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701.
Zhang Y Ou Y Cheng M Saadi HS Thundathil JC van der Hoorn FA 《Developmental biology》2012,366(2):101-110
Kinesin light chain 3 (KLC3) is the only known kinesin light chain expressed in post-meiotic male germ cells. We have reported that in rat spermatids KLC3 associates with outer dense fibers and mitochondrial sheath. KLC3 is able to bind to mitochondria in vitro and in vivo employing the conserved tetratrico-peptide repeat kinesin light chain motif. The temporal expression and association of KLC3 with mitochondria coincides with the stage in spermatogenesis when mitochondria move from the spermatid cell periphery to the developing midpiece suggesting a role in midpiece formation. In fibroblasts, expression of KLC3 results in formation of large KLC3 aggregates close to the nucleus that contain mitochondria. However, the molecular basis of the aggregation of mitochondria by KLC3 and its role in sperm tail midpiece formation are not clear. Here we show that KLC3 expression from an inducible system causes mitochondrial aggregation within 6h in a microtubule dependent manner. We identified the mitochondrial outer membrane porin protein VDAC2 as a KLC3 binding partner. To analyze a role for KLC3 in spermatids we developed a transgenic mouse model in which a KLC3ΔHR mutant protein is specifically expressed in spermatids: this KLC3 mutant protein binds mitochondria and causes aggregate formation, but cannot bind outer dense fibers. Male transgenic mice display significantly reduced reproductive efficiency siring small sized litters. We observed defects in the mitochondrial sheath structure in a number of transgenic spermatids. Transgenic males have a significantly reduced sperm count and produce spermatozoa that exhibit abnormal motility parameters. Our results indicate that KLC3 plays a role during spermiogenesis in the development of the midpiece and in the normal function of spermatozoa. 相似文献
702.
Badrul Haque Kazi Mohibur Rahman Azharul Hoque ATM Hasibul Hasan Rajib Nayan Chowdhury Sharif Uddin Khan Mondal Badrul Alam Mansur Habib Quazi Deen Mohammad 《BMC neurology》2012,12(1):1-4
Background
The correlation between intracranial pressure (ICP) and intraocular pressure (IOP) is still controversial in literature and hence whether IOP can be used as a non-invasive surrogate of ICP remains unknown. The aim of the current study was to further clarify the potential correlation between ICP and IOP.Methods
The IOP measured with Goldmann applanation tonometer was carried out on 130 patients whose ICP was determined via lumber puncture. The Pearson correlation coefficient between ICP and IOP was calculated, the fisher line discriminated analysis to evaluate the effectivity of using IOP to predict the ICP level.Results
A significant correlation between ICP and IOP was found. ICP was correlated significantly with IOP of the right eyes (p?<?0.001) and IOP of the left eyes (p?=?0.001) and mean IOP of both eyes (p?<?0.001), respectively. However, using IOP as a measurement to predict ICP, the accuracy rate was found to be 65.4%.Conclusion
Our data suggested that although a significant correlation exists between ICP and IOP, caution needs to be taken when using IOP readings by Goldmann applanation tonometer as a surrogate for direct cerebrospinal fluid pressure measurement of ICP. 相似文献703.
704.
Background
The oxidation of proteins by endogenously generated free radicals causes structural modifications in the molecules that lead to generation of neo-antigenic epitopes that have implications in various autoimmune disorders, including rheumatoid arthritis (RA). Collagen induced arthritis (CIA) in rodents (rats and mice) is an accepted experimental model for RA.Methodology/Principal Findings
Hydroxyl radicals were generated by the Fenton reaction. Collagen type II (CII) was modified by •OH radical (CII-OH) and analysed by ultraviolet-visible (UV-VIS), fluorescence and circular dichroism (CD) spectroscopy. The immunogenicity of native and modified CII was checked in female Lewis rats and specificity of the induced antibodies was ascertained by enzyme linked immunosorbent assay (ELISA). The extent of CIA was evaluated by visual inspection. We also estimated the oxidative and inflammatory markers in the sera of immunized rats. A slight change in the triple helical structure of CII as well as fragmentation was observed after hydroxyl radical modification. The modified CII was found to be highly arthritogenic and immunogenic as compared to the native form. The CII-OH immunized rats exhibited increased oxidative stress and inflammation as compared to the CII immunized rats in the control group.Conclusions/Significance
Neo-antigenic epitopes were generated on •OH modified CII which rendered it highly immunogenic and arthritogenic as compared to the unmodified form. Since the rodent CIA model shares many features with human RA, these results illuminate the role of free radicals in human RA. 相似文献705.
706.
Lorna R. Fiedler Kathryn Chapman Min Xie Evie Maifoshie Micaela Jenkins Pelin Arabacilar Golforoush Mohamed Bellahcene Michela Noseda Dörte Faust Ashley Jarvis Gary Newton Marta Abreu Paiva Mutsuo Harada Daniel J. Stuckey Weihua Song Josef Habib Priyanka Narasimham Rehan Aqil Michael D. Schneider 《Cell Stem Cell》2019,24(4):579-591.e12
707.
