首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   9094篇
  免费   697篇
  国内免费   758篇
  2024年   15篇
  2023年   108篇
  2022年   254篇
  2021年   499篇
  2020年   307篇
  2019年   439篇
  2018年   401篇
  2017年   251篇
  2016年   427篇
  2015年   589篇
  2014年   698篇
  2013年   786篇
  2012年   885篇
  2011年   764篇
  2010年   436篇
  2009年   432篇
  2008年   454篇
  2007年   396篇
  2006年   357篇
  2005年   257篇
  2004年   248篇
  2003年   202篇
  2002年   149篇
  2001年   133篇
  2000年   121篇
  1999年   102篇
  1998年   101篇
  1997年   91篇
  1996年   83篇
  1995年   71篇
  1994年   64篇
  1993年   46篇
  1992年   78篇
  1991年   47篇
  1990年   33篇
  1989年   37篇
  1988年   22篇
  1987年   25篇
  1986年   25篇
  1985年   24篇
  1984年   11篇
  1983年   9篇
  1982年   10篇
  1981年   6篇
  1980年   5篇
  1979年   9篇
  1976年   4篇
  1973年   5篇
  1971年   4篇
  1968年   6篇
排序方式: 共有10000条查询结果,搜索用时 46 毫秒
141.
142.
IsoBAs, stereoisomers of primary and secondary BAs, are found in feces and plasma of human individuals. BA signaling via the nuclear receptor FXR is crucial for regulation of hepatic and intestinal physiology/pathophysiology. Aim: Investigate the ability of BA-stereoisomers to bind and modulate FXR under physiological/pathological conditions. Methods: Expression-profiling, luciferase-assays, fluorescence-based coactivator-association assays, administration of (iso)-BAs to WT and cholestatic mice. Results: Compared to CDCA/isoCDCA, administration of DCA/isoDCA, UDCA/isoUDCA only slightly increased mRNA expression of FXR target genes; the induction was more evident looking at pre-mRNAs. Notably, almost 50% of isoBAs were metabolized to 3-oxo-BAs within 4 h in cell-based assays, making it difficult to study their actions. FRET-based real-time monitoring of FXR activity revealed that isoCDCA>CDCA stimulated FXR, and isoDCA and isoUDCA allowed fully activated FXR to be re-stimulated by a second dose of GW4064. In vivo co-administration of a single dose of isoBAs followed by GW4064 cooperatively activated FXR, as did feeding of UDCA in a background of endogenous FXR ligands. However, in animals with biliary obstruction and concomitant loss of intestinal BAs, UDCA was unable to increase intestinal Fgf15. In contrast, mice with an impaired enterohepatic circulation of BAs (Asbt?/?, Ostα?/?), administration of UDCA was still able to induce ileal Fgf15 and repress hepatic BA-synthesis, arguing that UDCA is only effective in the presence of endogenous FXR ligands. Conclusion: Secondary (iso)BAs cooperatively activate FXR in the presence of endogenous BAs, which is important to consider in diseases linked to disturbances in BA enterohepatic cycling.  相似文献   
143.
Pathogens secrete a large number of effectors that manipulate host processes to create an environment conducive to pathogen colonization. However, the underlying mechanisms by which Plasmopara viticola effectors manipulate host plant cells remain largely unclear. In this study, we reported that RXLR31154, a P. viticola RXLR effector, was highly expressed during the early stages of P. viticola infection. In our study, stable expression of RXLR31154 in grapevine (Vitis vinifera) and Nicotiana benthamiana promoted leaf colonization by P. viticola and Phytophthora capsici, respectively. By yeast two-hybrid screening, the 23-kDa oxygen-evolving enhancer 2 (VpOEE2 or VpPsbP), encoded by the PsbP gene, in Vitis piasezkii accession Liuba-8 was identified as a host target of RXLR31154. Overexpression of VpPsbP enhanced susceptibility to P. viticola in grapevine and P. capsici in N. benthamiana, and silencing of NbPsbPs, the homologs of PsbP in N. benthamiana, reduced P. capcisi colonization, indicating that PsbP is a susceptibility factor. RXLR31154 and VpPsbP protein were co-localized in the chloroplast. Moreover, VpPsbP reduced H2O2 accumulation and activated the 1O2 signaling pathway in grapevine. RXLR31154 could stabilize PsbP. Together, our data revealed that RXLR31154 reduces H2O2 accumulation and activates the 1O2 signaling pathway through stabilizing PsbP, thereby promoting disease.  相似文献   
144.
145.
Protein engineering through directed evolution is an effective way to obtain proteins with novel functions with the potential applications as tools for diagnosis or therapeutics. Many natural proteins have undergone directed evolution in vitro in the test tubes in the laboratories worldwide, resulting in the numerous protein variants with novel or enhanced functions. we constructed here an SH2 variant library by randomizing 8 variable residues in its phosphotyrosine (pTyr) binding pocket. Selection of this library by a pTyr peptide led to the identification of SH2 variants with enhanced affinities measured by EC50. Fluorescent polarization was then applied to quantify the binding affinities of the newly identified SH2 variants. As a result, three SH2 variants, named V3, V13 and V24, have comparable binding affinities with the previously identified SH2 triple‐mutant superbinder. Biolayer Interferometry assay was employed to disclose the kinetics of the binding of these SH2 superbinders to the phosphotyrosine peptide. The results indicated that all the SH2 superbinders have two‐orders increase of the dissociation rate when binding the pTyr peptide while there was no significant change in their associate rates. Intriguingly, though binding the pTyr peptide with comparable affinity with other SH2 superbinders, the V3 does not bind to the sTyr peptide. However, variant V13 and V24 have cross‐reactivity with both pTyr and sTyr peptides. The newly identified superbinders could be utilized as tools for the identification of pTyr‐containing proteins from tissues under different physiological or pathophysiological conditions and may have the potential in the therapeutics.  相似文献   
146.
