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51.
间隔子和分株影响克隆植物的空间分布和资源获取,二者之间关系的研究有助于理解克隆植物的生态适应机制。按照恢复时间设置I(5a)、II(15a)、III(25a)3个梯度,研究了永昌北海子国家湿地公园沼泽湿地恢复演替过程中朝天委陵菜(Potentilla supina)间隔子长度、直径与分枝强度之间的关系。结果表明:随着沼泽湿地恢复演替的进行,湿地群落的高度、盖度和生物量逐渐增大,土壤含水量、有机质逐渐增大,土壤容重逐渐降低;湿地群落的优势植物种群由朝天委陵菜转为黑麦草;朝天委陵菜间隔子长度和直径增大,分株数减小;间隔子长度、直径与分枝强度均呈显著负相关关系(P<0.05)。沼泽湿地恢复演替过程中,朝天委陵菜由选择垄断区域资源转向逃避或忍耐不利生境,体现了湿地克隆植物在异质性生境中独特的适应性。 相似文献
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Xin Shen Mei Tian Xueping Meng Huilian Liu Hanliang Cheng Changbao Zhu Fangqing Zhao 《Comparative biochemistry and physiology. Part D, Genomics & proteomics》2012,7(3):248-253
Next-generation sequencing (NGS) has proven a valuable platform for fast and easy obtaining of large numbers of sequences at relatively low cost. In this study we use shot-gun sequencing method on Illumina HiSeq 2000, to obtain enough sequences for the assembly of the bryozoan Membranipora grandicella (Bryozoa: Cheilostomatida) mitochondrial genome, which is the first representative of the suborder Malacostegina. The complete mitochondrial genome is 15,861 bp in length, which is relatively larger than other studied bryozoans. The mitochondrial genome contains 13 protein-coding genes, 2 ribosomal RNAs and 20 transfer RNAs. To investigate the phylogenetic position and the inner relationships of the phylum Bryozoa, phylogenetic trees were constructed with amino acid sequences of 11 PCGs from 30 metazoans. Two superclades of protostomes, namely Lophotrochozoa and Ecdysozoa, are recovered as monophyletic with strong support in both ML and Bayesian analyses. Somewhat to surprise, Bryozoa appears as the sister group of Chaetognatha with moderate or high support. The relationship among five bryozoans is Tubulipora flabellaris + (M. grandicella + (Flustrellidra hispida + (Bugula neritina + Watersipora subtorquata))), which supports for the view that Cheilostomatida is not a natural, monophyletic clade. NGS proved to be a quick and easy method for sequencing a complete mitochondrial genome. 相似文献
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Xingyuan Shi Xueping Luo Ting Chen Wei Guo Chanjin Liang Sihan Tang Jianming Mo 《Journal of cellular and molecular medicine》2021,25(5):2563-2571
Lung cancer is one of the major cause for high-death rate all over the world, due to increased metastasize and difficulties in diagnosis. Naringenin is naturally occurring flavonoid found in various fruits including tomatoes, citrus fruit and figs. Naringenin is known to have several therapeutic effects including anti-atherogenic, antimicrobial, anti-inflammatory, hepatoprotective, anticancer and anti-mutagenic. The present study was aimed to analyse the naringenin induced anti-proliferative and apoptosis effects in human lung cancer cells. Cells were treated with various concentrations of naringenin (10, 100 & 200 µmol/L) for 48 hours. Cisplatin (20 µg/mL) was used as positive control. Cell viability, apoptosis, migration and mRNA, and protein expression of caspase-3, matrixmetallo proteinases-2 (MMP-2) and MMP-9 were determined. The cell viability was 93.7 ± 7.5, 51.4 ± 4.4 and 32.1 ± 2.1 at 10, 100 and 200 µmol/L of naringenin respectively. Naringenin significantly increased apoptotic cells. The 100 and 200 µmol/L of naringenin significantly suppressed the larger wounds of cultured human cancer cells compared with the untreated lung cancer cells. Naringenin increased d the expression of caspase-3 and reduced the expression of MMP-2 and MMP-9. Taking all these data together, it is suggested that the naringenin was effective against human lung cancer proliferation, migration and metastasis. 相似文献
