全文获取类型
收费全文 | 1253篇 |
免费 | 125篇 |
国内免费 | 62篇 |
专业分类
化学 | 415篇 |
晶体学 | 1篇 |
力学 | 188篇 |
综合类 | 41篇 |
数学 | 162篇 |
物理学 | 633篇 |
出版年
2024年 | 1篇 |
2023年 | 12篇 |
2022年 | 21篇 |
2021年 | 70篇 |
2020年 | 38篇 |
2019年 | 37篇 |
2018年 | 26篇 |
2017年 | 42篇 |
2016年 | 60篇 |
2015年 | 59篇 |
2014年 | 75篇 |
2013年 | 76篇 |
2012年 | 61篇 |
2011年 | 72篇 |
2010年 | 57篇 |
2009年 | 62篇 |
2008年 | 51篇 |
2007年 | 47篇 |
2006年 | 77篇 |
2005年 | 76篇 |
2004年 | 64篇 |
2003年 | 73篇 |
2002年 | 50篇 |
2001年 | 42篇 |
2000年 | 49篇 |
1999年 | 20篇 |
1998年 | 21篇 |
1997年 | 15篇 |
1996年 | 11篇 |
1995年 | 12篇 |
1994年 | 9篇 |
1993年 | 12篇 |
1992年 | 11篇 |
1991年 | 5篇 |
1990年 | 5篇 |
1989年 | 4篇 |
1988年 | 3篇 |
1987年 | 2篇 |
1986年 | 3篇 |
1985年 | 1篇 |
1984年 | 2篇 |
1983年 | 1篇 |
1981年 | 1篇 |
1980年 | 1篇 |
1978年 | 2篇 |
1973年 | 1篇 |
排序方式: 共有1440条查询结果,搜索用时 31 毫秒
41.
A combination of "black box" and "calendar-time" methods for the determination of calibration intervals of an analytical
measuring instrument is discussed. Since the methods require information on the distributions of the calibration parameters,
such information is described for an atomic absorption spectrophotometer, as an example. The hypotheses on the normal distribution
of the calibration parameters are tested using the ω2-criterion and accepted at 0.90–0.95 levels of confidence. Corresponding control charts are designed for indication of warning
and action limits of the calibration parameters, and diagnoses of outliers in further calibrations. Control charts indicate
also when the calibration should be done according to the full program of the equipment manufacturer.
Received: 15 April 2000 / Accepted: 24 July 2000 相似文献
42.
43.
A method is described for the simultaneous quantitative determination of monoamines and related compounds from urine and brain tissue samples in the pg-range, using a GC/MF instrument LKB-2091 provided with a multiple ion detection (MID) system and capillary columns. The simultaneous detection of “fingerprints” with fourteen and more compounds during one single GC run was achieved after the intoduction of “time gates” for the detection of the different characteristic masses. Several modifications to the LKB equipment permitted exact reproducibility of retention times, which is essential for the use of “time gates”. The detection of “fingerprints” with these acidic, basic and alcoholic substances was achieved by the extraction of the dried biological samples with silylating agents. 相似文献
44.
We report the design and validation of a fast empirical function for scoring RNA-ligand interactions, and describe its implementation within RiboDock, a virtual screening system for automated flexible docking. Building on well-known protein-ligand scoring function foundations, features were added to describe the interactions of common RNA-binding functional groups that were not handled adequately by conventional terms, to disfavour non-complementary polar contacts, and to control non-specific charged interactions. The results of validation experiments against known structures of RNA-ligand complexes compare favourably with previously reported methods. Binding modes were well predicted in most cases and good discrimination was achieved between native and non-native ligands for each binding site, and between native and non-native binding sites for each ligand. Further evidence of the ability of the method to identify true RNA binders is provided by compound selection ('enrichment factor') experiments based around a series of HIV-1 TAR RNA-binding ligands. Significant enrichment in true binders was achieved amongst high scoring docking hits, even when selection was from a library of structurally related, positively charged molecules. Coupled with a semi-automated cavity detection algorithm for identification of putative ligand binding sites, also described here, the method is suitable for the screening of very large databases of molecules against RNA and RNA-protein interfaces, such as those presented by the bacterial ribosome. 相似文献
45.
46.
47.
Weihe Xu Kenneth Lauer Yong Chu Evgeny Nazaretski 《Journal of synchrotron radiation》2014,21(6):1367-1369
A rotational stage is a key component of every X‐ray instrument capable of providing tomographic or diffraction measurements. To perform accurate three‐dimensional reconstructions, runout errors due to imperfect rotation (e.g. circle of confusion) must be quantified and corrected. A dedicated instrument capable of full characterization and circle of confusion mapping in rotary stages down to the sub‐10 nm level has been developed. A high‐stability design, with an array of five capacitive sensors, allows simultaneous measurements of wobble, radial and axial displacements. The developed instrument has been used for characterization of two mechanical stages which are part of an X‐ray microscope. 相似文献
48.
49.
Non-small cell lung cancer (NSCLC) is a lethal non-immunogenic malignancy and proto-oncogene ROS-1 tyrosine kinase is one of its clinically relevant oncogenic markers. The ROS-1 inhibitor, crizotinib, demonstrated resistance due to the Gly2032Arg mutation. To curtail this resistance, researchers developed lorlatinib against the mutated kinase. In the present study, a receptor-ligand pharmacophore model exploiting the key features of lorlatinib binding with ROS-1 was exploited to identify inhibitors against the wild-type (WT) and the mutant (MT) kinase domain. The developed model was utilized to virtually screen the TimTec flavonoids database and the retrieved drug-like hits were subjected for docking with the WT and MT ROS-1 kinase. A total of 10 flavonoids displayed higher docking scores than lorlatinib. Subsequent molecular dynamics simulations of the acquired flavonoids with WT and MT ROS-1 revealed no steric clashes with the Arg2032 (MT ROS-1). The binding free energy calculations computed via molecular mechanics/Poisson-Boltzmann surface area (MM/PBSA) demonstrated one flavonoid (Hit) with better energy than lorlatinib in binding with WT and MT ROS-1. The Hit compound was observed to bind in the ROS-1 selectivity pocket comprised of residues from the β-3 sheet and DFG-motif. The identified Hit from this investigation could act as a potent WT and MT ROS-1 inhibitor. 相似文献
50.