全文获取类型
收费全文 | 82940篇 |
免费 | 4493篇 |
国内免费 | 2584篇 |
出版年
2023年 | 1096篇 |
2022年 | 1287篇 |
2021年 | 3716篇 |
2020年 | 2483篇 |
2019年 | 3574篇 |
2018年 | 2387篇 |
2017年 | 1600篇 |
2016年 | 2089篇 |
2015年 | 4103篇 |
2014年 | 7912篇 |
2013年 | 7380篇 |
2012年 | 5458篇 |
2011年 | 6306篇 |
2010年 | 4287篇 |
2009年 | 3853篇 |
2008年 | 3855篇 |
2007年 | 4170篇 |
2006年 | 2794篇 |
2005年 | 2360篇 |
2004年 | 1514篇 |
2003年 | 1231篇 |
2002年 | 1090篇 |
2001年 | 744篇 |
2000年 | 665篇 |
1999年 | 678篇 |
1998年 | 632篇 |
1997年 | 520篇 |
1996年 | 553篇 |
1995年 | 641篇 |
1994年 | 542篇 |
1993年 | 576篇 |
1992年 | 539篇 |
1991年 | 551篇 |
1990年 | 454篇 |
1989年 | 450篇 |
1988年 | 460篇 |
1987年 | 381篇 |
1986年 | 326篇 |
1985年 | 553篇 |
1984年 | 869篇 |
1983年 | 559篇 |
1982年 | 755篇 |
1981年 | 742篇 |
1980年 | 543篇 |
1979年 | 551篇 |
1978年 | 340篇 |
1977年 | 357篇 |
1976年 | 321篇 |
1974年 | 239篇 |
1973年 | 244篇 |
排序方式: 共有10000条查询结果,搜索用时 296 毫秒
991.
992.
Parthasarathy Manavalan Alan E. Smith John M. McPherson 《Journal of Protein Chemistry》1993,12(3):279-290
A sequence comparison of the two membrane-associated (MA) domains of the cystic fibrosis transmembrane conductance regulator (CFTR), multidrug resistance transporter (MDR), and -factor pheromone export system (STE6) proteins, each of which are believed to contain a total of 12 transmembrane (TM) segments, reveals significant amino acid homology and length conservation in the loop regions that connect individual TM sequences. Similar structural homology is observed between these proteins, hemolysin B (HLYB) and the major histocompatibility-linked peptide transporter, HAM1, the latter two which contain a single MA domain composed of six TM segments. In addition, there are specific sequences that are conserved within the TM segments of the five different membrane proteins. This observation suggests that the folding topologies of the MA domains of MDR, STE6, and CFTR in the plasma membrane are likely to be very similar. The sequence analysis also reveals that there are three characteristic motifs (a pair of aromatic residues, LTLXXXXXXP and GXXL) that are conserved in MDR, STE6, HLYB, HAM1, but not in CFTR. We propose that although CFTR may be evolutionarily related to these other membrane proteins, it belongs to a separate subclass. 相似文献
993.
Dietmar Helmut Pieper Karin Stadler-Fritzsche Karl-Heinrich Engesser Hans-Joachim Knackmuss 《Archives of microbiology》1993,160(3):169-178
2-Chloro-4-methylphenoxyacetate is not a growth substrate for Alcaligenes eutrophus JMP 134 and JMP 1341. It is, however, being transformed by enzymes of 2,4-dichlorophenoxyacetic acid metabolism to 2-chloro-4-methyl-cis, cis-muconate, which is converted by enzymatic 1,4-cycloisomerization to 4-carboxymethyl-2-chloro-4-methylmuconolactone as a dead end metabolite. Chemically, only 3,6-cycloisomerization occurs, giving rise to both diastereomers of 4-carboxychloromethyl-3-methylbut-2-en-4-olide. Those lactones harbonring a chlorosubstituent on the 4-carboxymethyl side chain were surprisingly stable under physiological as well as acidic conditions. 相似文献
994.
