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151.
提出一族求解非线性方程的修正Chebyshev-Halley迭代方法.该方法避免了计算函数的二阶导数,且具有至少三阶收敛的性质,当参数选取特殊值时,可以得到四阶收敛方法.收敛性分析和数值实验结果表明,该方法与具有同阶收敛性质的算法相比效率更高. 相似文献
152.
Chiang C Jacobsen JC Ernst C Hanscom C Heilbut A Blumenthal I Mills RE Kirby A Lindgren AM Rudiger SR McLaughlan CJ Bawden CS Reid SJ Faull RL Snell RG Hall IM Shen Y Ohsumi TK Borowsky ML Daly MJ Lee C Morton CC MacDonald ME Gusella JF Talkowski ME 《Nature genetics》2012,44(4):390-7, S1
We defined the genetic landscape of balanced chromosomal rearrangements at nucleotide resolution by sequencing 141 breakpoints from cytogenetically interpreted translocations and inversions. We confirm that the recently described phenomenon of 'chromothripsis' (massive chromosomal shattering and reorganization) is not unique to cancer cells but also occurs in the germline, where it can resolve to a relatively balanced state with frequent inversions. We detected a high incidence of complex rearrangements (19.2%) and substantially less reliance on microhomology (31%) than previously observed in benign copy-number variants (CNVs). We compared these results to experimentally generated DNA breakage-repair by sequencing seven transgenic animals, revealing extensive rearrangement of the transgene and host genome with similar complexity to human germline alterations. Inversion was the most common rearrangement, suggesting that a combined mechanism involving template switching and non-homologous repair mediates the formation of balanced complex rearrangements that are viable, stably replicated and transmitted unaltered to subsequent generations. 相似文献
153.
Heritable and inducible genetic interference by double-stranded RNA encoded by transgenes 总被引:56,自引:0,他引:56
Double-stranded RNA interference (RNAi) is an effective method for disrupting expression of specific genes in Caenorhabditis elegans and other organisms. Applications of this reverse-genetics tool, however, are somewhat restricted in nematodes because introduced dsRNA is not stably inherited. Another difficulty is that RNAi disruption of late-acting genes has been generally less consistent than that of embryonically expressed genes, perhaps because the concentration of dsRNA becomes lower as cellular division proceeds or as developmental time advances. In particular, some neuronally expressed genes appear refractory to dsRNA-mediated interference. We sought to extend the applicability of RNAi by in vivo expression of heritable inverted-repeat (IR) genes. We assayed the efficacy of in vivo-driven RNAi in three situations for which heritable, inducible RNAi would be advantageous: (i) production of large numbers of animals deficient for gene activities required for viability or reproduction; (ii) generation of large populations of phenocopy mutants for biochemical analysis; and (iii) effective gene inactivation in the nervous system. We report that heritable IR genes confer potent and specific gene inactivation for each of these applications. We suggest that a similar strategy might be used to test for dsRNA interference effects in higher organisms in which it is feasible to construct transgenic animals, but impossible to directly or transiently introduce high concentrations of dsRNA. 相似文献
154.
用原位聚合法以脲醛树脂为壁材,制备除草剂稀禾定微胶囊.考察了预聚反应介质pH值、预聚反应温度、缩聚反应催化剂及缩聚反应终点pH值对微胶囊的结构、包覆效果和包埋率等的影响.结果表明:预聚反应pH值为8.0,预聚反应温度为70℃,反应时间60 min,可得到以二羟甲脲为主的水溶性透明黏稠预聚物,用此预聚物进行缩聚反应,以NH4Cl做缩聚催化剂,芯皮比为1∶1.5(质量比),控制缩聚反应终点pH值为3.0,可制得结构紧密、包埋率为30.6%的流动性球形缓释性固体微胶囊. 相似文献
155.
