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61.
CD3单抗诱导幼龄小鼠胸腺细胞凋亡研究 总被引:1,自引:0,他引:1
用抗小鼠CD3单抗刺激幼龄小鼠胸腺细胞,培养不同时间后,检测小鼠胸腺细胞的凋亡情况。结果表明,胸腺细胞呈现了凋亡的典型形态学改变。流式细胞仪检测可见凋亡细胞特有的AP峰,CD3单抗刺激未成熟胸腺细胞可以通过内源性的凋亡途径引起细胞死亡。 相似文献
62.
63.
Sébastien Personnic Isabelle Domaizon Ursula Dorigo Lyria Berdjeb Stéphan Jacquet 《Hydrobiologia》2009,627(1):99-116
Flow cytometry (FCM) was used to assess microbial community abundances and patterns in three natural, large and deep peri-alpine
hydrosystems, i.e., lakes Annecy (oligotrophic), Bourget, and Geneva (mesotrophic). Picocyanobacteria, small eukaryotic autotrophs,
heterotrophic prokaryotes, and viruses were studied in the 0–50 m surface layers to highlight the impact of both physical
and chemical parameters as well as possible biotic interactions on the functioning of microbial communities. Some specificities
were recorded according to the trophic status of each ecosystem such as the higher number of viruses and heterotrophic bacteria
in mesotrophic environments (i.e., Lakes Geneva and Bourget) or the higher abundance of picocyanobacteria in the oligotrophic
Lake Annecy. However, both seasonal (temperature) and spatial (depth) variations were comparatively more important than the
trophic status in driving the microbial communities’ abundances in these three lakes, as revealed by principal component analysis
(PCA). A strong viral termination of the heterotrophic bacterial blooms could be observed in autumn for each lake, in parallel
to the mixing of the upper lit layers. As virus to bacteria ratio (VBR) was indeed very high at this period with values varying
between 87 and 114, such important relationships between viruses and bacteria were likely. The magnitudes of seasonal variations
in VBR, with the highest values ever reported so far, were largely greater than the magnitude of theoretical variations due
to the trophic status, suggesting also a strong seasonality in virioplankton production associated to prokaryotic dynamics.
FCM analyses allowed discriminating several viral groups. Virus-Like Particles group 1 (VLP1) and group 2 (VLP2) were always
observed and significantly correlated to bacteria for the former and chlorophyll a and picocyanobacteria for the latter, suggesting that most of VLP1 and VLP2 could be bacteriophages and cyanophages, respectively.
On the basis of these results, new ways of investigation emerge concerning the study of relationships between specific picoplanktonic
groups; and overall these results provide new evidence of the necessity to consider further viruses for a better understanding
of lake plankton ecology.
Handling editor: Luigi Naselli-Flores 相似文献
64.
《Biochemical and biophysical research communications》2020,521(2):290-295
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in PKD1 or PKD2, the genes encoding polycystin 1 (PC1) and polycystin 2 (PC2), respectively. PC1 and PC2 localize to the primary cilium and form a protein complex, which is thought to regulate signaling events. PKD1 mutations are associated with a stronger phenotype than PKD2, suggesting the existence of PC1 specific functions in renal tubular cells. However, the evidence for diverging molecular functions is scant. The bending of cilia by fluid flow induces a reduction in cell size through a mechanism that involves the kinase LKB1 but not PC2. Here, using different in vitro approaches, we show that contrary to PC2, PC1 regulates cell size under flow and thus phenocopies the loss of cilia. PC1 is required to couple mechanical deflection of cilia to mTOR in tubular cells. This study pinpoints divergent functions of the polycystins in renal tubular cells that may be relevant to disease severity in ADPKD. 相似文献
65.
