about
Crosstalk regulation among group 2-sigma factors in Synechocystis PCC6803Robust reconstruction of gene expression profiles from reporter gene data using linear inversion.The carbon assimilation network in Escherichia coli is densely connected and largely sign-determined by directions of metabolic fluxesInference of quantitative models of bacterial promoters from time-series reporter gene dataExperimental and computational validation of models of fluorescent and luminescent reporter genes in bacteriaQualitative simulation of genetic regulatory networks using piecewise-linear models.A quantitative UV laser footprinting analysis of the interaction of IHF with specific binding sites: re-evaluation of the effective concentration of IHF in the cell.WellReader: a MATLAB program for the analysis of fluorescence and luminescence reporter gene data.The tRNA function of SsrA contributes to controlling repression of bacteriophage Mu prophage.Long-term experimental evolution in Escherichia coli. XII. DNA topology as a key target of selection.Parallel changes in global protein profiles during long-term experimental evolution in Escherichia coli.Characterization of the Escherichia coli σ(S) core regulon by Chromatin Immunoprecipitation-sequencing (ChIP-seq) analysisDynamical Allocation of Cellular Resources as an Optimal Control Problem: Novel Insights into Microbial Growth Strategies.A physical model for the translocation and helicase activities of Escherichia coli transcription termination protein RhoStructural kinetics of transcription activation at the malT promoter of Escherichia coli by UV laser footprintingUnderstanding carbon catabolite repression in Escherichia coli using quantitative models.A simple polypyrimidine repeat acts as an artificial Rho-dependent terminator in vivo and in vitro.Resource Reallocation in Bacteria by Reengineering the Gene Expression Machinery.Shared control of gene expression in bacteria by transcription factors and global physiology of the cell.Repression of flagellar genes in exponential phase by CsgD and CpxR, two crucial modulators of Escherichia coli biofilm formation.A synthetic growth switch based on controlled expression of RNA polymerase.Improvement of pCVD442, a suicide plasmid for gene allele exchange in bacteria.Mathematical modelling of microbes: metabolism, gene expression and growth.Qualitative simulation of the initiation of sporulation in Bacillus subtilis.Expression dynamics of RpoS/Crl-dependent genes in Escherichia coli.Genetic Network Analyzer: qualitative simulation of genetic regulatory networks.The glucosyl-1-phosphate transferase WchA (Cap8E) primes the capsular polysaccharide repeat unit biosynthesis of Streptococcus pneumoniae serotype 8.Crl, a low temperature-induced protein in Escherichia coli that binds directly to the stationary phase sigma subunit of RNA polymerase.Genetic network analyzer: a tool for the qualitative modeling and simulation of bacterial regulatory networks.Control of bacteriophage mu lysogenic repression.A sensitive reporter gene system using bacterial luciferase based on a series of plasmid cloning vectors compatible with derivatives of pBR322.Physical properties of the Escherichia coli transcription termination factor rho. 2. Quaternary structure of the rho hexamer.An ensemble of mathematical models showing diauxic growth behaviourQualitative modelling and simulation of developmental regulatory networksMaximal transcriptional activation by the IHF protein of Escherichia coli depends on optimal DNA bending by the activatorMutual regulation of Crl and Fur in Escherichia coli W3110
P50
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P50
description
researcher ORCID ID = 0000-0002-1329-7558
@en
wetenschapper
@nl
name
Johannes Geiselmann
@ast
Johannes Geiselmann
@en
Johannes Geiselmann
@es
Johannes Geiselmann
@nl
type
label
Johannes Geiselmann
@ast
Johannes Geiselmann
@en
Johannes Geiselmann
@es
Johannes Geiselmann
@nl
prefLabel
Johannes Geiselmann
@ast
Johannes Geiselmann
@en
Johannes Geiselmann
@es
Johannes Geiselmann
@nl
P106
P1153
6701582645
P2456
P31
P496
0000-0002-1329-7558