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   132篇
  免费   2篇
  134篇
  2014年   6篇
  2013年   9篇
  2012年   4篇
  2011年   5篇
  2010年   6篇
  2009年   3篇
  2008年   2篇
  2007年   3篇
  2005年   2篇
  2001年   4篇
  1998年   2篇
  1995年   2篇
  1994年   2篇
  1993年   2篇
  1992年   3篇
  1989年   2篇
  1985年   1篇
  1984年   1篇
  1983年   1篇
  1982年   1篇
  1980年   1篇
  1977年   1篇
  1975年   1篇
  1971年   1篇
  1962年   1篇
  1958年   1篇
  1951年   4篇
  1945年   1篇
  1943年   1篇
  1929年   1篇
  1928年   1篇
  1927年   2篇
  1925年   2篇
  1922年   1篇
  1921年   1篇
  1920年   2篇
  1917年   2篇
  1916年   1篇
  1915年   1篇
  1914年   2篇
  1912年   3篇
  1911年   7篇
  1910年   2篇
  1909年   4篇
  1908年   5篇
  1907年   3篇
  1906年   4篇
  1905年   3篇
  1903年   1篇
  1902年   1篇
排序方式: 共有134条查询结果,搜索用时 15 毫秒
51.
52.
53.
54.
55.
Human papillomavirus 58 (HPV58) ranks the second or third in East Asian cervical cancers. Current studies on HPV58 are scarce and focus on the prototype. Previously, we identified the three most common circulating HPV58 E7 strains contained amino acid alterations: G41R/G63D (51%), T20I/G63S (22%) and T74A/D76E (14%) respectively. Among them, the T20I/G63S variant (V1) had a stronger epidemiological association with cervical cancer. We therefore suggested that V1 possessed stronger oncogenicity than the other two variants. Here, we performed phenotypic assays to characterize and compare their oncogenicities with HPV58 E7 prototype. Our results showed that overexpression of V1 conferred a higher colony‐forming ability to primary murine epithelial cells than prototype (< 0.05) and other variants, implicating its higher immortalising potential. Further experiments showed that both V1 and prototype enhanced the anchorage‐independent growth of NIH/3T3 cells (< 0.001), implicating their stronger transforming power than the two other variants. Moreover, they possessed an increased ability to degrade pRb (< 0.001), which is a major effector pathway of E7‐driven oncogenesis. Our work represents the first study to compare the oncogenicities of HPV58 E7 prototype and variants. These findings deepened our understanding of HPV58 and might inform clinical screening and follow‐up strategy.  相似文献   
56.
57.
58.
The procedures used in the organization and operation of a special study on diarrheal diseases involving federal, state, and local agencies are outlined. The integration of such a project into a local routine program is discussed and the possible benefits derived by the various agencies are briefly evaluated.  相似文献   
59.
Current experimental research on mammalian limb muscle structureand function is compared to that on mammalian jaw muscles. Twomajor areas of comparison are stressed: structural and functional.Comparisons of limbs and jaws are made from the point of viewof the impact of recent studies on simple mechanical modelsof limb/jaw muscle function. Limb muscle structure is comparedto jaw muscles at the level of muscle architecture, muscle histochemicaland motor unit properties, and the organization of motor unitsinto neuromuscular compartments. Such comparisons reveal thatalthough limb muscles and jaw muscles might be organized insimilar ways, fundamental differences exist, both in terms ofmuscle structure and the functional conclusions which have beenbased on studies of muscle structure. The comparisons also demonstratethat much recent evidence from structural studies have had littledirect impact on simple models of muscle function but a muchlarger influence on the assumptions of the models. Comparisonsof limb/jaw muscle function from kinematic and EMG studies,indicate that many masticatory strategies are used by differentmammals but the basic problems of posture and locomotion havebeen met with essentially similar solutions, even among diversemammalian groups. The results of such comparisons demonstratethat both limb and jaw muscle function are sufficiently complexthat new or re-vitalized models are needed if the relationshipbetween structure and function are ever to be understood.  相似文献   
60.
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