Beno?te Bourdin Behzad Shakeri Marie-Philippe Tétreault Rémy Sauvé Sylvie Lesage Lucie Parent 《The Journal of biological chemistry》2015,290(5):2854-2869
L-type Ca2+ channels play a critical role in cardiac rhythmicity. These ion channels are oligomeric complexes formed by the pore-forming CaVα1 with the auxiliary CaVβ and CaVα2δ subunits. CaVα2δ increases the peak current density and improves the voltage-dependent activation gating of CaV1.2 channels without increasing the surface expression of the CaVα1 subunit. The functional impact of genetic variants of CACNA2D1 (the gene encoding for CaVα2δ), associated with shorter repolarization QT intervals (the time interval between the Q and the T waves on the cardiac electrocardiogram), was investigated after recombinant expression of the full complement of L-type CaV1.2 subunits in human embryonic kidney 293 cells. By performing side-by-side high resolution flow cytometry assays and whole-cell patch clamp recordings, we revealed that the surface density of the CaVα2δ wild-type protein correlates with the peak current density. Furthermore, the cell surface density of CaVα2δ mutants S755T, Q917H, and S956T was not significantly different from the cell surface density of the CaVα2δ wild-type protein expressed under the same conditions. In contrast, the cell surface expression of CaVα2δ D550Y, CaVα2δ S709N, and the double mutant D550Y/Q917H was reduced, respectively, by ≈30–33% for the single mutants and by 60% for the latter. The cell surface density of D550Y/Q917H was more significantly impaired than protein stability, suggesting that surface trafficking of CaVα2δ was disrupted by the double mutation. Co-expression with D550Y/Q917H significantly decreased CaV1.2 currents as compared with results obtained with CaVα2δ wild type. It is concluded that D550Y/Q917H reduced inward Ca2+ currents through a defect in the cell surface trafficking of CaVα2δ. Altogether, our results provide novel insight in the molecular mechanism underlying the modulation of CaV1.2 currents by CaVα2δ. 相似文献
66.
We investigated the flow pattern and mixing behavior of a poly(γ‐glutamic acid) (γ‐PGA) solution in a bioreactor equipped with two Rushton turbines by simulation and experiment. Computational fluid dynamics (CFD) is used to solve the three‐dimensional hydrodynamics in the bioreactor and to obtain the flow patterns and tracer concentration at every point. The flow circulation patterns by inter‐impeller clearance and viscosity and their effects on overall mixing time were studied. Based on the results we can conclude that the impeller clearance should not be larger than 0.2 D for the efficient mixing under non‐aerated condition when the liquid viscosity is above 20 cp, which corresponds to concentrations of 20 g/L or above for γ‐PGA. 相似文献
67.
L. A. Siena M. E. Sartor F. Espinoza C. L. Quarin J. P. A. Ortiz 《Sexual plant reproduction》2008,21(3):205-215
Gametophytic apomixis is an asexual mode of reproduction by seeds. This trait is present in several plant families and is
strongly associated with polyploidy. Paspalum rufum is a forage grass with sexual self-incompatible diploids (2n = 2x = 20) and aposporous-apomictic pseudogamous tetraploids (2n = 4x = 40). In previous work embryological observations of the diploid genotype Q3754 showed 8.8–26.8% of the ovaries having one
meiotic plus an aposporous-like embryo sac, suggesting some capability for apomictic reproduction. The objective of this work
was to characterize progenies derived from Q3754 to determine if aposporous sacs were functional and generated progenies via
apomixis at the diploid level. Re-examination of Q3754 ovaries showed that 12.5% of them contained one sexual plus an aposporous
sac confirming previous results. Progeny tests were carried out on two experimental families (H1 and S1) employing heterozygous RAPD marker loci. Family H1 was obtained crossing Q3754 with a natural diploid genotype (Q3861) and S1 derived from the induced self-pollination of Q3754. Genetic analysis of H1 showed that all individuals derived from sexual reproduction. However, 5 out of 95 plants from S1 showed the same heterozygous state as the mother plant for 14 RAPD loci suggesting a clonal origin. Further experiments,
designed to test the functionality of aposporous sacs by flow cytometric analyses, were carried out on a third family (M1) obtained by crossing Q3754 with the tetraploid plant Q3785. Histograms of 20 M1 plants showed 15 diploids (75%), 4 triploids (20%) and 1 tetraploid (5%). Triploids and the tetraploid may have originated
from functional aposporous embryo sacs. Likewise, the reconstruction of the developmental route of 40 individual seeds demonstrated
that 11 of them (27.5%) derived from fertilized aposporic sacs. The results presented in this work indicate that gametophytic
apomixis is effectively expressed at the diploid level in Paspalum rufum and could be the foundation of a recurrent auto-polyploidization process in the species. 相似文献
68.
