全文获取类型
收费全文 | 512篇 |
免费 | 18篇 |
出版年
2022年 | 2篇 |
2021年 | 6篇 |
2020年 | 2篇 |
2019年 | 3篇 |
2018年 | 4篇 |
2017年 | 7篇 |
2016年 | 8篇 |
2015年 | 7篇 |
2014年 | 17篇 |
2013年 | 20篇 |
2012年 | 26篇 |
2011年 | 28篇 |
2010年 | 14篇 |
2009年 | 13篇 |
2008年 | 27篇 |
2007年 | 20篇 |
2006年 | 25篇 |
2005年 | 37篇 |
2004年 | 47篇 |
2003年 | 28篇 |
2002年 | 28篇 |
2001年 | 31篇 |
2000年 | 23篇 |
1999年 | 23篇 |
1998年 | 5篇 |
1997年 | 2篇 |
1996年 | 5篇 |
1995年 | 4篇 |
1994年 | 2篇 |
1993年 | 1篇 |
1992年 | 7篇 |
1991年 | 8篇 |
1990年 | 10篇 |
1989年 | 9篇 |
1988年 | 4篇 |
1987年 | 3篇 |
1986年 | 5篇 |
1985年 | 4篇 |
1984年 | 1篇 |
1983年 | 1篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1980年 | 1篇 |
1976年 | 2篇 |
1974年 | 1篇 |
1971年 | 2篇 |
1970年 | 3篇 |
1968年 | 1篇 |
1965年 | 1篇 |
排序方式: 共有530条查询结果,搜索用时 15 毫秒
81.
Three lignicolous freshwater ascomycetes from rivers in Akkeshi, Hokkaido, northern Japan are reported. All of these are new
species belonging to the Lophiostomataceae and described as Lophiostoma breviappendiculatum, Massarina clionina, and Massariosphaeria maxima. Morphological differences between each species and its similar taxa are noted. All three species have been observed to produce
only ascomatal states in artificial culture. 相似文献
82.
T. Ariizumi M. Amagai D. Shibata K. Hatakeyama M. Watanabe K. Toriyama 《Plant cell reports》2002,21(1):90-96
Promoter sequences of three anther-specific genes, each of which shows sequence identity to lipid transfer protein (LTP12), xyloglucan endotransglucosylase/hydrolase (XTH3), and polygalacturonase (PGA4), were obtained from Arabidopsis thaliana, fused to the #-glucuronidase (GUS) gene, and then introduced into A. thaliana. Histochemical GUS assay showed that the PGA4 promoter was active in the tapetum at the bicellular pollen stage and in tricellular pollen. The promoter of LTP12 and XTH3 directed GUS expression exclusively in the tapetum. The LTP12 promoter was activated from the uninucleate microspore stage, while the XTH3 promoter was activated from the bicellular pollen stage. This type of activation pattern at the late developmental stage of the tapetum has not been reported previously. The promoter sequences employed in this study will be useful for the characterization of genes differentially expressed in anthers. 相似文献
83.
T Niidome H Murakami M Kawazoe T Hatakeyama Y Kobashigawa M Matsushita Y Kumaki M Demura K Nitta H Aoyagi 《Bioorganic & medicinal chemistry letters》2001,11(14):1893-1896
We have designed and synthesized of carbohydrate-binding peptides, gramicidin S analogues. Asn/Asp/Gln and Trp residues in the peptides were employed as the binding sites for carbohydrates by hydrogen-bonding interaction and the creation units for hydrophobic pocket to promote the interaction, respectively. The data of fluorescence spectroscopy and affinity column chromatography indicated that the peptides possessed the binding ability for some carbohydrates in aqueous medium. As a result of 1H NMR study, nuclear Overhauser effects between aromatic side chains of a peptide, [Gln(1,1'),Trp(3,3')]-gramisidin S and mannose were observed, indicating that the interaction of the peptide with the sugar occurred in the hydrophobic environment formed by Trp and Phe residues. 相似文献
84.
