeper retinal vessels and in the neuronal
tissue of the outer plexiform layer. In the eyes that had ischaemia followed by reperfusion, there was moderate cellular oedema
with retinal swelling, and mitoses in the inner nuclear and plexiform layers. There were no changes evident at the immunohistochemical
level either in the intensity or distribution of stores of basic FGF. We conclude from these data that stores of basic FGF
are not altered dramatically under the conditions of transient experimental ischaemia and reperfusion in the rat, despite
the presence of cellular proliferation. 相似文献
16.
17.
A. Kanamori K. Kitajima Y. Inoue S. Inoue Z. Xulei C. Zuber J. Roth J. Ye F. A. Troy II 《Histochemistry and cell biology》1994,101(5):333-340
Two particular types of sialoglycoproteins have been detected in fish: polysialoglycoproteins containing 28-linked polysialic acid (8Neu5Gc2)
n
present in unfertilized Salmonidae fish eggs, and glycoproteins bearing oligo/polymers of deaminated neuraminic acids (KDN) found in the vitelline envelope of the eggs and ovarian fluid. We report the preparation and characterization of a monoclonal antibody specifically recognizing oligo/polymers of KDN sequences in glycoproteins and its application in immunohistochemistry. Fusion of spleen cells from a BALB/c mouse immunized with a KDN-rich glycoprotein (KDN-gp) containing (8KDN2)
n
6(KDN23Gal13GlNAc13) GalNAc1 residues, with mouse myeloma cells yielded a hybrid cell line producing a monoclonal antibody that bound to KDN-gp, but not to KDN-gp depleted of KDN residues. The specificity of the monoclonal antibody, designated mAb.kdn8kdn, was determined by an enzyme-linked immunosorbent assay using KDN-gp samples that varied in KDN content. These antigens were prepared by the selective removal of KDN residues from the native KDN-gp. The mAb.kdn8kdn reacted most strongly with the intact KDN-gp and less strongly with KDN-gp samples containing decreased numbers of KDN residues. The mAb.kdn8kdn was shown specifically to recognize the 28-linked oligo/polyKDN sequences, (8KDN2)
n
, and to be able to distinguish specifically (8KDN2)
n
chains from (8Neu5Ac2)
n
and (8Neu5Gc2)
n
chains. The antibody was used successfully for the immunohistochemical detection of reactive KDN epitopes in sections of paraffin embedded rat pancreas. Several controls verified the specificity of the immunohistochemical staining, thus providing the first demonstration of (8KDN2)
n
sequences in a mammalian tissue. The mAb.kdn8kdn can now be used to search further for glycoconjugates containing (8KDN2)
n
chains and will facilitate studies on their biosynthesis, intracellular localization and function. 相似文献
18.
Yoshihito Shirai Masaaki Yamaguchi Atsuko Kobayashi Akihiro Nishi Hisao Nakamura Hiroki Murakami 《Cytotechnology》1994,14(2):129-146
The growth yields for glucose and glutamine of murine hybridoma cells entrapped in collagen gel particles were examined during the growth phase. The immobilized hybridoma cells were cultivated in a fluidized bed fermenter where the medium was circulating to supply oxygen separately. Procedures to supply an alkaline solution for adjusting the pH level strongly affected the growth yields. A direct supply of the alkaline solution to the cultivation system reduced both the growth yields for glucose and glutamine, probably due to a local increase in pH level. On the other hand, when fresh medium in which the pH was adjusted to around 8.5 was added to the cultivation system, the growth yields were unchanged even at the same pH level as when direct alkaline supply was used. These results suggest that an indirect alkaline supply could be recommended to ajust the pH level when using medium-circulating-fermenters. 相似文献
19.
K Kanamori R W Kondrat B D Ross 《Cellular and molecular biology, including cyto-enzymology》2003,49(5):819-836
13C-enrichment analysis of glutamate in the extracellular fluid (GLU(ECF): 2-3 microM) by gas-chromatography/mass-spectrometry (GCMS) was combined with in vivo NMR observation of whole-brain GLU (approximately10 mM) to study neurotransmitter uptake. Brain GLU C5 was 13C-enriched by intravenous [2,5-13C]glucose infusion. GLU(ECF) was collected by microdialysis from the cortico-striatal region of awake rats. The 13C-enrichment of basal dialysate GLU C5 during 0.75-1.25 hr of infusion was 0.263 +/- 0.01, very close to the enrichment of whole-brain GLU C5. The result strongly suggests that dialysate GLU consists predominantly of neurotransmitter GLU. For selective 13C-enrichment of neurotransmitter GLU, the whole-brain 13C-enrichment was followed by [12C]glucose infusion to chase 13C from the small glial GLU pool. This leaves [5-13C]GLU mainly in the large neuronal metabolic pool and the vesicular neurotransmitter pool. The uptake of synaptic [5-13C]GLU(ECF) into glia and metabolism to glutamine (GLN) were monitored in vivo by NMR observation of [5-13C,15N]GLN formed during 15NH4Ac infusion. The rate of GLN synthesis, derived from neurotransmitter GLU(ECF) (which provided 80-90% of the substrate) was 6.4 +/- 0.44 micromol/g/hr. Hence, the observed rate represents a reasonable estimate for the rate of glial uptake of GLU(ECF), a process that is crucial for protecting the brain from GLU excitotoxicity. 相似文献
20.
Akihiro Yoshida Kuniaki Takata Toshiko Kasahara Toshio Aoyagi Shozo Saito Hiroshi Hirano 《The Histochemical journal》1995,27(5):420-426
Summary Glucose is actively absorbed in the intestine by the action of the Na+-dependent glucose transporter. Using an antibody against the rabbit intestinal Na+-dependent glucose transporter (SGLT1), we examined the localization of SGLT1 immunohistochemically along the rat digestive
tract (oesophagus, stomach, duodenum, jejunum, ileum, colon and rectum). SGLT1 was detected in the small intestine (duodenum,
jejunum and ileum), but not in the oesophagus, stomach, colon or rectum. SGLT1 was localized at the brush border of the absorptive
epithelium cells in the small intestine. Electron microscopical examination showed that SGLT1 was localized at the apical
plasma membrane of the absorptive epithelial cells. SGLT1 was not detected at the basolateral plasma membrane. Along the crypt-villus
axis, all the absorptive epithelial cells in the villus were positive for SGLT1, whose amount increased from the bottom of
the villus to its tip. On the other hand, cells in the crypts exhibited little or no staining for SGLT1. Goblet cells scattered
throughout the intestinal epithelium were negative for SGLT1. These observations show that SGLT1 is specific to the apical
plasma membrane of differentiated absorptive epithelial cells in the small intestine, and suggest that active uptake of glucose
occurs mainly in the absorptive epithelial cells in the small intestine. 相似文献