全文获取类型
收费全文 | 2433篇 |
免费 | 207篇 |
国内免费 | 354篇 |
出版年
2024年 | 6篇 |
2023年 | 65篇 |
2022年 | 101篇 |
2021年 | 183篇 |
2020年 | 124篇 |
2019年 | 142篇 |
2018年 | 139篇 |
2017年 | 85篇 |
2016年 | 124篇 |
2015年 | 166篇 |
2014年 | 206篇 |
2013年 | 185篇 |
2012年 | 244篇 |
2011年 | 221篇 |
2010年 | 113篇 |
2009年 | 109篇 |
2008年 | 133篇 |
2007年 | 80篇 |
2006年 | 83篇 |
2005年 | 68篇 |
2004年 | 60篇 |
2003年 | 54篇 |
2002年 | 71篇 |
2001年 | 23篇 |
2000年 | 26篇 |
1999年 | 24篇 |
1998年 | 14篇 |
1997年 | 18篇 |
1996年 | 20篇 |
1995年 | 6篇 |
1994年 | 17篇 |
1993年 | 9篇 |
1992年 | 7篇 |
1991年 | 9篇 |
1990年 | 7篇 |
1989年 | 10篇 |
1988年 | 7篇 |
1987年 | 4篇 |
1985年 | 4篇 |
1984年 | 3篇 |
1983年 | 2篇 |
1982年 | 2篇 |
1980年 | 2篇 |
1979年 | 3篇 |
1977年 | 3篇 |
1976年 | 3篇 |
1975年 | 4篇 |
1974年 | 1篇 |
1973年 | 1篇 |
1950年 | 1篇 |
排序方式: 共有2994条查询结果,搜索用时 31 毫秒
21.
Five new ent-pimarane diterpenes ( 1 – 5 ) and five known analogs ( 6 – 10 ) were isolated from the aerial parts of Siegesbeckia pubescens. Their structures, including absolute configurations, were determined by comprehensive spectroscopic methods especially 1D and 2D NMR and quantum chemical electronic circular dichroism calculations. All the isolated compounds were evaluated for their cytotoxicity against human BT549, A549 and H157 cancer cell lines. Among them, compounds 1 and 2 showed mild cytotoxicity against lung cancer cell lines H157 with IC50 values of 16.35±2.59 and 18.86±4.83 μM, respectively. 相似文献
22.
23.
硒对培养人胚肝细胞Ⅲ型前胶原,羟脯氨酸合成的影响 总被引:7,自引:0,他引:7
原代培养人胚肝细胞经1.156×10 ̄(-7)mol/L硒预处理4h,加入20mmol/L四氟化碳作用20h,观察硒对其Ⅲ型前胶原(PCⅢ)和羟脯氨酸(Hyp)生成的影响。结果培养液中PCⅢ水平、细胞内Hyp含量及细胞内外丙二醛(MDA)水平均降低,与未加硒对照组比较差别有显著性(P<0.01)。而硒谷腕甘肽过氧化物酶(Se-GSH-PX)活性则较对照组显著增高(P<0.001),且PCⅢ水平与Se-GSH-P_X/MDA比值呈负相关(r=-0.9156,P<0.01)。提示硒可提高Se-GSH-P_X/MDA比值,抑制脂质过氧化激发的肝细胞胶原合成。 相似文献
24.
黄芪有效成分对氧自由基清除作用的ESR研究 总被引:81,自引:0,他引:81
用电子自旋共振技术研究了黄芪总黄酮(TFA)、黄芪总皂甙(TSA)和黄芪总多糖(TPA)对次黄嘌呤/黄嘌呤氧化酶体系产生的超氧阴离子自由基和H2O2-Fe2+体系产生的羟自由基的清除作用.结果表明,这3种成分均有清除氧自由基的作用;对超氧阴离子自由基的清除效能大于对羟自由基的清除作用;其作用强度依次为TFA>TSA>TPA.结果提示清除氧自由基可能是黄芪抗衰老的主要机理之一,TFA和TSA是黄芪抗氧化作用的主要药理活性成分. 相似文献
25.
Human genes for glutathione S-transferases 总被引:11,自引:2,他引:9
The tissue distribution of different glutathione S-transferases (GST) is analysed by electrophoresis. The existence of GST"e" (erythrocyte), GST3, GST1, and GST2 is confirmed. GST"e" the fastest and most thermolabile of different GST analysed is observed only in erythrocyte cells. GST3 which migrates more slowly than GST"e" is present in all tissues and cells analysed, excepted for erythrocyte cells in which only GST"e" is observed. GST1 presents a polymorphism with four phenotypes, 1, 1/2, 2, and 0 controlled by three alleles 1, 2, and 0 (null). With the sample of 56 livers analysed the different frequencies obtained are 9%, 5%, 43%, 43% for the phenotypes 1, 1/2, 2, and 0 respectively and 0.074 (p), 0.279 (q), 0.647 (r) for the alleles, 1, 2, and 0 (null). GST2 presents variant patterns due probably, in the majority of cases, to post-synthetic modifications rather than allelic variation. Two new GST are described, GST4 and GST5. GST4 abundant in muscle tissue is a dimeric protein. GST4 forms with GST1 a heterodimeric band. GST5 is observed in brain homogenates. For the chromosome localization the results obtained by man (leucocytes)-mouse somatic cell hybrid analysis indicate that the gene for leucocytes GST is on chromosome 11. This gene is the structural GST3 gene. 相似文献
26.
C. Julier D. Weil P. Couillin J. C. Côté Cong Van Nguyen C. Foubert A. Boué J. P. Thirion J. C. Kaplan C. Junien 《Human genetics》1984,67(2):174-177
Summary We used a cloned human cDNA probe homologous to the placenta chorionic gonadotropin subunit (CGB) and to the pituitary luteinizing hormone subunit (LHB) and Southern blotting techniques to analyse DNA from a series of rodent x human somatic cell hybrids for the presence of specific gonadotropin subunit related sequences. Our results provide evidence for the assignment and linkage of the eight genes (or pseudogenes) coding for the subunit of these glycoprotein hormones to chromosome 19. Moreover, we observed a strict concordance between the permissivity of mouse x man hybrid cells to enteroviruses (which is linked to the presence of specific cell receptors encoded by human chromosome 19) and the presence of CGB and LHB related sequences, thus confirming the localization of the structural genes for the subunits on chromosome 19.This work was supported in part by INSERM grants CRL 81 1041 and by MRC grant MT 4860 相似文献
27.
H. de Verneuil B. Grandchamp Chantal Foubert Dominique Weil Cong Van N'Guyen Marie-Sylvie Gross Shigeru Sassa Y. Nordmann 《Human genetics》1984,66(2-3):202-205
Summary A specific enzyme immunoassay of uroporphyrinogen decarboxylase was developed and applied to the detection of the human enzyme in man-rodent somatic cell hybrids. This method allowed to assign the gene for uroporphyrinogen decarboxylase to human chromosome 1. 相似文献
28.
29.