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1.
Phenylephrine enhances glutamate release in the medial prefrontal cortex through interaction with N‐type Ca2+ channels and release machinery 下载免费PDF全文
Fei Luo Si‐hai Li Hua Tang Wei‐ke Deng Yu Zhang Ying Liu 《Journal of neurochemistry》2015,132(1):38-50
α1‐adrenoceptors (α1‐ARs) stimulation has been found to enhance excitatory processes in many brain regions. A recent study in our laboratory showed that α1‐ARs stimulation enhances glutamatergic transmission via both pre‐ and post‐synaptic mechanisms in layer V/VI pyramidal cells of the rat medial prefrontal cortex (mPFC). However, a number of pre‐synaptic mechanisms may contribute to α1‐ARs‐induced enhancement of glutamate release. In this study, we blocked the possible post‐synaptic action mediated by α1‐ARs to investigate how α1‐ARs activation regulates pre‐synaptic glutamate release in layer V/VI pyramidal neurons of mPFC. We found that the α1‐ARs agonist phenylephrine (Phe) induced a significant enhancement of glutamatergic transmission. The Phe‐induced potentiation was mediated by enhancing pre‐synaptic glutamate release probability and increasing the number of release vesicles via a protein kinase C‐dependent pathway. The mechanisms of Phe‐induced potentiation included interaction with both glutamate release machinery and N‐type Ca2+ channels, probably via a pre‐synaptic Gq/phospholipase C/protein kinase C pathway. Our results may provide a cellular and molecular mechanism that helps explain α1‐ARs‐mediated influence on PFC cognitive functions.
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Young Rae Ji Hei Jung Kim Dong Hun Yu Ki Beom Bae Seo Jin Park Si Jun Park Woo Young Jang Min-Cheol Kang Jain Jeong Yong Hun Sung Minjee Choi Taejun Park Taesun Park Jong Won Yun Hyun-Shik Lee Sanggyu Lee Myoung Ok Kim Zae Young Ryoo 《Biochemical and biophysical research communications》2014
Chronic hepatitis is a major cause of liver cancer, so earlier treatment of hepatitis might be reducing liver cancer incidence. Hepatitis can be induced in mice by treatment with Concanavalin A (Con A); the resulting liver injury causes significant CD4+ T cell activation and infiltration. In these T cells, Roquin, a ring-type E3 ubiquitin ligase, is activated. To investigate the role of Roquin, we examined Con A-induced liver injury and T cell infiltration in transgenic (Tg) mice overexpressing Roquin specifically in T cells. In Roquin Tg mice, Con A treatment caused greater increases in both the levels of liver injury enzymes and liver tissue apoptosis, as revealed by TUNEL and H&E staining, than wild type (WT) mice. Further, Roquin Tg mice respond to Con A treatment with greater increases in the T cell population, particularly Th17 cells, though Treg cell counts are lower. Roquin overexpression also enhances increases in pro-inflammatory cytokines, including IFN-γ, TNF-α and IL-6, upon liver injury. Furthermore, Roquin regulates the immune response and apoptosis in Con A induced hepatitis via STATs, Bax and Bcl2. These findings suggest that over-expression of Roquin exacerbates T-cell mediated hepatitis. 相似文献
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The insulin receptor (IR) binds insulin and plays important roles in glucose homeostasis by regulating the tyrosine kinase activity at its C-terminus. Its transmembrane domain (TMD) is shown to be important for transferring conformational changes induced by insulin across the cell membrane to regulate kinase activity. In this study, a construct IR940–988 containing the TMD was expressed and purified for structural studies. Its solution structure in dodecylphosphocholine (DPC) micelles was determined. The sequence containing residues L962 to Y976 of the TMD of the IR in micelles adopts a well-defined helical structure with a kink formed by glycine and proline residues present at its N-terminus, which might be important for its function. Paramagnetic relaxation enhancement (PRE) and relaxation experimental results suggest that residues following the TMD are flexible and expose to aqueous solution. Although purified IR940–988 in micelles existed mainly as a monomeric form verified by gel filtration and relaxation analysis, cross-linking study suggests that it may form a dimer or oligomers under micelle conditions. 相似文献
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Zhaowei Teng Yun Zhu Feihu Wu Yanhong Zhu Xiguang Zhang Chuanlin Zhang Shuangneng Wang Lei Zhang 《PloS one》2015,10(6)
Objective
To evaluate the association between chronic opioid use for non-cancer pain and fracture risk by conducting a meta-analysis of cohort studies.Methods
Cohort studies were identified by searching PubMed and EMBASE from their inception to July 2014. A fracture was considered an endpoint. The information was extracted by two authors independently. When the heterogeneity was significant, a random-effects model was used to calculate the overall pooled risk estimates.Results
Eight cohort studies were included in the final meta-analysis. On the basis of the Newcastle-Ottawa Scale (NOS), six studies were considered to be of high quality. The overall combined relative risk for the use of opioids and fractures was 1.88 (95% confidence interval [CI] 1.51-2.34). A subgroup analysis revealed the sources of heterogeneity. The sensitivity analysis indicated stable results, and no publication bias was observed.Conclusions
This meta-analysis of cohort studies demonstrates that opioids significantly increase the risk of fractures. 相似文献8.
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经口激光显微手术(transoral laser microsurgery,TLM)应用于声门型喉癌(glottic carcinoma,GC)具有显著的优越性:安全有效,局部复发率低,喉保留率高,实现了GC的微创治疗。大量的研究表明TLM应用于早期GC的疗效与放射治疗和喉裂开术相似。因其不但损伤更小,更加精确,而且患者术后生活质量更好,为早期GC的首选治疗方式。目前将TLM推广应用到中晚期GC、前联合喉癌以及挽救放疗或TLM后早期复发性GC的治疗中,可能为有效保留喉部功能的治疗方式,但是国内相关的文献报道较少,较多的报道了开放性手术仍是GC主要的治疗方式。因此,本文就TLM治疗GC的现状、手术疗效、优越性、应用前景等方面做一综述,进一步研究及认识TLM对GC的治疗有非常重要的临床应用价值。 相似文献
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Genome‐wide analysis identifies an african‐specific variant in SEMA4D associated with body mass index 下载免费PDF全文
Jie Zhou Lin Lei Amy R. Bentley Fasil Tekola-Ayele Sally N. Adebamowo Jennifer L. Baker Olufemi Fasanmade Godfrey Okafor Benjamin Eghan Jr. Kofi Agyenim‐Boateng Albert Amoah Clement Adebamowo Joseph Acheampong Thomas Johnson Johnnie Oli Daniel Shriner Adebowale A. Adeyemo Charles N. Rotimi 《Obesity (Silver Spring, Md.)》2017,25(4):794-800