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991.
Atsushi Kurata Yuto Yamaura Takumi Tanaka Chiaki Kato Kaoru Nakasone Noriaki Kishimoto 《World journal of microbiology & biotechnology》2017,33(4):73
Aneurinibacillus: sp. YR247 was newly isolated from the deep-sea sediment inside the Calyptogena community at a depth of 1171 m in Sagami Bay. The strain exhibited antifungal activity against the filamentous fungus Aspergillus brasiliensis NBRC9455. A crude extract prepared from the YR247 cells by ethanol extraction exhibited broad antimicrobial activities. The antifungal compound is stable at 4–70?°C and pH 2.0–12.0. After treatment with proteinase K, the antifungal activity was not detected, indicating that the antifungal compound of strain YR247 is a peptidic compound. Electrospray ionization mass spectrometry of the purified antifungal compound indicated that the peptidic compound has an average molecular weight of 1167.9. The molecular weight of the antifungal compound from strain YR247 is different from those of antimicrobial peptides produced by the related Aneurinibacillus and Bacillus bacteria. The antifungal peptidic compound from the deep-sea bacterium Aneurinibacillus sp. YR247 may be useful as a biocontrol agent. 相似文献
992.
Kyoko Sugai Suzuki Setsuko Teruyoshi Nagamitsu Noriaki Murakami Hidetoshi Kato Hiroshi Yoshimaru 《Journal of plant research》2013,126(6):763-774
Gene flow between populations in different environmental conditions can be limited due to divergent natural selection, thus promoting genetic differentiation. Elaeocarpus photiniifolia, an endemic tree species in the Bonin Islands, is distributed in two types of habitats, dry scrubs and mesic forests. We aim to elucidate the genetic differentiation in E. photiniifolia within and between islands and between the habitat types. We investigated genotypes of 639 individuals from 19 populations of E. photiniifolia and its closely-related E. sylvestris at 24 microsatellite loci derived from expressed sequence tags. The data revealed genetic differentiation (1) between E. photiniifolia and E. sylvestris (0.307 ≤ F ST ≤ 0.470), (2) between the E. photiniifolia populations of the Chichijima and Hahajima Island Groups in the Bonin Islands (0.033 ≤ F ST ≤ 0.121) and (3) between E. photiniifolia populations associated with dry scrubs and mesic forests in the Chichijima Island Group (0.005 ≤ F ST ≤ 0.071). Principal coordinate analysis and Bayesian clustering analysis also showed that genetically distinct groups were associated with the habitat types, and isolation by distance was not responsible for the genetic differentiation. These findings suggest that E. photiniifolia is divided into genetically differentiated groups associated with different environmental conditions in the Bonin Islands. 相似文献
993.
Haruka Aoki Tamotsu Ishizuka Akihiro Ono Noriaki Sunaga Fumikazu Okajima Masatomo Mori 《Biochemical and biophysical research communications》2010,400(1):128-133
Resolvin E1 (RvE1) is an anti-inflammatory lipid mediator derived from the omega-3 fatty acid eicosapentaenoic acid (EPA), and strongly acts in the resolution of inflammation. We previously reported that RvE1 dampens airway inflammation and hyperresponsiveness in a murine model of asthma. In the present study, to elucidate the effects of RvE1 on the development of asthmatic airway inflammation, we investigated whether RvE1 acts on different phases of an OVA-sensitized and -challenged mouse model of asthma. RvE1 treatments at the time of either OVA sensitization or at the time of OVA challenge were investigated and compared with RvE1 treatments at the time of both OVA sensitization and challenge. After RvE1 was administered to mice intraperitoneally at the time of both OVA sensitization and challenge, there were decreases in airway eosinophil and lymphocyte recruitment, as well as a reduction in Th2 cytokine and airway hyperresponsiveness. RvE1 treatment at the time of either OVA sensitization or challenge also improved AHR and airway inflammation. Our results suggest that RvE1 acts on several phases of asthmatic inflammation and may have anti-inflammatory effects on various cell types. 相似文献
994.
Sasaki M Anast J Bassett W Kawakami T Sakuragi N Dahiya R 《Biochemical and biophysical research communications》2003,309(2):305-309
Methylation-specific PCR (MSP) is frequently used to distinguish methylated alleles in the genome. Sequences that have been incompletely converted during bisulfite treatment are frequently co-amplified during MSP. For accurate MSP, it is important to detect methylated sequences in a background of unconverted DNA with a high level of sensitivity. We report here sensitive techniques, bisulfite conversion-specific MSP (BS-MSP) to accurately evaluate CpG methylation. BS-MSP provides accurate results across a wide spectrum of bisulfite conversion levels. BS-MSP is also confirmed to be a useful technique for the routine analysis of clinical tumor specimens that were paraffin-embedded and microdissected. BS-MSP thus provides the powerful features of ease of use and compatibility with paraffin sections. We recommend that methylation analysis should include a step to eliminate unconverted DNA to avoid overestimation of the DNA methylation level in the samples. 相似文献
995.
