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991.
992.
Acute β-Hydroxy-β-Methyl Butyrate Suppresses Regulators of Mitochondrial Biogenesis and Lipid Oxidation While Increasing Lipid Content in Myotubes 下载免费PDF全文
Jamie K. Schnuck Michele A. Johnson Lacey M. Gould Nicholas P. Gannon Roger A. Vaughan 《Lipids》2016,51(10):1127-1136
Leucine modulates synthetic and degradative pathways in muscle, possibly providing metabolic benefits for both athletes and diseased populations. Leucine has become popular among athletes for improving performance and body composition, however little is known about the metabolic effects of the commonly consumed leucine‐derived metabolite β‐hydroxy‐β‐methyl butyrate (HMB). Our work measured the effects of HMB on metabolic protein expression, mitochondrial content and metabolism, as well as lipid content in skeletal muscle cells. Specifically, cultured C2C12 myotubes were treated with either a control or HMB ranging from 6.25 to 25 μM for 24 h and mRNA and/or protein expression, oxygen consumption, glucose uptake, and lipid content were measured. Contrary to leucine's stimulatory effect on metabolism, HMB‐treated cells exhibited significantly reduced regulators of lipid oxidation including peroxisome proliferator‐activated receptor alpha (PPARα) and PPARβ/δ, as well as downstream target carnitine palmitoyl transferase, without alterations in glucose or palmitate oxidation. Furthermore, HMB significantly inhibited activation of the master regulator of energetics, AMP‐activated protein kinase. As a result, HMB‐treated cells also displayed reduced total mitochondrial content compared with true control or cells equivocally treated with leucine. Additionally, HMB treatment amplified markers of lipid biosynthesis (PPARγ and fatty acid synthase) as well as consistently promoted elevated total lipid content versus control cells. Collectively, our results demonstrate that HMB did not improve mitochondrial metabolism or content, and may promote elevated cellular lipid content possibly through heightened PPARγ expression. These observations suggest that HMB may be most beneficial for populations interested in stimulating anabolic cellular processes. 相似文献
993.
Farshid Nouri-Ahangarani Mehdi Nekoomanesh-Haghighi Milad Karbalaie 《Designed Monomers and Polymers》2016,19(5):394-405
In this article, polymerization of 1-hexene with FeCl3-doped Mg(OET)2/TiCl4/electron donor (ED) catalytic system is presented. For this purpose, first a number of TiCl4 catalysts supported on Mg(OEt)2 and Fe-doped Mg(OEt)2 supports were prepared with ethylbenzoate or dibutylphthalate as the internal EDs. After successive catalysts synthesis, they were employed in 1-hexene polymerization using cyclohexyl methyl dimethoxysilane as external ED as well as without it. The catalysts activity and molecular weight distribution (MWD) of poly 1-hexenes (PHs) were influenced strongly by both FeCl3 doping and donor presence so that a remarkable increase in the catalyst activity was seen in doped catalysts. Deconvolution of MWD curves revealed that increase in the type of active centers by introducing FeCl3 into the support should be responsible for the broadening of MWD of PHs. 13CNMR analysis indicated that while isotacticity does not change considerably by Fe doping, EDs increase its amount as high as 8–21%. Second, the stereoselective behavior of active Ti species in doped and undoped catalysts was fully explored by molecular modeling using density functional theory (DFT) method. Finally, with the aid of rheological measurements, the processability of polymers were evaluated and then the gel permeation chromatography (GPC) results were approved through the values obtained from model fitting as well as changes in moduli crossover modulus. 相似文献
994.
Majid Ghashang Hadi Taghrir Mohammad Najafi Biregan Negar Heydari Fateme Azimi 《Journal of Sulfur Chemistry》2016,37(1):61-69
An eco-friendly procedure for synthesis of 2-(2-oxo-2H-chromen-4-yl)-3-arylthiazolidin-4-one derivatives by three-component reaction of 2-oxo-2H-chromene-4-carbaldehydes, aromatic amines and thioglycolic acid, with tetramethylbutane-1,4-diammonium acetate as a low-cost ionic liquid catalyst under reflux condition is described. The use of an ionic liquid as a catalyst has the advantages of high yields, short reaction time and environmentally friendly reaction media. 相似文献
995.
Pervaporation removal of volatile organic compounds from aqueous solutions using the highly permeable PIM‐1 membrane 下载免费PDF全文
Xin Mei Wu Qiu Gen Zhang Faizal Soyekwo Qing Lin Liu Ai Mei Zhu 《American Institute of Chemical Engineers》2016,62(3):842-851
Wastewater containing volatile organic compounds (VOCs) is generated in various industrial processes and is seriously harmful to the natural environment and human health. Its treatment has become extremely important due to increasing environment concerns. Here, a high permeable membrane for fast and high‐efficient VOCs removal from aqueous solutions by pervaporation is reported. The as‐prepared PIM‐1 membrane allows ultrafast permeation of VOCs and exhibits excellent VOCs selectivity, particularly for ethyl acetate, dimethyl ether, and acetonitrile. Typically, the PIM‐1 membrane exhibits an ultrahigh flux and separation factor of 39.5 kg μm m?2 h?1 and 189, respectively, in the pervaporation of 1.0 mol% aqueous ethyl acetate solution. Furthermore, the solubility‐diffusion mechanism is revealed in the pervaporation of 10 kinds of 1.0 mol% VOCs solutions. It is found that the pervaporation performance is affected directly by physicochemical properties of VOCs. Moreover, effects of feed composition and temperature on the pervaporation are studied in details. © 2015 American Institute of Chemical Engineers AIChE J, 62: 842–851, 2016 相似文献
996.
