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排序方式: 共有253条查询结果,搜索用时 15 毫秒
1.
Development ofPostgraduate Education There were only postgraduates were honored master degree from the year to in old China. While after the establishment of new China the postgraduate educationhas developed in a certain degree there were postgraduates were enrolled from to there were no postgraduates during the period of to due to the"culture revolution".…… 《广西师范大学学报(自然科学版)》2003,21(Z1):231-232
1 Development of Postgraduate Education
There were only 200 postgraduates were honored master degree from the year 1935 to 1949 in old China. While, after the establishment of new China, the postgraduate education has developed in a certain degree, there were 23,000 postgraduates were enrolled from 1950 to 1965, and there were no postgraduates during the period of 1966 to 1977 due to the "culture revolution". 相似文献
2.
In modernindustry thin film on the substratc has much important role to decide the properties ofproduct especially for electrical optical wear-resistant etc production. There aresome technical methods to prepare thin film including plasma spray physical vapordeposition 《广西师范大学学报(自然科学版)》2003,21(Z4):284-285
In modern industry,thin film on the substratc has much important role to decide the properties of product, especially for electrical, optical and wear-resistant etc, production. There are some technical methods to prepare thin film,including plasma spray,physical vapor deposition (PVD),chemical vapor deposition (CVD) and sol-gel,etc. Among of them,sol-gel method has been developed a popular tech nique for preparing thin films. 相似文献
3.
对H型钢梁与矩形钢管柱平齐式端板单向螺栓连接节点承载性能进行试验和理论分析研究.通过对3种不同形式的平齐式端板单向螺栓连接节点进行单调静力加载试验,获得了各试件的破坏模式和弯矩-转角曲线,讨论了螺栓破坏、端板破坏、柱壁破坏等3种破坏模式.基于试验现象提出了节点螺栓力理论分布模式,并给出了螺栓强度控制的节点抗弯承载力计算公式.通过将端板和钢梁腹板等效为T形件,得出了端板屈服控制的节点抗弯承载力计算公式.基于试验现象并利用屈服线理论提出了钢管柱壁的屈服线模型,运用虚功原理得出由柱壁强度控制的节点抗弯承载力计算公式.研究表明螺栓、端板、柱壁间的相对强弱关系直接影响节点的破坏模式,理论计算值与试验相比结果偏安全.给出了H型钢梁与矩形钢管柱平齐式端板单向螺栓连接节点的设计准则和建议. 相似文献
4.
针对采用码相位循环移位获得的M元扩频需要额外同步信息的问题,提出一种改进型扩频通信算法.该算法采用m序列及其倒序序列构成系统扩频码集;在同相支路上利用扩频码的码极性调制进行传输,同时在正交支路利用扩频码码相位调制,实现M元扩频.该算法利用2种扩频方式的自身特点可快速准确地获取载波相位信息,具有不需要额外提供同步资源的优势.仿真结果表明,该算法可有效提高系统资源的利用率. 相似文献
5.
Cdk1 is sufficient to drive the mammalian cell cycle 总被引:1,自引:0,他引:1
Santamaría D Barrière C Cerqueira A Hunt S Tardy C Newton K Cáceres JF Dubus P Malumbres M Barbacid M 《Nature》2007,448(7155):811-815
6.
Spin-orbit (SO) coupling--the interaction between a quantum particle's spin and its momentum--is ubiquitous in physical systems. In condensed matter systems, SO coupling is crucial for the spin-Hall effect and topological insulators; it contributes to the electronic properties of materials such as GaAs, and is important for spintronic devices. Quantum many-body systems of ultracold atoms can be precisely controlled experimentally, and would therefore seem to provide an ideal platform on which to study SO coupling. Although an atom's intrinsic SO coupling affects its electronic structure, it does not lead to coupling between the spin and the centre-of-mass motion of the atom. Here, we engineer SO coupling (with equal Rashba and Dresselhaus strengths) in a neutral atomic Bose-Einstein condensate by dressing two atomic spin states with a pair of lasers. Such coupling has not been realized previously for ultracold atomic gases, or indeed any bosonic system. Furthermore, in the presence of the laser coupling, the interactions between the two dressed atomic spin states are modified, driving a quantum phase transition from a spatially spin-mixed state (lasers off) to a phase-separated state (above a critical laser intensity). We develop a many-body theory that provides quantitative agreement with the observed location of the transition. The engineered SO coupling--equally applicable for bosons and fermions--sets the stage for the realization of topological insulators in fermionic neutral atom systems. 相似文献
7.
