On the public citation graph
Staying in the loop to make ends meet: roles and regulation of GlmR in Bacillus subtilis
0 signed · 138 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cbic.200900557openalex-snapshot
Wall Teichoic Acid Function, Biosynthesis, and Inhibition
inferredcites →https://doi.org/10.1002/iub.2664openalex-snapshot
Biosynthesis of uridine diphosphate N‐Acetylglucosamine: An underexploited pathway in the search for novel antibiotics?
inferredcites →https://doi.org/10.1002/jobm.200800306openalex-snapshot
Diversity and phylogeny of culturable spore‐forming Bacilli isolated from marine sediments
inferredcites →https://doi.org/10.1002/pro.70111openalex-snapshot
Functional and structural characterization of Staphylococcus aureus N‐acetylglucosamine 1‐phosphate uridyltransferase ( GlmU ) reveals a redox‐sensitive acetyltransferase activity
inferredcites →https://doi.org/10.1007/978-1-0716-2233-9_11openalex-snapshot
Genome Editing Methods for Bacillus subtilis
inferredcites →https://doi.org/10.1007/s00294-016-0600-8openalex-snapshot
Replenishing the cyclic-di-AMP pool: regulation of diadenylate cyclase activity in bacteria
inferredcites →https://doi.org/10.1016/0006-291x(80)91557-0openalex-snapshot
Accumulation of cell-bound α-amylase in cells in the presence of tunicamycin
inferredcites →https://doi.org/10.1016/0147-619x(84)90061-1openalex-snapshot
Construction of a cloning site near one end of Tn917 into which foreign DNA may be inserted without affecting transposition in Bacillus subtilis or expression of the transposon-borne erm gene
inferredcites →https://doi.org/10.1016/j.celrep.2025.115268openalex-snapshot
A mutation in RNA polymerase imparts resistance to β-lactams by preventing dysregulation of amino acid and nucleotide metabolism
inferredcites →https://doi.org/10.1016/j.cels.2016.12.013openalex-snapshot
Construction and Analysis of Two Genome-Scale Deletion Libraries for Bacillus subtilis
inferredcites →https://doi.org/10.1016/j.chembiol.2005.09.006openalex-snapshot
Ligand Requirements for glmS Ribozyme Self-Cleavage
inferredcites →https://doi.org/10.1016/j.cub.2019.04.062openalex-snapshot
Mechanistic Origin of Cell-Size Control and Homeostasis in Bacteria
inferredcites →https://doi.org/10.1016/j.cub.2020.04.030openalex-snapshot
Biphasic Cell-Size and Growth-Rate Homeostasis by Single Bacillus subtilis Cells
inferredcites →https://doi.org/10.1016/j.drudis.2018.05.020openalex-snapshot
Structural basis for selective inhibition of antibacterial target MraY, a membrane-bound enzyme involved in peptidoglycan synthesis
inferredcites →https://doi.org/10.1016/j.ejps.2015.12.013openalex-snapshot
UDP-GlcNAc pathway: Potential target for inhibitor discovery against M. tuberculosis
inferredcites →https://doi.org/10.1016/j.jbc.2021.101317openalex-snapshot
Structural basis for the inhibition of the Bacillus subtilis c-di-AMP cyclase CdaA by the phosphoglucomutase GlmM
inferredcites →https://doi.org/10.1016/j.jbc.2022.102144openalex-snapshot
Structural basis for c-di-AMP–dependent regulation of the bacterial stringent response by receptor protein DarB
inferredcites →https://doi.org/10.1016/j.jmb.2008.12.031openalex-snapshot
PknB-Mediated Phosphorylation of a Novel Substrate, N-Acetylglucosamine-1-Phosphate Uridyltransferase, Modulates Its Acetyltransferase Activity
inferredcites →https://doi.org/10.1016/j.jmb.2021.166968openalex-snapshot
Molecular Mechanisms for Bacterial Potassium Homeostasis
inferredcites →https://doi.org/10.1016/j.jprot.2022.104767openalex-snapshot
Global landscape of lysine acylomes in Bacillus subtilis
inferredcites →https://doi.org/10.1016/j.mib.2021.01.015openalex-snapshot
Resource sharing between central metabolism and cell envelope synthesis
inferredcites →https://doi.org/10.1016/s0092-8674(01)00287-2openalex-snapshot
Control of Cell Shape in Bacteria
inferredcites →https://doi.org/10.1016/s0378-1119(96)00404-0openalex-snapshot
