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991.
对于外延膜多尺度应变模型的求解,设计了一类代数多重网格方法,进而以该代数多重网格为预条件子,结合其轭梯度法,得到一种预处理技术。数值实验结果表明,我们构造的代数多重网格算法是健壮的,具有很好的计算效率。 相似文献
992.
系统可靠性预计的上(下)限法 总被引:3,自引:0,他引:3
施军 《系统工程与电子技术》1994,(9)
用文献[1]提出的上限计算法预计的系统可靠度的上限会单调收敛至一个小于精确值的错误数值,并使系统可靠度的单一预计值过于保守。本文提出一种计算系统可靠度上限的新方法,并给出了完全对偶的、实用的上下限计算公式。实例表明,对于任何非单纯串联的复杂系统,应用本文的公式均能保证使计算结果单调收敛至真值,并使系统可靠度的单一预计值具有较高的精度。 相似文献
993.
1 .INTRODUCTIONTheabilityofpositioningmobileobjects (MOs) ,in cludingvehiclesandtravelersholdingmobiletermi nals,isafundamentalfunctionforsomeITSsubsys tems,suchasemergencyrescue,securitysystem ,au tomaticnavigationsystem ,andtrafficinducementsystem[1 ] .Atpresent,therearethreedominatingtypes[2 ]ofwirelesspositioningtechnologies,i.e.positioningbasedonsatellites,positioningbasedondedicatedcommunicationsystemsandpositioningbasedonpub liclandwirelesstelecommunicationsystems (PLMTS) ,respe… 相似文献
994.
史及民 《山西师范大学学报:自然科学版》1994,(4)
众所周知,在数据分析的拟合优度检验中,检验一总体是否服从某一有限的离散概率分布时,通过使用英国统计学家K.Pearson所引入的x~2统计量:x~e=sum from i=1 to r(λ_i(n_i/n-p_i)~2)其中λ_i=n/P_i,n_1 … n_λ=n,P_1 … P_r=1.本文分析K.Pearson x~2统计量的构造源渊,指出其弊端,并引入了结构上更合理的检验用统计量x~2_D,研究了它的均值,方差及渐近分布. 相似文献
995.
Five hybridomas secreting monoclonal antibody to E. coli L-asparaginase were isolated. These monoclonal antibodies were classified into 3 different subclasses; Ig G1 (1 clone), Ig G2 (2 clones) and Ig G3 (2 clones). One of them possessed anti-L-asparaginase neutralizing activity. Four antibodies examined demonstrated a linear Langmuir binding plot and binding affinities, with equilibrium dissociation constant (Kd) ranging between 2.5 X 10(-9) M and 6.3 X 10(-10) M. The monoclonal antibodies should be useful probes for investigation of the enzyme activity. 相似文献
996.
S. Benvenuti A. Gagliardo T. Guilford P. Luschi 《Cellular and molecular life sciences : CMLS》1996,52(6):608-612
In order to investigate the pigeon's compass mechanism, a series of overcast tests with clock-shifted birds were run at two familiar release sites. While controls were able to assume a correct homeward direction, the experimental birds' initial orientation cannot be explained either on the basis of a time-compensated sun compass or of a time-independent magnetic compass. Speculative explanations of our paradoxical results are attempted. 相似文献
997.
W T Clusin 《Nature》1983,301(5897):248-250
Electrical excitation of cardiac muscle may sometimes be due to initiation of inward current by the presence of Ca2+ ions at the inner surface of the cell membrane. During digitalis toxicity and other conditions that abnormally augment cellular Ca2+ stores, premature release of Ca2+ from the sarcoplasmic reticulum leads to a transient inward current, which is large enough to initiate premature beats and is accompanied by a transient contractile response. This inward current may be mediated either by electrogenic sodium-calcium exchange or by specific Ca2+-activated cation channels that have recently been characterized in tissue cultures of cardiac myocytes. An obvious question raised by these observations is whether release of the sequestered Ca2+ stores during each normal beat exerts a similar influence on membrane potential. To explore this, chick embryonic myocardial cell aggregates were voltage-clamped during abrupt exposure to caffeine, which is known to release Ca2+ from the sarcoplasmic reticulum. The speed of the perfusion system and the relative absence of diffusion barriers in the tissue-cultured cells allowed the effects of caffeine-induced Ca2+ release to be studied on a time scale comparable to that of a single normal beat. We report here that abrupt exposure of the cells to caffeine produced a transient inward current having similar features to that of digitalis toxicity, and which was both large enough and rapid enough to potentially contribute to the action potential. 相似文献
998.
Structure of an adenine-cytosine base pair in DNA and its implications for mismatch repair 总被引:30,自引:0,他引:30
Mutational pathways rely on introducing changes in the DNA double helix. This may be achieved by the incorporation of a noncomplementary base on replication or during genetic recombination, leading to substitution mutation. In vivo studies have shown that most combinations of base-pair mismatches can be accommodated in the DNA double helix, albeit with varying efficiencies. Fidelity of replication requires the recognition and excision of mismatched bases by proofreading enzymes and post-replicative mismatch repair systems. Rates of excision vary with the type of mismatch and there is some evidence that these are influenced by the nature of the neighbouring sequences. However, there is little experimental information about the molecular structure of mismatches and their effect on the DNA double helix. We have recently determined the crystal structures of several DNA fragments with guanine X thymine and adenine X guanine mismatches in a full turn of a B-DNA helix and now report the nature of the base pairing between adenine and cytosine in an isomorphous fragment. The base pair found in the present study is novel and we believe has not previously been demonstrated. Our results suggest that the enzymatic recognition of mismatches is likely to occur at the level of the base pairs and that the efficiency of repair can be correlated with structural features. 相似文献
999.
1000.
Structure of pre-pro-von Willebrand factor and its expression in heterologous cells 总被引:30,自引:0,他引:30
D T Bonthron R I Handin R J Kaufman L C Wasley E C Orr L M Mitsock B Ewenstein J Loscalzo D Ginsburg S H Orkin 《Nature》1986,324(6094):270-273
Von Willebrand factor (vWF), a multifunctional haemostatic glycoprotein derived from endothelial cells and megakaryocytes, mediates platelet adhesion to injured subendothelium and binds coagulation factor VIII in the circulation. Native vWF is a disulphide-bonded homopolymer; the monomeric subunits, of apparent relative molecular mass (Mr) 220,000 (220K) are derived from an intracellular precursor estimated at 260-275K. Multimer assembly is preceded by the formation of dimers, linked near their C-termini, which then assemble into filamentous polymers. The importance of the removal of the large vWF pro-polypeptide during multimer assembly, and whether this or other stages of the complex post-translational processing require components specific to endothelial cells or megakaryocytes, is unknown. Here we report an analysis of the complete sequence of pre-pro-vWF and expression of the molecule in heterologous cells. The vWF precursor is composed of several repeated subdomains. When expressed in COS and CHO cells, it is cleaved and assembled into biologically active high relative molecular mass disulphide bonded multimers. This suggests that the information for assembly of this complex molecule resides largely within its primary structure. 相似文献