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951.
Yok-Ai Que Ronen Hazan Benjamin Strobel Damien Maura Jianxin He Meenu Kesarwani Panagiotis Panopoulos Amy Tsurumi Marlyse Giddey Julie Wilhelmy Michael N. Mindrinos Laurence G. Rahme 《PloS one》2013,8(12)
Bacteria can be refractory to antibiotics due to a sub-population of dormant cells, called persisters that are highly tolerant to antibiotic exposure. The low frequency and transience of the antibiotic tolerant “persister” trait has complicated elucidation of the mechanism that controls antibiotic tolerance. In this study, we show that 2’ Amino-acetophenone (2-AA), a poorly studied but diagnostically important small, volatile molecule produced by the recalcitrant gram-negative human pathogen Pseudomonas aeruginosa, promotes antibiotic tolerance in response to quorum-sensing (QS) signaling. Our results show that 2-AA mediated persister cell accumulation occurs via alteration of the expression of genes involved in the translational capacity of the cell, including almost all ribosomal protein genes and other translation-related factors. That 2-AA promotes persisters formation also in other emerging multi-drug resistant pathogens, including the non 2-AA producer Acinetobacter baumannii implies that 2-AA may play an important role in the ability of gram-negative bacteria to tolerate antibiotic treatments in polymicrobial infections. Given that the synthesis, excretion and uptake of QS small molecules is a common hallmark of prokaryotes, together with the fact that the translational machinery is highly conserved, we posit that modulation of the translational capacity of the cell via QS molecules, may be a general, widely distributed mechanism that promotes antibiotic tolerance among prokaryotes. 相似文献
952.
Jianxin Hu Kelly Hu Tong Liu Matthew K. Stern Rajendra Mistry R. A. John Challiss Stefano Costanzi Jürgen Wess 《The Journal of biological chemistry》2013,288(48):34777-34790
Class A G protein-coupled receptors (GPCRs) are able to form homodimers and/or oligomeric arrays. We recently proposed, based on bioluminescence resonance energy transfer studies with the M3 muscarinic receptor (M3R), a prototypic class A GPCR, that the M3R is able to form multiple, structurally distinct dimers that are probably transient in nature (McMillin, S. M., Heusel, M., Liu, T., Costanzi, S., and Wess, J. (2011) J. Biol. Chem. 286, 28584–28598). To provide more direct experimental support for this concept, we employed a disulfide cross-linking strategy to trap various M3R dimeric species present in a native lipid environment (transfected COS-7 cells). Disulfide cross-linking studies were carried out with many mutant M3Rs containing single cysteine (Cys) substitutions within two distinct cytoplasmic M3R regions, the C-terminal portion of the second intracellular loop (i2) and helix H8 (H8). The pattern of cross-links that we obtained, in combination with molecular modeling studies, was consistent with the existence of two structurally distinct M3R dimer interfaces, one involving i2/i2 contacts (TM4-TM5-i2 interface) and the other one characterized by H8-H8 interactions (TM1-TM2-H8 interface). Specific H8-H8 disulfide cross-links led to significant impairments in M3R-mediated G protein activation, suggesting that changes in the structural orientation or mobility of H8 are critical for efficient receptor-G protein coupling. Our findings provide novel structural and functional insights into the mechanisms involved in M3R dimerization (oligomerization). Because the M3R shows a high degree of sequence similarity with many other class A GPCRs, our findings should be of considerable general interest. 相似文献
953.
Nelson L. S. Chan Jinzhen Guo Tianyi Zhang Guogen Mao Caixia Hou Fenghua Yuan Jian Huang Yanbin Zhang Jianxin Wu Liya Gu Guo-Min Li 《The Journal of biological chemistry》2013,288(21):15015-15022
Expansion of CAG/CTG trinucleotide repeats causes certain familial neurological disorders. Hairpin formation in the nascent strand during DNA synthesis is considered a major path for CAG/CTG repeat expansion. However, the underlying mechanism is unclear. We show here that removal or retention of a nascent strand hairpin during DNA synthesis depends on hairpin structures and types of DNA polymerases. Polymerase (pol) δ alone removes the 3′-slipped hairpin using its 3′-5′ proofreading activity when the hairpin contains no immediate 3′ complementary sequences. However, in the presence of pol β, pol δ preferentially facilitates hairpin retention regardless of hairpin structures. In this reaction, pol β incorporates several nucleotides to the hairpin 3′-end, which serves as an effective primer for the continuous DNA synthesis by pol δ, thereby leading to hairpin retention and repeat expansion. These findings strongly suggest that coordinated processing of 3′-slipped (CAG)n/(CTG)n hairpins by polymerases δ and β on during DNA synthesis induces CAG/CTG repeat expansions. 相似文献
954.
