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41.
Gregori G Ravasio A Murphy CD Schaar K Baird A Bell AR Benuzzi-Mounaix A Bingham R Constantin C Drake RP Edwards M Everson ET Gregory CD Kuramitsu Y Lau W Mithen J Niemann C Park HS Remington BA Reville B Robinson AP Ryutov DD Sakawa Y Yang S Woolsey NC Koenig M Miniati F 《Nature》2012,481(7382):480-483
The standard model for the origin of galactic magnetic fields is through the amplification of seed fields via dynamo or turbulent processes to the level consistent with present observations. Although other mechanisms may also operate, currents from misaligned pressure and temperature gradients (the Biermann battery process) inevitably accompany the formation of galaxies in the absence of a primordial field. Driven by geometrical asymmetries in shocks associated with the collapse of protogalactic structures, the Biermann battery is believed to generate tiny seed fields to a level of about 10(-21)?gauss (refs 7, 8). With the advent of high-power laser systems in the past two decades, a new area of research has opened in which, using simple scaling relations, astrophysical environments can effectively be reproduced in the laboratory. Here we report the results of an experiment that produced seed magnetic fields by the Biermann battery effect. We show that these results can be scaled to the intergalactic medium, where turbulence, acting on timescales of around 700 million years, can amplify the seed fields sufficiently to affect galaxy evolution. 相似文献
42.
Novel mutations target distinct subgroups of medulloblastoma 总被引:1,自引:0,他引:1
Robinson G Parker M Kranenburg TA Lu C Chen X Ding L Phoenix TN Hedlund E Wei L Zhu X Chalhoub N Baker SJ Huether R Kriwacki R Curley N Thiruvenkatam R Wang J Wu G Rusch M Hong X Becksfort J Gupta P Ma J Easton J Vadodaria B Onar-Thomas A Lin T Li S Pounds S Paugh S Zhao D Kawauchi D Roussel MF Finkelstein D Ellison DW Lau CC Bouffet E Hassall T Gururangan S Cohn R Fulton RS Fulton LL Dooling DJ Ochoa K Gajjar A Mardis ER Wilson RK Downing JR Zhang J Gilbertson RJ 《Nature》2012,488(7409):43-48
Medulloblastoma is a malignant childhood brain tumour comprising four discrete subgroups. Here, to identify mutations that drive medulloblastoma, we sequenced the entire genomes of 37 tumours and matched normal blood. One-hundred and thirty-six genes harbouring somatic mutations in this discovery set were sequenced in an additional 56 medulloblastomas. Recurrent mutations were detected in 41 genes not yet implicated in medulloblastoma; several target distinct components of the epigenetic machinery in different disease subgroups, such as regulators of H3K27 and H3K4 trimethylation in subgroups 3 and 4 (for example, KDM6A and ZMYM3), and CTNNB1-associated chromatin re-modellers in WNT-subgroup tumours (for example, SMARCA4 and CREBBP). Modelling of mutations in mouse lower rhombic lip progenitors that generate WNT-subgroup tumours identified genes that maintain this cell lineage (DDX3X), as well as mutated genes that initiate (CDH1) or cooperate (PIK3CA) in tumorigenesis. These data provide important new insights into the pathogenesis of medulloblastoma subgroups and highlight targets for therapeutic development. 相似文献
43.
为精确识别细颗粒物(PM_(2. 5))浓度超标的区域空间,依据卫星遥感与站点监测在PM_(2. 5)浓度观测方面的特点,建立遥感反演数据与站点监测数据间的临界映射分析法,综合卫星遥感覆盖面广和站点监测准确性高的技术优势。通过该方法研究珠三角区域2013年灰霾污染过程的PM_(2. 5)浓度超标区域,结果表明,利用星地结合的方法可以精确识别出PM_(2. 5)浓度超标的区域空间;广州市西部和南部、佛山市大部、肇庆市主城区及东南部、东莞市西部和北部、中山市北部和中部、江门市主城区及东部是珠三角PM_(2. 5)污染的高发地区,应作为防控重点。 相似文献
44.