996.
Tetsuya Niihori Meri Ouchi-Uchiyama Yoji Sasahara Takashi Kaneko Yoshiko Hashii Masahiro Irie Atsushi Sato Yuka Saito-Nanjo Ryo Funayama Takeshi Nagashima Shin-ichi Inoue Keiko Nakayama Keiichi Ozono Shigeo Kure Yoichi Matsubara Masue Imaizumi Yoko Aoki 《American journal of human genetics》2015,97(6):848-854
997.
Hitoki Yamanaka Tai Nakanishi Toshikazu Takagi Makiko Ohsawa Noriaki Kubo Naoto Yamamoto Takahira Takemoto Kazutaka Ohsawa 《Experimental Animals》2015,64(4):375-382
Helicobacter sp. MIT 01-6451 has been detected in SPF mice kept in
Japan. To characterize strain MIT 01-6451, its infection route during fetal and neonatal
life and effects on pregnancy were investigated using immunocompetent and immunodeficient
mouse strains (BALB/c, C57BL/6, and SCID). MIT 01-6451 was detected in the uterus, vagina,
and mammary glands of 50% of infected SCID mice, whereas these tissues were all negative
in immunocompetent mice. No fetal infections with MIT 01-6451 were detected at 16–18 days
after pregnancy in any mouse strain. In newborn mice, MIT 01-6451 was detected in
intestinal tissue of C57BL/6 and SCID mice at 9–11 days after birth, but not in BALB/c
mice. The IgA and IgG titers to MIT 01-6451 in sera of C57BL/6 female mice were
significantly lower than those of BALB/c mice. Although no significant differences in the
number of newborns per litter were observed between MIT 01-6451-infected and MIT
01-6451-free dams, the birth rate was lower in infected SCID mice than in control SCID
mice. The present results indicated that MIT 01-6451 infects newborn mice after birth
rather than by vertical transmission to the fetus via the placenta and that MIT 01-6451
infection shows opportunistically negative effects on the birth rate. In addition, the
maternal immune response may affect infection of newborn mice with MIT 01-6451 through
breast milk. 相似文献
998.
Ryanodine receptor (RyR) mutations linked with some congenital skeletal and cardiac diseases are localized to three easily definable regions: region 1 (N-terminal domain), region 2 (central domain), and a rather broad region 3 containing the channel pore. As shown in our recent studies, the interdomain interaction between regions 1 and 2 plays a critical role in channel regulation and pathogenesis. Here we present evidence that within region 3 there is a similar channel regulation mechanism mediated by an interdomain interaction. DP15, a peptide corresponding to RyR1 residues 4820-4841, produced significant activation of [3H]ryanodine binding above threshold Ca2+ concentrations (>or=0.3 microM), but MH mutations (L4823P or L4837V) made in DP15 almost completely abolished its channel activating function. To identify the DP15 binding site(s) within RyR1, DP15 (labeled with a fluorescent probe Alexa Fluor 680 and a photoaffinity cross-linker APG) was cross-linked to RyR1, and the site of cross-linking was identified by gel analysis of fluorescently labeled proteolytic fragments with the aid of Western blotting with site-specific antibodies. The shortest fluorescently labeled band was a 96 kDa fragment which was stained with an antibody directed to the region of residues 4114-4142 of RyR1, indicating that the interaction between the region of residues 4820-4841 adjacent to the channel pore and the 96 kDa segment containing the region of residues 4114-4142 is involved in the mechanism of Ca2+-dependent channel regulation. In further support of this concept, anti-DP15 antibody and cardiac counterpart of DP15 produced channel activation similar to that of DP15. 相似文献
999.
Sato F Imaizumi T Sashinami H Yoshida H Kusumi T Mori F Wakabayashi K Nakane A Satoh K Kijima H 《Biochemical and biophysical research communications》2007,354(2):608-612
We investigated the effect of heat-killed Listeria monocytogenes (HKLM) on the expression of vascular endothelial growth factor (VEGF) in RAW264.7 macrophage-like cells. The expression of VEGF was induced in RAW264.7 cells treated with HKLM. Pretreatment of cells with cycloheximide, a protein synthesis inhibitor, inhibited the induction of VEGF mRNA by HKLM. Induction of VEGF by HKLM was partially inhibited by treatment of cells with SB203580, a p38 mitogen-activated protein kinase (MAPK) inhibitor, or a neutralizing antibody against tumor necrosis factor-alpha (TNF-alpha). In addition, HKLM induced phosphorylation of p38 MAPK. These results suggest that p38 MAPK and TNF-alpha are involved in the VEGF expression induced by HKLM in RAW264.7 cells. We confirmed that increased VEGF expression is immunohistochemically detected in splenic macrophages of mice infected with L. monocytogenes (L. monocytogenes). VEGF is thought to be involved in inflammatory reactions induced by L. monocytogenes infection. 相似文献
1000.