Plasmids for ectopic integration in Bacillus subtilis
inferredcites →https://doi.org/10.1021/acs.biochem.4c00726openalex-snapshot
Metals in Motion: Understanding Labile Metal Pools in Bacteria
inferredcites →https://doi.org/10.1021/acschembio.3c00452openalex-snapshot
Phosphonate and Thiasugar Analogues of Glucosamine-6-phosphate: Activation of the glmS Riboswitch and Antibiotic Activity
inferredcites →https://doi.org/10.1021/acssynbio.1c00250openalex-snapshot
Modular and Single-Cell Sensors of Bacterial Ser/Thr Kinase Activity
inferredcites →https://doi.org/10.1021/cb100269fopenalex-snapshot
Synthetic Lethal Compound Combinations Reveal a Fundamental Connection between Wall Teichoic Acid and Peptidoglycan Biosyntheses in Staphylococcus aureus
inferredcites →https://doi.org/10.1038/emboj.2009.25openalex-snapshot
Distinct and essential morphogenic functions for wall‐ and lipo‐teichoic acids in Bacillus subtilis
inferredcites →https://doi.org/10.1038/embor.2011.77openalex-snapshot
c‐di‐AMP reports DNA integrity during sporulation in Bacillus subtilis
inferredcites →https://doi.org/10.1038/ja.2016.49openalex-snapshot
Quinovosamycins: new tunicamycin-type antibiotics in which the α, β-1″,11′-linked N-acetylglucosamine residue is replaced by N-acetylquinovosamine
inferredcites →https://doi.org/10.1038/nature02362openalex-snapshot
Control of gene expression by a natural metabolite-responsive ribozyme
inferredcites →https://doi.org/10.1038/nchembio.1363openalex-snapshot
Riboswitches in eubacteria sense the second messenger c-di-AMP
inferredcites →https://doi.org/10.1038/nchembio.1606openalex-snapshot
c-di-AMP binds the ydaO riboswitch in two pseudo-symmetry–related pockets
inferredcites →https://doi.org/10.1038/nchembio.1607openalex-snapshot
Structural insights into recognition of c-di-AMP by the ydaO riboswitch
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nsmb.1989openalex-snapshot
The glmS riboswitch integrates signals from activating and inhibitory metabolites in vivo
inferredcites →https://doi.org/10.1038/s41467-021-21306-0openalex-snapshot
A meet-up of two second messengers: the c-di-AMP receptor DarB controls (p)ppGpp synthesis in Bacillus subtilis
inferredcites →https://doi.org/10.1038/s41467-023-38944-1openalex-snapshot
Cyclic di-AMP traps proton-coupled K+ transporters of the KUP family in an inward-occluded conformation
inferredcites →https://doi.org/10.1038/s41467-023-39723-8openalex-snapshot
On the mechanisms of lysis triggered by perturbations of bacterial cell wall biosynthesis
inferredcites →https://doi.org/10.1038/s41467-024-49785-xopenalex-snapshot
Molecular motor tug-of-war regulates elongasome cell wall synthesis dynamics in Bacillus subtilis
inferredcites →https://doi.org/10.1038/s41467-024-49952-0openalex-snapshot
Acetyl-CoA synthetase activity is enzymatically regulated by lysine acetylation using acetyl-CoA or acetyl-phosphate as donor molecule
inferredcites →https://doi.org/10.1038/s41467-025-57842-2openalex-snapshot
Regulation of acetyl-CoA biosynthesis via an intertwined acetyl-CoA synthetase/acetyltransferase complex
inferredcites →https://doi.org/10.1038/s41564-019-0439-0openalex-snapshot
Bacillus subtilis cell diameter is determined by the opposing actions of two distinct cell wall synthetic systems
inferredcites →https://doi.org/10.1038/s41564-023-01329-7openalex-snapshot
Growth rate is modulated by monitoring cell wall precursors in Bacillus subtilis
inferredcites →https://doi.org/10.1038/s41564-025-02027-2openalex-snapshot
Cyclic-di-AMP modulates cellular turgor in response to defects in bacterial cell wall synthesis
inferredcites →https://doi.org/10.1038/s41564-026-02368-6openalex-snapshot
Wall teichoic acids regulate peptidoglycan synthesis to maintain rod shape in Bacillus subtilis
inferredcites →https://doi.org/10.1038/s41598-017-04064-2openalex-snapshot