Many enzymes are subject to allosteric control, often with inhibitors and activators binding to the same effector site. Phosphofructokinase in Escherichia coli is such an enzyme, being inhibited by phosphoenolpyruvate (PEP) and activated by ADP and GDP. How do individual interactions with effectors affect the balance between activation and inhibition, especially when both ligands share aspects of the same binding site? We find that mutation of a single residue in the effector site, Glu----Ala 187, leads to PEP being an activator rather than an inhibitor. With low concentrations of the substrate fructose-6-phosphate, the mutant enzyme is more than one hundred times more active than wild-type enzyme at millimolar concentrations of PEP. The classical Monod-Wyman-Changeux two-state model is too simple to account for the properties of the mutant enzyme. 相似文献
45.
This paper reports a recent development of a yarn modification process to produce torque balanced singles spun yarns. Taking advantages of the core-sheath structure of unconventional spun yarns, we have developed a yarn modification process and applied it to singles yarns spun by rotor spinning. Torque free singles yarns have been produced from 100% cotton fibers. The spirality of resultant single jersey knit fabrics has been greatly reduced or, in some cases, completely eliminated. Properties and performance characteristics of both parent and modified yarns as well as their resultant fabrics have been evaluated including the yarn tensile properties, surface properties, handle, air permeability, burst strength, and pilling resistance of the fabrics. 相似文献
46.
47.
A Functional Framework for Integrating eCRM with Workflow Management Based on Customer Value 总被引:2,自引:0,他引:2
Introduction No other inventions in recent years have had such a deep influence on how companies manage their customer relationships and how they do business as the Internet. Use of the Internet has changed customers’ purchase expectations to a totally n… 相似文献
48.
Classical unidimensional scaling provides a difficult combinatorial task. A procedure formulated as a nonlinear programming
(NLP) model is proposed to solve this problem. The new method can be implemented with standard mathematical programming software.
Unlike the traditional procedures that minimize either the sum of squared error (L
2 norm) or the sum pf absolute error (L
1 norm), the proposed method can minimize the error based on any L
p
norm for 1 ≤p < ∞. Extensions of the NLP formulation to address a multidimensional scaling problem under the city-block model are also
discussed. 相似文献
49.
Lau LF 《Cellular and molecular life sciences : CMLS》2011,68(19):3149-3163
CCN1 (CYR61) is a dynamically expressed, multifunctional matricellular protein that plays essential roles in cardiovascular
development during embryogenesis, and regulates inflammation, wound healing and fibrogenesis in the adult. Aberrant CCN1 expression
is associated with myriad pathologies, including various cancers and diseases associated with chronic inflammation. CCN1 promotes
diverse and sometimes opposing cellular responses, which can be ascribed, as least in part, to disparate activities mediated
through its direct binding to distinct integrins in different cell types and contexts. Accordingly, CCN1 promotes cell proliferation,
survival and angiogenesis by binding to integrin αvβ3, and induces apoptosis and senescence through integrin α6β1 and heparan sulfate proteoglycans. The ability of CCN1 to trigger the accumulation of a robust and sustained level of reactive
oxygen species underlies some of its unique activities as a matrix cell-adhesion molecule. Emerging studies suggest that CCN1
might be useful as a biomarker or therapeutic target in certain diseases. 相似文献
50.
CL Cheung KS Lau AY Ho KK Lee SC Tiu EY Lau J Leung MW Tsang KW Chan CY Yeung YC Woo EY Cheung VH Hung HK Pang CS Hung PC Sham AW Kung 《Nature genetics》2012,44(9):1026-1029
Thyrotoxic periodic paralysis (TPP) is a potentially life-threatening complication of thyrotoxicosis. We conducted a genome-wide association study (GWAS) and a replication study with a total of 123 southern Chinese with TPP (cases) and 1,170 healthy controls and identified a susceptibility locus on chromosome 17q24.3 near KCNJ2 (rs312691: odds ratio (OR) = 3.3; P(meta-analysis) = 1.8 × 10(-14)). All subjects with TPP also had Graves' disease, and subsequent TPP versus Graves' disease comparison confirmed that the association at 17q24.3 was specific to TPP. The area under the curve (AUC) of rs312691 genotype for risk prediction of TPP in subjects with Graves' disease was 0.73. Expression quantitative trait locus (eQTL) analysis identified SNPs in the region flanking rs312691 (±10 kb) that could potentially affect KCNJ2 expression (P = 0.0001). Our study has identified a susceptibility locus associated with TPP and provides insight into the causes of TPP. 相似文献