about
Interaction specificity, toxicity and regulation of a paralogous set of ParE/RelE-family toxin-antitoxin systems.A structural model of anti-anti-σ inhibition by a two-component receiver domain: the PhyR stress response regulatorGeneral Stress Signaling in the AlphaproteobacteriaA cell cycle and nutritional checkpoint controlling bacterial surface adhesionFine-scale time-lapse analysis of the biphasic, dynamic behaviour of the two Vibrio cholerae chromosomesThe Brucella abortus virulence regulator, LovhK, is a sensor kinase in the general stress response signalling pathwayStructure and function of HWE/HisKA2-family sensor histidine kinases.A photosensory two-component system regulates bacterial cell attachment.Identification of the PhoB Regulon and Role of PhoU in the Phosphate Starvation Response of Caulobacter crescentusComparisons of pollen coat genes across Brassicaceae species reveal rapid evolution by repeat expansion and diversificationProper Control of Caulobacter crescentus Cell Surface Adhesion Requires the General Protein Chaperone DnaK.The LovK-LovR two-component system is a regulator of the general stress pathway in Caulobacter crescentusExperimental evolution of diverse Escherichia coli metabolic mutants identifies genetic loci for convergent adaptation of growth rate.Molecular control of gene expression by Brucella BaaR, an IclR-type transcriptional repressor.Gene network analysis identifies a central post-transcriptional regulator of cellular stress survival.Feedback regulation of Caulobacter crescentus holdfast synthesis by flagellum assembly via the holdfast inhibitor HfiAA Genome-Wide Analysis of Adhesion in Identifies New Regulatory and Biosynthetic Components for Holdfast AssemblyRegulation of bacterial surface attachment by a network of sensory transduction proteins.Alterations in CER6, a gene identical to CUT1, differentially affect long-chain lipid content on the surface of pollen and stemsGene families from the Arabidopsis thaliana pollen coat proteomePolarity factors play a role in antibiotic resistancePeriplasmic protein EipA determines envelope stress resistance and virulence in Brucella abortusBrucella Periplasmic Protein EipB Is a Molecular Determinant of Cell Envelope Integrity and VirulenceA Carbonic Anhydrase Pseudogene Sensitizes Select Brucella Lineages to Low CO2 Tension
P50
Q24605823-1F99BB92-F7FA-40A2-A331-365AB1223BCDQ27664153-14CE1711-431F-4828-9F07-29AD6361E07CQ28085365-AD2CBA7C-4139-474B-BD86-2DC39324F954Q28539050-24369C74-1BA7-4A68-AB8A-5E67135379A8Q30491746-28BDB436-C4CB-4418-B3CD-C596E8D831C0Q34490455-DE91C4E8-F595-45B0-B700-B6DC92C9E392Q34551140-9A9630D6-4B13-46BC-AA55-3C160DD97A5EQ36156921-65C4C4F3-F8F9-483E-8AE8-97CB06A20B59Q36390613-2E8D97FE-1721-45DA-A5CC-DBCCEC678519Q36855319-68D875DD-AE52-45C2-8C92-53ACF2FE359BQ41065130-6121EF45-9C5E-4FE8-A3D0-9CAA057CD84CQ42190336-98BE594F-952F-436C-8F2E-B4AF1A556B8CQ52340379-DBF79205-52D1-40B3-AD17-1972FE6A683CQ54250549-5F3969AC-D248-490A-80A8-244A140929EFQ54256188-2E17F2BA-5C7C-48B3-8A33-FA883171BF4EQ63514531-E3022570-3B63-426E-B22E-7CD99FEFCCFDQ64238722-4950F812-1B1A-4096-B083-E800483162D3Q64891517-CEB2C429-B4DD-4A88-832D-32B46F2C9AA0Q73102589-C0ACDF2A-ECB7-4C26-B0DE-DFBF2E443B82Q74115284-9FC8D7EE-E790-4FC0-B9B0-8F3220F7601DQ87937898-4E3E0A7A-EDB8-45CB-987E-60353A65056BQ90402689-4EA0D54E-A3D7-4B7C-BDBD-91A44D057A8BQ92766605-5A20CAD2-7E0F-4774-9099-4872672EA9E4Q93086006-2EA1A609-9848-47B6-AA75-DACA7CF43D96
P50
description
researcher, ORCID id # 0000-0002-0612-5029
@en
wetenschapper
@nl
name
Aretha Fiebig
@ast
Aretha Fiebig
@en
Aretha Fiebig
@es
Aretha Fiebig
@nl
type
label
Aretha Fiebig
@ast
Aretha Fiebig
@en
Aretha Fiebig
@es
Aretha Fiebig
@nl
prefLabel
Aretha Fiebig
@ast
Aretha Fiebig
@en
Aretha Fiebig
@es
Aretha Fiebig
@nl
P106
P31
P496
0000-0002-0612-5029