YvcK, a protein required for cell wall integrity and optimal carbon source utilization, binds uridine diphosphate-sugars
inferredcites →https://doi.org/10.1038/s41598-017-15107-zopenalex-snapshot
The Bacillus BioBrick Box 2.0: expanding the genetic toolbox for the standardized work with Bacillus subtilis
inferredcites →https://doi.org/10.1038/s41598-018-20145-2openalex-snapshot
Dual regulation of activity and intracellular localization of the PASTA kinase PrkC during Bacillus subtilis growth
inferredcites →https://doi.org/10.1038/s41598-020-72854-2openalex-snapshot
Uridine diphosphate N-acetylglucosamine orchestrates the interaction of GlmR with either YvcJ or GlmS in Bacillus subtilis
inferredcites →https://doi.org/10.1038/s41598-020-74609-5openalex-snapshot
Cell morphology maintenance in Bacillus subtilis through balanced peptidoglycan synthesis and hydrolysis
inferredcites →https://doi.org/10.1038/s41598-021-04294-5openalex-snapshot
Magnesium rescues the morphology of Bacillus subtilis mreB mutants through its inhibitory effect on peptidoglycan hydrolases
inferredcites →https://doi.org/10.1038/s41598-022-09276-9openalex-snapshot
Arginine glycosylation regulates UDP-GlcNAc biosynthesis in Salmonella enterica
inferredcites →https://doi.org/10.1038/s42003-024-07420-xopenalex-snapshot
Membrane-embedded CdaA is required for efficient synthesis of second messenger cyclic di-AMP
inferredcites →https://doi.org/10.1039/c7ra00086copenalex-snapshot
Mutational analysis to identify the residues essential for the acetyltransferase activity of GlmU in Bacillus subtilis
inferredcites →https://doi.org/10.1039/d2ra02044kopenalex-snapshot
GlmU inhibitor from the roots of Euphorbia ebracteolata as an anti-tuberculosis agent
inferredcites →https://doi.org/10.1073/pnas.1000928107openalex-snapshot
Biosynthesis and functions of bacillithiol, a major low-molecular-weight thiol in Bacilli
inferredcites →https://doi.org/10.1073/pnas.2318666121openalex-snapshot
c-di-AMP determines the hierarchical organization of bacterial RCK proteins
inferredcites →https://doi.org/10.1074/jbc.m112.395491openalex-snapshot
Cyclic Di-AMP Homeostasis in Bacillus subtilis
inferredcites →https://doi.org/10.1074/jbc.m114.562496openalex-snapshot
PrkC-mediated Phosphorylation of Overexpressed YvcK Protein Regulates PBP1 Protein Localization in Bacillus subtilis mreB Mutant Cells
inferredcites →https://doi.org/10.1091/mbc.e24-07-0302openalex-snapshot
GpsB interacts with FtsZ in multiple species and may serve as an accessory Z-ring anchor
inferredcites →https://doi.org/10.1093/nar/gkad1120openalex-snapshot
Co-transcriptional folding of the glmS ribozyme enables a rapid response to metabolite
inferredcites →https://doi.org/10.1093/nar/gkae957openalex-snapshot
A new framework for Subti Wiki, the database for the model organism Bacillus subtilis
inferredcites →https://doi.org/10.1093/nar/gkr032openalex-snapshot
Rapid changes in gene expression: DNA determinants of promoter regulation by the concentration of the transcription initiating NTP in Bacillus subtilis
inferredcites →https://doi.org/10.1099/00221287-136-12-2527openalex-snapshot
The effects of osmotic upshock on the intracellular solute pools of Bacillus subtilis
inferredcites →https://doi.org/10.1099/mic.0.28172-0openalex-snapshot
YvcK of Bacillus subtilis is required for a normal cell shape and for growth on Krebs cycle intermediates and substrates of the pentose phosphate pathway
inferredcites →https://doi.org/10.1111/1462-2920.15008openalex-snapshot
An extracytoplasmic protein and a moonlighting enzyme modulate synthesis of c‐di‐AMP in Listeria monocytogenes
inferredcites →https://doi.org/10.1111/1751-7915.14257openalex-snapshot
A model industrial workhorse: Bacillus subtilis strain 168 and its genome after a quarter of a century
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06601.xopenalex-snapshot
Regulation of cell wall morphogenesis in Bacillus subtilis by recruitment of PBP1 to the MreB helix
