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1.
胶原/壳聚糖复合膜的制备及止血效果的研究 总被引:5,自引:1,他引:5
目的 以胶原和壳聚糖制备复合膜,检验其止血效果,并探讨其止血原因。材料与方法:以酸解法从牛腱中提取胶原,用甲壳素制得壳聚糖,以胶原和壳聚制成复合膜,通过动物实验测不同配比的复合膜对出血创面的止血时间,并与其它止血材料做对比。结果:各种配比的复合膜的止血效果均比明胶等一般止血材料好。结论:胶原/壳聚糖复合膜有良好的止血作用,可望在外科手术上得到广泛应用。 相似文献
2.
Comparative study of symmetric and asymmetric somatic hybridization between common wheat and Haynaldia villosa 总被引:1,自引:0,他引:1
Symmetric and asymmetric protoplast fusion between long term cell suspension-derived protoplasts of Triticum aestivum (cv. Jinan 177) and protoplasts of Haynaldia villosa prepared from one-year-old embryogeneric calli was performed by PEG method. In asymmetric fusion, donor calli were treated with gamma ray at a dose of 40, 60, 80 Gy (1.3 Gy/min) respectively and then used to isolate protoplasts. Results of morphological, cytological, biochemical (isozyme) and 5S rDNA spacer sequence analysis revealed that we obtained somatic hybrid lines at high frequency from both symmetric and asymmetric fusion. Hybrid plants were recovered from symmetric and low dose γ-fusion combinations. GISH (genomic in situ hybridization) analysis proved exactly the existence of both parental chromosomes and the common occurrence of several kinds of translocation between them in the hybrid clones regenerated from symmetric and asymmetric fusion. And the elimination of donor DNA in hybrid clones regenerated from asymmetric fusion 相似文献
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[目的] 探究青藏高原不同地区高寒草原紫花针茅根际和体内真菌群落的组成、多样性等特征,及与土壤环境因子(理化性质和酶活性)间的相互关系。[方法] 从青藏高原不同地区采集紫花针茅样品,应用土壤化学方法分析根际土壤理化性质和酶活性,并采用Illumina Miseq高通量测序技术,解析根际土壤和体内真菌群落组成和丰度、Alpha多样性和菌群结构,同时分析了紫花针茅根际真菌种群多样性与土壤环境因子的相关性,厘清了影响紫花针茅根际真菌区系的土壤环境因素。[结果] 三个采样地的根际土壤呈中性偏碱,土壤理化性质和酶活性变化各异。高通量测序共得到314801条有效序列和4491个OTUs;XZ样地的紫花针茅真菌多样性和丰富度相对偏低,GS样地最高。在门分类水平上,子囊菌门Ascomycota和担子菌门Basidiomycota是主要内生真菌类群,占总菌群的88.28%。不同采样地区紫花针茅体内真菌群落结构存在明显差异,而根际土壤真菌群落结构差异不大。相关性分析表明,紫花针茅真菌多样性与土壤pH、有效钾、铁、钙、镁、多酚氧化酶、过氧化物酶和脱氢酶呈显著(P<0.05)或极显著(P<0.01)正相关,而与海拔、土壤酸性磷酸酶呈极显著负相关。RDA分析发现,紫花针茅根际土壤真菌不同,影响的土壤环境因子也不同。[结论] 青藏高原高寒草地紫花针茅根际和体内栖息着丰富的真菌群落,其组成和多样性受多种土壤环境因子影响,且影响不同真菌群落的主要土壤环境因子也不同。本研究对于有益微生物资源的开发、利用及保护具有重要意义,并为紫花针茅草原保育和合理开发利用提供科学依据。 相似文献
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再论假裸枝叠层石科* 总被引:4,自引:1,他引:4
内蒙古桌子山地区中奥陶统公乌素组遗迹化石十分丰富.本文共鉴定、描述14个遗迹属、17个遗迹种,其中1新遗迹属——Biscopulatichnus、4新遗种和6未定种.并根据不同遗迹属在不同层位中的相对丰度,建立了4个遗迹组合,自下而上的顺序是:1. Taenidium-Phycodes 组合;2. Volkichnium 组合;3. Helminthopsis 组合;4. Granularia-Circulichnus 组合,大致相当于 Seilacher (1967) 的 Zoophycos 遗迹相,反映出公乌素组沉积期,水体较深且宁静、缺氧、有机质含量高,推测应为大陆斜坡环境. 相似文献
6.