955.
Jing Li Xin Wang Jason Diaz Sabrina H. Tsang Christopher B. Buck Jianxin You 《Journal of virology》2013,87(16):9173-9188
Clonal integration of Merkel cell polyomavirus (MCV) DNA into the host genome has been observed in at least 80% of Merkel cell carcinoma (MCC). The integrated viral genome typically carries mutations that truncate the C-terminal DNA binding and helicase domains of the MCV large T antigen (LT), suggesting a selective pressure to remove this MCV LT region during tumor development. In this study, we show that MCV infection leads to the activation of host DNA damage responses (DDR). This activity was mapped to the C-terminal helicase-containing region of the MCV LT. The MCV LT-activated DNA damage kinases, in turn, led to enhanced p53 phosphorylation, upregulation of p53 downstream target genes, and cell cycle arrest. Compared to the N-terminal MCV LT fragment that is usually preserved in mutants isolated from MCC tumors, full-length MCV LT shows a decreased potential to support cellular proliferation, focus formation, and anchorage-independent cell growth. These apparently antitumorigenic effects can be reversed by a dominant-negative p53 inhibitor. Our results demonstrate that MCV LT-induced DDR activates p53 pathway, leading to the inhibition of cellular proliferation. This study reveals a key difference between MCV LT and simian vacuolating virus 40 LT, which activates a DDR but inhibits p53 function. This study also explains, in part, why truncation mutations that remove the MCV LT C-terminal region are necessary for the oncogenic progression of MCV-associated cancers. 相似文献
956.
Yongchen Hao Xuehui Liu Xiangfeng Lu Xueli Yang Laiyuan Wang Shufeng Chen Hongfan Li Jianxin Li Jie Cao Jichun Chen Ying Li Liancheng Zhao Yongyong Shi Chong Shen Weili Yan Jiang He Jianfeng Huang Dongfeng Gu 《Human genetics》2013,132(6):681-689
Human height is a complex genetic trait with high heritability but discovery efforts in Asian populations are limited. We carried out a meta-analysis of genome-wide association studies (GWAS) for height in 6,534 subjects with in silico replication of 1,881 subjects in Han Chinese. We identified three novel loci reaching the genome-wide significance threshold (P < 5 × 10?8), which mapped in or near ZNF638 (rs12612930, P = 2.02 × 10?10), MAML2 (rs11021504, P = 7.81 × 10?9), and C18orf12 (rs11082671, P = 1.87 × 10?8). We also confirmed two loci previously reported in European populations including CS (rs3816804, P = 2.63 × 10?9) and CYP19A1 (rs3751599, P = 4.80 × 10?10). In addition, we provided evidence supporting 35 SNPs identified by previous GWAS (P < 0.05). Our study provides new insights into the genetic determination of biological regulation of human height. 相似文献
957.
John M. Fevig Jianxin Feng Karen A. Rossi Keith J. Miller Ginger Wu Chen-Pin Hung Thao Ung Sarah E. Malmstrom Ge Zhang William J. Keim Mary Jane Cullen Kenneth W. Rohrbach Qinling Qu Jinping Gan Mary Ann Pelleymounter Jeffrey A. Robl 《Bioorganic & medicinal chemistry letters》2013,23(1):330-335
A series of 2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-ones is described, several examples of which exhibit potent 5-HT2C agonism with excellent selectivity over the closely related 5-HT2A and 5-HT2B receptors. Compounds such as 38 and 44 were shown to be effective in reducing food intake in an acute rat feeding model. 相似文献
958.