Peça J Feliciano C Ting JT Wang W Wells MF Venkatraman TN Lascola CD Fu Z Feng G 《Nature》2011,472(7344):437-442
Autism spectrum disorders (ASDs) comprise a range of disorders that share a core of neurobehavioural deficits characterized by widespread abnormalities in social interactions, deficits in communication as well as restricted interests and repetitive behaviours. The neurological basis and circuitry mechanisms underlying these abnormal behaviours are poorly understood. SHANK3 is a postsynaptic protein, whose disruption at the genetic level is thought to be responsible for the development of 22q13 deletion syndrome (Phelan-McDermid syndrome) and other non-syndromic ASDs. Here we show that mice with Shank3 gene deletions exhibit self-injurious repetitive grooming and deficits in social interaction. Cellular, electrophysiological and biochemical analyses uncovered defects at striatal synapses and cortico-striatal circuits in Shank3 mutant mice. Our findings demonstrate a critical role for SHANK3 in the normal development of neuronal connectivity and establish causality between a disruption in the Shank3 gene and the genesis of autistic-like behaviours in mice. 相似文献
8.
Regulation of primary cilia formation and left-right patterning in zebrafish by a noncanonical Wnt signaling mediator, duboraya 总被引:1,自引:0,他引:1
Oishi I Kawakami Y Raya A Callol-Massot C Izpisúa Belmonte JC 《Nature genetics》2006,38(11):1316-1322
Primary cilia are microtubule-based organelles that project from the surface of nearly every animal cell. Although important functions of primary cilia in morphogenesis and tissue homeostasis have been identified, the mechanisms that control the formation of primary cilia are not understood. Here we characterize a zebrafish gene, termed duboraya (dub), that is essential for ciliogenesis. Knockdown of dub in zebrafish embryos results in both defects in primary cilia formation in Kupffer's vesicle and randomization of left-right organ asymmetries. We show that, at the molecular level, the function of dub in ciliogenesis is regulated by phosphorylation, which in turn depends on Frizzled-2-mediated noncanonical Wnt signaling. We also provide evidence that, at the cellular level, dub function is essential for actin organization in the cells lining Kupffer's vesicle. Taken together, our findings identify a molecular factor that links noncanonical Wnt signaling with the control of left-right axis specification, and provide an entry point for analyzing the mechanisms that regulate primary cilia formation. 相似文献
9.
Alcázar R García AV Kronholm I de Meaux J Koornneef M Parker JE Reymond M 《Nature genetics》2010,42(12):1135-1139
Accumulation of genetic incompatibilities within species can lead to reproductive isolation and, potentially, speciation. In this study, we show that allelic variation at SRF3 (Strubbelig Receptor Family 3), encoding a receptor-like kinase, conditions the occurrence of incompatibility between Arabidopsis thaliana accessions. The geographical distribution of SRF3 alleles reveals that allelic forms causing epistatic incompatibility with a Landsberg erecta allele at the RPP1 resistance locus are present in A. thaliana accessions in central Asia. Incompatible SRF3 alleles condition for an enhanced early immune response to pathogens as compared to the resistance-dampening effect of compatible SRF3 forms in isogenic backgrounds. Variation in disease susceptibility suggests a basis for the molecular patterns of a recent selective sweep detected at the SRF3 locus in central Asian populations. 相似文献
10.
Roscioli T Kamsteeg EJ Buysse K Maystadt I van Reeuwijk J van den Elzen C van Beusekom E Riemersma M Pfundt R Vissers LE Schraders M Altunoglu U Buckley MF Brunner HG Grisart B Zhou H Veltman JA Gilissen C Mancini GM Delrée P Willemsen MA Ramadža DP Chitayat D Bennett C Sheridan E Peeters EA Tan-Sindhunata GM de Die-Smulders CE Devriendt K Kayserili H El-Hashash OA Stemple DL Lefeber DJ Lin YY van Bokhoven H 《Nature genetics》2012,44(5):581-585
Walker-Warburg syndrome (WWS) is an autosomal recessive multisystem disorder characterized by complex eye and brain abnormalities with congenital muscular dystrophy (CMD) and aberrant a-dystroglycan glycosylation. Here we report mutations in the ISPD gene (encoding isoprenoid synthase domain containing) as the second most common cause of WWS. Bacterial IspD is a nucleotidyl transferase belonging to a large glycosyltransferase family, but the role of the orthologous protein in chordates is obscure to date, as this phylum does not have the corresponding non-mevalonate isoprenoid biosynthesis pathway. Knockdown of ispd in zebrafish recapitulates the human WWS phenotype with hydrocephalus, reduced eye size, muscle degeneration and hypoglycosylated a-dystroglycan. These results implicate ISPD in a-dystroglycan glycosylation in maintaining sarcolemma integrity in vertebrates. 相似文献