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   40326篇
  免费   107篇
  国内免费   183篇
系统科学   203篇
丛书文集   722篇
教育与普及   66篇
理论与方法论   160篇
现状及发展   19283篇
研究方法   1553篇
综合类   18095篇
自然研究   534篇
  2013年   321篇
  2012年   507篇
  2011年   1040篇
  2010年   214篇
  2008年   651篇
  2007年   711篇
  2006年   732篇
  2005年   702篇
  2004年   805篇
  2003年   655篇
  2002年   646篇
  2001年   1169篇
  2000年   1087篇
  1999年   765篇
  1992年   748篇
  1991年   551篇
  1990年   618篇
  1989年   633篇
  1988年   578篇
  1987年   667篇
  1986年   636篇
  1985年   805篇
  1984年   616篇
  1983年   508篇
  1982年   472篇
  1981年   506篇
  1980年   604篇
  1979年   1291篇
  1978年   1084篇
  1977年   1031篇
  1976年   834篇
  1975年   932篇
  1974年   1259篇
  1973年   1085篇
  1972年   1100篇
  1971年   1272篇
  1970年   1598篇
  1969年   1223篇
  1968年   1242篇
  1967年   1212篇
  1966年   1020篇
  1965年   757篇
  1964年   249篇
  1959年   411篇
  1958年   727篇
  1957年   496篇
  1956年   411篇
  1955年   417篇
  1954年   405篇
  1948年   271篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
L B Knee  C M Brunt 《Nature》2001,412(6844):308-310
A large fraction of the mass of the interstellar medium in our Galaxy is in the form of warm (103-104 K) and cool (50-100 K) atomic hydrogen (H i) gas. Cold (10-30 K) regions are thought to be dominated by dense clouds of molecular hydrogen. Cold H i is difficult to observe, and therefore our knowledge of its abundance and distribution in the interstellar medium is poor. The few known clouds of cold H i are much smaller in size and mass than typical molecular clouds. Here we report the discovery that the H i supershell GSH139-03-69 is very cold (10 K). It is about 2 kiloparsecs in size and as massive as the largest molecular complexes. The existence of such an immense structure composed of cold atomic hydrogen in the interstellar medium runs counter to the prevailing view that cold gas resides almost exclusively in clouds dominated by molecular hydrogen.  相似文献   
992.
993.
本文建立了同时考虑轴颈径向位移和歪斜时的滑动轴承动力学模型.对于这种模型,油膜力将扩展为四个广义力分量.文章将相应的动力系数矩阵分解为对称和反对称两部分并讨论其物理性质.然后,本文推导得出该模型的正交变换矩阵,在此基础上导得各向同性的动力系数矩阵表达式,并讨论了诸元素的物理意义.文章最后引入动力系数椭圆的概念以分析非对称动力系数矩阵的变换性质.  相似文献   
994.
LEED强度的多重散射分析,进一步确定Zr与氧作用在低覆盖量下(<1ML),形成(2×2)-O结构,是氧吸附后进入Zr表面原子层下,占据八面体空位,形成有两层氧的under layer结构,Zr表面原子层有Fcc重构。分析得到的Zt-O键距为0.232nm,而Zr-Zr间距增大为0.268nm,比原来的距离增大约4.3%,这是由于氧插入的结果。  相似文献   
995.
本文报导用活性炭盒吸附方法对香港室内氡浓度的测量结果及其浓度分布规律。对室内氡浓度与建筑物表面氡析出率的关系进行了分析研究。证实室内空气中的氡主要来源于建材中的镭,而氡浓度水平只决定于室内建筑物表面氡的析出率及通风状况。  相似文献   
996.
T Tanabe  B A Adams  S Numa  K G Beam 《Nature》1991,352(6338):800-803
Membrane depolarization causes many kinds of ion channels to open, a process termed activation. For both Na+ channels and Ca2+ channels, kinetic analysis of current has suggested that during activation the channel undergoes several conformational changes before reaching the open state. Structurally, these channels share a common motif: the central element is a large polypeptide with four repeating units of homology (repeats I-IV), each containing a voltage-sensing region, the S4 segment. This suggests that the distinct conformational transitions inferred from kinetic analysis may be equated with conformational changes of the individual structural repeats. To investigate the molecular basis of channel activation, we constructed complementary DNAs encoding chimaeric Ca2+ channels in which one or more of the four repeats of the skeletal muscle dihydropyridine receptor are replaced by the corresponding repeats derived from the cardiac dihydropyridine receptor. We report here that repeat I determines whether the chimaeric Ca2+ channel shows slow (skeletal muscle-like) or rapid (cardiac-like) activation.  相似文献   
997.
