全文获取类型
收费全文 | 1816篇 |
免费 | 176篇 |
国内免费 | 9篇 |
出版年
2023年 | 12篇 |
2022年 | 11篇 |
2021年 | 57篇 |
2020年 | 44篇 |
2019年 | 50篇 |
2018年 | 56篇 |
2017年 | 56篇 |
2016年 | 77篇 |
2015年 | 132篇 |
2014年 | 111篇 |
2013年 | 117篇 |
2012年 | 181篇 |
2011年 | 159篇 |
2010年 | 91篇 |
2009年 | 79篇 |
2008年 | 102篇 |
2007年 | 103篇 |
2006年 | 86篇 |
2005年 | 65篇 |
2004年 | 55篇 |
2003年 | 53篇 |
2002年 | 51篇 |
2001年 | 15篇 |
2000年 | 11篇 |
1999年 | 19篇 |
1998年 | 18篇 |
1997年 | 12篇 |
1996年 | 4篇 |
1995年 | 8篇 |
1994年 | 11篇 |
1992年 | 9篇 |
1991年 | 6篇 |
1990年 | 11篇 |
1989年 | 11篇 |
1988年 | 7篇 |
1987年 | 10篇 |
1986年 | 9篇 |
1982年 | 8篇 |
1981年 | 4篇 |
1980年 | 4篇 |
1979年 | 8篇 |
1977年 | 6篇 |
1974年 | 3篇 |
1973年 | 4篇 |
1972年 | 3篇 |
1971年 | 6篇 |
1970年 | 4篇 |
1969年 | 4篇 |
1968年 | 3篇 |
1967年 | 5篇 |
排序方式: 共有2001条查询结果,搜索用时 328 毫秒
41.
Andrea G. Marshall Jennifer A. Watson Jada J. Hallengren Brandon J. Walters Lynn E. Dobrunz Ludwig Francillon Julie A. Wilson Scott E. Phillips Scott M. Wilson 《PloS one》2013,8(12)
In this study, we identified and characterized an N-ethyl-N-nitrosourea (ENU) induced mutation in Usp14 (nmf375) that leads to adult-onset neurological disease. The nmf375 mutation causes aberrant splicing of Usp14 mRNA, resulting in a 95% reduction in USP14. We previously showed that loss of USP14 in ataxia (ax
J) mice results in reduced ubiquitin levels, motor endplate disease, Purkinje cell axonal dystrophy and decreased hippocampal paired pulse facilitation (PPF) during the first 4-6 weeks of life, and early postnatal lethality by two months of age. Although the loss of USP14 is comparable between the nmf375 and ax
J mice, the nmf375 mice did not exhibit these ax
J developmental abnormalities. However, by 12 weeks of age the nmf375 mutants present with ubiquitin depletion and motor endplate disease, indicating a continual role for USP14-mediated regulation of ubiquitin pools and neuromuscular junction (NMJ) structure in adult mice. The observation that motor endplate disease was only seen after ubiquitin depletion suggests that the preservation of NMJ structure requires the stable maintenance of synaptic ubiquitin pools. Differences in genetic background were shown to affect ubiquitin expression and dramatically alter the phenotypes caused by USP14 deficiency. 相似文献
42.
目的:早期液体复苏对感染性休克患者血流动力学的影响。方法:选取2012年2月-2013年2月我院ICU收治的26例感染性休克患者作为研究对象,随机分为对照组和试验组,各13例。两组患者均采用PICCO监测,并根据早期复苏目标导向(Earlygoaldirectedtherapy,EGDT)进行早期液体复苏治疗。对照组和试验组复苏液分别为林格液和6%羟乙基淀粉130/0.4氯化钠溶液。分别于复苏开始时(Oh)、8h和24h收集患者的血流动力学参数。结果:两组患者CO及PAWP水平均随着时间的延长下降,而CI、CVP及SVR水平均随着时间的增加上升。除对照组CI外,与开始复苏(oh)相比较试验组和对照组的C0、CI、CVP、SVR及PAWP与开始复苏(O小时)相比较均有显著差异(P值均〈0.05)。经重复测量资料的.方差分析进行比较发现,与对照组相比较,试验组CVP和SVR上升水平及PAWP下降水平明显,差异具有统计学意义(P值均〈0.05)。结论:感染性休克患者使用6%羟乙基淀粉130/0.4氯化钠溶液进行复苏,能更好的改善患者的血流动力学指标。 相似文献
43.