Agopian A Ronzon F Sauzéat E Sodoyer R El Habib R Buchet R Chevalier M 《Biochimica et biophysica acta》2007,1774(3):351-358
The formulation of human vaccines often includes adjuvants such as aluminum hydroxide that are added to enhance the immune responses to vaccine antigens. However, these adjuvants may also affect the conformation of antigenic proteins. Such structural modifications could lead to changes in antigenicity such that suboptimal protective immune responses could be generated relative to those induced by the vaccine antigens alone. Here, we used attenuated total reflectance infrared spectroscopy (ATR-FTIR) to compare the secondary structures of recombinant HIV-1-gp41 (gp41) in solution or adsorbed to aluminum hydroxide. The gp41 secondary structure content was 72% alpha-helices and 28% beta-sheets in 5 mM formate buffer p(2)H 2.5, while it was 66% beta-sheets and 34% random coil in acetonitril/(2)H(2)O (95/5:v/v). A fully reversible conformational change of gp41 in acetonitril/(2)H(2)O (95/5:v/v) was observed upon addition of either 35 mM formate p(2)H 2.5 or 0.1% (w/v) detergent (Tween 20, Hecameg, Brij 35 or beta-d-octyl-glucopyranoside). When gp41 was adsorbed to aluminum hydroxide in the presence of 0.1% (w/v) detergent, in either formate or in acetonitril/(2)H(2)O (95/5:v/v) its secondary structure remained stable and was identical to that of gp41 in 5 mM formate buffer p(2)H 2.5. The method described here could be applied for the characterization of gp41 conformers for use in immunological screening of antigens, and more generally to all antigenic proteins adsorbed to aluminum hydroxide. 相似文献
708.
Tamir A Basagila E Kagahzian A Jiao L Jensen S Nicholls J Tate P Stamp G Farzaneh F Harrison P Stauss H George AJ Habib N Lechler RI Lombardi G 《Cancer immunology, immunotherapy : CII》2007,56(12):2017-2016
Background Dendritic cells (DCs) are the most effective antigen-presenting cells. In the last decade, the use of DCs for immunotherapy
of cancer patients has been vastly increased. High endocytic capacity together with a unique capability of initiating primary
T-cell responses have made DCs the most potent candidates for this purpose. Although DC vaccination occasionally leads to
tumor regression, clinical efficacy, and immunogenicity of DCs in clinical trials has not been yet clarified. The present
study evaluated the safety and effectiveness of tumor-lysate loaded DC vaccines in advanced colorectal cancer (CRC) patients
with carcinoembryonic antigen (CEA) positive tumors.
Results Six patients HLA-A*0201-positive were vaccinated with autologous DCs loaded with tumor lysates (TL) together with tetanus
toxoid antigen, hepatitis B, and influenza matrix peptides. Two additional patients were injected with DCs that were generated
from their sibling or parent with one haplotype mismatch. All patients received the vaccines every 2 weeks, with a total of
three intra-nodal injections per patient. The results indicated that DC vaccination was safe and well tolerated by the patients.
Specific immune responses were detected and in some patients, transient stabilization or even reduction of CEA levels were
observed. The injection of haplotype mismatched HLA-A*0201-positive DCs resulted in some enhancement of the anti-tumor response
in vitro and led to stabilization/reduction of CEA levels in the serum, compared to the use of autologous DCs.
Conclusion Altogether, these results suggest that TL-pulsed DCs may be an effective vaccine method in CRC patients. Elimination of regulatory
mechanisms as well as adjustment of the vaccination protocol may improve the efficacy of DC vaccination.
An erratum to this article can be found at 相似文献
709.
Cd-induced growth reduction in the halophyte <Emphasis Type="Italic">Sesuvium portulacastrum</Emphasis> is significantly improved by NaCl 总被引:2,自引:0,他引:2
Ghnaya T Slama I Messedi D Grignon C Ghorbel MH Abdelly C 《Journal of plant research》2007,120(2):309-316
The effects of Cd2+ and NaCl, applied together or separately, on growth and uptake of Cd2+ were determined for the halophyte Sesuvium portulacastrum L. Seedlings were cultivated in the presence of 50 or 100 μmol L−1 Cd2+ alone or combined with 100 or 400 mmol L−1 NaCl. Data showed that alone, Cd2+ induced chlorosis, necrosis, and inhibited growth. Addition of NaCl to Cd2+-containing medium restored growth and alleviated the toxicity, however. NaCl also enhanced the amounts of Cd2+ accumulated in the shoots. All Cd2+ treatment reduced K+ and Ca2+ uptake and transport to the shoots. Accumulation of Na+ in the shoots was not affected by Cd2+, however. Thus S. portulacastrum maintained its halophytic characteristics in the presence of Cd2+. We suggest this halophyte could be used for phytoextraction of Cd2+ from salt-contaminated sites. 相似文献
710.
To understand the role of glutathione (GSH) in the protection of cells from arsenite toxicity, we studied the mechanism of apoptotic cell death in cells genetically unable to synthesize GSH (GCS-2 cells). Arsenite stimulated an increase in protein ubiquitination in GCS-2 cells while the wild-type cells were unaffected. Arsenite treatment increased lipid peroxidation and induced ubiquitination of molecular chaperone Hsp90 and impaired its ability to bind cochaperone p50(Cdc-37) and client proteins Plk-1 and Cdk-4 in GCS-2 cells. Treatment with arsenite also partially inhibited proteasome activity in GCS-2 cells. In these cells stably transfected with GFP(u) (a reporter consisting of a short degron fused to the COOH-terminus of GFP), intracellular fluorescence increased, suggesting the accumulation of GFP aggregates. GCS-2 cells underwent apoptosis accompanied by release of cytochrome c into the cytoplasm. Taken together, these data suggest that a possible mechanism of arsenite-induced apoptosis is the accumulation of ubiquitinated proteins and impairment of the protein degradative pathway. Further, protection from arsenite-induced ubiquitination is mediated by GSH and to a lesser extent by available reducing equivalents in the cells. 相似文献