Karin Schubert Dieter Reiml Jean-Pierre Accolas Franz Fiedler 《Archives of microbiology》1993,160(3):222-228
The primary structure of the peptidoglycan and the teichoic acids of two coryneform isolates from the surface flora of French cooked cheeses, CNRZ 925 and CNRZ 926, have been determined. In the peptidoglycan, meso-diaminopimelic acid was localized in position three of the peptide subunit. It contained an d-glutamyl-d-aspartyl interpeptide bridge, connecting meso-diaminopimelic acid and d-alanine residues of adjacent peptide subunits. The -carboxyl group of d-glutamic acid in position two of peptide subunits was substituted with glycine amide. The teichoic acid pattern and composition differed between the strains: both contained an erythritol teichoic acid and strain CNRZ 925 also contained an N-acetylglucosaminylphosphate polymer. The erythritol teichoic acids differed in terms of the quality and quantity of substituents, but they both had N,N-diacetyl-2,3-diamino-2,3-dideoxyglucuronic acid in common.Abbreviations DNP
dinitrophenyl
- Ery
erythritol
- Gal
galactose
- GlcN
glucosamine
- GlcNAc
N-acetylglucosamine
- GlcUANAc2
N,N-diacetyl-2,3-diamino-2,3-dideoxyglucuronic acid
- Hex UANAc2
N,N-diacetyl-2,3-diamino-2,3-dideoxyhexuronic
- acid
m-Dpm, meso-diaminopimelic acid
- Mur
muramic acid
- MurNAc
N-acetylmuramic acid 相似文献
995.
G. K. Haines G. D. Ghadge S. Becker M. Kies H. Pelzer B. Thimmappaya J. A. Radosevich 《Virchows Archiv. B, Cell pathology including molecular pathology》1993,63(1):289-295
p68 is an inducible protein kinase which is believed to be an important factor in the regulation of both viral and cellular
protein synthesis. We have produced a monoclonal antibody (TJ4C4) which specifically detects p68, and which can be used to
detect this antigen in formalin-fixed, paraffin-embedded tissues. Because p68 plays an important role in cellular protein
synthesis, we hypothesized that it may correlate with normal and neoplastic cellular differentiation. One hundred and seventy-seven
head and neck squamous cell carcinoma specimens, representing 82 patients, were studied. The relative amount, frequency, and
distribution of p68 expression were determined by microscopic evaluation of ABC immunoperoxidase-stained specimens. A spectrum
of immunoreactivity was detected in 156 of 177 tumors, as well as within the normal squamous epithelium. Normal, actively
proliferating cells, such as the basal layer of squamous epithelium, expressed comparatively little p68. Increased p68 expression
was noted to parallel the morphologic features of cellular differentiation. In neoplastic tissue, p68 expression also increased
with the degree of cellular differentiation. These data demonstrate that the expression of p68 parallels the degree of cellular
differentiation in squamous cell carcinoma of the head and neck region, as well as within normal squamous mucosa. Therefore,
p68 may provide an objective biologic measure of cellular differentiation which does not depend on morphologic features. 相似文献
996.
采用SDS聚丙烯酰胺凝胶电泳银染色的方法,对58例肺癌患者和32例肺结核患者的血清蛋白进行比较分析,发现有五种特异蛋白,分别存在于A区、C区、F区和G区。肺癌组和肺结核组比较,存在极显著性差异(P<0.01),提示有早期诊断肺癌的价值,有可能成为临床诊断肺癌的一个重要参考指标。 相似文献
997.
本文对11例肺癌患者胸水13种游离氨基酸作了分析,并与28例正常人血浆游离氨基酸水平作了对照,结果表明:肺癌患者胸水的必需及非必需氨基酸普遍高于正常人血浆游离氨基酸,但其胸水谷氨酰胺水平则明显低于正常人血浆水平。 相似文献
998.
