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   17篇
  免费   0篇
现状及发展   8篇
研究方法   2篇
综合类   7篇
  2012年   1篇
  2008年   1篇
  2007年   1篇
  2006年   1篇
  2002年   1篇
  1987年   1篇
  1979年   1篇
  1978年   2篇
  1974年   2篇
  1973年   2篇
  1971年   4篇
排序方式: 共有17条查询结果,搜索用时 250 毫秒
1.
Nitrogenase catalyses the ATP-dependent reduction of N2 to NH3, and is composed of two proteins, dinitrogenase (MoFe protein or component I) and dinitrogenase reductase (Fe protein or component II). Dinitrogenase contains a unique prosthetic group (iron-molybdenum cofactor, FeMoco) comprised of Fe, Mo and S, which has been proposed as the site of N2 reduction. Biochemical and genetic studies of Nif- (nitrogen fixation) mutants of Klebsiella pneumoniae which are defective in nitrogen fixation, have shown that the nifB, nifQ, nifN, nifE and nifV genes are required for the biosynthesis of FeMo-co. Recently, a system for in vitro synthesis of FeMoco was described. The assay requires at least the nifB, nifN and nifE gene products, and a low-molecular-weight factor (V factor) produced in the presence of the nifV gene product. We have used this system to study FeMoco biosynthesis. We report here the isolation of V factor and identify it as homocitric acid ([R]2-hydroxy-1,2,4-butanetricarboxylic acid).  相似文献   
2.
Zusammenfassung Immunologische Toleranz konnte in Mäusen durch hohe Dosen vonE. coli Lipopolysaccharid erreicht werden. Der Effekt war mit Hilfe der passiven hämolytischen «plaque»-Methode besser zu erfassen als im direkten bakteriologischen System.

Supported in part by grants from the U.S. National Science Foundation and the National Institutes of Health, Bethesda, Maryland.  相似文献   
3.
4.
Zusammenfassung Nachweis, dass «Plaque»-bildende Antikörperzellen gegen somatische Antigene vonVibrio cholerae sich in der Milz immunisierter Mäuse schnell und «treppenartig» nach übereinstimmender Latenzzeit von 42 h entwickeln, ohne dass dabei ein «background» an Antikörper bildenden Zellen zu erfassen war.  相似文献   
5.
Membrane antigens of murine leukaemia cells   总被引:1,自引:0,他引:1  
J Cerny  M Essex 《Nature》1974,251(5477):742-745
  相似文献   
6.
Fu ZQ  Guo M  Jeong BR  Tian F  Elthon TE  Cerny RL  Staiger D  Alfano JR 《Nature》2007,447(7142):284-288
  相似文献   
7.
A therapeutic strategy for treating cancer is to target and eradicate cancer stem cells (CSCs) without harming their normal stem cell counterparts. The success of this approach relies on the identification of molecular pathways that selectively regulate CSC function. Using BCR-ABL-induced chronic myeloid leukemia (CML) as a disease model for CSCs, we show that BCR-ABL downregulates the Blk gene (encoding B-lymphoid kinase) through c-Myc in leukemic stem cells (LSCs) in CML mice and that Blk functions as a tumor suppressor in LSCs but does not affect normal hematopoietic stem cells (HSCs) or hematopoiesis. Blk suppresses LSC function through a pathway involving an upstream regulator, Pax5, and a downstream effector, p27. Inhibition of this Blk pathway accelerates CML development, whereas increased activity of the Blk pathway delays CML development. Blk also suppresses the proliferation of human CML stem cells. Our results show the feasibility of selectively targeting LSCs, an approach that should be applicable to other cancers.  相似文献   
8.
Résumé Les souris infectées par le virus de la leucémie de Friend avaient le meme nombre de cellules spléniques capables de se lier à des érythrocytes de mouton grâc à un récepteur immunolgobuline que les souris normales, non infectées, et servant de contrôle, possédent également. De plus, les souris infectées par le virus répondent à l'immunisation par des érythrocytes de mouton defacon nettement diminuée.  相似文献   
9.
G Kelsoe  J Cerny 《Nature》1979,279(5711):333-334
  相似文献   
10.
Chronic pancreatitis is a common inflammatory disease of the pancreas. Mutations in the genes encoding cationic trypsinogen (PRSS1) and the pancreatic secretory trypsin inhibitor (SPINK1) are associated with chronic pancreatitis. Because increased proteolytic activity owing to mutated PRSS1 enhances the risk for chronic pancreatitis, mutations in the gene encoding anionic trypsinogen (PRSS2) may also predispose to disease. Here we analyzed PRSS2 in individuals with chronic pancreatitis and controls and found, to our surprise, that a variant of codon 191 (G191R) is overrepresented in control subjects: G191R was present in 220/6,459 (3.4%) controls but in only 32/2,466 (1.3%) affected individuals (odds ratio 0.37; P = 1.1 x 10(-8)). Upon activation by enterokinase or trypsin, purified recombinant G191R protein showed a complete loss of trypsin activity owing to the introduction of a new tryptic cleavage site that renders the enzyme hypersensitive to autocatalytic proteolysis. In conclusion, the G191R variant of PRSS2 mitigates intrapancreatic trypsin activity and thereby protects against chronic pancreatitis.  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