inferredcites →https://doi.org/10.1111/j.1365-2958.2009.06805.xopenalex-snapshot
Partial functional redundancy of MreB isoforms, MreB, Mbl and MreBH, in cell morphogenesis of Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2011.07587.xopenalex-snapshot
The YvcK protein is required for morphogenesis via localization of PBP1 under gluconeogenic growth conditions in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2011.07953.xopenalex-snapshot
Analysis of the role ofBacillus subtilisσMin β‐lactam resistance reveals an essential role for c‐di‐AMP in peptidoglycan homeostasis
inferredcites →https://doi.org/10.1111/mmi.12335openalex-snapshot
Differentiated roles for MreB ‐actin isologues and autolytic enzymes in B acillus subtilis morphogenesis
inferredcites →https://doi.org/10.1111/mmi.13281openalex-snapshot
Cyclic‐di‐ AMP synthesis by the diadenylate cyclase CdaA is modulated by the peptidoglycan biosynthesis enzyme GlmM in L actococcus lactis
inferredcites →https://doi.org/10.1126/science.1206848openalex-snapshot
Condition-Dependent Transcriptome Reveals High-Level Regulatory Architecture in Bacillus subtilis
inferredcites →https://doi.org/10.1128/aac.01617-16openalex-snapshot
Transposon-Sequencing Analysis Unveils Novel Genes Involved in the Generation of Persister Cells in Uropathogenic Escherichia coli
inferredcites →https://doi.org/10.1128/iai.00766-20openalex-snapshot
Beyond Homeostasis: Potassium and Pathogenesis during Bacterial Infections
inferredcites →https://doi.org/10.1128/iai.02207-14openalex-snapshot
Mycobacterial Gene cuvA Is Required for Optimal Nutrient Utilization and Virulence
inferredcites →https://doi.org/10.1128/jb.00023-23openalex-snapshot
All DACs in a Row: Domain Architectures of Bacterial and Archaeal Diadenylate Cyclases
inferredcites →https://doi.org/10.1128/jb.00102-23openalex-snapshot
Bacillus subtilis, a Swiss Army Knife in Science and Biotechnology
inferredcites →https://doi.org/10.1128/jb.00183-16openalex-snapshot
YodL and YisK Possess Shape-Modifying Activities That Are Suppressed by Mutations in Bacillus subtilis mreB and mbl
inferredcites →https://doi.org/10.1128/jb.00202-23openalex-snapshot
Bacillus subtilis YisK possesses oxaloacetate decarboxylase activity and exhibits Mbl-dependent localization
inferredcites →https://doi.org/10.1128/jb.00375-22openalex-snapshot
Magnesium Modulates Bacillus subtilis Cell Division Frequency
inferredcites →https://doi.org/10.1128/jb.00462-18openalex-snapshot
Making and Breaking of an Essential Poison: the Cyclases and Phosphodiesterases That Produce and Degrade the Essential Second Messenger Cyclic di-AMP in Bacteria
inferredcites →https://doi.org/10.1128/jb.00564-15openalex-snapshot
An Essential Poison: Synthesis and Degradation of Cyclic Di-AMP in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.00576-20openalex-snapshot
Simulations of Proposed Mechanisms of FtsZ-Driven Cell Constriction
inferredcites →https://doi.org/10.1128/jb.01256-09openalex-snapshot
Muropeptide Rescue in Bacillus subtilis Involves Sequential Hydrolysis by β- N -Acetylglucosaminidase and N -Acetylmuramyl- l -Alanine Amidase
inferredcites →https://doi.org/10.1128/jb.01336-06openalex-snapshot
Wall Teichoic Acid Polymers Are Dispensable for Cell Viability in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.01497-08openalex-snapshot
The Cell Wall Regulator σISpecifically Suppresses the Lethal Phenotype ofmblMutants inBacillus subtilis
inferredcites →https://doi.org/10.1128/jb.174.21.6852-6856.1992openalex-snapshot
Identification of tms-26 as an allele of the gcaD gene, which encodes N-acetylglucosamine 1-phosphate uridyltransferase in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.177.3.765-773.1995openalex-snapshot
Bacillus subtilis possesses a second determinant with extensive sequence similarity to the Escherichia coli mreB morphogene
inferredcites →https://doi.org/10.1128/jb.184.9.2500-2520.2002openalex-snapshot