Based on small-scale synthesis (0.3 g), a 100-g scale-up synthesis of crude [Aib8, Arg34]-glucagon-like peptide-1 (GLP-1) (7–37) was completed. The crude [Aib8, Arg34]-GLP-1 (7–37) was purified using a dynamic axial compression column 200 (DAC-200). Approximately 61 g of [Aib8, Arg34]-GLP-1 (7–37) with a purity of >99% was obtained through one-step reverse-phase chromatography. The purification yield was approximately 92%. The yield from the total reaction was approximately 60%. In summary, we developed an economical and environmentally friendly route to the synthesis and purification of crude [Aib8, Arg34]-GLP-1 (7–37), laying a foundation for subsequent industrial production. 相似文献
999.
Seyede Saba Hosseini Seyed Omar Ebrahimi Maryam Haji Ghasem Kashani Somayeh Reiisi 《Cell biology international》2023,47(1):98-109
Naturally-derived drugs have drawn much attention in recent decades. Efficiency, lower toxicity, and economic reasons are some of their advantages that justify this broad range of administration for different diseases, including cancer. If we can find a specific combination that boosts the effects of their single therapy, leading to synergism effect, increased efficiency, and decreased toxicity, they can act even better. Quercetin and fisetin, two well-known flavonoids, have been used to fight against various cancers. In this study, we investigated their possible synergism quercetin and fisetin on MCF7, MDA-MB-231, BT549, T47D, and 4T1 breast cancer cell lines. Then the optimum combined dose was used to study their impacts on wound healing abilities and clonogenic properties. The real-time qPCR was used to study the expression of their validated downstream effectors in predicted pathways. A significant synergism effect (p < .01, combination index: <1) was observed for all cell lines. Combination therapy was significantly more effective in colony formation (p < .0001) and wound healing assays (p < .001) compared to single therapies. The expression level of potential effectors was also showed a greater change. In vivo study confirmed the in vitro results and showed how significantly (p < .001) their synergism promotes their singular function in inhibiting cancer progression. The breast cancer mouse models receiving combined therapy lived longer with higher average body weight and smaller tumor sizes. These results exhibit that quercetin and fisetin inhibit cancer cell proliferation, migration and colony formation synergistically, and matrix metalloproteinase signaling and apoptotic pathways are relatively responsible for inhibitory activities. 相似文献
1000.
The protective effect of arbutin against potassium bromate-induced oxidative damage in the rat brain
H. Turan Akkoyun Ahmet Uyar Mahire Bayramoglu Akkoyun Aydın Şükrü Bengü Şule Melek Fatma Karagözoğlu Sevinç Aydın Suat Ekin Sinem Aslan Erdem 《Journal of biochemical and molecular toxicology》2023,37(2):e23248
This study aimed to investigate the protective effects of arbutin (ARB) against brain injury induced in rats with potassium bromate (KBrO3). The rats were divided into four groups as Group 1: Control (0.9% NaCl ml/kg/day p.), Group 2: KBrO3 (100 mg/kg (gavage), Group 3: ARB (50 mg/kg/day p.), and Group 4: KBrO3 + ARB (100 mg/kg (gavage) + 50 mg/kg/day p.). At the end of the fifth day of the study, the rats in all groups were killed, and their brain tissues were collected. In the collected brain tissues, malondialdehyde (MDA), superoxide dismutase (SOD), and catalase (CAT) levels were measured, and routine histopathological examinations were made. The MDA levels in the group that was exposed to KBrO3 were significantly higher than those in the control group (p ˂ 0.001). In comparison to the KBrO3 group, the MDA levels in the KBrO3 + ARB group were significantly lower (p ˂ 0.001). It was observed that SOD and CAT enzyme activity levels were significantly lower in the KBrO3 group compared to the control group (p ˂ 0.001), while these levels were significantly higher in the KBrO3 + ARB group than in the KBrO3 group (p ˂ 0.001). Additionally, the group that was subjected to KBrO3 toxicity, as well as ARB administration, had much lower levels of histopathologic signs than the group that was subjected to KBrO3 toxicity only. Consequently, it was found that KBrO3 exposure led to injury in the brain tissues of the rats, and using ARB was effective in preventing this injury. 相似文献