On the public citation graph

Metabolism Shapes the Cell

https://doi.org/10.1128/jb.00039-17
0 signed · 175 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/pmic.201000791openalex-snapshot
An expanded protein–protein interaction network in Bacillus subtilis reveals a group of hubs: Exploration by an integrative approach
inferredcites →https://doi.org/10.1016/j.bpj.2015.06.026openalex-snapshot
Cell-Shape Homeostasis in Escherichia coli Is Driven by Growth, Division, and Nucleoid Complexity
inferredcites →https://doi.org/10.1016/j.bpj.2015.07.002openalex-snapshot
Cell-Size Homeostasis and the Incremental Rule in a Bacterial Pathogen
inferredcites →https://doi.org/10.1016/j.cell.2007.05.043openalex-snapshot
A Metabolic Sensor Governing Cell Size in Bacteria
inferredcites →https://doi.org/10.1016/j.cell.2014.11.022openalex-snapshot
A Constant Size Extension Drives Bacterial Cell Size Homeostasis
inferredcites →https://doi.org/10.1016/j.cell.2016.05.003openalex-snapshot
A Comprehensive, CRISPR-based Functional Analysis of Essential Genes in Bacteria
inferredcites →https://doi.org/10.1016/j.cell.2016.05.045openalex-snapshot
Relative Rates of Surface and Volume Synthesis Set Bacterial Cell Size
inferredcites →https://doi.org/10.1016/j.cub.2014.12.009openalex-snapshot
Cell-Size Control and Homeostasis in Bacteria
inferredcites →https://doi.org/10.1016/j.devcel.2009.10.024openalex-snapshot
Coupling Prokaryotic Cell Fate and Division Control with a Bifunctional and Oscillating Oxidoreductase Homolog
inferredcites →https://doi.org/10.1016/j.femsre.2004.11.002openalex-snapshot
The PEP—pyruvate—oxaloacetate node as the switch point for carbon flux distribution in bacteria: We dedicate this paper to Rudolf K. Thauer, Director of the Max-Planck-Institute for Terrestrial Microbiology in Marburg, Germany, on the occasion of his 65th birthday
inferredcites →https://doi.org/10.1016/j.mib.2013.09.003openalex-snapshot
Do the divisome and elongasome share a common evolutionary past?
inferredcites →https://doi.org/10.1016/j.mib.2015.01.011openalex-snapshot
Growth rate and cell size: a re-examination of the growth law
inferredcites →https://doi.org/10.1016/j.tim.2015.11.007openalex-snapshot
You Are What You Eat: Metabolic Control of Bacterial Division
inferredcites →https://doi.org/10.1016/j.ymben.2010.10.001openalex-snapshot
Physical interactions between tricarboxylic acid cycle enzymes in Bacillus subtilis: Evidence for a metabolon
inferredcites →https://doi.org/10.1016/j.ymben.2016.09.001openalex-snapshot
CRISPRi engineering E. coli for morphology diversification
inferredcites →https://doi.org/10.1016/s0021-9258(18)68091-3openalex-snapshot
Properties of Escherichia coli mutants lacking membrane-derived oligosaccharides.
inferredcites →https://doi.org/10.1016/s0021-9258(18)92940-6openalex-snapshot
Biosynthesis of membrane-derived oligosaccharides. Membrane-bound glucosyltransferase system from Escherichia coli requires polyprenyl phosphate
inferredcites →https://doi.org/10.1021/acschembio.6b00523openalex-snapshot
Direct Evidence for Metabolon Formation and Substrate Channeling in Recombinant TCA Cycle Enzymes
inferredcites →https://doi.org/10.1038/emboj.2013.129openalex-snapshot
Direct interaction of FtsZ and MreB is required for septum synthesis and cell division in Escherichia coli
inferredcites →https://doi.org/10.1038/nature03239openalex-snapshot
Interaction network containing conserved and essential protein complexes in Escherichia coli
inferredcites →https://doi.org/10.1038/nature14562openalex-snapshot
A noisy linear map underlies oscillations in cell size and gene expression in bacteria
inferredcites →https://doi.org/10.1038/ncb2087openalex-snapshot
The metabolic enzyme CTP synthase forms cytoskeletal filaments
inferredcites →https://doi.org/10.1038/nchembio.1689openalex-snapshot
Lipid-linked cell wall precursors regulate membrane association of bacterial actin MreB
inferredcites →https://doi.org/10.1038/ncomms11423openalex-snapshot
Phosphotransferase-dependent accumulation of (p)ppGpp in response to glutamine deprivation in Caulobacter crescentus
inferredcites →https://doi.org/10.1038/ncomms12340openalex-snapshot
