全文获取类型
收费全文 | 1586篇 |
免费 | 116篇 |
国内免费 | 111篇 |
出版年
2024年 | 2篇 |
2023年 | 20篇 |
2022年 | 31篇 |
2021年 | 71篇 |
2020年 | 55篇 |
2019年 | 54篇 |
2018年 | 48篇 |
2017年 | 46篇 |
2016年 | 72篇 |
2015年 | 97篇 |
2014年 | 109篇 |
2013年 | 120篇 |
2012年 | 113篇 |
2011年 | 139篇 |
2010年 | 79篇 |
2009年 | 74篇 |
2008年 | 87篇 |
2007年 | 74篇 |
2006年 | 93篇 |
2005年 | 58篇 |
2004年 | 60篇 |
2003年 | 36篇 |
2002年 | 35篇 |
2001年 | 20篇 |
2000年 | 17篇 |
1999年 | 29篇 |
1998年 | 21篇 |
1997年 | 24篇 |
1996年 | 26篇 |
1995年 | 20篇 |
1994年 | 13篇 |
1993年 | 9篇 |
1992年 | 9篇 |
1991年 | 9篇 |
1990年 | 4篇 |
1989年 | 9篇 |
1988年 | 5篇 |
1987年 | 5篇 |
1986年 | 1篇 |
1985年 | 2篇 |
1984年 | 3篇 |
1983年 | 4篇 |
1982年 | 2篇 |
1980年 | 1篇 |
1979年 | 1篇 |
1978年 | 1篇 |
1977年 | 1篇 |
1976年 | 1篇 |
1975年 | 2篇 |
1972年 | 1篇 |
排序方式: 共有1813条查询结果,搜索用时 31 毫秒
191.
192.
Wei J Ouyang H Wang Y Pang D Cong NX Wang T Leng B Li D Li X Wu R Ding Y Gao F Deng Y Liu B Li Z Lai L Feng H Liu G Deng X 《The FEBS journal》2012,279(1):91-99
Hypertriglyceridemia has recently been considered to be an independent risk factor for coronary heart disease, in which apolipoprotein (Apo)CIII is one of the major contributory factors, as it is strongly correlated with plasma triglyceride levels. Although ApoCIII transgenic mice have been generated as an animal model for the study of hypertriglyceridemia, the features of lipoprotein metabolism in mice differ greatly from those in humans. Because of the great similarity between pigs and humans with respect to lipid metabolism and cardiovascular physiology, we generated transgenic miniature pigs expressing human ApoCIII by the transfection of somatic cells combined with nuclear transfer. The expression of human ApoCIII was detected in the liver and intestine of the transgenic pigs. As compared with nontransgenic controls, transgenic pigs showed significantly increased plasma triglyceride levels (83 ± 36 versus 38 ± 4 mg·dL(-1), P < 0.01) when fed a chow diet. Plasma lipoprotein profiling by FPLC in transgenic animals showed a higher peak in large-particle fractions corresponding to very low-density lipoprotein/chylomicrons when triglyceride content in the fractions was assayed. There was not much difference in cholesterol content in FPLC fractions, although a large low-density lipoprotein peak was identified in both nontransgenic and transgenic animals, resembling that found in humans. Further analysis revealed markedly delayed clearance of plasma triglyceride, accompanied by significantly reduced lipoprotein lipase activity in post-heparin plasma, in transgenic pigs as compared with nontransgenic controls. In summary, we have successfully generated a novel hypertriglyceridemic ApoCIII transgenic miniature pig model that could be of great value for studies on hyperlipidemia in relation to atherosclerotic disorders. 相似文献
193.
The pathophysiology of spinal cord injury (SCI) is characterized by the initial, primary injury followed by secondary injury processes in which oxidative stress is a critical component. Secondary injury processes not only exacerbate pathology at the site of primary injury, but also result in spreading of injuries to the adjacent, otherwise healthy tissue. The lipid peroxidation byproduct acrolein has been implicated as one potential mediator of secondary injury. To further and rigorously elucidate the role of acrolein in secondary injury, a unique ex vivo model is utilized to isolate the detrimental effects of mechanical injury from toxins such as acrolein that are produced endogenously following SCI. We demonstrate that (i) acrolein-Lys adducts are capable of diffusing from compressed tissue to adjacent, otherwise uninjured tissue; (ii) secondary injury by itself produces significant membrane damage and increased superoxide production; and (iii) these injuries are significantly attenuated by the acrolein scavenger hydralazine. Furthermore, hydralazine treatment results in significantly less membrane damage 2 h following compression injury, but not immediately after. These findings support our hypothesis that, following SCI, acrolein is increased to pathologic concentrations, contributes significantly to secondary injury, and thus represents a novel target for scavenging to promote improved recovery. 相似文献
194.
Foliar δ13C values of Calligogum kozlovi and Haloxylon ammodendron ranged from −13.13 to −15.11 ‰, while those of the rest 11 species were in the range of −22.22 to −27.73 ‰. This indicates
that two of 13 dominant plant species in the Qaidam Basin possess a C4 photosynthetic pathway. Significant differences were observed for the average foliar δ13C values between C3 or C4 plant communities, between grass and shrub communities, even between the same species derived from different sites. Precipitation
accounted for the major part of the differences. 相似文献
195.
196.
