全文获取类型
收费全文 | 2285篇 |
免费 | 179篇 |
国内免费 | 2篇 |
专业分类
2466篇 |
出版年
2023年 | 12篇 |
2022年 | 28篇 |
2021年 | 51篇 |
2020年 | 23篇 |
2019年 | 25篇 |
2018年 | 56篇 |
2017年 | 39篇 |
2016年 | 60篇 |
2015年 | 102篇 |
2014年 | 97篇 |
2013年 | 157篇 |
2012年 | 156篇 |
2011年 | 187篇 |
2010年 | 111篇 |
2009年 | 110篇 |
2008年 | 145篇 |
2007年 | 117篇 |
2006年 | 117篇 |
2005年 | 120篇 |
2004年 | 125篇 |
2003年 | 116篇 |
2002年 | 86篇 |
2001年 | 18篇 |
2000年 | 21篇 |
1999年 | 23篇 |
1998年 | 26篇 |
1997年 | 17篇 |
1996年 | 27篇 |
1995年 | 22篇 |
1994年 | 14篇 |
1993年 | 24篇 |
1992年 | 15篇 |
1991年 | 11篇 |
1990年 | 13篇 |
1989年 | 8篇 |
1988年 | 8篇 |
1987年 | 15篇 |
1986年 | 8篇 |
1985年 | 11篇 |
1984年 | 12篇 |
1983年 | 14篇 |
1982年 | 15篇 |
1981年 | 11篇 |
1980年 | 14篇 |
1979年 | 14篇 |
1978年 | 9篇 |
1977年 | 6篇 |
1976年 | 11篇 |
1975年 | 7篇 |
1973年 | 5篇 |
排序方式: 共有2466条查询结果,搜索用时 15 毫秒
51.
CpG-DNA and its related synthetic CpG oligodeoxynucleotides (CpG-ODNs) play an important role in immune cell survival. It has been suggested that Akt is one of the CpG-DNA-responsive serine/threonine kinases; however, the target protein of CpG-DNA that leads to Akt activation has not been elucidated. Here, we report that ex vivo stimulation of bone marrow-derived macrophages (BMDMs) from mice lacking the catalytic subunit of DNA-dependent protein kinase (DNA-PKcs) results in defective phosphorylation and activation of Akt by CpG-DNA. Unexpectedly, loss of the Toll-like receptor 9 has a minimal effect on Akt activation in response to CpG-DNA. Further in vitro analysis using purified DNA-PK and recombinant Akt proteins reveals that DNA-PK directly induces phosphorylation and activation of Akt. In addition, in BMDMs, DNA-PKcs associates with Akt upon CpG-DNA stimulation and triggers transient nuclear translocation of Akt. Thus, our findings establish a novel role for DNA-PKcs in CpG-DNA signaling and define a CpG-DNA/DNA-PKcs/Akt pathway. 相似文献
52.
Andrea Gloria‐Soria Diego Ayala Ambicadutt Bheecarry Olger Calderon‐Arguedas Dave D. Chadee Marina Chiappero Maureen Coetzee Khouaildi Bin Elahee Ildefonso Fernandez‐Salas Hany A. Kamal Basile Kamgang Emad I. M. Khater Laura D. Kramer Vicki Kramer Alma Lopez‐Solis Joel Lutomiah Ademir Martins Jr Maria Victoria Micieli Christophe Paupy Alongkot Ponlawat Nil Rahola Syed Basit Rasheed Joshua B. Richardson Amag A. Saleh Rosa Maria Sanchez‐Casas Gonçalo Seixas Carla A. Sousa Walter J. Tabachnick Adriana Troyo Jeffrey R. Powell 《Molecular ecology》2016,25(21):5377-5395
Mosquitoes, especially Aedes aegypti, are becoming important models for studying invasion biology. We characterized genetic variation at 12 microsatellite loci in 79 populations of Ae. aegypti from 30 countries in six continents, and used them to infer historical and modern patterns of invasion. Our results support the two subspecies Ae. aegypti formosus and Ae. aegypti aegypti as genetically distinct units. Ae. aegypti aegypti populations outside Africa are derived from ancestral African populations and are monophyletic. The two subspecies co‐occur in both East Africa (Kenya) and West Africa (Senegal). In rural/forest settings (Rabai District of Kenya), the two subspecies remain genetically distinct, whereas in urban settings, they introgress freely. Populations outside Africa are highly genetically structured likely due to a combination of recent founder effects, discrete discontinuous habitats and low migration rates. Ancestral populations in sub‐Saharan Africa are less genetically structured, as are the populations in Asia. Introduction of Ae. aegypti to the New World coinciding with trans‐Atlantic shipping in the 16th to 18th centuries was followed by its introduction to Asia in the late 19th century from the New World or from now extinct populations in the Mediterranean Basin. Aedes mascarensis is a genetically distinct sister species to Ae. aegypti s.l. This study provides a reference database of genetic diversity that can be used to determine the likely origin of new introductions that occur regularly for this invasive species. The genetic uniqueness of many populations and regions has important implications for attempts to control Ae. aegypti, especially for the methods using genetic modification of populations. 相似文献
53.
54.