Brandon Faubert Gino Boily Said Izreig Takla Griss Bozena Samborska Zhifeng Dong Fanny Dupuy Christopher Chambers Benjamin J. Fuerth Benoit Viollet Orval A. Mamer Daina Avizonis Ralph J. DeBerardinis Peter M. Siegel Russell G. Jones 《Cell metabolism》2013,17(1):113-124
Highlights? Loss of AMPKα1 cooperates with the Myc oncogene to accelerate lymphomagenesis ? AMPKα dysfunction enhances aerobic glycolysis (Warburg effect) ? Inhibiting HIF-1α reverses the metabolic effects of AMPKα loss ? HIF-1α mediates the growth advantage of tumors with reduced AMPK signaling 相似文献
44.
Allison D. Ebert Brandon C. Shelley Amanda M. Hurley Marco Onorati Valentina Castiglioni Teresa N. Patitucci Soshana P. Svendsen Virginia B. Mattis Jered V. McGivern Andrew J. Schwab Dhruv Sareen Ho Won Kim Elena Cattaneo Clive N. Svendsen 《Stem cell research》2013,10(3):417-427
We have developed a simple method to generate and expand multipotent, self-renewing pre-rosette neural stem cells from both human embryonic stem cells (hESCs) and human induced pluripotent stem cells (iPSCs) without utilizing embryoid body formation, manual selection techniques, or complex combinations of small molecules. Human ESC and iPSC colonies were lifted and placed in a neural stem cell medium containing high concentrations of EGF and FGF-2. Cell aggregates (termed EZ spheres) could be expanded for long periods using a chopping method that maintained cell–cell contact. Early passage EZ spheres rapidly down-regulated OCT4 and up-regulated SOX2 and nestin expression. They retained the potential to form neural rosettes and consistently differentiated into a range of central and peripheral neural lineages. Thus, they represent a very early neural stem cell with greater differentiation flexibility than other previously described methods. As such, they will be useful for the rapidly expanding field of neurological development and disease modeling, high-content screening, and regenerative therapies based on pluripotent stem cell technology. 相似文献
45.
Jessica L. Miller Sara Murray Ashley M. Vaughan Anke Harupa Brandon Sack Michael Baldwin Ian N. Crispe Stefan H. I. Kappe 《PloS one》2013,8(4)
The liver stages of Plasmodium parasites are important targets for the development of anti-malarial vaccine candidates and chemoprophylaxis approaches that aim to prevent clinical infection. Analyzing the impact of interventions on liver stages in the murine malaria model system Plasmodium yoelii has been cumbersome and requires terminal procedures. In vivo imaging of bioluminescent parasites has previously been shown to be an effective and non-invasive alternative to monitoring liver stage burden in the Plasmodium berghei model. Here we report the generation and characterization of a transgenic P. yoelii parasite expressing the reporter protein luciferase throughout the parasite life cycle. In vivo bioluminescent imaging of these parasites allows for quantitative analysis of P. yoelii liver stage burden and parasite development, which is comparable to quantitative RT-PCR analysis of liver infection. Using this system, we show that both BALB/cJ and C57BL/6 mice show comparable susceptibility to P. yoelii infection with sporozoites and that bioluminescent imaging can be used to monitor protective efficacy of attenuated parasite immunizations. Thus, this rapid, simple and noninvasive method for monitoring P. yoelii infection in the liver provides an efficient system to screen and evaluate the effects of anti-malarial interventions in vivo and in real-time. 相似文献
46.
Stephanie Melkonian Maria Argos Megan N. Hall Yu Chen Faruque Parvez Brandon Pierce Hongyuan Cao Briseis Aschebrook-Kilfoy Alauddin Ahmed Tariqul Islam Vesna Slavcovich Mary Gamble Parvez I. Haris Joseph H. Graziano Habibul Ahsan 《PloS one》2013,8(11)
Background
We utilized data from the Health Effects of Arsenic Longitudinal Study (HEALS) in Araihazar, Bangladesh, to evaluate the association of steamed rice consumption with urinary total arsenic concentration and arsenical skin lesions in the overall study cohort (N=18,470) and in a subset with available urinary arsenic metabolite data (N=4,517).Methods
General linear models with standardized beta coefficients were used to estimate associations between steamed rice consumption and urinary total arsenic concentration and urinary arsenic metabolites. Logistic regression models were used to estimate prevalence odds ratios (ORs) and their 95% confidence intervals (CIs) for the associations between rice intake and prevalent skin lesions at baseline. Discrete time hazard models were used to estimate discrete time (HRs) ratios and their 95% CIs for the associations between rice intake and incident skin lesions.Results
Steamed rice consumption was positively associated with creatinine-adjusted urinary total arsenic (β=0.041, 95% CI: 0.032-0.051) and urinary total arsenic with statistical adjustment for creatinine in the model (β=0.043, 95% CI: 0.032-0.053). Additionally, we observed a significant trend in skin lesion prevalence (P-trend=0.007) and a moderate trend in skin lesion incidence (P-trend=0.07) associated with increased intake of steamed rice.Conclusions
This study suggests that rice intake may be a source of arsenic exposure beyond drinking water. 相似文献47.
