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   306篇
  免费   0篇
  国内免费   1篇
系统科学   10篇
现状及发展   48篇
研究方法   26篇
综合类   205篇
自然研究   18篇
  2017年   1篇
  2013年   1篇
  2012年   15篇
  2011年   33篇
  2010年   5篇
  2008年   16篇
  2007年   9篇
  2006年   17篇
  2005年   12篇
  2004年   8篇
  2003年   15篇
  2002年   8篇
  2001年   12篇
  2000年   14篇
  1999年   6篇
  1998年   1篇
  1997年   2篇
  1996年   2篇
  1993年   1篇
  1992年   8篇
  1991年   2篇
  1990年   9篇
  1989年   8篇
  1988年   5篇
  1987年   3篇
  1986年   1篇
  1985年   5篇
  1984年   2篇
  1983年   3篇
  1982年   3篇
  1981年   1篇
  1980年   1篇
  1979年   3篇
  1978年   7篇
  1977年   4篇
  1976年   4篇
  1975年   6篇
  1974年   4篇
  1973年   7篇
  1971年   4篇
  1970年   12篇
  1969年   5篇
  1968年   5篇
  1967年   4篇
  1966年   6篇
  1965年   5篇
  1963年   1篇
  1962年   1篇
排序方式: 共有307条查询结果,搜索用时 15 毫秒
31.
Alteration in crossbridge kinetics caused by mutations in actin   总被引:6,自引:0,他引:6  
D R Drummond  M Peckham  J C Sparrow  D C White 《Nature》1990,348(6300):440-442
The generation of force during muscle contraction results from the interaction of myosin and actin. The kinetics of this force generation vary between different muscle types and within the same muscle type in different species. Most attention has focused on the role of myosin isoforms in determining these differences. The role of actin isoforms has received little attention, largely because of the lack of a suitable cell type in which the myosin isoform remains constant yet the actin isoforms vary. An alternative approach would be to examine the effect of actin mutations, however, most of these cause such gross disruption of muscle structure that mechanical measurements are impossible. We have now identified two actin mutations which, despite involving conserved amino acids, can assemble into virtually normal myofibrils. These amino-acid changes in actin significantly affect the kinetics of force generation by muscle fibres. One of the mutations is not in the putative myosin-binding site, demonstrating the importance of long-range effects of amino acids on actin function.  相似文献   
32.
The known Mountain Plover population breeding on the Myton Bench, Duchesne County, Utah, is small, composed roughly of 30 adults and young after each breeding season. Currently, its location is peripheral to the species main range. This shrub-steppe breeding habitat differs from the shortgrass prairie habitat with which this bird is historically associated. Between 1996 and 1998 we made observations at nesting sites located consistently in 2 concentrated areas surrounded by large tracts of similar habitat. Activity may be focused in these specific areas because of breeding-site fidelity; this behavior is common among most shorebirds and has been documented for the Mountain Plover in Colorado. Also, Mountain Plovers are social and tend to choose nest sites near others. Most nests in Utah were located within close proximity of mounds of white-tailed prairie dogs ( Cynomys leucurus ), and all were situated near roadways or oil well pads. Mountain Plovers were often observed with broods on these bare areas at night. We conclude that Mountain Plovers on the Myton Bench are distributed in clumped breeding colonies within large areas of apparently favorable habitat.  相似文献   
33.
Nucleosome mobilization catalysed by the yeast SWI/SNF complex.   总被引:18,自引:0,他引:18  
  相似文献   
34.
Hemodilution with 40 ml/kg of Fluosol or saline reduced the acetaminophen Vd and the acetaminophen sulfate ClM at 48 or 72 h, respectively. Fluosol hemodilution increased the acetaminophen renal excretion at 24 and 72 h. But at 48 h, Fluosol hemodilution either inhibited the renal secretion of acetaminophen or enhanced its reabsorption.  相似文献   
35.
A bacteriophage infective toXenorhabdus luminescens, a bacterial symbiont of heterorhabditid nematodes, was recovered from insects that supported poor nematode development. Plaque tests showed the phage particles to be infective only to primary and not secondary colonies ofX. luminescens. The phage was not infective toX. nenatophilus primaries or secondaries. The bacteriophage particles ranged 80–90 nm in length, with the head ranging from 40 to 50 nm in diameter. Restriction analysis was performed on isolated bacteriophage DNA. This first report of a bacteriophage fromXenorhabdus species has pratical implications since it could be detrimental to cultures ofHeterorhabditis nematodes that are being produced throughout the world for the biological control of insects.  相似文献   
36.
In vitro synthesis of Hb Hammersmith (CDI phe-ser)   总被引:3,自引:0,他引:3  
J M White  J V Dacie 《Nature》1970,225(5235):860-861
  相似文献   
37.
Charcot-Marie-Tooth disease 1A (CMT1A) is a hereditary demyelinating peripheral neuropathy, associated with a DNA duplication on chromosome 17p11.2. A related disorder in the mouse, trembler (Tr), maps to mouse chromosome 11 which has syntenic homology to human chromosome 17p. Recently, the peripheral myelin protein-22 (pmp-22) gene was identified as the likely Tr locus. We have constructed a partial yeast artificial chromosome contig spanning the CMT1A gene region and mapped the PMP-22 gene to the duplicated region. These observations further implicate PMP-22 as a candidate gene for CMT1A, and suggest that over-expression of this gene may be one mechanism that produces the CMT1A phenotype.  相似文献   
38.
39.
New partial skeleton of Homo habilis from Olduvai Gorge, Tanzania   总被引:1,自引:0,他引:1  
A new partial skeleton of an adult hominid from lower Bed I (about 1.8 Myr ago), Olduvai Gorge, is described. This specimen's craniodental anatomy indicates attribution to Homo habilis, but its postcranial anatomy, including small body size and relatively long arms, is strikingly similar to that of some early Australopithecus individuals.  相似文献   
40.
Résumé Les auteurs ont effectué de nouvelles préparations chimiques anticancéreuses en utilisant une forme des agents alkylants déactivés du type moutarde nitrogénée quaternaire. Un mode d'action est proposé par lequel ces préparations peuvent être activées in vivo.

Sponsored by the Cancer Chemotherapy National Service Center, National Cancer Institute, National Institutes of Health, Contract No. SA-43-ph-4360.  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