Bacillus subtilisfunctional genomics: global characterization of the stringent response by proteome and transcriptome analysis
inferredcites →https://doi.org/10.1128/jb.188.7.2692-2700.2006openalex-snapshot
The Intestinal Life Cycle of Bacillus subtilis and Close Relatives
inferredcites →https://doi.org/10.1128/mbio.00073-23openalex-snapshot
Listeria monocytogenes GlmR Is an Accessory Uridyltransferase Essential for Cytosolic Survival and Virulence
inferredcites →https://doi.org/10.1128/mbio.00092-22openalex-snapshot
A Central Role for Magnesium Homeostasis during Adaptation to Osmotic Stress
inferredcites →https://doi.org/10.1128/mbio.00341-18openalex-snapshot
Cyclic di-AMP Acts as an Extracellular Signal That Impacts Bacillus subtilis Biofilm Formation and Plant Attachment
inferredcites →https://doi.org/10.1128/mbio.00475-23openalex-snapshot
A Decrease in Fatty Acid Synthesis Rescues Cells with Limited Peptidoglycan Synthesis Capacity
inferredcites →https://doi.org/10.1128/mbio.01625-20openalex-snapshot
(p)ppGpp and c-di-AMP Homeostasis Is Controlled by CbpB in Listeria monocytogenes
inferredcites →https://doi.org/10.1128/mbio.01760-23openalex-snapshot
An exhaustive multiple knockout approach to understanding cell wall hydrolase function in Bacillus subtilis
inferredcites →https://doi.org/10.1128/mbio.02667-22openalex-snapshot
Insights into the Roles of Lipoteichoic Acids and MprF in Bacillus subtilis
inferredcites →https://doi.org/10.1128/mbio.02773-23openalex-snapshot
A CRISPRi-based genetic resource to study essential Staphylococcus aureus genes
inferredcites →https://doi.org/10.1128/mbio.03798-24openalex-snapshot
Pyruvate kinase directly generates GTP in glycolysis, supporting growth and contributing to guanosine toxicity
inferredcites →https://doi.org/10.1128/microbiolspec.tbtb2-0005-2015openalex-snapshot
Epigenetic Phosphorylation Control of Mycobacterium tuberculosis Infection and Persistence
inferredcites →https://doi.org/10.1128/mmbr.00014-06openalex-snapshot
The Bacterial Actin-Like Cytoskeleton
inferredcites →https://doi.org/10.1128/mmbr.00029-16openalex-snapshot
The Blueprint of a Minimal Cell: MiniBacillus
inferredcites →https://doi.org/10.1128/msphere.00321-24openalex-snapshot
Identification of novel genetic factors that regulate c-di-AMP production in Staphylococcus aureus using a riboswitch-based biosensor
inferredcites →https://doi.org/10.1128/msystems.00005-16openalex-snapshot
Temporal Regulation of the Bacillus subtilis Acetylome and Evidence for a Role of MreB Acetylation in Cell Wall Growth
inferredcites →https://doi.org/10.1128/msystems.01131-24openalex-snapshot
Allosteric regulation of pyruvate kinase enables efficient and robust gluconeogenesis by preventing metabolic conflicts and carbon overflow
inferredcites →https://doi.org/10.1128/spectrum.02011-24openalex-snapshot
Sirtuin-dependent reversible lysine acetylation of the o -succinylbenzoyl-coenzyme A synthetase of Bacillus subtilis
inferredcites →https://doi.org/10.1146/annurev-micro-020518-115943openalex-snapshot
Cyclic di-AMP Signaling in Bacteria
inferredcites →https://doi.org/10.1146/annurev-micro-092412-155620openalex-snapshot
Wall Teichoic Acids of Gram-Positive Bacteria
inferredcites →https://doi.org/10.1186/1471-2164-10-291openalex-snapshot
Comprehensive identification of essential Staphylococcus aureus genes using Transposon-Mediated Differential Hybridisation (TMDH)
inferredcites →https://doi.org/10.1186/s12864-015-1361-3openalex-snapshot
A new platform for ultra-high density Staphylococcus aureus transposon libraries
inferredcites →https://doi.org/10.1261/rna.2266506openalex-snapshot
Characteristics of the glmS ribozyme suggest only structural roles for divalent metal ions
inferredcites →https://doi.org/10.1271/bbb1961.40.447openalex-snapshot
Tunicamycin inhibits the formation of lipid intermediate in cell-free peptidoglycan synthesis of bacteria.