目的分析广西地区近8年2型糖尿病患者的住院费用情况。方法收集广西医科大学第一附属医院2004年4月~2011年12月出院的2型糖尿病患者的病案资料,按有无并发症分为无并发症组2050例,有并发症组4795例,用两样本比较的秩和检验比较两组住院费用的差异。按并发症个数将有并发症组分为3个亚组,即B组(1个并发症组2478例)、C组(2个并发症1444例)、D组(3个及3个以上并发症组873例),用多个样本比较Kruskal-Wallis H检验,组间比较用扩增t检验。按有无大血管病变将患者分为2型糖尿病无大血管病变组5711例,2型糖尿病并大血管病变组1134例,采用秩和检验比较两组住院费用的差异。结果 2型糖尿病患者中位住院费用为7009.55元;无并发症组的中位住院费用为5702.2元,有并发症组的中位住院费用为7726.65元;1个并发症组中位住院费用为6999.89元,2个并发症组的中位住院费用为8060.78元,3个及3个以上并发症组中位住院费用为10396.24元;2型糖尿病无大血管病变中位住院费用为6525.84元,2型糖尿病并大血管病变中位住院费用为11215.13元。结论有并发症较无并发症住院费用更高,有大血管病变较无大血管病变的2型糖尿病费用更高,并发症个数越多,费用越高。 相似文献
959.
通过对山羊臭虎耳草6个花形态及其发育阶段、授粉过程的连续观察和对花粉活性、柱头可授性的连续检测,报道了一种新的延迟自动自花授粉机制,即山羊臭虎耳草花丝运动引导的延迟自动自花授粉。利用电子显微镜研究了花粉囊的破裂方式和柱头结构,同时利用苏丹Ⅲ研究了花粉的组织化学性质。结果显示:(1)第四生长阶段,当花丝引导大部分花粉囊运动至柱头上方时,花粉和柱头的可授性才均达到峰值[可授性分别为(94±6)%和(96±13)%],这种运动消除了第三生长阶段花粉活性较高[(90±8)%]而柱头可授性较低[(6±17)%]的异花授粉特征,即消除了花粉与柱头的时空隔离;自动自花授粉发生于异花授粉特征消除之后,因此山羊臭虎耳草具有典型的延迟自动自交行为。(2)第四发育阶段柱头空腔的大量柱状突起和花粉鞘的油脂性特征,增加了花粉和柱头的接触表面,并且使花粉更好地互相堆积粘附在柱头上,提高授粉效率。(3)对山羊臭虎耳草的繁育系统研究表明,强制自花授粉和人工自花授粉产种量无明显差异,2007年和2008年的自交系数高达0.92和0.91,说明山羊臭虎耳草具有很好的自交能力并且不存在花粉数量限制;人工异花授粉的产种率显著高于人工自花授粉,说明自花花粉的质量显著低于异花花粉,虎耳草延迟自动自花授粉存在生殖衰退,生殖保障系数2007年为0.92,2008年为0.91,表明在极端环境下自动自花授粉为该植物提供了繁殖保障,但极端环境下,没有观察到有效的授粉昆虫。研究表明,作为高山冰缘植物的山羊臭虎耳草,保留了开花植物异花授粉的特征,在极端环境下利用延迟自动自花授粉机制完成授粉,保障生殖。 相似文献
960.
11 kDa蛋白作为B19病毒的一个非结构蛋白,可能在病毒复制周期中发挥重要作用。为了研究11 kDa蛋白对细胞内NF-κB信号通路的影响,首先通过原核表达纯化获得GST-11 kDa融合蛋白,并制备免疫血清,利用免疫血清验证了11 kDa蛋白在Hela细胞呈胞浆定位。荧光素酶检测系统发现11 kDa蛋白能上调细胞内NF-κB转录活性,Western blotting进一步表明11 kDa蛋白能够引起细胞内IκB-α的降解。同时,11 kDa蛋白还能够上调细胞内炎性因子IL6启动子的活性,而该反应主要依赖于NF-κB通路。结果表明,11 kDa蛋白通过参与细胞内信号途径激活相关炎性因子的表达。 相似文献