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231.
Using model-theoretic methods we prove:
Theorem A If G is a Nash group over the real or p-adic field, then there is a Nash isomorphism between neighbourhoods of the identity
of G and of the set of F-rational points of an algebraic group defined over F.
Theorem B Let G be a connected affine Nash group over ℝ. Then G is Nash isogeneous with the (real) connected component of the set of
real points of an algebraic group defined over ℝ.
Theorem C Let G be a group definable in a pseudo-finite field F. Then G is definably virtually isogeneous with the set of F-rational
points of an algebraic group defined over F.
Both authors supported by NSF grants. 相似文献
232.
Uniform oscillations in spatially extended systems resonate with temporal periodic forcing within the Arnold tongues of single forced oscillators. The Arnold tongues are wedge-like domains in the parameter space spanned by the forcing amplitude and frequency, within which the oscillator's frequency is locked to a fraction of the forcing frequency. Spatial patterning can modify these domains. We describe here two pattern formation mechanisms affecting frequency locking at half the forcing frequency. The mechanisms are associated with phase-front instabilities and a Turing-like instability of the rest state. Our studies combine experiments on the ruthenium catalyzed light-sensitive Belousov-Zhabotinsky reaction forced by periodic illumination, and numerical and analytical studies of two model systems, the FitzHugh-Nagumo model and the complex Ginzburg-Landau equation, with additional terms describing periodic forcing. 相似文献
233.
Fiona M. Fennessy Andriy Fedorov Sandeep N. Gupta Ehud J. Schmidt Clare M. Tempany Robert V. Mulkern 《Magnetic resonance imaging》2012
There are many challenges in developing robust imaging biomarkers that can be reliably applied in a clinical trial setting. In the case of dynamic contrast-enhanced (DCE) MRI, one such challenge is to obtain accurate precontrast T1 maps for subsequent use in two-compartment pharmacokinetic models commonly used to fit the MR enhancement time courses. In the prostate, a convenient and common approach for this task has been to use the same 3D spoiled gradient-echo sequence used to collect the DCE data, but with variable flip angles (VFAs) to collect data suitable for T1 mapping prior to contrast injection. However, inhomogeneous radiofrequency conditions within the prostate have been found to adversely affect the accuracy of this technique. Herein we demonstrate the sensitivity of DCE pharmacokinetic parameters to precontrast T1 values and examine methods to improve the accuracy of T1 mapping with flip angle-corrected VFA SPGR methods, comparing T1 maps from such methods with “gold standard” reference T1 maps generated with saturation recovery experiments performed with fast spin-echo (FSE) sequences. 相似文献
234.
Let X be a k-vector space, and U a maximal proper filter of subspaces of X. Then the ring of endomorphisms of X that are “continuous” with respect to U modulo the ideal of those that are “trivial” with respect to U forms a division ring E(U). (These division rings can also be described as the endomorphism rings of the simple left End(X)-modules.) We study this and the dual construction, based on maximal cofiIters of subspaces of X, in particular, the relation between the constructed division rings and the original field or division ring k. We end by examining a more general construction in which X is a module over a general ring, given with both a filter and a cofilter of submodules. 相似文献
235.
Shon A. Levkovich Prof. Ehud Gazit Dr. Dana Laor Bar-Yosef 《Angewandte Chemie (International ed. in English)》2023,62(38):e202217622
The vital role of metabolites across all branches of life and their involvement in various disorders have been investigated for decades. Many metabolites are poorly soluble in water or in physiological buffers and tend to form supramolecular aggregates. On the other hand, in the cell, they should be preserved in a pool and be readily available for the execution of biochemical functions. We thus propose that a quality-control network, termed “metabolostasis”, has evolved to regulate the storage and retrieval of aggregation-prone metabolites. Such a system should control metabolite concentration, subcellular localization, supramolecular arrangement, and interaction in dynamic environments, thus enabling normal cellular physiology, healthy development, and preventing disease onset. The paradigm-shifting concept of metabolostasis calls for a reevaluation of the traditional view of metabolite storage and dynamics in physiology and pathology and proposes unprecedented directions for therapeutic targets under conditions where metabolostasis is imbalanced. 相似文献