全文获取类型
收费全文 | 1388篇 |
免费 | 84篇 |
出版年
2022年 | 12篇 |
2021年 | 16篇 |
2019年 | 8篇 |
2018年 | 19篇 |
2017年 | 9篇 |
2016年 | 25篇 |
2015年 | 37篇 |
2014年 | 34篇 |
2013年 | 66篇 |
2012年 | 70篇 |
2011年 | 68篇 |
2010年 | 42篇 |
2009年 | 42篇 |
2008年 | 63篇 |
2007年 | 57篇 |
2006年 | 52篇 |
2005年 | 75篇 |
2004年 | 79篇 |
2003年 | 67篇 |
2002年 | 43篇 |
2001年 | 66篇 |
2000年 | 52篇 |
1999年 | 45篇 |
1998年 | 21篇 |
1997年 | 13篇 |
1996年 | 19篇 |
1995年 | 11篇 |
1994年 | 15篇 |
1993年 | 14篇 |
1992年 | 27篇 |
1991年 | 25篇 |
1990年 | 18篇 |
1989年 | 24篇 |
1988年 | 29篇 |
1987年 | 24篇 |
1986年 | 22篇 |
1985年 | 17篇 |
1984年 | 12篇 |
1983年 | 17篇 |
1982年 | 11篇 |
1981年 | 7篇 |
1980年 | 14篇 |
1979年 | 14篇 |
1978年 | 6篇 |
1977年 | 8篇 |
1976年 | 6篇 |
1974年 | 5篇 |
1973年 | 6篇 |
1971年 | 9篇 |
1966年 | 5篇 |
排序方式: 共有1472条查询结果,搜索用时 15 毫秒
161.
Superoxide dismutase (SOD) as a potential inhibitory mediator of inflammation via neutrophil apoptosis 总被引:1,自引:0,他引:1
Yasui K Kobayashi N Yamazaki T Agematsu K Matsuzaki S Ito S Nakata S Baba A Koike K 《Free radical research》2005,39(7):755-762
Superoxide dismutase (SOD) is supposed to be an effective agent for neutrophil-mediated inflammation in the area of critical medicine. We investigated the involvement of SOD in the regulation of neutrophil apoptosis. Exogenously added SOD effectively induced neutrophil apoptosis, and the fluorescence patterns determined using annexin-V and the 7-AAD were similar to those seen in Fas-mediated neutrophil apoptosis. Neutrophils are short-lived leukocytes that need to be removed safely by apoptosis. The clearance of apoptotic neutrophils from sites of inflammation is a crucial determinant of the resolution of inflammation. Catalase inhibited the neutrophil apoptosis and caspase-3 activation. Spontaneous apoptosis, hydrogen peroxide and anti-Fas antibody-induced apoptosis of neutrophils were accelerated in Down's syndrome patients, in whom the SOD gene is overexpressed. Hydrogen peroxide was thought to be a possible major mediator of ROS-induced neutrophil apoptosis in caspase-dependent manner. Neutrophil apoptosis represents a crucial step in the mechanism governing the resolution of inflammation and has been suggested as a possible target for the control of neutrophil-mediated tissue injury. SOD may be a potential inhibitory mediator of neutrophil-mediated inflammation. 相似文献
162.
LSD1 is a recently identified human lysine (K)-specific histone demethylase. LSD1 is associated with HDAC1/2; CoREST, a SANT domain-containing corepressor; and BHC80, a PHD domain-containing protein, among others. We show that CoREST endows LSD1 with the ability to demethylate nucleosomal substrates and that it protects LSD1 from proteasomal degradation in vivo. We find hyperacetylated nucleosomes less susceptible to CoREST/LSD1-mediated demethylation, suggesting that hypoacetylated nucleosomes may be the preferred physiological substrates. This raises the possibility that histone deacetylases and LSD1 may collaborate to generate a repressive chromatin environment. Consistent with this model, TSA treatment results in derepression of LSD1 target genes. While CoREST positively regulates LSD1 function, BHC80 inhibits CoREST/LSD1-mediated demethylation in vitro and may therefore confer negative regulation. Taken together, these findings suggest that LSD1-mediated histone demethylation is regulated dynamically in vivo. This is expected to have profound effects on gene expression under both physiological and pathological conditions. 相似文献
163.
164.