Antimicrobial peptides trigger a division block in Escherichia coli through stimulation of a signalling system
inferredcites →https://doi.org/10.1038/ncomms3856openalex-snapshot
Discovery of chlamydial peptidoglycan reveals bacteria with murein sacculi but without FtsZ
inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00930.xopenalex-snapshot
A UDP glucosyltransferase from Bacillus subtilis successively transfers up to four glucose residues to 1,2‐diacylglycerol: expression of ypfP in Escherichia coli and structural analysis of its reaction products
inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00974.xopenalex-snapshot
Analysis of the effect of ppGpp on the ftsQAZ operon in Escherichia coli
inferredcites →https://doi.org/10.1073/pnas.1004304107openalex-snapshot
Teichoic acids are temporal and spatial regulators of peptidoglycan cross-linking in Staphylococcus aureus
inferredcites →https://doi.org/10.1073/pnas.1511751112openalex-snapshot
Antagonism screen for inhibitors of bacterial cell wall biogenesis uncovers an inhibitor of undecaprenyl diphosphate synthase
inferredcites →https://doi.org/10.1073/pnas.72.8.2999openalex-snapshot
Distinct penicillin binding proteins involved in the division, elongation, and shape of Escherichia coli K12.
inferredcites →https://doi.org/10.1074/jbc.270.49.29096openalex-snapshot
Pleiotropic Regulation of Central Carbohydrate Metabolism in Escherichia coli via the Gene csrA
inferredcites →https://doi.org/10.1074/jbc.m113.522623openalex-snapshot
Benzothiazinones Mediate Killing of Corynebacterineae by Blocking Decaprenyl Phosphate Recycling Involved in Cell Wall Biosynthesis
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/10.1074/jbc.m309849200openalex-snapshot
Bifunctional Phosphoglucose/Phosphomannose Isomerases from the Archaea Aeropyrum pernix and Thermoplasma acidophilum Constitute a Novel Enzyme Family within the Phosphoglucose Isomerase Superfamily
inferredcites →https://doi.org/10.1074/jbc.m703536200openalex-snapshot
Identification of a Soluble Diacylglycerol Kinase Required for Lipoteichoic Acid Production in Bacillus subtilis
inferredcites →https://doi.org/10.1074/mcp.m800546-mcp200openalex-snapshot
Novel Activities of Glycolytic Enzymes in Bacillus subtilis
inferredcites →https://doi.org/10.1089/mdr.2014.0035openalex-snapshot
Deciphering the Metabolism of Undecaprenyl-Phosphate: The Bacterial Cell-Wall Unit Carrier at the Membrane Frontier
inferredcites →https://doi.org/10.1093/jac/3.suppl_b.13openalex-snapshot
The mechanism of action of mecillinam
inferredcites →https://doi.org/10.1099/00221287-19-3-592openalex-snapshot
Dependency on Medium and Temperature of Cell Size and Chemical Composition during Balanced Growth of Salmonella typhimurium
inferredcites →https://doi.org/10.1099/mic.0.022475-0openalex-snapshot
CpgA, EF-Tu and the stressosome protein YezB are substrates of the Ser/Thr kinase/phosphatase couple, PrkC/PrpC, in 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/febs.13959openalex-snapshot
Regulation of bacterial cell wall growth
inferredcites →https://doi.org/10.1111/j.1365-2958.1991.tb00751.xopenalex-snapshot
Cell division and peptidoglycan assembly in Eschenchia coli
inferredcites →https://doi.org/10.1111/j.1365-2958.1994.tb00482.xopenalex-snapshot
ppGpp concentration, growth without PBP2 activity, and growth‐rate control in Escherichia coli
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04367.xopenalex-snapshot
The morphogenetic MreBCD proteins of Escherichia coli form an essential membrane‐bound complex
inferredcites →https://doi.org/10.1111/j.1365-2958.2005.04506.xopenalex-snapshot
A magnesium‐dependent mreB null mutant: implications for the role of mreB in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2005.04736.xopenalex-snapshot
Roles for MreC and MreD proteins in helical growth of the cylindrical cell wall in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06210.xopenalex-snapshot
Control of the cell elongation–division cycle by shuttling of PBP1 protein in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06483.xopenalex-snapshot
A matter of life and death: cell wall homeostasis and the WalKR (YycGF) essential signal transduction pathway
