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This paper deals with the parallel simulation of delamination problems at the meso-scale by means of multi-scale methods, the aim being the Virtual Delamination Testing of Composite parts. In the non-linear context, Domain Decomposition Methods are mainly used as a solver for the tangent problem to be solved at each iteration of a Newton-Raphson algorithm. In case of strongly non linear and heterogeneous problems, this procedure may lead to severe difficulties. The paper focuses on methods to circumvent these problems, which can now be expressed using a relatively general framework, even though the different ingredients of the strategy have emerged separately. We rely here on the micro-macro framework proposed in [Ladevèze, Loiseau, and Dureisseix, 2001]. The method proposed in this paper introduces three additional features: (i) the adaptation of the macro-basis to situations where classical homogenization does not provide a good preconditioner, (ii) the use of non-linear relocalization to decrease the number of global problems to be solved in the case of unevenly distributed non-linearities, (iii) the adaptation of the approximation of the local Schur complement which governs the convergence of the proposed iterative technique. Computations of delamination and delamination-buckling interaction with contact on potentially large delaminated areas are used to illustrate those aspects. 相似文献
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Melanomas develop with high frequency in transgenic mice in which oncogenic sequences of the SV40 DNA tumor virus have been specifically targeted to melanocytes. To investigate the role of SV40 in melanomagenesis, cultured human melanocytes were transformed with a retroviral shuttle vector encoding the SV40 large T antigen and examined for changes in cell-cycle kinetics and growth-factor dependence. Colonies expressing the viral oncogene were morphologically indistinguishable from their non-T-antigen-transformed counterparts. Also like normal melanocytes, the infected cells remained anchorage dependent and non-tumorigenic in nude mice. However, T-antigen-positive cultures exhibited significantly accelerated population doubling times, increased saturation densities with highly confluent monolayers and a three- to fourfold extended life span. Most interestingly, cell-cycle analysis revealed a measurable shift from quiescent to cycling cells in T-antigen-expressing cultures and an acquired ability to progress more rapidly through G1. Moreover, T-antigen-positive melanocytes proliferated in the absence of PMA and required markedly reduced levels of exogenous bFGF. These studies indicate that the viral oncogen of simian virus 40 provides melanocytes with distinct growth advantages that may render these cells unusually susceptible to additional environmental challenges necessary for full expression of the malignant phenotype. 相似文献
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While loss-of-function mutations in Gsalpha are invariably associated with the short stature and brachydactyly of Albright hereditary osteodystrophy (AHO), the association with hormone resistance (to parathyroid hormone and thyrotropin) typical of pseudohypoparathyroidism type Ia (PHP-Ia) is much more variable. Observational studies and DNA polymorphism analysis suggest that maternal transmission of the Gsalpha mutation may be required for full expression of clinical hormone resistance. To test this hypothesis, we studied transmission of a frameshift mutation in Gsalpha through three generations of a pedigree affected by AHO and PHP-Ia. While all family members carrying this loss-of-function mutation in one Gsalpha allele had AHO, neither the presence of the mutation nor the degree of reduction of erythrocyte Gsalpha bioactivity allowed prediction of phenotype (AHO alone versus AHO and PHP-Ia). Paternal transmission of the mutation (from the patriarch of the first generation to three members of the second generation) was not associated with concurrent PHP-Ia, but maternal transmission (from two women in the second generation to four children in the third generation) was invariably associated with PHP-Ia. No expansion of an upstream short CCG nucleotide repeat region was detected, nor was there evidence of uniparental disomy by polymorphism analysis. This report, the first to document the effects across three generations of both paternal and maternal transmission of a specific Gsalpha mutation, strongly supports the hypothesis that a maternal factor determines full expression of Gsalpha dysfunction as PHP-Ia. 相似文献
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CA Manogue 《Canadian Metallurgical Quarterly》1987,35(12):3783-3795
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