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Fu M Rao M Bouras T Wang C Wu K Zhang X Li Z Yao TP Pestell RG 《The Journal of biological chemistry》2005,280(17):16934-16941
The cyclin D1 gene encodes the labile serum-inducible regulatory subunit of a holoenzyme that phosphorylates and inactivates the retinoblastoma protein. Overexpression of cyclin D1 promotes cellular proliferation and normal physiological levels of cyclin D1 function to inhibit adipocyte differentiation in vivo. We have previously shown that cyclin D1 inhibits peroxisome proliferator-activated receptor (PPAR)gamma-dependent activity through a cyclin-dependent kinase- and retinoblastoma protein-binding-independent mechanism. In this study, we determined the molecular mechanism by which cyclin D1 regulated PPARgamma function. Herein, murine embryonic fibroblast (MEF) differentiation by PPARgamma ligand was associated with a reduction in histone deacetylase (HDAC1) activity. Cyclin D1-/- MEFs showed an increased propensity to undergo differentiation into adipocytes. Genetic deletion of cyclin D1 reduced HDAC1 activity. Reconstitution of cyclin D1 into the cyclin D1-/- MEFs increased HDAC1 activity and blocked PPARgamma-mediated adipogenesis. PPARgamma activity was enhanced in cyclin D1-/- cells. Reintroduction of cyclin D1 inhibited basal and ligand-induced PPARgamma activity and enhanced HDAC repression of PPARgamma activity. Cyclin D1 bound HDAC in vivo and preferentially physically associated with HDAC1, HDAC2, HDAC3, and HDAC5. Chromatin immunoprecipitation assay demonstrated that cyclin D1 enhanced recruitment of HDAC1 and HDAC3 and histone methyltransferase SUV39H1 to the PPAR response element of the lipoprotein lipase promoter and decreased acetylation of total histone H3 and histone H3 lysine 9. Collectively, these studies suggest an important role of cyclin D1 in regulation of PPARgamma-mediated adipocyte differentiation through recruitment of HDACs to regulate PPAR response element local chromatin structure and PPARgamma function. 相似文献
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在干旱半干旱生态脆弱区,地下水是限制植物种类组成、数量和生长发育的关键因素之一。近年来由于气候变化与土地利用强度的增加,我国北方普遍出现以极端气候变化、地表水体萎缩和地下水位下降为特征的生态过程,对区域生态系统安全和可持续发展构成严重威胁。而有关干旱半干旱区地下水埋深变化驱动退化植被恢复和稳定性维持方面的系统研究尚存不足。系统总结了地下水埋深变化分别对植物、土壤产生的影响及其三者间相互作用关系,比较分析了前人的研究成果,归纳总结了地下水埋深变化的驱动作用和影响因素,以及干旱半干旱区地下水埋深变化对植物土壤系统影响的预测模型研究,以期为今后应对地下水埋深变化制定生态保护策略提供理论指导依据。对本研究做了展望。 相似文献
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Daw-Yang Hwang Stefan Kohl Xueping Fan Asaf Vivante Stefanie Chan Gabriel C. Dworschak Julian Schulz Albertien M. van Eerde Alina C. Hilger Heon Yung Gee Tracie Pennimpede Bernhard G. Herrmann Glenn van de Hoek Kirsten Y. Renkema Christoph Schell Tobias B. Huber Heiko M. Reutter Neveen A. Soliman Natasa Stajic Radovan Bogdanovic Elijah O. Kehinde Richard P. Lifton Velibor Tasic Weining Lu Friedhelm Hildebrandt 《Human genetics》2015,134(8):905-916