首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   29篇
  免费   2篇
耳鼻咽喉   1篇
基础医学   5篇
内科学   4篇
皮肤病学   6篇
特种医学   7篇
外科学   4篇
预防医学   1篇
肿瘤学   3篇
  2021年   2篇
  2015年   2篇
  2014年   2篇
  2012年   6篇
  2011年   4篇
  2010年   3篇
  2008年   1篇
  2007年   1篇
  2006年   2篇
  2005年   1篇
  2003年   1篇
  1999年   1篇
  1997年   1篇
  1993年   2篇
  1985年   2篇
排序方式: 共有31条查询结果,搜索用时 640 毫秒
1.
2.
We report our first experience of brain DaTSCAN SPECT imaging using cadmium-zinc-telluride gamma camera (CZT-GC) in 2 cases: a 64-year-old patient suffering from essential tremor and a 73-year-old patient presenting with atypical bilateral extrapyramidal syndrome. In both cases, 2 different acquisitions were performed and compared, using a double-head Anger-GC, followed immediately by a second acquisition on CZT-GC. There were no significant visual differences between images generated by different GC. Our first result suggests that DaTSCAN SPECT is feasible on CZT-GC, allowing both injected dose and acquisition time reductions without compromising image quality. This experience needs to be evaluated in larger series.  相似文献   
3.
4.
A continuum of water populations can exist in nanoscale layered materials, which impacts transport phenomena relevant for separation, adsorption, and charge storage processes. Quantification and direct interrogation of water structure and organization are important in order to design materials with molecular-level control for emerging energy and water applications. Through combining molecular simulations with ambient-pressure X-ray photoelectron spectroscopy, X-ray diffraction, and diffuse reflectance infrared Fourier transform spectroscopy, we directly probe hydration mechanisms at confined and nonconfined regions in nanolayered transition-metal carbide materials. Hydrophobic (K+) cations decrease water mobility within the confined interlayer and accelerate water removal at nonconfined surfaces. Hydrophilic cations (Li+) increase water mobility within the confined interlayer and decrease water-removal rates at nonconfined surfaces. Solutes, rather than the surface terminating groups, are shown to be more impactful on the kinetics of water adsorption and desorption. Calculations from grand canonical molecular dynamics demonstrate that hydrophilic cations (Li+) actively aid in water adsorption at MXene interfaces. In contrast, hydrophobic cations (K+) weakly interact with water, leading to higher degrees of water ordering (orientation) and faster removal at elevated temperatures.

Geologic clays are minerals with variable amounts of water trapped within the bulk structure (1) and are routinely used as hydraulic barriers where water and contaminant transport must be controlled (2, 3). These layered materials can exhibit large degrees of swelling when intercalated with a hydrated cation (4). Fundamentally, water adsorption at exposed interfaces and transport in confined channels is dictated by geometry, morphology, and chemistry (e.g., surface chemistry, local solutes, etc.) (5). Understanding water adsorption and swelling in natural clay materials has significant implications for understanding water interactions in nanoscale layered materials. At the nanoscale, the ability to control the interlayer swelling and water adsorption can lead to more precise control over mass and reactant transport, resulting in enhancement in properties necessary for next-generation energy storage (power and capacity) (68), membranes (selectivity, salt rejection, and water permeability), catalysis (913), and adsorption (14).Two-dimensional (2D) and multilayered transition-metal carbides and nitrides (MXenes) are a recent addition to the few-atom-thick materials and have been widely studied in their applications to energy storage (6, 9, 15, 16), membranes (13), and adsorption (17). MXenes (Mn+1XnTx) are produced via selective etching of A elements from ceramic MAX (Mn+1 AXn) phase materials (11, 18). The removal of A element results in thin Mn+1 Xn nanosheets with negative termination groups (Tx). MXene’s hydrophilic and negatively charged surface properties promote spontaneous intercalation of a wide array of ions and compounds. Cation intercalation properties in MXenes have been vigorously explored due to their demonstrated high volumetric capacitance, which may enable high-rate energy storage (6, 19). In addition, their unique and rich surface chemistry may enable selective ion adsorption, making them promising candidates for water purification and catalytic applications (2022).Water and ion transport within multilayered MXenes is governed by the presence of a continuum of water populations. The configuration of