斑鳢、乌鳢及其杂种细胞核DNA流式含量分析 总被引:1,自引:0,他引:1
以斑鳢(Channa maculata)、乌鳢(C.argus)及其正交杂种斑乌鳢(斑鳢♀×乌鳢♂)和反交杂种乌斑鳢(乌鳢♀×斑鳢♂)的红细胞为材料,以鸡(Gallus gallus)血细胞为DNA标准(2.5 pg/2c,2c指2倍体),采用流式细胞仪测定了这4种鱼的细胞核DNA含量。斑鳢、乌鳢、斑乌鳢及乌斑鳢这4种鱼血细胞DNA的绝对含量分别为(1.488±0.035)pg/2c、(1.489±0.034)pg/2c、(1.522±0.077)pg/2c和(1.520±0.033)pg/2c。斑鳢和乌鳢的细胞核DNA含量差异不显著(P0.05),斑鳢和乌鳢与两种杂交鳢的DNA含量差异显著(P0.05),两种杂交鳢之间的细胞核DNA含量差异不显著(P0.05)。杂交鳢细胞核DNA含量显著高于亲本,可以作为杂种鉴定的依据。 相似文献
69.
利用PKH 26和CFSE两种荧光染料对靶细胞染色,建立了一种通过流式细胞术进行马传染性贫血症病毒(Equine infectious anemia virus,EIAV)抗原特异性细胞毒性T淋巴细胞(Cytotoxic T lymphocytes,CTL)反应的新方法,避免了经典的Cr51释放法对检测人员的放射线威胁,降低了本底释放,提高了检测的灵敏度.将该检测方法用于检测EIAV疫苗毒接种马和嵌合克隆接种马的细胞免疫反应变化趋势,数据显示细胞免疫反应在接种后3个月达到成熟阶段而后保持在较高的反应水平.该方法的成功建立和应用为研究EIAV减毒疫苗的免疫机制提供了好的研究手段,也为其他病毒的免疫学研究提供了新的参考方法. 相似文献
70.
Mazen Amatoury Vera Merheb Jessica Langer Xin Maggie Wang Russell Clive Dale Fabienne Brilot 《Journal of visualized experiments : JoVE》2013,(81)
Over the recent years, antibodies against surface and conformational proteins involved in neurotransmission have been detected in autoimmune CNS diseases in children and adults. These antibodies have been used to guide diagnosis and treatment. Cell-based assays have improved the detection of antibodies in patient serum. They are based on the surface expression of brain antigens on eukaryotic cells, which are then incubated with diluted patient sera followed by fluorochrome-conjugated secondary antibodies. After washing, secondary antibody binding is then analyzed by flow cytometry. Our group has developed a high-throughput flow cytometry live cell-based assay to reliably detect antibodies against specific neurotransmitter receptors. This flow cytometry method is straight forward, quantitative, efficient, and the use of a high-throughput sampler system allows for large patient cohorts to be easily assayed in a short space of time. Additionally, this cell-based assay can be easily adapted to detect antibodies to many different antigenic targets, both from the central nervous system and periphery. Discovering additional novel antibody biomarkers will enable prompt and accurate diagnosis and improve treatment of immune-mediated disorders. 相似文献