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   144篇
  免费   8篇
  2022年   5篇
  2021年   12篇
  2020年   3篇
  2019年   3篇
  2018年   5篇
  2017年   3篇
  2016年   9篇
  2015年   7篇
  2014年   6篇
  2013年   11篇
  2012年   2篇
  2011年   8篇
  2010年   1篇
  2009年   6篇
  2008年   5篇
  2007年   9篇
  2006年   8篇
  2005年   7篇
  2004年   4篇
  2003年   3篇
  2002年   4篇
  2001年   2篇
  2000年   3篇
  1998年   1篇
  1997年   2篇
  1994年   1篇
  1991年   2篇
  1990年   2篇
  1986年   1篇
  1984年   2篇
  1981年   1篇
  1979年   2篇
  1978年   3篇
  1976年   1篇
  1975年   2篇
  1971年   2篇
  1969年   1篇
  1968年   1篇
  1967年   2篇
排序方式: 共有152条查询结果,搜索用时 46 毫秒
151.

Proteins of the Bcl-2 protein family, including pro-apoptotic Bax and anti-apoptotic Bcl-xL, are critical for mitochondrial-mediated apoptosis regulation. Since yeast lacks obvious orthologs of Bcl-2 family members, heterologous expression of these proteins has been used to investigate their molecular and functional aspects. Active Bax is involved in the formation of mitochondrial outer membrane pores, through which cytochrome c (cyt c) is released, triggering a cascade of downstream apoptotic events. However, when in its inactive form, Bax is largely cytosolic or weakly bound to mitochondria. Given the central role of Bax in apoptosis, studies aiming to understand its regulation are of paramount importance towards its exploitation as a therapeutic target. So far, studies taking advantage of heterologous expression of human Bax in yeast to unveil regulation of Bax activation have relied on the use of artificial mutated or mitochondrial tagged Bax for its activation, rather than the wild type Bax (Bax α). Here, we found that cell death could be triggered in yeast cells heterologoulsy expressing Bax α with concentrations of acetic acid that are not lethal to wild type cells. This was associated with Bax mitochondrial translocation and cyt c release, closely resembling the natural Bax function in the cellular context. This regulated cell death process was reverted by co-expression with Bcl-xL, but not with Bcl-xLΔC, and in the absence of Rim11p, the yeast ortholog of mammalian GSK3β. This novel system mimics human Bax α regulation by GSK3β and can therefore be used as a platform to uncover novel Bax regulators and explore its therapeutic modulation.

  相似文献   
152.
Some methodological aspects are discussed of the investigation of acute infarct myocarditis (AIM) in relation to weather fronts. Results of a new method of analysis are given. Data were analysed from about the hour of the onset of symptoms, and led to the diagnosis of AIM either immediately or within a few hours or days (3019 cases observed over 4.5 years during 1982–1986 in Plzen, Czechoslovakia). Weather classification was based on three factors (the type of the foregoing front, the type of the subsequent front, the time section of the time interval demarcated by the passage of the surfaces of the fronts). AIM occurrence increased in particular types of weather fronts: (i) by 30% during 7–12 h after a warm front, if the time span between fronts exceeded 24 h; (ii) by 10% in time at least 36 h distant from the foregoing cold or occlusion front and from the succeeding warm or occlusion front; (iii) by 20% during 0–2 h before the passage of the front, provided the foregoing front was not warm and the interval between fronts exceeded 5 h. AIM occurrence decreased by 15%–20% for time span between fronts > 24 h at times 6–11, 6–23 and 6–35 h before a coming warm or occlusion front (for interfrontal intervals 25–48, 49–72 and possibly > 72 h), and also at 12–23 and possibly 12–35 h before a cold front (for intervals 49–72 and possibly > 72 h), if the foregoing front was cold or an occlusion front.  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