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.1365-2958.2010.07472.xopenalex-snapshot
Enzymatic activities and functional interdependencies of Bacillus subtilis lipoteichoic acid synthesis enzymes
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07483.xopenalex-snapshot
A new morphogenesis pathway in bacteria: unbalanced activity of cell wall synthesis machineries leads to coccus-to-rod transition and filamentation in ovococci
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.1365-2958.2011.07663.xopenalex-snapshot
Circuitry linking the Csr and stringent response global regulatory systems
inferredcites →https://doi.org/10.1111/j.1365-2958.2012.08100.xopenalex-snapshot
Chlamydia co‐opts the rod shape‐determining proteins MreB and Pbp2 for cell division
inferredcites →https://doi.org/10.1111/j.1574-6976.2007.00090.xopenalex-snapshot
Morphogenesis of rod-shaped sacculi
inferredcites →https://doi.org/10.1111/mmi.12007openalex-snapshot
Changes in the oligomerization potential of the division inhibitor UgtP co‐ordinate B acillus subtilis cell size with nutrient availability
inferredcites →https://doi.org/10.1111/mmi.12150openalex-snapshot
Colocalization and interaction between elongasome and divisome during a preparative cell division phase in E scherichia coli
inferredcites →https://doi.org/10.1111/mmi.13279openalex-snapshot
Structure of the bacterial cell division determinant GpsB and its interaction with penicillin‐binding proteins
inferredcites →https://doi.org/10.1111/mmi.13284openalex-snapshot
Dead‐end intermediates in the enterobacterial common antigen pathway induce morphological defects in Escherichia coli by competing for undecaprenyl phosphate
inferredcites →https://doi.org/10.1111/mmi.13613openalex-snapshot
Suppression and synthetic‐lethal genetic relationships of Δgps B mutations indicate that G ps B mediates protein phosphorylation and penicillin‐binding protein interactions in S treptococcus pneumoniae D 39
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.04819-14openalex-snapshot
Amdinocillin (Mecillinam) Resistance Mutations in Clinical Isolates and Laboratory-Selected Mutants of Escherichia coli
inferredcites →https://doi.org/10.1128/aem.00310-09openalex-snapshot
Substrate Specificity of a Mannose-6-Phosphate Isomerase from Bacillus subtilis and Its Application in the Production of l -Ribose
inferredcites →https://doi.org/10.1128/aem.71.1.39-45.2005openalex-snapshot
Bacillus subtilis α-Phosphoglucomutase Is Required for Normal Cell Morphology and Biofilm Formation
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.00099-08openalex-snapshot
Glutamate Metabolism in Bacillus subtilis : Gene Expression and Enzyme Activities Evolved To Avoid Futile Cycles and To Allow Rapid Responses to Perturbations of the System
inferredcites →https://doi.org/10.1128/jb.00180-16openalex-snapshot
Classic Spotlight: Staying in Shape and Discovery of the mrdAB and mreBCD Operons
inferredcites →https://doi.org/10.1128/jb.00197-06openalex-snapshot
Lesions in Teichoic Acid Biosynthesis in Staphylococcus aureus Lead to a Lethal Gain of Function in the Otherwise Dispensable Pathway
inferredcites →https://doi.org/10.1128/jb.00507-13openalex-snapshot
The Conserved DNA-Binding Protein WhiA Is Involved in Cell Division in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.00550-16openalex-snapshot
Interrupting Biosynthesis of O Antigen or the Lipopolysaccharide Core Produces Morphological Defects in Escherichia coli by Sequestering Undecaprenyl Phosphate
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.01034-15openalex-snapshot
Colanic Acid Intermediates Prevent De Novo Shape Recovery of Escherichia coli Spheroplasts, Calling into Question Biological Roles Previously Attributed to Colanic Acid
inferredcites →https://doi.org/10.1128/jb.01217-13openalex-snapshot
Defects in the Flagellar Motor Increase Synthesis of Poly-γ-Glutamate in Bacillus subtilis
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.01938-06openalex-snapshot
Mutations Blocking Side Chain Assembly, Polymerization, or Transport of a Wzy-DependentStreptococcus pneumoniaeCapsule Are Lethal in the Absence of Suppressor Mutations and Can Affect Polymer Transfer to the Cell Wall