water in confined (interlayer) and nonconfined state (surface) influences the material system’s physical properties (13, 2327). However, our current understanding of water–surface interactions and water structure at the molecular scale is incomplete due to limited characterization approaches (28). Most modern observations are limited to macroscopic measurements (e.g., transport measurement, contact angle, etc.), which do not capture the impact of local heterogeneity due to surface roughness, surface chemistry, solutes, etc. (29). Herein, we address this gap via combining theory with an ensemble of direct and indirect interrogation techniques. Water structure and sorption properties at MXene interfaces are directly probed by using ambient-pressure X-ray photoelectron spectroscopy (APXPS), X-ray diffraction (XRD), and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). APXPS enables detection of local chemically specific signatures and quantitative analysis at near-ambient pressures (30). This technique provides the ability to spatially resolve the impact of surface chemistry and solutes on water sorption/desorption at water–solid interfaces. Model hydrophobic (e.g., K+) and hydrophilic (e.g., Li+) cations were intercalated into the layers via ion exchange to systematically probe the impacts of charged solutes on water orientation and sorption. Prior reports suggest that water within the confined interlayer transforms from bulk-like to crystalline when intercalated with bulky cations (31, 32). Furthermore, it has been demonstrated that water ordering is correlated with ion size (33, 34). Here, we expand upon this early work and examine the role that solute hydrophobicity and hydrophilicity impacts water adsorption on solid interfaces. Water mobility within the interlayer is impacted by the hydration energy of that cation. Results shed light on the intertwined role that surface counterions and terminating groups play on the dynamics of hydration and dehydration.  相似文献   
5.
6.
The aim of the presented study was to perform a global sensitivity analysis of various design parameters affecting the lost motion of the harmonic drive. A detailed virtual model of a harmonic drive was developed, including the wave generator, the flexible ball bearing, the flexible spline and the circular spline. Finite element analyses were performed to observe which parameter from the harmonic drive geometry parameter group affects the lost motion value most. The analyses were carried out using 4% of the rated harmonic drive output torque by the locked wave generator and fixed circular spline according the requirements for the high accuracy harmonic drive units. The described approach was applied to two harmonic drive units with the same ratio, but various dimensions and rated power were used to generalize and interpret the global sensitivity analysis results properly. The most important variable was for both harmonic drives the offset from the nominal tooth shape.  相似文献   
7.
8.
9.
Genetic alterations occur during the adenoma-carcinoma sequence of colon cancer formation and drive the initiation and progression of colon cancer formation. The aberrant methylation of genes is an alternate, epigenetic mechanism for silencing tumor suppressor genes in colon cancer. The aim of this study was to determine on a global and gene-specific level the role of CpG island methylation in the initiation and progression of colon cancer. Consequently, we assessed the frequency of gene methylation in tumors representative of the commonly recognized histological steps of the adenoma-carcinoma progression sequence through the analysis of eight genes previously identified to be methylated in colon cancer, MGMT, HLTF, MLH1, p14(ARF), CDKN2A, TIMP3, THBS1, and CDH1. We observed that the proportion of tumors carrying methylated alleles increased from adenomas to adenocarcinomas but that the proportion of tumors with methylated alleles was not different between adenocarcinomas and metastases (69% versus 90%, P = 0.01 and 90% versus 81%, P > 0.05). The most substantial difference occurred between early and advanced adenomas (47% versus 84%, P = 0.018). Furthermore, we observed that the frequency of gene methylation at the different steps of the progression sequence varied between genes. Thus, the aberrant methylation of genes appears to increase most significantly during the progression of early adenomas to advanced adenomas, and the frequency of specific gene methylation at the different steps of the adenoma-carcinoma progression sequence varies in a gene-specific fashion.  相似文献   
10.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号