全文获取类型
收费全文 | 18832篇 |
免费 | 1398篇 |
国内免费 | 5篇 |
专业分类
20235篇 |
出版年
2021年 | 131篇 |
2020年 | 111篇 |
2019年 | 117篇 |
2018年 | 294篇 |
2017年 | 263篇 |
2016年 | 453篇 |
2015年 | 786篇 |
2014年 | 731篇 |
2013年 | 1061篇 |
2012年 | 1293篇 |
2011年 | 1250篇 |
2010年 | 754篇 |
2009年 | 601篇 |
2008年 | 1110篇 |
2007年 | 1114篇 |
2006年 | 1061篇 |
2005年 | 1014篇 |
2004年 | 932篇 |
2003年 | 863篇 |
2002年 | 820篇 |
2001年 | 414篇 |
2000年 | 449篇 |
1999年 | 400篇 |
1998年 | 195篇 |
1997年 | 148篇 |
1996年 | 138篇 |
1995年 | 142篇 |
1994年 | 142篇 |
1993年 | 119篇 |
1992年 | 241篇 |
1991年 | 236篇 |
1990年 | 220篇 |
1989年 | 172篇 |
1988年 | 183篇 |
1987年 | 159篇 |
1986年 | 147篇 |
1985年 | 135篇 |
1984年 | 122篇 |
1983年 | 96篇 |
1982年 | 93篇 |
1981年 | 120篇 |
1980年 | 89篇 |
1979年 | 118篇 |
1978年 | 106篇 |
1977年 | 87篇 |
1976年 | 100篇 |
1975年 | 79篇 |
1974年 | 97篇 |
1973年 | 70篇 |
1971年 | 82篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
991.
Tejiokem MC Faye A Penda IC Guemkam G Ateba Ndongo F Chewa G Rekacewicz C Rousset D Kfutwah A Boisier P Warszawski J;ARNS -PEDIACAM study group 《PloS one》2011,6(7):e21840
Background
Early infant diagnosis (EID) of HIV is a key-point for the implementation of early HAART, associated with lower mortality in HIV-infected infants. We evaluated the EID process of HIV according to national recommendations, in urban areas of Cameroon.Methods/Findings
The ANRS12140-Pediacam study is a multisite cohort in which infants born to HIV-infected mothers were included before the 8th day of life and followed. Collection of samples for HIV DNA/RNA-PCR was planned at 6 weeks together with routine vaccination. The HIV test result was expected to be available at 10 weeks. A positive or indeterminate test result was confirmed by a second test on a different sample. Systematic HAART was offered to HIV-infected infants identified. The EID process was considered complete if infants were tested and HIV results provided to mothers/family before 7 months of age. During 2007–2009, 1587 mother-infant pairs were included in three referral hospitals; most infants (n = 1423, 89.7%) were tested for HIV, at a median age of 1.5 months (IQR, 1.4–1.6). Among them, 51 (3.6%) were HIV-infected. Overall, 1331 (83.9%) completed the process by returning for the result before 7 months (median age: 2.5 months (IQR, 2.4–3.0)). Incomplete process, that is test not performed, or result of test not provided or provided late to the family, was independently associated with late HIV diagnosis during pregnancy (adjusted odds ratio (aOR) = 1.8, 95%CI: 1.1 to 2.9, p = 0.01), absence of PMTCT prophylaxis (aOR = 2.4, 95%CI: 1.4 to 4.3, p = 0.002), and emergency caesarean section (aOR = 2.5, 95%CI: 1.5 to 4.3, p = 0.001).Conclusions
In urban areas of Cameroon, HIV-infected women diagnosed sufficiently early during pregnancy opt to benefit from EID whatever their socio-economic, marital or disclosure status. Reduction of non optimal diagnosis process should focus on women with late HIV diagnosis during pregnancy especially if they did not receive any PMTCT, or if complications occurred at delivery. 相似文献992.
Leucine supplementation in rats induced a delay in muscle IR/PI3K signaling pathway associated with overall impaired glucose tolerance 总被引:1,自引:0,他引:1
Michèle Balage Joëlle DupontIsabelle Mothe-Satney Sophie TesseraudLaurent Mosoni Dominique Dardevet 《The Journal of nutritional biochemistry》2011,22(3):219-226
Although activation of the mammalian target of rapamycin complex/p70 S6 kinase (S6K1) pathway by leucine is efficient to stimulate muscle protein synthesis, it can also exert inhibition on the early steps of insulin signaling leading to insulin resistance. We investigated the impact of 5-week leucine supplementation on insulin signaling and sensitivity in 4-month old rats fed a 15% protein diet supplemented (LEU) or not (C) with 4.5% leucine. An oral glucose tolerance test was performed in each rat at the end of the supplementation and glucose transport was measured in vitro using isolated epitrochlearis muscles incubated with 2-deoxy-d-[3H]-glucose under increasing insulin concentrations. Insulin signaling was assessed on gastrocnemius at the postabsorptive state or 30 and 60 min after gavage with a nutrient bolus. Tyrosine phosphorylation of IRβ, IRS1 and PI3 kinase activity were reduced in LEU group 30 min after feeding (−36%, −36% and −38% respectively, P<.05) whereas S6K1, S6rp and 4EBP1 phosphorylations were similar. Overall glucose tolerance was reduced in leucine-supplemented rats and was associated with accumulation of perirenal adipose tissue (+27%, P<.05). Conversely, in vitro insulin-response of muscle glucose transport tended to be improved in leucine-supplemented rats. In conclusion, dietary leucine supplementation in adult rats induced a delay in the postprandial stimulation in the early steps of muscle insulin signaling without muscle resistance on insulin-induced glucose uptake. However, it resulted in overall glucose intolerance linked to increased local adiposity. Further investigations are necessary to clearly define the beneficial and/or deleterious effects of chronic dietary leucine supplementation in healthy subjects. 相似文献
993.