inferredcites →https://doi.org/10.1128/jb.107.1.210-216.1971openalex-snapshot
Effect of Nutrient Concentration on the Growth of Escherichia coli
inferredcites →https://doi.org/10.1128/jb.123.1.7-19.1975openalex-snapshot
Control of cell length in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.135.2.559-574.1978openalex-snapshot
Dimensions of Escherichia coli at various growth rates: model for envelope growth
inferredcites →https://doi.org/10.1128/jb.137.2.839-845.1979openalex-snapshot
High and selective resistance to mecillinam in adenylate cyclase-deficient or cyclic adenosine 3',5'-monophosphate receptor protein-deficient mutants of Escherichia coli
inferredcites →https://doi.org/10.1128/jb.141.1.52-57.1980openalex-snapshot
Cluster of mrdA and mrdB genes responsible for the rod shape and mecillinam sensitivity of Escherichia coli
inferredcites →https://doi.org/10.1128/jb.170.1.65-70.1988openalex-snapshot
Cyclic AMP and cell division in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.171.6.3025-3030.1989openalex-snapshot
Penicillin-binding protein 2 is essential in wild-type Escherichia coli but not in lov or cya mutants
inferredcites →https://doi.org/10.1128/jb.174.17.5748-5752.1992openalex-snapshot
Cloning and sequencing of Escherichia coli murZ and purification of its product, a UDP-N-acetylglucosamine enolpyruvyl transferase
inferredcites →https://doi.org/10.1128/jb.175.15.4744-4755.1993openalex-snapshot
Identification and molecular characterization of csrA, a pleiotropic gene from Escherichia coli that affects glycogen biosynthesis, gluconeogenesis, cell size, and surface properties
inferredcites →https://doi.org/10.1128/jb.175.20.6704-6710.1993openalex-snapshot
Penicillin-binding protein 2 inactivation in Escherichia coli results in cell division inhibition, which is relieved by FtsZ overexpression
inferredcites →https://doi.org/10.1128/jb.177.14.4194-4197.1995openalex-snapshot
MurA (MurZ), the enzyme that catalyzes the first committed step in peptidoglycan biosynthesis, is essential in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.178.13.3818-3828.1996openalex-snapshot
Mecillinam resistance in Escherichia coli is conferred by loss of a second activity of the AroK protein
inferredcites →https://doi.org/10.1128/jb.179.21.6692-6698.1997openalex-snapshot
Topological analysis of the membrane-bound glucosyltransferase, MdoH, required for osmoregulated periplasmic glucan synthesis in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.179.21.6858-6861.1997openalex-snapshot
Inactivation of mdoH leads to increased expression of colanic acid capsular polysaccharide in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.180.3.547-555.1998openalex-snapshot
Bacillus subtilis Cell Cycle as Studied by Fluorescence Microscopy: Constancy of Cell Length at Initiation of DNA Replication and Evidence for Active Nucleoid Partitioning
inferredcites →https://doi.org/10.1128/jb.180.5.1053-1062.1998openalex-snapshot
Control of ftsZ Expression, Cell Division, and Glutamine Metabolism in Luria-Bertani Medium by the Alarmone ppGpp in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.184.22.6109-6114.2002openalex-snapshot
The PrpC Serine-Threonine Phosphatase and PrkC Kinase Have Opposing Physiological Roles in Stationary-Phase Bacillus subtilis Cells
inferredcites →https://doi.org/10.1128/jb.185.22.6666-6677.2003openalex-snapshot
Localization of the Vegetative Cell Wall Hydrolases LytC, LytE, and LytF on the Bacillus subtilis Cell Surface and Stability of These Enzymes to Cell Wall-Bound or Extracellular Proteases
inferredcites →https://doi.org/10.1128/jb.186.11.3516-3524.2004openalex-snapshot
Transcriptome Analysis of Crp-Dependent Catabolite Control of Gene Expression in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.187.1.54-64.2005openalex-snapshot
Localization of MreB inRhodobacter sphaeroidesunder Conditions Causing Changes in Cell Shape and Membrane Structure
inferredcites →https://doi.org/10.1128/jb.188.5.1667-1679.2006openalex-snapshot
Use of Thymine Limitation and Thymine Starvation To Study Bacterial Physiology and Cytology
inferredcites →https://doi.org/10.1128/jb.94.5.1783-1784.1967openalex-snapshot