Seiji Sugimoto Yoshiharu Yokoo Noritaka Hatakeyama Akira Yotsuji Sadao Teshiba Hiroshi Hagino 《Biotechnology letters》1991,13(6):385-388
Summary Higher culture pH of 7.6 was shown to be preferable for the inclusion body formation of salmon growth hormone (SGH) inEscherichia
coli harboring a recombinant plasmid. High-level formation of SGH inclusion bodies was achieved at 33°C (pH 7.6). Growth inhibition by soluble SGH was also observed. 相似文献
85.
H Kouriki-Nagatomo T Hatakeyama M Jelokhani-Niaraki M Kondo T Ehara N Yamasaki 《Bioscience, biotechnology, and biochemistry》1999,63(7):1279-1284
The pore-forming activity of CEL-III, a Gal/GalNAc specific lectin from the Holothuroidea Cucumaria echinata, was examined using artificial lipid membranes as a model system of erythrocyte membrane. The carboxyfluorescein (CF)-leakage studies clearly indicated that CEL-III induced the formation of pores in the dipalmitoyl phosphatidyl choline (DPPC)-lactosyl ceramide (LacCer) liposomes effectively but not in the DPPC-glucosyl ceramide (GlcCer) liposomes or DPPC liposomes. Such a leakage of CF was strongly inhibited by lactose, a potent inhibitor of CEL-III, suggesting that the leakage is mediated through the specific binding of CEL-III to the carbohydrate chains on the surface of the liposomes. The leakage of CF from the DPPC-lactosyl ceramide liposomes was pH-dependent, and it increased with increasing pH. The immunoblotting analysis and circular dichroism data indicated that upon interaction with liposomes, CEL-III associated to form an oligomer concomitantly with a marked conformational change. Furthermore, channel measurements showed that CEL-III has an ability to form small ion channels in the planar lipid bilayers consisting of diphytanoylphosphatidylcholine and human globoside (Gb4Cer)/LacCer. 相似文献
86.
Takashi Hatakeyama Miki Okada Seiko Shimamoto Yasuo Kubota Ryoji Kobayashi 《European journal of biochemistry》2004,271(18):3765-3775
In this report, we have focused our attention on identifying intracellular mammalian proteins that bind S100A12 in a Ca2+-dependent manner. Using S100A12 affinity chromatography, we have identified cytosolic NADP+-dependent isocitrate dehydrogenase (IDH), fructose-1,6-bisphosphate aldolase A (aldolase), glyceraldehyde-3-phosphate dehydrogenese (GAPDH), annexin V, S100A9, and S100A12 itself as S100A12-binding proteins. Immunoprecipitation experiments indicated the formation of stable complexes between S100A12 and IDH, aldolase, GAPDH, annexin V and S100A9 in vivo. Surface plasmon resonance analysis showed that the binding to S100A12, of S100A12, S100A9 and annexin V, was strictly Ca2+-dependent, whereas that of GAPDH and IDH was only weakly Ca2+-dependent. To localize the site of S100A12 interaction, we examined the binding of a series of C-terminal truncation mutants to the S100A12-immobilized sensor chip. The results indicated that the S100A12-binding site on S100A12 itself is located at the C-terminus (residues 87-92). However, cross-linking experiments with the truncation mutants indicated that residues 87-92 were not essential for S100A12 dimerization. Thus, the interaction between S100A12 and S100A9 or immobilized S100A12 should not be viewed as a typical S100 homo- or heterodimerization model. Ca2+-dependent affinity chromatography revealed that C-terminal residues 75-92 are not necessary for the interaction of S100A12 with IDH, aldolase, GAPDH and annexin V. To analyze the functional properties of S100A12, we studied its action in protein folding reactions in vitro. The thermal aggregation of IDH or GAPDH was facilitated by S100A12 in the absence of Ca2+, whereas in the presence of Ca2+ the protein suppressed the aggregation of aldolase to less than 50%. These results suggest that S100A12 may have a chaperone/antichaperone-like function which is Ca2+-dependent. 相似文献
87.