Xinqing Ye Jinan Guo Hongxiang Zhang Qinggui Meng Yun Ma Rui Lin Xianlin Yi Haoyuan Lu Xianzhong Bai Jiwen Cheng 《Journal of cellular biochemistry》2019,120(8):13841-13852
Estrogen-related receptor α (ERRα) belongs to the superfamily of nuclear orphan receptors. However, the role of ERRα in bladder cancer remains unknown. This study examined the expression of ERRα in bladder cancer tissues and explored the molecular mechanisms of ERRα in bladder cancer progression. The expression of ERRα in bladder cancer tissues from 61 patients was determined by immunohistochemistry. We performed quantitative real-time polymerase chain reaction assay to detect the gene expression levels and carried out Western blot assay to measure protein levels. In vitro functional assays, including colony formation, Cell Counting Kit-8, Transwell invasion, and migration assays, were performed to detect bladder cancer cell growth, proliferation, invasion, and migration, respectively. Flow cytometry was used to determine the cell apoptotic rate of bladder cancer cells. Among the 61 detected bladder cancer tissues, 39 bladder cancer tissues showed positive ERRα immunoreactivity. Higher ERRα immunoreactivity score was significantly associated with TNM stage, tumor grade, distant metastasis, and poor survival in patients with bladder cancer. Univariate and multivariate analyses showed that ERRα immunoreactivity was an independent prognostic factor for overall survival in patients with bladder cancer. ERRα was found to be upregulated in bladder cancer cell lines, and knockdown of ERRα suppressed bladder cancer cell growth, proliferation, invasion, and migration; promoted bladder cancer cell apoptosis; and inhibited the epithelial-mesenchymal transition of bladder cancer cells. On the other hand, bladder cancer cell proliferation, invasion, and migration were significantly enhanced after cells were transfected with an ERRα-overexpressing vector. In vivo tumor growth and metastasis assays showed that ERRα knockdown resulted in remarkable inhibition of tumor growth and tumor metastasis in nude mice. Collectively, our results suggest that the enhanced expression of ERRα may play a key role in the development and progression of bladder cancer and ERRα may serve as an important prognostic factor for bladder cancer. 相似文献
7.
Estimation of Cellobiohydrolase I Activity by Numerical Differentiation of Dynamic Ultraviolet Spectroscopy 总被引:1,自引:0,他引:1
Bin WU Yue ZHAO Pei-Ji GAO The State Key Laboratory of Microbial Technology Shandong University Jinan China 《Acta biochimica et biophysica Sinica》2006,(6)
1,4-β-D-glucan cellobiohydrolase I (CBH I),p-nitrophenyl β-D-cellobioside,p-nitrophenol andcellobiose show distinct ultraviolet spectra,allowing the design of an assay to track the dynamic process ofp-nitrophenyl β-D-cellobioside hydrolysis by CBH I.Based on the linear relationship between p-nitrophenolformation in the hydrolysate and its first derivative absorption Curve of AUC340_400_(nm)(area under the curve),a new sensitive assay for the determination of CBH I activity was developed.The dynamic parameters ofcatalysis reaction,such as Vm and k_(cat),can all be derived from this result.The influence of β-glucosidase andendoglucanase in crude enzyme sample on the assay was discussed in detail.This approach is useful foraccurate determination of the activity of CBHs. 相似文献
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Wang S Wang Z Lin S Zheng W Wang R Jin S Chen J Jin L Li Y 《The Biochemical journal》2012,446(1):79-87
Retinoids display anti-tumour activity on various cancer cells and therefore have been used as important therapeutic agents. However, adverse side effects and RA (retinoic acid) resistance limit further development and clinical application of retinoid-based therapeutic agents. We report in the present paper the identification of a natural marine product that activates RARs (RA receptors) with a chemical structure distinct from retinoids by high-throughput compound library screening. Luffariellolide was uncovered as a novel RAR agonist by inducing co-activator binding to these receptors in vitro, further inhibiting cell growth and regulating RAR target genes in various cancer cells. Structural and molecular studies unravelled a unique binding mode of this natural ligand to RARs with an unexpected covalent modification on the RAR. Functional characterization further revealed that luffariellolide displays chemotherapeutic potentials for overcoming RA resistance in colon cancer cells, suggesting that luffariellolide may represent a unique template for designing novel non-retinoid compounds with advantages over current RA drugs. 相似文献
10.
Zhang H Li J Barrington RA Liang G Qin G Liu DX 《Biochemical and biophysical research communications》2007,359(2):285-291
C1 inhibitor (C1INH), a complement regulatory protein, prevents endotoxin shock via a direct interaction of the amino-terminal domain with gram-negative bacterial lipopolysaccharide (LPS). Importantly, the cleaved, inactive C1INH still is an anti-endotoxin effector indicating the anti-endotoxin peptide that generates from the amino-terminal domain of C1INH. In this study, we first identified that a cleaved fragment within the major part of the amino-terminal domain in in vitro proteolytic analysis of C1INH had an ability to bind to LPS. We synthesized several peptides overlapping the C1INH cleaved fragment. Among these synthetic peptides, a 13-mer derivative peptide at position from 18 to 30, named N2((18-30)), exhibited the most powerful anti-endotoxin activity in vitro, enlightening that it was most strong at binding to LPS, inhibiting the interaction of LPS with LPS-binding protein (LBP), blocking LPS binding to CD14(+) cells, and suppressing production of tumor necrosis factor (TNF)-alpha by murine macrophages, RAW 264.7. In the murine endotoxin shock model, the peptide N2((18-30)) protected mice from LPS-induced lethal septic shock by inhibiting macrophage activation. These data indicate that the peptide N2((18-30)) derived from the amino-terminal region of C1INH is anti-endotoxin. 相似文献