Changes in landscape pattern of alpine wetlands on the Zoige Plateau in the past four decades 总被引:2,自引:0,他引:2
下载免费PDF全文
![点击此处可从《农业工程》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Based on RS, GIS and Apack software, the indices of landscape pattern such as landscape area index, landscape diversity index and landscape fragmentation index were chosen in order to describe changes in the spatial pattern of alpine wetland landscape on the Zoige Plateau during 1966–2000. Results showed that alpine wetland landscape was characteristic of marsh wetlands, which had the biggest patch number and the largest area. The alpine wetland landscape had higher spatial heterogeneity. The largest area appeared in Zoige County with the highest wetland ratio; comparatively, Aba County and Luqu County had much lower wetland ratio. The total area of alpine wetland landscape decreased rapidly during 1966–1986, but it began to increase after 1986. The wetland landscape area shrank by 59857.83 hm2 during 1966–2000. The alpine wetland landscape showed the characteristics of concentrated distribution in the past four decades, with higher convergence and dominance indices. The centroid of wetland landscape moved 12.54 km in the northwest direction firstly, 11.33 km in the southeast direction, and then 1.1 km in the north direction. 相似文献
197.
Variation in gene expression may give rise to a significant fraction of inter-individual phenotypic variation. Studies searching for the underlying genetic controls for such variation have been conducted in model organisms and humans in recent years. In our previous effort of assessing conserved underlying haplotype patterns across ethnic populations, we constructed common haplotypes using SNPs having conserved linkage disequilibrium (LD) across ethnic populations. These common haplotypes cluster into a simple evolutionary structure based on their frequencies, defining only up to three conserved clusters termed 'haplotype frameworks'. One intriguing preliminary finding was that a significant portion of reported variants strongly associated with cis-regulation tags these globally conserved haplotype frameworks. Here we expand the investigation by collecting genes showing stringently determined cis-association between genotypes and expression phenotypes from major studies. We conducted phylogenetic analysis of current major haplotypes along with the corresponding haplotypes derived from chimpanzee reference sequences. Our analysis reveals that, for the vast majority of such cis-regulatory genes, the tagging SNPs showing the strongest association also tag the haplotype lineages directly separated from ancestry, inferred from either chimpanzee reference sequences or the allele frequency-derived haplotype frameworks, suggesting that the differentially expressed phenotypes were evolved relatively early in human history. Such evolutionary signatures provide keys for a more effective identification of globally-conserved candidate regulatory haplotypes across human genes in future epidemiologic and pharmacogenetic studies. 相似文献
198.
199.
Kyriazis GA Wei Z Vandermey M Jo DG Xin O Mattson MP Chan SL 《The Journal of biological chemistry》2008,283(37):25492-25502
Central to the pathogenesis of Alzheimer disease is the aberrant processing of the amyloid precursor protein (APP) to generate amyloid beta-peptide (Abeta), the principle component of amyloid plaques. The cell fate determinant Numb is a phosphotyrosine binding domain (PTB)-containing endocytic adapter protein that interacts with the carboxyl-terminal domain of APP. The physiological relevance of this interaction is unknown. Mammals produce four alternatively spliced variants of Numb that differ in the length of their PTB and proline-rich region. In the current study, we determined the influence of the four human Numb isoforms on the intracellular trafficking and processing of APP. Stable expression of Numb isoforms that differ in the PTB but not in the proline-rich region results in marked differences in the sorting of APP to the recycling and degradative pathways. Neural cells expressing Numb isoforms that lack the insert in the PTB (short PTB (SPTB)) exhibited marked accumulation of APP in Rab5A-labeled early endosomal and recycling compartments, whereas those expressing isoforms with the insertion in the PTB (long PTB (LPTB)) exhibited reduced amounts of cellular APP and its proteolytic derivatives relative to parental control cells. Neither the activities of thebeta- and gamma-secretases nor the expression of APP mRNA were significantly different in the stably transfected cells, suggesting that the differential effects of the Numb proteins on APP metabolism is likely to be secondary to altered APP trafficking. In addition, the expression of SPTB-Numb increases at the expense of LPTB-Numb in neuronal cultures subjected to stress, suggesting a role for Numb in stress-induced Abeta production. Taken together, these results suggest distinct roles for the human Numb isoforms in APP metabolism and may provide a novel potential link between altered Numb isoform expression and increased Abeta generation. 相似文献
200.
Xiong B Li S Ai JS Yin S Ouyang YC Sun SC Chen DY Sun QY 《Biology of reproduction》2008,79(4):718-726
BRCA1 as a tumor suppressor has been widely investigated in mitosis, but its functions in meiosis are unclear. In the present study, we examined the expression, localization, and function of BRCA1 during mouse oocyte meiotic maturation. We found that expression level of BRCA1 was increased progressively from germinal vesicle to metaphase I stage, and then remained stable until metaphase II stage. Immunofluorescent analysis showed that BRCA1 was localized to the spindle poles at metaphase I and metaphase II stages, colocalizing with centrosomal protein gamma-tubulin. Taxol treatment resulted in the presence of BRCA1 onto the spindle microtubule fibers, whereas nocodazole treatment induced the localization of BRCA1 onto the chromosomes. Depletion of BRCA1 by both antibody injection and siRNA injection caused severely impaired spindles and misaligned chromosomes. Furthermore, BRCA1-depleted oocytes could not arrest at the metaphase I in the presence of low-dose nocodazole, suggesting that the spindle checkpoint is defective. Also, in BRCA1-depleted oocytes, gamma-tubulin dissociated from spindle poles and MAD2L1 failed to rebind to the kinetochores when exposed to nocodazole at metaphase I stage. Collectively, these data indicate that BRCA1 regulates not only meiotic spindle assembly, but also spindle assembly checkpoint, implying a link between BRCA1 deficiency and aneuploid embryos. 相似文献