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1.
Patricia A. Miguez Stephen A. Tuin Adam G. Robinson Joyce Belcher Prapaporn Jongwattanapisan Kimberly Perley Vinicius de Paiva Gon«alves Arash Hanifi Nancy Pleshko Elisabeth R. Barton 《International journal of molecular sciences》2021,22(6)
This study evaluated the direct effect of a phytochemical, hesperidin, on pre-osteoblast cell function as well as osteogenesis and collagen matrix quality, as there is little known about hesperidin’s influence in mineralized tissue formation and regeneration. Hesperidin was added to a culture of MC3T3-E1 cells at various concentrations. Cell proliferation, viability, osteogenic gene expression and deposited collagen matrix analyses were performed. Treatment with hesperidin showed significant upregulation of osteogenic markers, particularly with lower doses. Mature and compact collagen fibrils in hesperidin-treated cultures were observed by picrosirius red staining (PSR), although a thinner matrix layer was present for the higher dose of hesperidin compared to osteogenic media alone. Fourier-transform infrared spectroscopy indicated a better mineral-to-matrix ratio and matrix distribution in cultures exposed to hesperidin and confirmed less collagen deposited with the 100-µM dose of hesperidin. In vivo, hesperidin combined with a suboptimal dose of bone morphogenetic protein 2 (BMP2) (dose unable to promote healing of a rat mandible critical-sized bone defect) in a collagenous scaffold promoted a well-controlled (not ectopic) pattern of bone formation as compared to a large dose of BMP2 (previously defined as optimal in healing the critical-sized defect, although of ectopic nature). PSR staining of newly formed bone demonstrated that hesperidin can promote maturation of bone organic matrix. Our findings show, for the first time, that hesperidin has a modulatory role in mineralized tissue formation via not only osteoblast cell differentiation but also matrix organization and matrix-to-mineral ratio and could be a potential adjunct in regenerative bone therapies. 相似文献
2.
Virginia Veronica Visconti Ida Cariati Simona Fittipaldi Riccardo Iundusi Elena Gasbarra Umberto Tarantino Annalisa Botta 《International journal of molecular sciences》2021,22(8)
DNA methylation is one of the most studied epigenetic mechanisms that play a pivotal role in regulating gene expression. The epigenetic component is strongly involved in aging-bone diseases, such as osteoporosis and osteoarthritis. Both are complex multi-factorial late-onset disorders that represent a globally widespread health problem, highlighting a crucial point of investigations in many scientific studies. In recent years, new findings on the role of DNA methylation in the pathogenesis of aging-bone diseases have emerged. The aim of this systematic review is to update knowledge in the field of DNA methylation associated with osteoporosis and osteoarthritis, focusing on the specific tissues involved in both pathological conditions. 相似文献
3.
某飞机用30CrMnSiA钢沉头螺栓在拆卸过程中发生断裂,同炉批未曾使用的螺栓经磁粉检测也存在裂纹。为查找失效分析原因,通过对断裂件和同炉批开裂的螺栓外观检查、断口宏微观分析、能谱分析、硬度检测、金相分析等方法对断裂和开裂的螺栓进行了分析。结果表明:断裂螺栓和开裂螺栓断裂类型为氢脆,螺栓氢脆断裂主要与抗拉强度和热处理工艺有关,通过改善热处理工艺参数,适当降低螺栓的强度,增加酸洗后的除氢时间降低氢含量,从而避免氢脆发生的可能性。 相似文献
4.
通过硬度、拉伸、冲击测试,以及光学显微镜(OM)、扫描电镜(SEM)等分析手段研究了C64钢在不同温度淬火过程中的显微组织和力学性能的变化。结果表明:当淬火温度低于950 ℃时,C64试验钢的显微组织中板条马氏体较为细小;当温度高于950 ℃时,板条马氏体急剧长大。随着淬火温度的升高,碳化物开始逐渐溶解,950 ℃时几乎全部溶解。钢的强度、硬度随着淬火温度的升高呈现下降的趋势;钢的伸长率、断面收缩率、冲击吸收能量随着淬火温度的升高表现出先升高后下降的趋势,并在950 ℃时达到最大值。试验钢最佳淬火温度为950 ℃,能够获得组织均匀、细小的板条状马氏体组织。此时,试验钢的抗拉强度为1122 MPa,屈服强度为1106 MPa,伸长率为11.40%,断面收缩率为25.20%,冲击吸收能量为191.0 J,能达到强韧化的最佳匹配。 相似文献
5.