Mendes FS González-Pajuelo M Cordier H François JM Vasconcelos I 《Applied microbiology and biotechnology》2011,92(3):519-527
In this work, the production of 1,3-propanediol from glucose and molasses was studied in a two-step process using two recombinant
microorganisms. The first step of the process is the conversion of glucose or other sugar into glycerol by the metabolic engineered
Saccharomyces cerevisiae strain HC42 adapted to high (>200 g l−1) glucose concentrations. The second step, carried out in the same bioreactor, was performed by the engineered strain Clostridium acetobutylicum DG1 (pSPD5) that converts glycerol to 1,3-propanediol. This two-step strategy led to a flexible process, resulting in a 1,3-propanediol
production and yield that depended on the initial sugar concentration. Below 56.2 g l−1 of sugar concentration, cultivation on molasses or glucose showed no significant differences. However, at higher molasses
concentrations, glycerol initially produced by yeast could not be totally converted into 1,3-propanediol by C. acetobutylicum and a lower 1,3-propanediol overall yield was observed. In our hand, the best results were obtained with an initial glucose
concentration of 103 g l−1, leading to a final 1,3-propanediol concentration of 25.5 g l−1, a productivity of 0.16 g l−1 h−1 and 1,3-propanediol yields of 0.56 g g−1 glycerol and 0.24 g g−1 sugar, which is the highest value reported for a two-step process. For an initial sugar concentration (from molasses) of
56.2 g l−1, 27.4 g l−1 of glycerol were produced, leading to 14.6 g l−1 of 1.3-propanediol and similar values of productivity, 0.15 g l−1 h−1, and overall yield, 0.26 g g−1 sugar. 相似文献
994.
Cobucci-Ponzano B Zorzetti C Strazzulli A Carillo S Bedini E Corsaro MM Comfort DA Kelly RM Rossi M Moracci M 《Glycobiology》2011,21(4):448-456
The large-scale production of oligosaccharides is a daunting task, hampering the study of the role of glycans in vivo and the testing of the efficacy of novel glycan-based drugs. Glycosynthases, mutated glycosidases that synthesize oligosaccharides in high yields, are becoming important chemo-enzymatic tools for the production of oligosaccharides. However, while β-glycosynthase can be produced with a rather well-established technology, examples of α-glycosynthases are thus far limited only to enzymes from glycoside hydrolase 29 (GH29), GH31 and GH95 families. α-L-Fucosynthases from GH29 use convenient glycosyl azide derivatives as a strategic alternative to glycosyl fluoride donors. However, the general applicability of this method to other α-glycosynthases is not trivial and remains to be confirmed. Here, β-D-galactopyranosyl azide was converted to α-galacto-oligosaccharides with good yields and high regioselectivity, catalyzed by a novel α-galactosynthase based on the GH36 α-galactosidase from the hyperthermophilic bacterium Thermotoga maritima. These results open a new avenue to the practical synthesis of biologically interesting α-galacto-oligosaccharides and demonstrate more widespread use of β-glycosyl-azide as donors, confirming their utility to expand the repertoire of glycosynthases. 相似文献
995.
996.
Human glioma cell culture: two FCS-free media could be recommended for clinical use in immunotherapy
Anne Clavreul Isabelle Jean Laurence Preisser Agnès Chassevent Anne Sapin Sophie Michalak Philippe Menei 《In vitro cellular & developmental biology. Animal》2009,45(9):500-511
Immunotherapy, particularly active vaccination, may be developed as an effective and safe treatment modality for malignant
gliomas, which continue to have a poor prognosis, despite advances in surgical techniques and adjuvant chemotherapy and radiotherapy.
Since no glioma-specific tumor-associated antigens (TAAs) have been discovered, autologous tumor cells or well-established
glioma cell lines could be used in future vaccination protocols to induce antitumour immunity against unknown TAAs. One obstacle
for clinical use of these tumour cell vaccines is related to foetal calf serum (FCS). Efforts are currently being directed
toward developing FCS-free media and serum-free alternatives to culture these cell vaccines. In this study, a medium containing
human serum and one serum-free medium (UltraCulture), supplemented or not with epidermal growth factor, were tested on morphology,
survival, DNA content and TAA expression of human glioma cell lines and glioma biopsy primary cultures. Their effects were
compared on FCS-containing medium. Results show that, whatever the medium used, no significant variations in morphology and
survival were observed. Furthermore, human serum-containing medium or UltraCulture preserved at early passage cultures the
cell population of interest present in the biopsies before culture. In addition, the expression profile of eight TAAs was
similar between these media. These data indicate that human serum-containing medium and UltraCulture serum-free medium could
be promising candidates to produce tumour-cell vaccines. 相似文献
997.
