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51.
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认知增强型无线传感器节点设计 总被引:3,自引:0,他引:3
为了提高无线传感器节点及其网络的吞吐量和频谱利用率,从节点设计的角度,引入认知方法增强节点的频谱感知能力,设计了基于低功耗高速率处理器的多射频接口认知增强无线传感器节点.节点采用STR911系列的ARM9微处理器,具有4个射频接口,覆盖了ISM频段和ZigBee频段.实验结果表明,相比基于Atmega128处理器的节点,该节点具有更强的认知能力,吞吐量提高了68.41%,平均信道感知时延缩短了1.4782ms;相比于CSMA/CA方法,通信时延缩短了11.86%,链路层控制方案能够有效避免干扰对节点间通信的影响. 相似文献
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Iwona Mazur-Michaek Katarzyna Kowalska Daniel Zielonka Marta Leniczak-Staszak Paulina Pietras Witold Szaflarski Mark Isalan Michal Mielcarek 《International journal of molecular sciences》2022,23(10)
Huntington’s disease (HD) is a fatal neurodegenerative disorder caused by a polyglutamine expansion in the huntingtin protein. HD-related pathological remodelling has been reported in HD mouse models and HD carriers. In this study, we studied structural abnormalities in the optic nerve by employing Spectral Domain Optical Coherence Tomography (SD-OCT) in pre-symptomatic HD carriers of Caucasian origin. Transmission Electron Microscopy (TEM) was used to investigate ultrastructural changes in the optic nerve of the well-established R6/2 mouse model at the symptomatic stage of the disease. We found that pre-symptomatic HD carriers displayed a significant reduction in the retinal nerve fibre layer (RNFL) thickness, including specific quadrants: superior, inferior and temporal, but not nasal. There were no other significant irregularities in the GCC layer, at the macula level and in the optic disc morphology. The ultrastructural analysis of the optic nerve in R6/2 mice revealed a significant thinning of the myelin sheaths, with a lamellar separation of the myelin, and a presence of myelonoid bodies. We also found a significant reduction in the thickness of myelin sheaths in peripheral nerves within the choroids area. Those ultrastructural abnormalities were also observed in HD photoreceptor cells that contained severely damaged membrane disks, with evident vacuolisation and swelling. Moreover, the outer segment of retinal layers showed a progressive disintegration. Our study explored structural changes of the optic nerve in pre- and clinical settings and opens new avenues for the potential development of biomarkers that would be of great interest in HD gene therapies. 相似文献
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提出了一种新的、以认知能力为基础的无线网络,称为无线认知网络。对无线认知网络进行了定义,对认知实体、认知进程和认知环境进行了分析和讨论,提出了无线认知网络的实体、网络、认知和控制4个关联层面,对无线认知网络的特点进行了阐述,并给出了技术上的挑战。在此基础上,从基础设施、层次结构和节点性质3个方面对无线认知网络进行了分类研究,在给出最小跨层设计原则与信息交换方法的基础上,提出了由基础层、网络适配层、应用开发环境层和应用逻辑层组成的4层软件体系结构。最后结合无线认知网络目前的惟一实例-认知无线电网络,对无线认知网络的实例化问题进行了讨论。 相似文献
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本文介绍在Visual Basic语言编程环境中,利用鼠标mousedown、mousemove和mouseup事件,建立一个可供写字或绘图的窗口,将其编译成在桌面上可执行的文件,代替教学用粉笔写字或绘图. 相似文献
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Shruti V. Patil Ramesh B. Kasetti J. Cameron Millar Gulab S. Zode 《International journal of molecular sciences》2022,23(13)
Glaucoma is a multifactorial disease leading to irreversible blindness. Primary open-angle glaucoma (POAG) is the most common form and is associated with the elevation of intraocular pressure (IOP). Reduced aqueous humor (AH) outflow due to trabecular meshwork (TM) dysfunction is responsible for IOP elevation in POAG. Extracellular matrix (ECM) accumulation, actin cytoskeletal reorganization, and stiffening of the TM are associated with increased outflow resistance. Transforming growth factor (TGF) β2, a profibrotic cytokine, is known to play an important role in the development of ocular hypertension (OHT) in POAG. An appropriate mouse model is critical in understanding the underlying molecular mechanism of TGFβ2-induced OHT. To achieve this, TM can be targeted with recombinant viral vectors to express a gene of interest. Lentiviruses (LV) are known for their tropism towards TM with stable transgene expression and low immunogenicity. We, therefore, developed a novel mouse model of IOP elevation using LV gene transfer of active human TGFβ2 in the TM. We developed an LV vector-encoding active hTGFβ2C226,228S under the control of a cytomegalovirus (CMV) promoter. Adult C57BL/6J mice were injected intravitreally with LV expressing null or hTGFβ2C226,228S. We observed a significant increase in IOP 3 weeks post-injection compared to control eyes with an average delta change of 3.3 mmHg. IOP stayed elevated up to 7 weeks post-injection, which correlated with a significant drop in the AH outflow facility (40.36%). Increased expression of active TGFβ2 was observed in both AH and anterior segment samples of injected mice. The morphological assessment of the mouse TM region via hematoxylin and eosin (H&E) staining and direct ophthalmoscopy examination revealed no visible signs of inflammation or other ocular abnormalities in the injected eyes. Furthermore, transduction of primary human TM cells with LV_hTGFβ2C226,228S exhibited alterations in actin cytoskeleton structures, including the formation of F-actin stress fibers and crossed-linked actin networks (CLANs), which are signature arrangements of actin cytoskeleton observed in the stiffer fibrotic-like TM. Our study demonstrated a mouse model of sustained IOP elevation via lentiviral gene delivery of active hTGFβ2C226,228S that induces TM dysfunction and outflow resistance. 相似文献
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