6.
Jian Zhou Chenyu Zhu Lihua Li Man Cheung Ng Kun Liu 《Journal of the American Ceramic Society》2021,104(1):243-255
The glass-to-mold adhesion in precision glass molding could severely degrade the quality of molded optics and shorten the lifespan of the precious molds. Since the consequences of adhesion take effect during the separation between glass and molds, it is important to investigate the debonding behaviors of a typical glass molding interface. To this end, here we perform a probe tack test procedure for borosilicate glass BK7, where debonding is conducted at molding temperature and specific velocity. We fully characterize the debonding behaviors using the peak adhesion stress σmax and the work of debonding Wdeb. Experiments show that when temperature is decreased from 690°C to 655°C at 10 μm/s, σmax continuously increases, while Wdeb first increases but then sharply decreases. When the debonding velocity is increased from 10 to 50 μm/s at 680°C, σmax also increases while Wdeb overall decreases. Therefore, the debonding behaviors are highly temperature and rate dependent. More importantly, depending on the debonding conditions, three debonding types are identified, that is, the cohesive bulk deformation, the cohesive-interfacial transition and the interfacial fracture. The cohesive type can be converted into the interfacial fracture, by either decreasing temperature or increasing the debonding velocity. Based on the Wdeb criterion, the three debonding regimes can be clearly distinguished. Finally, analyses on the temperature and velocity experimental results are unified by incorporating the reduced crack velocity aTvc. The dependences of both viscoelasticity and Wdeb on aTvc qualitatively explain the transition condition for different debonding types. Concerning these findings, the work of debonding not only supplements the characterization of adhesion strength, but also throws insightful light on revealing the debonding mechanisms. 相似文献
7.
Jacques Hernigou Pascale Vertongen Joanne Rasschaert Philippe Hernigou 《International journal of molecular sciences》2021,22(8)
The value of bone marrow aspirate concentrates for treatment of human knee cartilage lesions is unclear. Most of the studies were performed with intra-articular injections. However, subchondral bone plays an important role in the progression of osteoarthritis. We investigated by a literature review whether joint, subchondral bone, or/and scaffolds implantation of fresh autologous bone marrow aspirate concentrated (BMAC) containing mesenchymal stem cells (MSCs) would improve osteoarthritis (OA). There is in vivo evidence that suggests that all these different approaches (intra-articular injections, subchondral implantation, scaffolds loaded with BMAC) can improve the patient. This review analyzes the evidence for each different approach to treat OA. We found that the use of intra-articular injections resulted in a significant relief of pain symptoms in the short term and was maintained in 12 months. However, the clinical trials indicate that the application of autologous bone marrow concentrates in combination with scaffolds or in injection in the subchondral bone was superior to intra-articular injection for long-term results. The tendency of MSCs to differentiate into fibrocartilage affecting the outcome was a common issue faced by all the studies when biopsies were performed, except for scaffolds implantation in which some hyaline cartilage was found. The review suggests also that both implantation of subchondral BMAC and scaffolds loaded with BMAC could reduce the need for further surgery. 相似文献
8.
9.
Samantha Donsante Biagio Palmisano Marta Serafini Pamela G. Robey Alessandro Corsi Mara Riminucci 《International journal of molecular sciences》2021,22(8)
Bone formation starts near the end of the embryonic stage of development and continues throughout life during bone modeling and growth, remodeling, and when needed, regeneration. Bone-forming cells, traditionally termed osteoblasts, produce, assemble, and control the mineralization of the type I collagen-enriched bone matrix while participating in the regulation of other cell processes, such as osteoclastogenesis, and metabolic activities, such as phosphate homeostasis. Osteoblasts are generated by different cohorts of skeletal stem cells that arise from different embryonic specifications, which operate in the pre-natal and/or adult skeleton under the control of multiple regulators. In this review, we briefly define the cellular identity and function of osteoblasts and discuss the main populations of osteoprogenitor cells identified to date. We also provide examples of long-known and recently recognized regulatory pathways and mechanisms involved in the specification of the osteogenic lineage, as assessed by studies on mice models and human genetic skeletal diseases. 相似文献
10.