Purification and cloning of amyloid precursor protein beta-secretase from human brain 总被引:40,自引:0,他引:40
Sinha S Anderson JP Barbour R Basi GS Caccavello R Davis D Doan M Dovey HF Frigon N Hong J Jacobson-Croak K Jewett N Keim P Knops J Lieberburg I Power M Tan H Tatsuno G Tung J Schenk D Seubert P Suomensaari SM Wang S Walker D Zhao J McConlogue L John V 《Nature》1999,402(6761):537-540
Proteolytic processing of the amyloid precursor protein (APP) generates amyloid beta (Abeta) peptide, which is thought to be causal for the pathology and subsequent cognitive decline in Alzheimer's disease. Cleavage by beta-secretase at the amino terminus of the Abeta peptide sequence, between residues 671 and 672 of APP, leads to the generation and extracellular release of beta-cleaved soluble APP, and a corresponding cell-associated carboxy-terminal fragment. Cleavage of the C-terminal fragment by gamma-secretase(s) leads to the formation of Abeta. The pathogenic mutation K670M671-->N670L671 at the beta-secretase cleavage site in APP, which was discovered in a Swedish family with familial Alzheimer's disease, leads to increased beta-secretase cleavage of the mutant substrate. Here we describe a membrane-bound enzyme activity that cleaves full-length APP at the beta-secretase cleavage site, and find it to be the predominant beta-cleavage activity in human brain. We have purified this enzyme activity to homogeneity from human brain using a new substrate analogue inhibitor of the enzyme activity, and show that the purified enzyme has all the properties predicted for beta-secretase. Cloning and expression of the enzyme reveals that human brain beta-secretase is a new membrane-bound aspartic proteinase. 相似文献
156.
技术与社会:工作组织的网络化实践研究 总被引:1,自引:0,他引:1
国内目前对网络技术在工作组织中具体实践的经验研究还较少,一定程度上限制了我们对网络一社会互动机制和水平的认识。通过将大学、企业、媒体组织个案置于全球网络化实践的背景下进行经验研究,显而易见,电脑网络的应用已经对我国工作组织的社会结构和社会行动产生了重要影响,但其影响的程度叉受到工作组织既有的社会结构和社会行动模式的制约和型塑。其具体特征表现出一定的差异性。 相似文献
157.
通过张量分析,给出一个具有一般形式的非负张量谱半径的上下界估计不等式,在特别情况下改进了相关非负张量谱半径的估计不等式. 相似文献
158.
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours. 总被引:226,自引:0,他引:226
L A Donehower M Harvey B L Slagle M J McArthur C A Montgomery J S Butel A Bradley 《Nature》1992,356(6366):215-221
Mutations in the p53 tumour-suppressor gene are the most frequently observed genetic lesions in human cancers. To investigate the role of the p53 gene in mammalian development and tumorigenesis, a null mutation was introduced into the gene by homologous recombination in murine embryonic stem cells. Mice homozygous for the null allele appear normal but are prone to the spontaneous development of a variety of neoplasms by 6 months of age. These observations indicate that a normal p53 gene is dispensable for embryonic development, that its absence predisposes the animal to neoplastic disease, and that an oncogenic mutant form of p53 is not obligatory for the genesis of many types of tumours. 相似文献
159.
水合锰(Ⅱ)结构的量子化学和ABEEM/MM研究 总被引:1,自引:0,他引:1
应用新一代可极化分子力场——原子-键电负性均衡浮动电荷分子力场ABEEM/MM,结合精密量子化学方法, 构建了精确的Mn2+-H2O 相互作用的势能函数, 确定了相关参数.将该势能函数用于计算[Mn(H2O)n]2+(n=1~12)的结构和结合能, 得到了与量子化学一致的结果. 进一步对Mn2+水溶液进行ABEEM/MM 动力学模拟, 得到的Mn2+–O 径向分布函数的第一和第二最高峰分别处于0.218 和0.435 nm 处, 积分得到第一和第二水合层的配位水分子数分别为7.03 和17.74; 对于O–Mn2+–O 角度分布函数, 其第一和第二最高峰分别位于80°和140°附近, 这些结果与实验和其他理论方法的结果有很好的一致性. Mn2+的极化作用使得第一水合层中水分子的键长明显增长, 键角明显减小; 而Mn2+对第二水合层及外层水分子的结构影响较小. 分析体系的电荷分布表明, 与ABEEM-7P 纯水相比, Mn2+水溶液中参与形成氢键的氢原子和孤对电子的电荷变化较大, 且Mn2+和其邻近的水分子间存在明显的电荷转移. 相似文献
160.
A novel metalloproteinase gene specifically expressed in stromal cells of breast carcinomas. 总被引:46,自引:0,他引:46
P Basset J P Bellocq C Wolf I Stoll P Hutin J M Limacher O L Podhajcer M P Chenard M C Rio P Chambon 《Nature》1990,348(6303):699-704
A gene has been identified that is expressed specifically in stromal cells surrounding invasive breast carcinomas. On the basis of its sequence, the product of this gene, named stromelysin-3, is a new member of the family of metalloproteinase enzymes which degrade the extracellular matrix. The suggestion is that stromelysin-3 is one of the stroma-derived factors that have long been postulated to play an important part in progression of epithelial malignancies. 相似文献