Terada N Ohno N Yamakawa H Ohara O Liao X Baba T Ohno S 《Histochemistry and cell biology》2005,124(3-4):303-311
Protein 4.1 families have recently been established as potential organizers of an adherens system. In the adult mouse testis,
protein 4.1G (4.1G) localized as a line pattern in both basal and adluminal compartments of the seminiferous tubules, attaching
regions of germ cells and Sertoli cells. By double staining for 4.1G and F-actin, their localizations were shown to be different,
indicating that 4.1G was localized in a region other than the basal and apical ectoplasmic specializations, which formed the
Sertoli–Sertoli cell junction and Sertoli–spermatid junction, respectively. By electron microscopy, immunoreactive products
were seen exclusively on the cell membranes of Sertoli cells, attaching to the various differentiating germ cells. The immunolocalization
of cadherin was identical to that of 4.1G, supporting the idea that 4.1G may be functionally interconnected with adhesion
molecules. In an experimental mouse model of cadmium treatment, in which tight and adherens junctions of seminiferous tubules
were disrupted, the 4.1G immunostaining in the seminiferous tubules was dramatically decreased. These results indicate that
4.1G may have a basic adhesive function between Sertoli cells and germ cells from the side of Sertoli cells. 相似文献
165.
Protein 4.1 G localizes in rodent microglia 总被引:2,自引:2,他引:0
Ohno N Terada N Tanaka J Yokoyama A Yamakawa H Fujii Y Baba T Ohara O Ohno S 《Histochemistry and cell biology》2005,124(6):477-486
Although it was reported that protein 4.1 G, a cytoskeletal protein characterized by its general expression in the body, interacts
with some signal transduction molecules in the central nervous system (CNS), its distribution and significance in vivo remained
to be elucidated. In the present study, we have identified 4.1 G-positive cells in the rodent CNS, and demonstrated its immunolocalization
in the developing mouse CNS. In the rodent CNS, 4.1 G was colocalized with markers for microglia, such as CD45, OX-42 and
ionized calcium-binding adapter molecule 1 (Iba1), but not with markers for neuronal or other glial cells. Additionally, colocalization
of 4.1 G and A1 adenosine receptor was observed in the mouse cerebrum. In a mixed glial culture, most OX-42-positive microglia
were positive for 4.1 G, and 4.1 G isoforms of the same molecular weight as in the rat brain were expressed in cultured microglia,
where 4.1 G mRNA was detected by RT-PCR. In the developing mouse cerebral cortex, 4.1 G was detected in immature microglia,
which were positive for Iba1. These results indicate that 4.1 G in the CNS is mainly distributed in microglia in vivo. Considering
the interactions between 4.1 G and the signal transduction molecules, putative roles have been propsed for 4.1 G in microglial
functions in the CNS. 相似文献
166.
Brain macrophages/microglia and astrocytes are known to be involved in the pathogenesis of HIV-1-associated dementia (HAD). To clarify their interaction and contribution to the pathogenesis, HIV-1-infected or uninfected macrophages were used as a model of brain macrophages/microglia, and their effects on human astrocytes in vitro were examined. The culture supernatants of HIV-1-infected or uninfected macrophages induced significant astrocyte proliferation, which was annihilated with a neutralizing antibody to stromal cell-derived factor (SDF)-1alpha or a matrix metalloproteinase (MMP) inhibitor. In these astrocytes, CXCR4, MMP, and tissue inhibitors of matrix metalloproteinase mRNA expression and SDF-1alpha production were significantly up-regulated. The supernatants of infected macrophages were always more effective than those of uninfected cells. Moreover, the enhanced production of SDF-1alpha was suppressed by the MMP inhibitor. These results indicate that the activated and HIV-1-infected macrophages can indirectly induce astrocyte proliferation through up-regulating SDF-1alpha and MMP production, which implies a mechanism of astrogliosis in HAD. 相似文献
167.
Difference in bacterial motion between forward and backward swimming caused by the wall effect 下载免费PDF全文
Magariyama Y Ichiba M Nakata K Baba K Ohtani T Kudo S Goto T 《Biophysical journal》2005,88(5):3648-3658
A bacterial cell that has a single polar flagellum alternately repeats forward swimming, in which the flagellum pushes the cell body, and backward swimming, in which the flagellum pulls the cell body. We have reported that the backward swimming speeds of Vibrio alginolyticus are on average greater than the forward swimming speeds. In this study, we quantitatively measured the shape of the trajectory as well as the swimming speed. The trajectory shape in the forward mode was almost straight, whereas that in the backward mode was curved. The same parameters were measured at different distances from a surface. The difference in the motion characteristics between swimming modes was significant when a cell swam near a surface. In contrast, the difference was indistinguishable when a cell swam >60 microm away from any surfaces. In addition, a cell in backward mode tended to stay near the surface longer than a cell in forward mode. This wall effect on the bacterial motion was independent of chemical modification of the glass surface. The macroscopic behavior is numerically simulated on the basis of experimental results and the significance of the phenomenon reported here is discussed. 相似文献
168.