Takasaki Takeshi Hatakeyama Katsunori Watanabe Masao Toriyama Kinya Isogai Akira Hinata Kokichi 《Plant molecular biology》1999,40(4):659-668
Self-incompatibility (SI) in Brassicaceae is genetically controlled by the S locus complex in which S locus glycoprotein (SLG) and S receptor kinase (SRK) genes have been identified, and these two genes encoding stigma proteins are believed to play important roles in SI recognition reaction. Here we introduced the SLG43 gene of Brassica rapa into a self-incompatible cultivar, Osome, of B. rapa, and examined the effect of this transgene on the SI behavior of the transgenic plants. Preliminary pollination experiments demonstrated that Osome carried S52 and S60, and both were codominant in stigma, but S52 was dominant to S60 in pollen. S43 was found to be recessive to S52 and codominant with S60 in stigma. The nucleotide sequence of SLG43 was more similar to that of SLG52 (87.8% identity) than to that of SLG60 (74.8% identity). Three of the ten primary transformants (designated No. 1 to No. 10) were either completely (No. 9) or partially (No. 6 and No. 7) self-compatible; the SI phenotype of the stigma was changed from S52S60 to S60, but the SI phenotype of the pollen was not altered. In these three plants, the mRNA and protein levels of both SLG43 and SLG52 were reduced, whereas those of SLG60 were not. All the plants in the selfed progeny of No. 9 and No. 6 regained SI and they produced a normal level of SLG52. These results suggest that the alteration of the SI phenotype of the stigma in the transformants Nos. 6, 7, and 9 was the result of specific co-suppression between the SLG43 transgene and the endogenous SLG52 gene. Three of the transformants (Nos. 5, 8 and 10) produced SLG43 protein, but their SI phenotype was not altered. The S60 homozygotes in the selfed progeny of No. 10 which produced the highest level of SLG43 were studied because S43 was codominant with S60 in the stigma. They produced SLG43 at approximately the same level as did S43S60 heterozygotes, but did not show S43 haplotype specificity at the stigma side. We conclude that SLG is necessary for the expression of the S haplotype specificity in the stigma but the introduction of SLG alone is not sufficient for conferring a novel S haplotype specificity to the stigma. 相似文献
88.
89.
Haruo Hashimoto Tomoo Eto Tsutomu Kamisako Naoko Hoya Teruhiko Hatakeyama Toshiro Arai Makoto Yokosuka Yasuyuki Ohnishi Mamoru Ito Kyoji Hioki Ryo Suzuki Mitsuru Ohsugi Muneo Saito Yoshito Ueyama Toshimasa Yamauchi Naoto Kubota Kazuyuki Tobe Takashi Kadowaki Norikazu Tamaoki Tatsuji Nomura Kinori Kosaka 《Experimental Animals》2008,57(4):407-411
Efficient reproduction using natural mating and reproduction technology [in vitro fertilization (IVF) and embryo transfer (ET)] was investigated in IRS2 deficient mice with C57BL/6JJcl genetic background (Irs2(-/-) mice) as a typical type 2 diabetes model. From the results using various combinations of Irs2(-/-) and Irs2(-/+) mice, the combination of female Irs2(-/+) x male Irs2(-/-) was found to be more efficient than other combinations. In applications of reproduction technology using IVF and ET, the combination of female Irs2(-/+) x male Irs2(-/-) involves the possibility of Irs2(-/-) production by repeats using female Irs2(-/+) mice. However, reproductive continuity using this combination is difficult because of dependence on human technique and the cost of ET. Therefore, we concluded that Irs2(-/-) mice should be produced by embryo transfer using Irs2(-/-) mice from a colony consisting of female Irs2(-/+) x male Irs2(-/-). 相似文献
90.