全文获取类型
收费全文 | 2139篇 |
免费 | 100篇 |
出版年
2022年 | 6篇 |
2021年 | 20篇 |
2020年 | 10篇 |
2019年 | 14篇 |
2018年 | 27篇 |
2017年 | 34篇 |
2016年 | 31篇 |
2015年 | 75篇 |
2014年 | 63篇 |
2013年 | 106篇 |
2012年 | 116篇 |
2011年 | 144篇 |
2010年 | 78篇 |
2009年 | 70篇 |
2008年 | 104篇 |
2007年 | 99篇 |
2006年 | 110篇 |
2005年 | 109篇 |
2004年 | 125篇 |
2003年 | 102篇 |
2002年 | 103篇 |
2001年 | 55篇 |
2000年 | 66篇 |
1999年 | 51篇 |
1998年 | 21篇 |
1997年 | 15篇 |
1996年 | 12篇 |
1995年 | 21篇 |
1994年 | 21篇 |
1993年 | 23篇 |
1992年 | 48篇 |
1991年 | 37篇 |
1990年 | 41篇 |
1989年 | 35篇 |
1988年 | 28篇 |
1987年 | 26篇 |
1986年 | 21篇 |
1985年 | 19篇 |
1984年 | 13篇 |
1983年 | 19篇 |
1982年 | 11篇 |
1981年 | 10篇 |
1980年 | 15篇 |
1979年 | 15篇 |
1978年 | 10篇 |
1977年 | 6篇 |
1975年 | 6篇 |
1974年 | 8篇 |
1968年 | 5篇 |
1967年 | 8篇 |
排序方式: 共有2239条查询结果,搜索用时 31 毫秒
991.
Uchiyama J Takemura I Satoh M Kato S Ujihara T Akechi K Matsuzaki S Daibata M 《PloS one》2011,6(10):e26648
Some bacterial strains of the multidrug-resistant Gram-positive bacteria Enterococcus faecalis can significantly reduce the efficacy of conventional antimicrobial chemotherapy. Thus, the introduction of bacteriophage (phage) therapy is expected, where a phage is used as a bioagent to destroy bacteria. E. faecalis phage ΦEF24C is known to be a good candidate for a therapeutic phage against E. faecalis. However, this therapeutic phage still produces nonuniform antimicrobial effects with different bacterial strains of the same species and this might prove detrimental to its therapeutic effects. One solution to this problem is the preparation of mutant phages with higher activity, based on a scientific rationale. This study isolated and analyzed a spontaneous mutant phage, ΦEF24C-P2, which exhibited higher infectivity against various bacterial strains when compared with phage ΦEF24C. First, the improved bactericidal effects of phage ΦEF24C-P2 were attributable to its increased adsorption rate. Moreover, genomic sequence scanning revealed that phage ΦEF24C-P2 had a point mutation in orf31. Proteomic analysis showed that ORF31 (mw, 203 kDa) was present in structural components, and immunological analysis using rabbit-derived antibodies showed that it was a component of a long, flexible fine tail fiber extending from the tail end. Finally, phage ΦEF24C-P2 also showed higher bactericidal activity in human blood compared with phage ΦEF24C using the in vitro assay system. In conclusion, the therapeutic effects of phage ΦEF24C-P2 were improved by a point mutation in gene orf31, which encoded a tail fiber component. 相似文献
992.
Okada Y Nobori H Shimizu M Watanabe M Yonekura M Nakai T Kamikawa Y Wakimura A Funahashi N Naruse H Watanabe A Yamasaki D Fukada S Yasui K Matsumoto K Sato T Kitajima K Nakano T Aird WC Doi T 《PloS one》2011,6(9):e24837
In previous studies on the mechanism underlying megakaryocyte-specific gene expression, several ETS motifs were found in each megakaryocyte-specific gene promoter. Although these studies suggested that several ETS family proteins regulate megakaryocyte-specific gene expression, only a few ETS family proteins have been identified. Platelet factor 4 (PF4) is a megakaryocyte-specific gene and its promoter includes multiple ETS motifs. We had previously shown that ETS-1 binds to an ETS motif in the PF4 promoter. However, the functions of the other ETS motifs are still unclear. The goal of this study was to investigate a novel functional ETS motif in the PF4 promoter and identify proteins binding to the motif. In electrophoretic mobility shift assays and a chromatin immunoprecipitation assay, FLI-1, ELF-1, and GABP bound to the -51 ETS site. Expression of FLI-1, ELF-1, and GABP activated the PF4 promoter in HepG2 cells. Mutation of a -51 ETS site attenuated FLI-1-, ELF-1-, and GABP-mediated transactivation of the promoter. siRNA analysis demonstrated that FLI-1, ELF-1, and GABP regulate PF4 gene expression in HEL cells. Among these three proteins, only FLI-1 synergistically activated the promoter with GATA-1. In addition, only FLI-1 expression was increased during megakaryocytic differentiation. Finally, the importance of the -51 ETS site for the activation of the PF4 promoter during physiological megakaryocytic differentiation was confirmed by a novel reporter gene assay using in vitro ES cell differentiation system. Together, these data suggest that FLI-1, ELF-1, and GABP regulate PF4 gene expression through the -51 ETS site in megakaryocytes and implicate the differentiation stage-specific regulation of PF4 gene expression by multiple ETS factors. 相似文献
993.
994.
995.