Bubikat A De Windt LJ Zetsche B Fabritz L Sickler H Eckardt D Gödecke A Baba HA Kuhn M 《The Journal of biological chemistry》2005,280(22):21594-21599
The crucial functions of atrial natriuretic peptide (ANP) and endothelial nitric oxide/NO in the regulation of arterial blood pressure have been emphasized by the hypertensive phenotype of mice with systemic inactivation of either the guanylyl cyclase-A receptor for ANP (GC-A-/-) or endothelial nitric-oxide synthase (eNOS-/-). Intriguingly, similar levels of arterial hypertension are accompanied by marked cardiac hypertrophy in GC-A-/-, but not in eNOS-/-, mice, suggesting that changes in local pathways regulating cardiac growth accelerate cardiac hypertrophy in the former and protect the heart of the latter. Our recent observations in mice with conditional, cardiomyocyte-restricted GC-A deletion demonstrated that ANP locally inhibits cardiomyocyte growth. Abolition of these local, protective effects may enhance the cardiac hypertrophic response of GC-A-/- mice to persistent increases in hemodynamic load. Notably, eNOS-/- mice exhibit markedly increased cardiac ANP levels, suggesting that increased activation of cardiac GC-A can prevent hypertensive heart disease. To test this hypothesis, we generated mice with systemic inactivation of eNOS and cardiomyocyte-restricted deletion of GC-A by crossing eNOS-/- and cardiomyocyte-restricted GC-A-deficient mice. Cardiac deletion of GC-A did not affect arterial hypertension but significantly exacerbated cardiac hypertrophy and fibrosis in eNOS-/- mice. This was accompanied by marked cardiac activation of both the mitogen-activated protein kinase (MAPK) ERK 1/2 and the phosphatase calcineurin. Our observations suggest that local ANP/GC-A/cyclic GMP signaling counter-regulates MAPK/ERK- and calcineurin/nuclear factor of activated T cells-dependent pathways of cardiac myocyte growth in hypertensive eNOS-/- mice. 相似文献
169.
Estrogen, insulin, and dietary signals cooperatively regulate longevity signals to enhance resistance to oxidative stress in mice 总被引:6,自引:0,他引:6
Baba T Shimizu T Suzuki Y Ogawara M Isono K Koseki H Kurosawa H Shirasawa T 《The Journal of biological chemistry》2005,280(16):16417-16426
To investigate the biological significance of a longevity mutation found in daf-2 of Caenorhabditis elegans, we generated a homologous murine model by replacing Pro-1195 of insulin receptors with Leu using a targeted knock-in strategy. Homozygous mice died in the neonatal stage from diabetic ketoacidosis, whereas heterozygous mice showed the suppressed kinase activity of the insulin receptor but grew normally without spontaneously developing diabetes during adulthood. We examined heterozygous insulin receptor mutant mice for longevity phenotypes. Under 80% oxygen, mutant female mice survived 33.3% longer than wild-type female mice, whereas mutant male mice survived 18.2% longer than wild-type male mice. These results suggested that mutant mice acquired more resistance to oxidative stress, but the benefit of the longevity mutation was more pronounced in females than males. Manganese superoxide dismutase activity in mutant mice was significantly upregulated, suggesting that the suppressed insulin signaling leads to an enhanced antioxidant defense. To analyze the molecular basis of the gender difference, we administered estrogen to mutant mice. It was found that the survival of mice under 80% oxygen was extended when they were administered estradiol. In contrast, mutant and wild-type female mice showed shortened survivals when their ovaries were removed. The influence of estrogen is remarkable in mutant mice compared with wild-type mice, suggesting that estrogen modulates insulin signaling in mutant mice. Furthermore, we showed additional extension of survival under oxidative conditions when their diet was restricted. Collectively, we show that three distinct signals; insulin, estrogen, and dietary signals work in independent and cooperative ways to enhance the resistance to oxidative stress in mice. 相似文献
170.
Yamada T Sakisaka T Hisata S Baba T Takai Y 《The Journal of biological chemistry》2005,280(38):33026-33034
Rap1 and Rho small G proteins have been implicated in the neurite outgrowth, but the functional relationship between Rap1 and Rho in the neurite outgrowth remains to be established. Here we identified a potent Rho GTPase-activating protein (GAP), RA-RhoGAP, as a direct downstream target of Rap1 in the neurite outgrowth. RA-RhoGAP has the RA and GAP domains and showed GAP activity specific for Rho, which was enhanced by the binding of the GTP-bound active form of Rap1 to the RA domain. Overexpression of RA-RhoGAP induced inactivation of Rho for promoting the neurite outgrowth in a Rap1-dependent manner. Knockdown of RA-RhoGAP reduced the Rap1-induced neurite outgrowth. These results indicate that RA-RhoGAP transduces a signal from Rap1 to Rho and regulates the neurite outgrowth. 相似文献