inferredcites →https://doi.org/10.1371/journal.pgen.1005275openalex-snapshot
The Eukaryotic-Like Ser/Thr Kinase PrkC Regulates the Essential WalRK Two-Component System in Bacillus subtilis
inferredcites →https://doi.org/10.1371/journal.pgen.1007689openalex-snapshot
A metabolic checkpoint protein GlmR is important for diverting carbon into peptidoglycan biosynthesis in Bacillus subtilis
inferredcites →https://doi.org/10.1371/journal.pgen.1008434openalex-snapshot
Bacillus subtilis PgcA moonlights as a phosphoglucosamine mutase in support of peptidoglycan synthesis
inferredcites →https://doi.org/10.1371/journal.pgen.1011215openalex-snapshot
Reciprocal regulation of enterococcal cephalosporin resistance by products of the autoregulated yvcJ-glmR-yvcL operon enhances fitness during cephalosporin exposure
inferredcites →https://doi.org/10.1371/journal.pone.0131169openalex-snapshot
Changes in the Acetylome and Succinylome of Bacillus subtilis in Response to Carbon Source
inferredcites →https://doi.org/10.1371/journal.pone.0204687openalex-snapshot
Protein lysine acetylation plays a regulatory role in Bacillus subtilis multicellularity
inferredcites →https://doi.org/10.1371/journal.ppat.1006001openalex-snapshot
The Listeria monocytogenes PASTA Kinase PrkA and Its Substrate YvcK Are Required for Cell Wall Homeostasis, Metabolism, and Virulence
inferredcites →https://doi.org/10.1371/journal.ppat.1007537openalex-snapshot
Inhibition of the Staphylococcus aureus c-di-AMP cyclase DacA by direct interaction with the phosphoglucosamine mutase GlmM
inferredcites →https://doi.org/10.2139/ssrn.4949024openalex-snapshot
Comprehensive Double-Mutant Analysis of the Bacillus subtilis Envelope Using Double-CRISPRi
inferredcites →https://doi.org/10.2741/354openalex-snapshot
Genistein stimulates the insulin-dependent signaling pathway
inferredcites →https://doi.org/10.3389/fcimb.2024.1408947openalex-snapshot
Bacterial protein acetylation: mechanisms, functions, and methods for study
inferredcites →https://doi.org/10.3389/fmicb.2018.00111openalex-snapshot
Turgor Pressure and Possible Constriction Mechanisms in Bacterial Division
inferredcites →https://doi.org/10.3389/fmicb.2021.697930openalex-snapshot
Metabolic Control of Cell Elongation and Cell Division in Bacillus subtilis
inferredcites →https://doi.org/10.3389/fmicb.2022.1004737openalex-snapshot
Mirubactin C rescues the lethal effect of cell wall biosynthesis mutations in Bacillus subtilis
inferredcites →https://doi.org/10.3389/fmicb.2024.1356733openalex-snapshot
Nε-lysine acetylation of the histone-like protein HBsu influences antibiotic survival and persistence in Bacillus subtilis
inferredcites →https://doi.org/10.3390/biom13050720openalex-snapshot
Recent Advances in Peptidoglycan Synthesis and Regulation in Bacteria
inferredcites →https://doi.org/10.3390/ijms24010455openalex-snapshot
Stress-Associated and Growth-Dependent Mutagenesis Are Divergently Regulated by c-di-AMP Levels in Bacillus subtilis
inferredcites →https://doi.org/10.3390/microorganisms12071309openalex-snapshot
Adaptation of Bacillus subtilis MreB Filaments to Osmotic Stress Depends on Influx of Potassium Ions
inferredcites →https://doi.org/10.3390/microorganisms9102148openalex-snapshot
Staphylococcus aureus Transcriptome Data and Metabolic Modelling Investigate the Interplay of Ser/Thr Kinase PknB, Its Phosphatase Stp, the glmR/yvcK Regulon and the cdaA Operon for Metabolic Adaptation
inferredcites →https://doi.org/10.3791/59905-vopenalex-snapshot
Live-Cell Fluorescence Microscopy to Investigate Subcellular Protein Localization and Cell Morphology Changes in Bacteria
inferredcites →https://doi.org/10.7554/elife.107679openalex-snapshot
The interplay of membrane tension and FtsZ filament condensation on the initiation and progression of cell division in B. subtilis
inferredcites →https://doi.org/10.7554/elife.57902openalex-snapshot
A regulatory pathway that selectively up-regulates elongasome function in the absence of class A PBPs
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.