The outer membrane proteins TolC and EefC from Enterobacter aerogenes are involved in multidrug resistance as part of two resistance-nodulation-division efflux systems. To gain more understanding in the molecular mechanism underlying drug efflux, we have undertaken an electrophysiological characterization of the channel properties of these two proteins. TolC and EefC were purified in their native trimeric form and then reconstituted in proteoliposomes for patch-clamp experiments and in planar lipid bilayers. Both proteins generated a small single channel conductance of about 80 pS in 0.5 M KCl, indicating a common gated structure. The resultant pores were stable, and no voltage-dependent openings or closures were observed. EefC has a low ionic selectivity (P(K)/P(Cl)= approximately 3), whereas TolC is more selective to cations (P(K)/P(Cl)= approximately 30). This may provide a possible explanation for the difference in drug selectivity between the AcrAB-TolC and EefABC efflux systems observed in vivo. The pore-forming activity of both TolC and EefC was severely inhibited by divalent cations entering from the extracellular side. Another characteristic of the TolC and EefC channels was the systematic closure induced by acidic pH. These results are discussed in respect to the physiological functions and structural models of TolC and EefC. 相似文献
998.
Müller P Ewers C Bertsche U Anstett M Kallis T Breukink E Fraipont C Terrak M Nguyen-Distèche M Vollmer W 《The Journal of biological chemistry》2007,282(50):36394-36402
Bacterial cell division requires the coordinated action of cell division proteins and murein (peptidoglycan) synthases. Interactions involving the essential cell division protein FtsN and murein synthases were studied by affinity chromatography with membrane fraction. The murein synthases PBP1A, PBP1B, and PBP3 had an affinity to immobilized FtsN. FtsN and PBP3, but not PBP1A, showed an affinity to immobilized PBP1B. The direct interaction between FtsN and PBP1B was confirmed by pulldown experiments and surface plasmon resonance. The interaction was also detected by bacterial two-hybrid analysis. FtsN and PBP1B could be cross-linked in intact cells of the wild type and in cells depleted of PBP3 or FtsW. FtsN stimulated the in vitro murein synthesis activities of PBP1B. Thus, FtsN could have a role in controlling or modulating the activity of PBP1B during cell division in Escherichia coli. 相似文献
999.
Halilagic A Ribes V Ghyselinck NB Zile MH Dollé P Studer M 《Developmental biology》2007,303(1):362-375
We have previously shown that retinoic acid (RA) synthesized by the retinaldehyde dehydrogenase 2 (RALDH2) is required in forebrain development. Deficiency in RA due to inactivation of the mouse Raldh2 gene or to complete absence of retinoids in vitamin-A-deficient (VAD) quails, leads to abnormal morphogenesis of various forebrain derivatives. In this study we show that double Raldh2/Raldh3 mouse mutants have a more severe phenotype in the craniofacial region than single null mutants. In particular, the nasal processes are truncated and the eye abnormalities are exacerbated. It has been previously shown that retinoids act mainly on cell proliferation and survival in the ventral forebrain by regulating SHH and FGF8 signaling. Using the VAD quail model, which survives longer than the Raldh-deficient mouse embryos, we found that retinoids act in maintaining the correct position of anterior and dorsal boundaries in the forebrain by modulating FGF8 anteriorly and WNT signaling dorsally. Furthermore, BMP4 and FGF8 signaling are affected in the nasal region and BMP4 is ventrally expanded in the optic vesicle. At the optic cup stage, Pax6, Tbx5 and Bmp4 are ectopically expressed in the presumptive retinal pigmented epithelium (RPE), while Otx2 and Mitf are not induced, leading to a dorsal transdifferentiation of RPE to neural retina. Therefore, besides being required for survival of ventral structures, retinoids are involved in restricting anterior identity in the telencephalon and dorsal identity in the diencephalon and the retina. 相似文献
1000.
Adle Martial Isabelle Gaillard Jean-Marc Engasser Annie Marc 《Enzyme and microbial technology》1995,17(12):1062-1066
A homemade serum-free medium containing a low protein level under 0.1 g l−1 has been proved to support long-term cultures of VO 208 hybridoma cells successfully up to 50 days. The low protein level was achieved by supplying the lipids through liposomes containing cholesterol, oleic acid,
- dipalmitoyl phosphatidylcholine, and bovine serum albumin. The influence of the liposome content in the feeding medium was studied in a continuous culture performed with step variations of the liposomes level, from 7.5 to 30 ml l−1. The cell density decreased at the highest liposomes content while it became higher with 7.5 or 12 ml l−1 of liposomes. For each step variation appeared a transitory activation of the specific rates of nutrient consumption, metabolite production and antibody secretion, as well as a transitory decrease of the specific cell growth rate. The overall structure of the antibodies was not affected during the culture. 相似文献