Paek  Hyo-Jin  Luo  Zhao-Bo  Choe  Hak-Myong  Quan  Biao-Hu  Gao  Kai  Han  Sheng-Zhong  Li  Zhou-Yan  Kang  Jin-Dan  Yin  Xi-Jun 《Transgenic research》2021,30(5):663-674
Transgenic Research - Herein, we investigate the high incidence of umbilical hernia and tippy-toe standing and their underlying changes in gene expression and proliferation in myostatin knockout...  相似文献   
147.
智尹  张育庆  王垚 《生态学报》2021,41(12):4676-4684
监测自然保护地生态承载力,对了解其时空分异规律及可持续发展有着重要意义。金石滩地质遗迹保护区是国家公园和风景名胜区的结合区域,是生态保护与地区发展间矛盾冲突所在之处,是多身份自然保护地的典型代表区域。以1998、2003、2007、2012、2015、2018年遥感影像和土地利用数据为基础,选取金石滩这个兼具保护与开发多种功能的自然保护地为研究区域,从弹性生态支撑系统、资源环境供容系统、社会经济协调系统3方面构建指标体系,运用模糊综合评价模型研究金石滩生态承载力的时空分异规律。结果表明:(1)在3个准则层中,弹性生态支撑力和资源环境供容力呈现出持续降低的剧烈下降趋势,社会经济协调力呈现先降后升、之后平稳发展的趋势。(2)金石滩生态承载力整体来看从强承载力演变为较弱承载力,1998-2018年自0.7572变为0.2940,近30年来承载力等级降低。(3)海陆生态承载力完全不同,陆地为强、较强承载力,海岸为弱、较弱承载力,自北部陆地向南部海岸逐渐减弱呈现极其不平衡的海陆空间分异。通过对金石滩1998-2018年生态承载力分析,能够反映区域的生态承载力变化情况,可为其他自然保护地的生态承载力评估和可持续发展提供参考。  相似文献   
148.
TMEM41B and VMP1 are integral membrane proteins of the endoplasmic reticulum (ER) and regulate the formation of autophagosomes, lipid droplets (LDs), and lipoproteins. Recently, TMEM41B was identified as a crucial host factor for infection by all coronaviruses and flaviviruses. The molecular function of TMEM41B and VMP1, which belong to a large evolutionarily conserved family, remains elusive. Here, we show that TMEM41B and VMP1 are phospholipid scramblases whose deficiency impairs the normal cellular distribution of cholesterol and phosphatidylserine. Their mechanism of action on LD formation is likely to be different from that of seipin. Their role in maintaining cellular phosphatidylserine and cholesterol homeostasis may partially explain their requirement for viral infection. Our results suggest that the proper sorting and distribution of cellular lipids are essential for organelle biogenesis and viral infection.  相似文献   
149.
Zhu  Yun  Xu  Baoping  Li  Changchong  Chen  Zhimin  Cao  Ling  Fu  Zhou  Shang  Yunxiao  Chen  Aihuan  Deng  Li  Bao  Yixiao  Sun  Yun  Ning  Limin  Yu  Shuilian  Gu  Fang  Liu  Chunyan  Yin  Ju  Shen  Adong  Xie  Zhengde  Shen  Kunling 《中国病毒学》2021,36(6):1543-1553
Virologica Sinica - Community-acquired pneumonia (CAP) is one of the leading causes of morbidity and mortality in children worldwide. In this study, we aimed to describe the aetiology of viral...  相似文献   
150.
本研究利用MISA软件对四种河鲀全基因组中的微卫星进行筛选并分析.结果如下:在红鳍东方鲀(Takifugu rubripes)(391.49 Mb)、菊黄东方鲀(T.flavidus)(366.29 Mb)、双斑东方鲀(T.bimaculatus)(371.68 Mb)及黑青斑河鲀(Tetraodon nigroviridis)(342.40 Mb)全基因组中,分别筛选出142 885个、135 009个、147 549个和179 703个完整型微卫星.相对丰度分别为365个/Mb,369个/Mb,397个/Mb和525个/Mb.微卫星总长度分别为2 876 322 bp,2 689 710 bp,3 140 445 bp 和3 615 069 bp,分别占基因组序列总长度的0.73%,0.73%,0.84%和1.06%.在1~6个不同碱基重复类型完整型微卫星中,四种河鲀的6种碱基类型数目排序是一致的.均是单碱基重复数目最多,然后依次是二碱基、三碱基、四碱基、五碱基和六碱基.其中AC,A,C,AG,AGG,AT,AAT和AAC是四种河鲀共有的常见核心重复类别.东方鲀属(Takifugu)三种河鲀基因组微卫星分布特征极为相似,分析红鳍东方鲀和双斑东方鲀的遗传距离可能更为接近.鲀属(Tetraodon)黑青斑河鲀与其他三种东方鲀属河鲀除部分微卫星特征相似外,在微卫星总数、微卫星相对丰度和密度、部分碱基类型数目及类别方面和东方鲀属差距较大.这可能与两属鱼类地理分布及进行滑动复制的碱基组成有关,推测东方鲀属和鲀属基因组可能具有独特的进化机制.本研究为多种河鲀基因组特征分析、多种河鲀微卫星引物设计、不同属种河鲀遗传距离及亲缘关系的探究等奠定了基础.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号