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   109篇
  免费   0篇
教育与普及   1篇
现状及发展   66篇
研究方法   10篇
综合类   32篇
  2012年   1篇
  2011年   2篇
  2008年   1篇
  2007年   2篇
  2006年   3篇
  2005年   1篇
  2004年   2篇
  2003年   4篇
  2002年   2篇
  2001年   3篇
  2000年   1篇
  1999年   4篇
  1992年   1篇
  1991年   2篇
  1990年   1篇
  1989年   1篇
  1988年   1篇
  1987年   2篇
  1981年   2篇
  1980年   2篇
  1979年   1篇
  1978年   7篇
  1977年   9篇
  1976年   4篇
  1975年   8篇
  1974年   6篇
  1973年   6篇
  1972年   3篇
  1971年   4篇
  1970年   1篇
  1969年   1篇
  1968年   8篇
  1967年   2篇
  1966年   1篇
  1965年   3篇
  1962年   1篇
  1959年   1篇
  1956年   1篇
  1955年   3篇
  1954年   1篇
排序方式: 共有109条查询结果,搜索用时 218 毫秒
101.
102.
Zusammenfassung Dissoziierte Nervenzellen der Gehirnhemisphären von Hühnerembryonen wurden inRose-Kammern mit und ohne Cellophanmembran kultiviert. Die Differenzierung der Neurone wurde mit Phasenkontrast und histochemischen Methoden untersucht.

Chargée de Recherche au CNRS.  相似文献   
103.
Phosphoinositides play a central role in the control of major eukaryotic cell signaling mechanisms. Accordingly, the list of phosphoinositide-metabolizing enzymes implicated in human diseases has considerably increased these last years. Here we will focus on myotubularin, the protein mutated in the X-linked myotubular myopathy (XLMTM) and the founding member of a family of 13 related proteins. Recent data demonstrate that myotubularin and several other members of the family are potent lipid phosphatases showing a marked specificity for phosphatidylinositol 3-phosphate [PtdIns(3)P]. This finding has raised considerable interest as PtdIns(3)P is implicated in vesicular trafficking and sorting through its binding to specific protein domains. The structure of myotubularin, the molecular mechanisms of its function and its implication in the etiology of XLMTM will be discussed, as well as the potential function and role of the other members of the family.Received 14 February 2003; received after revision 10 April 2003; accepted 14 April 2003  相似文献   
104.
The amnionless gene, Amn, on mouse chromosome 12 encodes a type I transmembrane protein that is expressed in the extraembryonic visceral layer during gastrulation. Mice homozygous with respect to the amn mutation generated by a transgene insertion have no amnion. The embryos are severely compromised, surviving to the tenth day of gestation but seem to lack the mesodermal layers that normally produce the trunk. The Amn protein has one transmembrane domain separating a larger, N-terminal extracellular region and a smaller, C-terminal cytoplasmic region. The extracellular region harbors a cysteine-rich domain resembling those occurring in Chordin, found in Xenopus laevis embryos, and Sog, found in Drosophila melanogaster. As these cysteine-rich domains bind bone morphogenetic proteins (Bmps), it has been speculated that the cysteine-rich domain in Amn also binds Bmps. We show that homozygous mutations affecting exons 1-4 of human AMN lead to selective malabsorption of vitamin B12 (a phenotype associated with megaloblastic anemia 1, MGA1; OMIM 261100; refs. 5,6) in otherwise normal individuals, suggesting that the 5' end of AMN is dispensable for embryonic development but necessary for absorption of vitamin B12. When the 5' end of AMN is truncated by mutations, translation is initiated from alternative downstream start codons.  相似文献   
105.
Résumé Des cellules, encore à un stade indifférencié, dissociées d'hémisphères cérébraux d'embryon de Poulet ont formé, en culture, des fibres nerveuses. La plupart des cellules se différencient en neuroblastes unipolaire et bipolaire; certaines évoluent vers le type multipolaire sans contact direct avec des cellules gliales.

Chargée de Recherche au CNRS.  相似文献   
106.
Summary The irradiation of the lens by a simple dose of 1400 r, gives a very important and lasting reduction of its hexokinase activity. Its ATPase activity shows an increase during the first four days and a return to normal again. The variations observed here (that isin vivo) are different from the ones noted after irradiation of these enzymesin vitro.

Travail effectué avec le concours matériel de l'Institut National d'Hygiène.  相似文献   
107.
108.
109.
Mandel CR  Kaneko S  Zhang H  Gebauer D  Vethantham V  Manley JL  Tong L 《Nature》2006,444(7121):953-956
Most eukaryotic messenger RNA precursors (pre-mRNAs) undergo extensive maturational processing, including cleavage and polyadenylation at the 3'-end. Despite the characterization of many proteins that are required for the cleavage reaction, the identity of the endonuclease is not known. Recent analyses indicated that the 73-kDa subunit of cleavage and polyadenylation specificity factor (CPSF-73) might be the endonuclease for this and related reactions, although no direct data confirmed this. Here we report the crystal structures of human CPSF-73 at 2.1 A resolution, complexed with zinc ions and a sulphate that might mimic the phosphate group of the substrate, and the related yeast protein CPSF-100 (Ydh1) at 2.5 A resolution. Both CPSF-73 and CPSF-100 contain two domains, a metallo-beta-lactamase domain and a novel beta-CASP (named for metallo-beta-lactamase, CPSF, Artemis, Snm1, Pso2) domain. The active site of CPSF-73, with two zinc ions, is located at the interface of the two domains. Purified recombinant CPSF-73 possesses RNA endonuclease activity, and mutations that disrupt zinc binding in the active site abolish this activity. Our studies provide the first direct experimental evidence that CPSF-73 is the pre-mRNA 3'-end-processing endonuclease.  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