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   1151篇
  免费   212篇
  国内免费   235篇
  2024年   3篇
  2023年   13篇
  2022年   34篇
  2021年   37篇
  2020年   52篇
  2019年   68篇
  2018年   36篇
  2017年   27篇
  2016年   35篇
  2015年   52篇
  2014年   112篇
  2013年   75篇
  2012年   158篇
  2011年   173篇
  2010年   113篇
  2009年   110篇
  2008年   102篇
  2007年   76篇
  2006年   50篇
  2005年   39篇
  2004年   31篇
  2003年   21篇
  2002年   12篇
  2001年   17篇
  2000年   5篇
  1999年   13篇
  1998年   6篇
  1997年   3篇
  1996年   4篇
  1991年   4篇
  1989年   4篇
  1988年   6篇
  1987年   10篇
  1986年   11篇
  1985年   9篇
  1984年   2篇
  1983年   4篇
  1981年   4篇
  1978年   2篇
  1976年   3篇
  1975年   5篇
  1974年   5篇
  1973年   9篇
  1972年   4篇
  1971年   7篇
  1970年   7篇
  1969年   4篇
  1968年   5篇
  1966年   4篇
  1965年   2篇
排序方式: 共有1598条查询结果,搜索用时 15 毫秒
1.
2.
Irradiation of a mouse thymocyte fraction enriched by T-lymphocyte precursors changes the antigenic phenotype of cells toward the increase of their highly differentiated forms. Similar changes in membrane marker antigens are produced by chemical inductors of differentiation and thymotropin. The changes in the cell phenotype induced by the above agents are associated with both membrane and intragenome rearrangements. The results of the experiments on preventing the expression of some antigens by puromycin and the data on the level of spontaneous genome lesions in thymocyte fractions have prompted an assumption that destabilization of the genome upon irradiation increases DNA injury above some critical level which may serve a stimulus for "sorting out" the most radiosensitive thymocyte fraction.  相似文献   
3.
In studying the main indices that characterize the neurochemical system of biosynthesis and degradation of a dopamine neuromediator, tyrosine hydroxylase-dopamine-monoamine oxidase, in different brain regions 5-6 min, 1 and 18 h after whole-body irradiation with high energy electrons (100 Gy) the authors have revealed a 25-40% inhibition of tyrosine hydroxylase and monoamine oxidase activity, and a 40% increase in the dopamine content of basal ganglia of the brain that control behavioural reactions of the organism. The neurochemical disturbances revealed are involved in the mechanisms of early transient incapacity after irradiation with superhigh doses.  相似文献   
4.
Musashi-2(MSI2)是一种RNA结合蛋白质,对维持造血干细胞功能具有重要作用。研究表明,MSI2高表达能促进急性髓系白血病(acute myelocytic leukemia, AML)进展,但其作用机制尚不明确。本研究稳定沉默HL60细胞MSI2后,第1、2、3、4 d对照组的相对细胞生长率分别为1.931 ± 0.027、3.070 ± 0.073、4.017 ± 0.092和4.215 ± 0.246;敲减组分别为1.927 ± 0.035、2.564 ± 0.090、2.825 ± 0.097和3.223 ± 0.182,两组相比具有统计学差异,P<0.001;细胞凋亡明显增加(7.967% ± 0.698% vs 3.400% ± 0.322%., P<0.01);G0/G1期细胞比例明显增高(67.430% ± 4.390% vs. 50.360% ± 2.160%, P<0.01);NUMB蛋白明显上调,LEF1明显下降。环状RNA(circular RNA, circRNA)芯片筛选和荧光定量PCR验证显示,MSI2沉默组circRNA_001214表达水平是对照组3.48倍。这一结果也在NALM6细胞得到证实。进一步用生物信息学分析,显示circRNA_001214最可能与miR-1273a、miR-1273e和miR 5095结合,进而影响参与细胞凋亡相关基因(CYCS、AKT1、BAX、TNFRSF10A、TNFRSF10D)、Wnt信号基因(WNT4、WNT2B、WNT7B、 DKK2、SFRP1、CSNKE1和LEF1)以及参与细胞代谢相关基因(RPE, PGAM4, PGAM1, TAT, CBS、RPE、SUCLG2、PGAM4、PGAM1和 IDNK)。总而言之,MSI2可能通过干扰circRNA_001214生成,减少靶miRNA对凋亡、Wnt信号及细胞代谢相关基因表达的影响,促进细胞生长。  相似文献   
5.
Using methods of G- and C-banding, a study was made of the karyotype of mouse myeloma cell line sp2/0-Ag14. The number of chromosomes varies from 58 to 65, the modal class being 61-62. 50 per cent of chromosomes are rearranged. Normal chromosomes 6, 12 and X were not detected in either examined cell of this line. Among the marker chromosomes there are an isochromosome (19/19), three dicentric markers and one marker with two interstitial C-bands. There is a specific marker t (12; 15) of mouse plasmacytomas in the karyotype sp2/0-Ag14. A possible association of specific translocations and segregations of the normal chromosomes with the phenotype of line sp2/0-Ag14 is discussed. The results obtained may be useful for cytogenetic analysis of hybridomas.  相似文献   
6.
The effects of osmotic pressure on inward sodium current during a change in temperature were investigated during experiments on isolated rat spinal ganglia neurons using techniques of intracellular perfusion and voltage clamping. It was found that the effect of osmotic pressure on the kinetic parameters of sodium current does not depend on temperature over a wide range of 8–40°C; the apparent values of activation energies for the activation and inactivation processes do not dependent on degree of osmolality. Overall findings would appear to indicate that the osmotic pressure effect is actually initiated by association with aqueous transmembrane flux. Opinions are expressed as to the location of the structures through which this aqueous flux passes and of the sodium channel gating mechanism, together which the molecular mechanisms of interaction between these two elements.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 18, No. 4, pp. 518–525, July–August, 1986.  相似文献   
7.
8.
在主动脉与肾动脉缩窄造成的慢性心功能不全大鼠,血浆儿茶酚胺浓度增高;心脏β-肾上腺素受体(β-AR)数量增加,其中β_1-AR及其mRNA增加,而β_2-AR及其mRNA不变;左心房异丙基肾上腺素(ISO)浓度-收缩效应曲线右移;而心肌ISO浓度-cAMP蓄积曲线无显著改变;血淋巴细胞β-AR数量显著减少.结果提示心功能不全时心脏β_1-AR数量增多,但其介导的正性变力效应反而降低,在cAMP生成以后的信号转导过程或心肌收缩成分功能存在障碍,而血淋巴细胞β-AR的改变与心脏β-AR的功能改变平行.  相似文献   
9.
Polypeptide fragments from Na+, K+-ATPase of cattle brain are obtained by the bromocyan-treatment of the protein and subsequent gel filtration via sephadexes; the fragments were reconstructed into bilayer lipid membranes (BLM). Polypeptides of fractions I and II induce cationic and polypeptides of fraction IV--cationic-anionic conductivity of BLM. Neither sodium nor potassium selectivity of BLM modified by protein fragments of fractions I and II was observed. Fluctuations of the modified membranes current are of spasmodic character, ATP and inhibitors of the sodium pump do not affect them. The induction of current fluctuations peculiar to channels into BLM is supposed to be a character of polypeptides obtained after the ATPase splitting but not of the cation-transport system of the sodium pump.  相似文献   
10.
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