Sugihara Y Taniguchi H Kushima R Tsuda H Kubota D Ichikawa H Sakamoto K Nakamura Y Tomonaga T Fujita S Kondo T 《Journal of Proteomics》2012,75(17):5342-5355
Novel candidates of biomarker and therapeutic target in colorectal cancer (CRC) were investigated using a proteomic approach. The proteome of normal colorectal epithelial tissues was compared with that of the tumor ones in 59 CRC patients using two-dimensional difference gel electrophoresis. Of 3458 protein spots, 110 exhibited statistically significant (p<0.01) differences in intensity (more than 2.5-folds) between the normal and tumor tissue groups. Of 67 unique gene products that were identified for 105 of the 110 protein spots, we focused on the higher expression of the adenoma polyposis coli-binding protein EB1 (EB1). EB1 was originally discovered as a binding protein of APC, which is a tumor suppressor gene product, and the expression of EB1 has been associated with poor prognosis in several malignancies but not in CRC. Immunohistochemical analysis of the 132 CRC cases revealed that EB1 was overexpressed in tumor cells in correlation with poor prognosis. Suppression of EB1 by RNAi inhibited CRC cell proliferation and invasion. In this study, the overexpression of EB1 in CRC tissues correlating with prognosis, and its functional contribution to the malignant phenotypes of CRC cells are described. The present findings indicate that EB1 is a potential biomarker and therapeutic target in CRC. 相似文献
996.
Honma M Tanaka K Konno K Tsuge K Okuno T Hashimoto M 《Bioorganic & medicinal chemistry》2012,20(12):3793-3798
Plipastatin A1 and fengycin IX were experimentally proven to be identical compounds, while these had been considered as diastereomers due to the permutation of the enantiomeric pair of Tyr in most papers. The (1)H NMR spectrum changed to become quite similar to that of plipastatin A1, when the sample which provided resembled spectrum of fengycin IX was treated with KOAc followed by LH-20 gel filtration. Our structural investigations disclosed that the structures of these molecules should be settled into that of plipastatin A1 by Umezawa (L-Tyr4 and D-Tyr10). 相似文献
997.
Ichikawa M Ohtsuka M Ohki H Haginoya N Itoh M Sugita K Usui H Suzuki M Terayama K Kanda A 《Bioorganic & medicinal chemistry》2012,20(9):3072-3093
In the present article, we have reported the design, synthesis, and identification of highly potent benzhydrol derivatives as squalene synthase inhibitors (compound 1). Unfortunately, the in vivo efficacies of the compounds were not enough for acquiring the clinical candidate. We continued our investigation to obtain a more in vivo efficacious template than the benzhydrol template. In our effort, we focused on a benzoxazepine ring and designed a new tricyclic scaffold by the incorporation of heterocycle into it. Prepared pyrrolobenzoxazepine derivatives showed further efficient in vitro and in vivo activities. 相似文献
998.
Migration patterns of juvenile Lutjanus argentimaculatus in a mangrove estuary in Trang province, Thailand, as revealed by ultrasonic telemetry 总被引:1,自引:0,他引:1
Matiss Zagars Kou Ikejima Nobuaki Arai Hiromichi Mitamura Kotaro Ichikawa Takashi Yokota Prasert Tongnunui 《Environmental Biology of Fishes》2012,94(2):377-388
Migrational patterns of mangrove jack Lutjanus argentimaculatus were studied in a mangrove estuary in Trang province, Thailand, using ultrasonic telemetry. Ultrasonic coded transmitters
were surgically implanted in 18 fish and 16 of them were subsequently monitored by nine fixed receivers installed along Sikao
Creek estuary in June and November 2006. Due to technical limitations all of the individuals were released in the middle of
the creek. Their movements were monitored for a period of up to 1 month, the data being used to describe short term migration
of juvenile Lutjanus argentimaculatus in the creek and to find possible environmental cues for the observed movements. All of the individuals showed a tide related
movement pattern, suggesting foraging in the small mangrove channels and/or mangrove forest during high tides. 50% of the
fish left the study area for the open coast area within a short time following release, indicating that a part of juvenile
L. argentimaculatus may move in between estuarine habitats instead of being site attached. As the fish were reared in fish cages for a certain
period of time before the study this behavior could partly be explained by the time spent in captivity. It was found that
L. argentimaculatus showed higher movement activity during night high tides possibly explained by an increased availability of the sough after
food items. 相似文献
999.
1000.
Replication factor C (RFC) is a five-subunit complex that loads proliferating cell nuclear antigen (PCNA) clamps onto primer-template DNA (ptDNA) during replication. RFC subunits belong to the AAA(+) superfamily, and their ATPase activity drives interactions between the clamp loader, the clamp, and the ptDNA, leading to topologically linked PCNA·ptDNA. We report the kinetics of transient events in Saccharomyces cerevisiae RFC-catalyzed PCNA loading, including ATP-induced RFC activation, PCNA opening, ptDNA binding, ATP hydrolysis, PCNA closing, and PCNA·ptDNA release. This detailed perspective enables assessment of individual RFC-A, RFC-B, RFC-C, RFC-D, and RFC-E subunit functions in the reaction mechanism. Functions have been ascribed to RFC subunits previously based on a steady-state analysis of 'arginine-finger' ATPase mutants; however, pre-steady-state analysis provides a different view. The central subunit RFC-C serves as a critical swivel point in the clamp loader. ATP binding to this subunit initiates RFC activation, and the clamp loader adopts a spiral conformation that stabilizes PCNA in a corresponding open spiral. The importance of RFC subunit response to ATP binding decreases as RFC-C>RFC-D>RFC-B, with RFC-A being unnecessary. RFC-C-dependent activation of RFC also enables ptDNA binding, leading to the formation of the RFC·ATP·PCNA(open)·ptDNA complex. Subsequent ATP hydrolysis leads to complex dissociation, with RFC-D activity contributing the most to rapid ptDNA release. The pivotal role of the RFC-B/C/D subunit ATPase core in clamp loading is consistent with the similar central location of all three ATPase active subunits of the Escherichia coli clamp loader. 相似文献