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J Richert

Publications and source records attributed to J Richert.

At least 19 recordsLinked to original sources
PubMed2003

Transient backbending behavior in the Ising model with fixed magnetization.

The physical origin of the backbendings in the equations of state of finite but not necessarily small systems is studied in the Ising model with fixed magnetization (IMFM) by means of the topological properties of the observable distributions and the analysis of the largest cluster with increasing lattice size. Looking at the convexity anomalies of the IMFM thermodynamic potential, it is shown that the order of the transition at the thermodynamic limit can be recognized in finite systems independently of the lattice size. General statistical mechanics arguments and analytical calculations suggest that the backbending in the caloric curve is a transient behavior which should not converge to a plateau in the thermodynamic limit, while the first-order transition (in the Ehrenfest sense) is still signaled by a discontinuity in the magnetization equation of state.

Journal Article↗
PubMed2003

Dynamics of many-particle fragmentation in a cellular automaton model.

A three-dimensional cellular automaton model developed by the authors to deal with the dynamics of N-body interactions has been adapted to investigate the head-on collision of two identical bound clusters of particles, and the ensuing process of fragmentation. The range of impact energies is chosen low enough, to secure that a compound bound cluster can be formed. The model is devised to simulate the laboratory set-up of fragmentation experiments as monitored by 4 pi detectors. The particles interact via a Lennard-Jones potential. At low impact energies the numerical experiments following the dynamics of the individual particles indicate a phase of energy sharing among all the particles of the compound cluster. Fragments of all sizes are then found to evaporate from the latter cluster. The cluster sizes, measured in our setup by simulated 4 pi detectors, conform to a power law of exponent approximately 2.6. In an attempt to duplicate the laboratory caloric curves related, in particular, to nuclear fragmentation processes, we introduce several temperature parameters (kinetic temperature of nucleons, kinetic temperature of fragments, reaction equilibrium temperatures). Theoretical caloric curves are then constructed for those temperature parameters, we regard as physically most relevant. Our results show that different temperature definitions generate different curve patterns, indicating that the fragmentation system remains far from thermodynamic equilibrium. The pattern of the laboratory caloric curve for Au-Au collision experiments as derived from a recent analysis [NuPECC Report, 1997 (unpublished)] is reproduced qualitatively by our reaction temperatures.

Journal Article↗
PubMed1999

Application of cellular automata to N-body systems.

A two-dimensional cellular automaton model is introduced to deal with the dynamics of a finite system of particles whose interactions are simulated by two-body step potentials. The method is illustrated for a potential approximating the standard Lennard-Jones potential, representative for the problem of heavy ion collisions in nuclear physics. From the cellular automaton dynamics thermodynamic equilibrium state variables are introduced in the usual way. The numerical experiments indicate the occurrence of a phase transition. Macroscopically the transition is marked by a singularity in the equation of state; microscopically it manifests itself by the formation of clusters of particles of all sizes, obeying a mass distribution in the form of a power law of exponent 1.35.

Journal Article↗
PubMed1991

A myelin basic protein peptide is recognized by cytotoxic T cells in the context of four HLA-DR types associated with multiple sclerosis.

We have examined previously the peptide specificity of the T cell response to myelin basic protein (MBP) in patients with multiple sclerosis (MS) and healthy controls, and demonstrated that an epitope spanning amino acids 87-106 was frequently recognized. Because this region is encephalitogenic in some experimental animals, it has been postulated that the response to the epitope may have relevance to MS. In this study, the fine specificity of this response is studied using four well-characterized, monospecific T cell lines from three MS patients and an identical twin of a patient. Each of the lines recognized a peptide with the same core sequence, amino acids 89-99, although the responses were affected to various degrees by truncations at the COOH- or NH2 terminal ends of the 87-106 epitope. Importantly, the epitope was recognized in conjunction with four different HLA-DR molecules. Also, the T cell receptor beta chain usage was heterogeneous, and each line expressed a different VDJ sequence. The four HLA-DR molecules restricting the response to this epitope have been shown to be overrepresented in MS populations in various geographic areas, suggesting that the response to this region of the MBP molecule may be relevant to the pathogenesis of MS. These findings may have important implications in designing therapeutic strategies for the disease.

Amino Acid Sequence↗
PubMed1990

Fine specificity and HLA restriction of myelin basic protein-specific cytotoxic T cell lines from multiple sclerosis patients and healthy individuals.

Myelin basic protein (MBP) is a candidate Ag for the autoimmune process believed to be involved in the pathogenesis of multiple sclerosis (MS). To investigate the fine specificity and HLA restriction of human MBP-specific CTL, long term T cell lines (TCL) were established from 22 MS patients and 16 healthy individuals by repeated antigenic restimulation. By using this approach, MBP-specific cytotoxic TCL were generated from 81% of the lines from MS patients and 69% of those from controls. TCL from both groups expressed the CD3+, CD4+, CD8- phenotype and secreted substantial amounts of IFN-gamma. By using large enzymatic and small synthetic peptides of MBP, TCL were primarily specific for the C-terminal part of the molecule and to a lesser extent for the N-terminal portion. Two regions of the molecule, MBP peptide 87-106 and MBP peptide 154-172, were recognized by the majority of the polyspecific lines and by four and three of 14 monospecific TCL, respectively. These highly immunogenic regions are of interest because they include sequences encephalitogenic in other species. The HLA restriction of each line was determined by using antibody blocking as well as various target cells including EBV-transformed B cells, homozygous typing cells, and fibroblasts transfected with cDNA for DR-alpha and DR-beta genes. All TCL were restricted by HLA-DR Ag. Several HLA-DR molecules restricted multiple cathepsin D-derived and synthetic MBP peptides, including the regions of peptides 87-106 and 154-172 which, respectively, were recognized in conjunction with four and three HLA-DR types. Three of these HLA-DR types are overrepresented in MS patients in different geographic regions. Together, these findings suggest that the MBP-specific cytotoxic T cell response, although not sufficient for disease, may be important for the pathogenesis of MS.

Amino Acid Sequence↗
PubMed1975

[Pancreatic secretion of patients with chronic renal insufficiency (author's transl)].

Pancreatic function tests were performed in 15 patients with advanced renal insufficiency. Pancreatic secretion was stimulated with CCK/PZ and secretin and 60 minutes later with bile given intraduodenally and CCK/PZ and secretin intravenously. The Wilcoxon-test showed that there were significantly higher lipase levels in serum and lower amylase amounts in duodenal juice compared to normal volunteers. No differences could be demonstratd for volume, maximal bicarbonate concentration, lipase and trypsin outputs. It could be shown by nonlinear discriminant analysis that pancreatic secretion might specifically be changed in patients with chronic renal failure. These patients can be definitely differentiated according to the secretion pattern from normal controls and patients with chronic pancreatitis, pancreatic carcinoma, chronic and acute duodenal ulcer.

Adult↗