Viki R. Chopda Timothy Holzberg Xudong Ge Brandon Folio Michael Tolosa Yordan Kostov Leah Tolosa Govind Rao 《Biotechnology and bioengineering》2020,117(4):981-991
Dissolved carbon dioxide (dCO2) is a well-known critical parameter in bioprocesses due to its significant impact on cell metabolism and on product quality attributes. Processes run at small-scale faces many challenges due to limited options for modular sensors for online monitoring and control. Traditional sensors are bulky, costly, and invasive in nature and do not fit in small-scale systems. In this study, we present the implementation of a novel, rate-based technique for real-time monitoring of dCO2 in bioprocesses. A silicone sampling probe that allows the diffusion of CO2 through its wall was inserted inside a shake flask/bioreactor and then flushed with air to remove the CO2 that had diffused into the probe from the culture broth (sensor was calibrated using air as zero-point calibration). The gas inside the probe was then allowed to recirculate through gas-impermeable tubing to a CO2 monitor. We have shown that by measuring the initial diffusion rate of CO2 into the sampling probe we were able to determine the partial pressure of the dCO2 in the culture. This technique can be readily automated, and measurements can be made in minutes. Demonstration experiments conducted with baker's yeast and Yarrowia lipolytica yeast cells in both shake flasks and mini bioreactors showed that it can monitor dCO2 in real-time. Using the proposed sensor, we successfully implemented a dCO2-based control scheme, which resulted in significant improvement in process performance. 相似文献
48.
Janousek Christopher N. Dugger Bruce D. Drucker Brandon M. Thorne Karen M. 《Hydrobiologia》2020,847(20):4311-4323
Hydrobiologia - Plant productivity is central to numerous ecosystem functions in tidal wetlands. We examined how productivity of brackish marsh plants in northern California responded to abiotic... 相似文献
49.
Naiomy D. Rios-Arce Andrew Dagenais Derrick Feenstra Brandon Coughlin Ho Jun Kang Susanne Mohr Laura R. McCabe Narayanan Parameswaran 《Journal of cellular physiology》2020,235(3):2350-2365
Type-1 diabetes (T1D) increases systemic inflammation, bone loss, and risk for bone fractures. Levels of the anti-inflammatory cytokine interleukin-10 (IL-10) are decreased in T1D, however their role in T1D-induced osteoporosis is unknown. To address this, diabetes was induced in male IL-10 knockout (KO) and wild-type (WT) mice. Analyses of femur and vertebral trabecular bone volume fraction identified bone loss in T1D-WT mice at 4 and 12 weeks, which in T1D-IL-10-KO mice was further reduced at 4 weeks but not 12 weeks. IL-10 deficiency also increased the negative effects of T1D on cortical bone. Osteoblast marker osterix was decreased, while osteoclast markers were unchanged, suggesting that IL-10 promotes anabolic processes. MC3T3-E1 osteoblasts cultured under high glucose conditions displayed a decrease in osterix which was prevented by addition of IL-10. Taken together, our results suggest that IL-10 is important for promoting osteoblast maturation and reducing bone loss during early stages of T1D. 相似文献
50.
Daniel C. B. Jeffery Brandon A. Wyse Muhammad Attiq Rehman Geoffrey W. Brown Zhiying You Roxanne Oshidari Hisao Masai Krassimir Y. Yankulov 《Nucleic acids research》2013,41(18):8475-8488
Position-effect variegation (PEV) phenotypes are characterized by the robust multigenerational repression of a gene located at a certain locus (often called gene silencing) and occasional conversions to fully active state. Consequently, the active state then persists with occasional conversions to the repressed state. These effects are mediated by the establishment and maintenance of heterochromatin or euchromatin structures, respectively. In this study, we have addressed an important but often neglected aspect of PEV: the frequency of conversions at such loci. We have developed a model and have projected various PEV scenarios based on various rates of conversions. We have also enhanced two existing assays for gene silencing in Saccharomyces cerevisiae to measure the rate of switches from repressed to active state and vice versa. We tested the validity of our methodology in Δsir1 cells and in several mutants with defects in gene silencing. The assays have revealed that the histone chaperone Chromatin Assembly Factor I is involved in the control of epigenetic conversions. Together, our model and assays provide a comprehensive methodology for further investigation of epigenetic stability and position effects. 相似文献