A locus segregating with familial Alzheimer's disease (AD) has been mapped to chromosome 21, close to the amyloid precursor protein (APP) gene. Recombinants between the APP gene and the AD locus have been reported which seemed to exclude it as the site of the mutation causing familial AD. But recent genetic analysis of a large number of AD families has demonstrated that the disease is heterogeneous. Families with late-onset AD do not show linkage to chromosome 21 markers. Some families with early-onset AD show linkage to chromosome 21 markers, but some do not. This has led to the suggestion that there is non-allelic genetic heterogeneity even within early onset familial AD. To avoid the problems that heterogeneity poses for genetic analysis, we have examined the cosegregation of AD and markers along the long arm of chromosome 21 in a single family with AD confirmed by autopsy. Here we demonstrate that in this kindred, which shows linkage to chromosome 21 markers, there is a point mutation in the APP gene. This mutation causes an amino-acid substitution (Val----Ile) close to the carboxy terminus of the beta-amyloid peptide. Screening other cases of familial AD revealed a second unrelated family in which this variant occurs. This suggests that some cases of AD could be caused by mutations in the APP gene.  相似文献   
998.
999.
G Varadi  P Lory  D Schultz  M Varadi  A Schwartz 《Nature》1991,352(6331):159-162
The L-type voltage-dependent calcium channel is an important link in excitation-contraction coupling of muscle cells (reviewed in refs 2 and 3). The channel has two functional characteristics: calcium permeation and receptor sites for calcium antagonists. In skeletal muscle the channel is a complex of five subunits, alpha 1, alpha 2, beta, gamma and delta. Complementary DNAs to these subunits have been cloned and their amino-acid sequences deduced. The skeletal muscle alpha 1 subunit cDNA expressed in L cells manifests as specific calcium-ion permeation, as well as sensitivity to the three classes of organic calcium-channel blockers. We report here that coexpression of the alpha 1 subunit with other subunits results in significant changes in dihydropyridine binding and gating properties. The available number of drug receptor sites increases 10-fold with an alpha 1 beta combination, whereas the affinity of the dihydropyridine binding site remains unchanged. Also, the presence of the beta subunit accelerates activation and inactivation kinetics of the calcium-channel current.  相似文献   
1000.
Effects of the steel gene product on mouse primordial germ cells in culture.   总被引:21,自引:0,他引:21  
I Godin  R Deed  J Cooke  K Zsebo  M Dexter  C C Wylie 《Nature》1991,352(6338):807-809
Mutations at the steel (sl) and dominant white spotting (W) loci in the mouse affect primordial germ cells (PGC), melanoblasts and haemopoietic stem cells. The W gene encodes a cell-surface receptor of the tyrosine kinase family, the proto-oncogene c-kit. In situ analysis has shown c-kit messenger RNA expression in PGC in the early genital ridges. The Sl gene encodes the ligand for this receptor, a peptide growth factor, called here stem cell factor (SCF). SCF mRNA is expressed in many regions of the early mouse embryo, including the areas of migration of these cell types. It is important now to identify the role of the Sl-W interaction in the development of these migratory embryonic stem cell populations. Using an in vitro assay system, we show that SCF increases both the overall numbers and colony sizes of migratory PGC isolated from wild-type mouse embryos, and cultured on irradiated feeder layers of STO cells (a mouse embryonic fibroblast line). In the absence of feeder cells, SCF causes a large increase in the initial survival and apparent motility of PGC in culture. But labelling with bromodeoxyuridine shows that SCF is not, by itself, a mitogen for PGC. SCF does not exert a chemotropic effect on PGC in in vitro assays. These results suggest that SCF in vivo is an essential requirement for PGC survival. This demonstrates the control of the early germ-line population by a specific trophic factor.  相似文献   
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