Gua JQ Wang Y Franzblau SG Montenegro G Timmermann BN 《Zeitschrift für Naturforschung. C, Journal of biosciences》2004,59(11-12):797-802
Antitubercular bioassay-guided fractionation of the dichloromethane extracts of the above-ground biomass and roots of Quinchamalium majus led to the identification of six known constituents, betulinic acid (1), daucosterol (2), 5,7-dihydroxyflavone (3), oleanolic acid (4), (-)-2S-pinocembrin (5), and ursolic acid (6), for the first time in this species. Their chemical structures were determined on the basis of spectroscopic evidence and chemical transformation methods. All of these compounds along with additional 11 analogues were evaluated for their antitubercular potential against Mycobacterium tuberculosis in a microplate alamar blue assay, and the primary structure-activity relationships (SARs) for 4 and 6 were discussed. In addition, all the isolates were tested for cytotoxicity against African green monkey Vero cells in order to evaluate for their selectivity potential. 相似文献
55.
Pereira RP Fachinetto R de Souza Prestes A Puntel RL Santos da Silva GN Heinzmann BM Boschetti TK Athayde ML Bürger ME Morel AF Morsch VM Rocha JB 《Neurochemical research》2009,34(5):973-983
Considering the important role of oxidative stress in the pathogenesis of several neurological diseases, and the growing evidence
of the presence of compounds with antioxidant properties in the plant extracts, the aim of the present study was to investigate
the antioxidant capacity of three plants used in Brazil to treat neurological disorders: Melissa officinalis, Matricaria recutita and Cymbopogon citratus. The antioxidant effect of phenolic compounds commonly found in plant extracts, namely, quercetin, gallic acid, quercitrin
and rutin was also examined for comparative purposes. Cerebral lipid peroxidation (assessed by TBARS) was induced by iron
sulfate (10 μM), sodium nitroprusside (5 μM) or 3-nitropropionic acid (2 mM). Free radical scavenger properties and the chemical
composition of plant extracts were assessed by 1′-1′ Diphenyl-2′ picrylhydrazyl (DPPH) method and by Thin Layer Chromatography
(TLC), respectively. M. officinalis aqueous extract caused the highest decrease in TBARS production induced by all tested pro-oxidants. In the DPPH assay, M. officinalis presented also the best antioxidant effect, but, in this case, the antioxidant potencies were similar for the aqueous, methanolic
and ethanolic extracts. Among the purified compounds, quercetin had the highest antioxidant activity followed by gallic acid,
quercitrin and rutin. In this work, we have demonstrated that the plant extracts could protect against oxidative damage induced
by various pro-oxidant agents that induce lipid peroxidation by different process. Thus, plant extracts could inhibit the
generation of early chemical reactive species that subsequently initiate lipid peroxidation or, alternatively, they could
block a common final pathway in the process of polyunsaturated fatty acids peroxidation. Our study indicates that M. officinalis could be considered an effective agent in the prevention of various neurological diseases associated with oxidative stress. 相似文献
56.
57.
58.
59.
Cortés-Sarabia Karen Bautista-Santos Isabel Cisneros-Sarabia Alondra Parra-Rojas Isela Estrada-Moreno Ana Karen Flores-Alfaro Eugenia Fernández-Tilapa Gloria Ramírez-Peralta Arturo Vences-Velázquez Amalia 《International journal of peptide research and therapeutics》2021,27(1):413-420
International Journal of Peptide Research and Therapeutics - Gardnerella vaginalis produces vaginolysin (VLY), a cholesterol-dependent cytolysin, responsible of the cellular lysis and epithelial... 相似文献
60.
Juan Del Coso Javier Portillo Gloria Muñoz Javier Abián-Vicén Cristina Gonzalez-Millán Jesús Muñoz-Guerra 《Amino acids》2013,44(6):1511-1519
The aim of this study was to determine the effects of a caffeine-containing energy drink on physical performance during a rugby sevens competition. A second purpose was to investigate the post-competition urinary caffeine concentration derived from the energy drink intake. On two non-consecutive days of a friendly tournament, 16 women from the Spanish National rugby sevens Team (mean age and body mass = 23 ± 2 years and 66 ± 7 kg) ingested 3 mg of caffeine per kg of body mass in the form of an energy drink (Fure®, ProEnergetics) or the same drink without caffeine (placebo). After 60 min for caffeine absorption, participants performed a 15-s maximal jump test, a 6 × 30 m sprint test, and then played three rugby sevens games against another national team. Individual running pace and instantaneous speed during the games were assessed using global positioning satellite (GPS) devices. Urine samples were obtained pre and post-competition. In comparison to the placebo, the ingestion of the energy drink increased muscle power output during the jump series (23.5 ± 10.1 vs. 25.6 ± 11.8 kW, P = 0.05), running pace during the games (87.5 ± 8.3 vs. 95.4 ± 12.7 m/min, P < 0.05), and pace at sprint velocity (4.6 ± 3.3 vs. 6.1 ± 3.4 m/min, P < 0.05). However, the energy drink did not affect maximal running speed during the repeated sprint test (25.0 ± 1.5 vs. 25.0 ± 1.7 km/h). The ingestion of the energy drink resulted in a higher post-competition urine caffeine concentration than the placebo (3.3 ± 0.7 vs. 0.2 ± 0.1 μg/mL; P < 0.05). In summary, 3 mg/kg of caffeine in the form of a commercially available energy drink considerably enhanced physical performance during a women’s rugby sevens competition. 相似文献