997.
Izchel Figarola-Centurin Martha Escoto-Delgadillo Gracia Viviana Gonzlez-Enríquez Juan Ernesto Gutirrez-Sevilla Eduardo Vzquez-Valls Blanca Miriam Torres-Mendoza 《International journal of molecular sciences》2022,23(2)
HIV-Associated neurocognitive disorder (HAND) is one of the major concerns since it persists in 40% of this population. Nowadays, HAND neuropathogenesis is considered to be caused by the infected cells that cross the brain–blood barrier and produce viral proteins that can be secreted and internalized into neurons leading to disruption of cellular processes. The evidence points to viral proteins such as Tat as the causal agent for neuronal alteration and thus HAND. The hallmarks in Tat-induced neurodegeneration are endoplasmic reticulum stress and mitochondrial dysfunction. Sirtuins (SIRTs) are NAD+-dependent deacetylases involved in mitochondria biogenesis, unfolded protein response, and intrinsic apoptosis pathway. Tat interaction with these deacetylases causes inhibition of SIRT1 and SIRT3. Studies revealed that SIRTs activation promotes neuroprotection in neurodegenerative diseases such Alzheimer’s and Parkinson’s disease. Therefore, this review focuses on Tat-induced neurotoxicity mechanisms that involve SIRTs as key regulators and their modulation as a therapeutic strategy for tackling HAND and thereby improving the quality of life of people living with HIV. 相似文献
998.
Elena V. Mitroshina Maria M. Loginova Roman S. Yarkov Mark D. Urazov Maria O. Novozhilova Mikhail I. Krivonosov Mikhail V. Ivanchenko Maria V. Vedunova 《International journal of molecular sciences》2022,23(2)
Ischemic brain injury is a widespread pathological condition, the main components of which are a deficiency of oxygen and energy substrates. In recent years, a number of new forms of cell death, including necroptosis, have been described. In necroptosis, a cascade of interactions between the kinases RIPK1 and RIPK3 and the MLKL protein leads to the formation of a specialized death complex called the necrosome, which triggers MLKL-mediated destruction of the cell membrane and necroptotic cell death. Necroptosis probably plays an important role in the development of ischemia/reperfusion injury and can be considered as a potential target for finding methods to correct the disruption of neural networks in ischemic damage. In the present study, we demonstrated that blockade of RIPK1 kinase by Necrostatin-1 preserved the viability of cells in primary hippocampal cultures in an in vitro model of glucose deprivation. The effect of RIPK1 blockade on the bioelectrical and metabolic calcium activity of neuron-glial networks in vitro using calcium imaging and multi-electrode arrays was assessed for the first time. RIPK1 blockade was shown to partially preserve both calcium and bioelectric activity of neuron-glial networks under ischemic factors. However, it should be noted that RIPK1 blockade does not preserve the network parameters of the collective calcium dynamics of neuron-glial networks, despite the maintenance of network bioelectrical activity (the number of bursts and the number of spikes in the bursts). To confirm the data obtained in vitro, we studied the effect of RIPK1 blockade on the resistance of small laboratory animals to in vivo modeling of hypoxia and cerebral ischemia. The use of Necrostatin-1 increases the survival rate of C57BL mice in modeling both acute hypobaric hypoxia and ischemic brain damage. 相似文献
999.
1000.
Mariia Belinskaia Tomas Zurawski Seshu Kumar Kaza Caren Antoniazzi J. Oliver Dolly Gary W. Lawrence 《International journal of molecular sciences》2022,23(2)
Nerve growth factor (NGF) is known to intensify pain in various ways, so perturbing pertinent effects without negating its essential influences on neuronal functions could help the search for much-needed analgesics. Towards this goal, cultured neurons from neonatal rat trigeminal ganglia—a locus for craniofacial sensory nerves—were used to examine how NGF affects the Ca2+-dependent release of a pain mediator, calcitonin gene-related peptide (CGRP), that is triggered by activating a key signal transducer, transient receptor potential vanilloid 1 (TRPV1) with capsaicin (CAP). Measurements utilised neurons fed with or deprived of NGF for 2 days. Acute re-introduction of NGF induced Ca2+-dependent CGRP exocytosis that was inhibited by botulinum neurotoxin type A (BoNT/A) or a chimera of/E and/A (/EA), which truncated SNAP-25 (synaptosomal-associated protein with Mr = 25 k) at distinct sites. NGF additionally caused a Ca2+-independent enhancement of the neuropeptide release evoked by low concentrations (<100 nM) of CAP, but only marginally increased the peak response to ≥100 nM. Notably, BoNT/A inhibited CGRP exocytosis evoked by low but not high CAP concentrations, whereas/EA effectively reduced responses up to 1 µM CAP and inhibited to a greater extent its enhancement by NGF. In addition to establishing that sensitisation of sensory neurons to CAP by NGF is dependent on SNARE-mediated membrane fusion, insights were gleaned into the differential ability of two regions in the C-terminus of SNAP-25 (181–197 and 198–206) to support CAP-evoked Ca2+-dependent exocytosis at different intensities of stimulation. 相似文献