Biosynthesis of the N-acyl-galactosaminase in cell walls of Bacillus subtilis
inferredcites →https://doi.org/10.1128/mbio.00935-14openalex-snapshot
Coordinating Bacterial Cell Division with Nutrient Availability: a Role for Glycolysis
inferredcites →https://doi.org/10.1128/mmbr.00042-10openalex-snapshot
Eukaryote-Like Serine/Threonine Kinases and Phosphatases in Bacteria
inferredcites →https://doi.org/10.1146/annurev-micro-092412-155620openalex-snapshot
Wall Teichoic Acids of Gram-Positive Bacteria
inferredcites →https://doi.org/10.1146/annurev.biochem.70.1.149openalex-snapshot
Channeling of Substrates and Intermediates in Enzyme-Catalyzed Reactions
inferredcites →https://doi.org/10.1155/2013/371429openalex-snapshot
Biosynthesis of Osmoregulated Periplasmic Glucans inEscherichia coli: The Phosphoethanolamine Transferase Is Encoded byopgE
inferredcites →https://doi.org/10.1159/000308512openalex-snapshot
In vitro Phosphorylation of Key Metabolic Enzymes from Bacillus subtilis: PrkC Phosphorylates Enzymes from Different Branches of Basic Metabolism
inferredcites →https://doi.org/10.1159/000464443openalex-snapshot
Synthetic, Switchable Enzymes
inferredcites →https://doi.org/10.1186/1475-2859-11-79openalex-snapshot
Manipulation of the carbon storage regulator system for metabolite remodeling and biofuel production in Escherichia coli
inferredcites →https://doi.org/10.1186/s13068-016-0630-yopenalex-snapshot
Examining Escherichia coli glycolytic pathways, catabolite repression, and metabolite channeling using Δpfk mutants
inferredcites →https://doi.org/10.1371/journal.pgen.1001119openalex-snapshot
The Metabolic Enzyme ManA Reveals a Link between Cell Wall Integrity and Chromosome Morphology
inferredcites →https://doi.org/10.1371/journal.pgen.1003663openalex-snapshot
A Moonlighting Enzyme Links Escherichia coli Cell Size with Central Metabolism
inferredcites →https://doi.org/10.1371/journal.pgen.1004731openalex-snapshot
Multiple Regulatory Systems Coordinate DNA Replication with Cell Growth in Bacillus subtilis
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.pone.0000447openalex-snapshot
Genetic Evidence for a Link Between Glycolysis and DNA Replication
inferredcites →https://doi.org/10.1371/journal.pone.0092229openalex-snapshot
AspC-Mediated Aspartate Metabolism Coordinates the Escherichia coli Cell Cycle
inferredcites →https://doi.org/10.1371/journal.ppat.1005590openalex-snapshot
Pathogenic Chlamydia Lack a Classical Sacculus but Synthesize a Narrow, Mid-cell Peptidoglycan Ring, Regulated by MreB, for Cell Division
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/10.15252/embj.201490730openalex-snapshot
A NAD‐dependent glutamate dehydrogenase coordinates metabolism with cell division in Caulobacter crescentus
inferredcites →https://doi.org/10.2174/138920312804871201openalex-snapshot
Bacterial Cell Division Regulation by Ser/Thr Kinases: A Structural Perspective
inferredcites →https://doi.org/10.3389/fmicb.2016.01492openalex-snapshot
Localization of Components of the RNA-Degrading Machine in Bacillus subtilis
inferredcites →https://doi.org/10.3390/metabo4010001openalex-snapshot
Regulation Systems of Bacteria such as Escherichia coli in Response to Nutrient Limitation and Environmental Stresses

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4095375openalex-extracted
Cone Photoreceptor Phosphodiesterase 6H Inhibition Regulates Cancer Cell Growth and Metabolism Replicating the Dark Retina Response
inferred← citeshttps://doi.org/10.1002/advs.202403067openalex-snapshot
Engineered Cell Elongation Promotes Extracellular Electron Transfer of Shewanella Oneidensis
inferred← citeshttps://doi.org/10.1007/978-3-030-90621-4_1openalex-snapshot
Toward a Comparative Systems Biology of the Alphaproteobacterial Cell Cycle
inferred← citeshttps://doi.org/10.1007/978-3-031-39094-4_6openalex-snapshot
Microbial Metabolomics: An Overview of Applications
inferred← citeshttps://doi.org/10.1007/s00281-018-0671-3openalex-snapshot
Antidromic neurogenic activity and cutaneous bacterial flora
inferred← citeshttps://doi.org/10.1007/s11356-021-17289-6openalex-snapshot
Nitric oxide–secreting probiotics as sustainable bio-cleaners for reverse osmosis membrane systems
inferred← citeshttps://doi.org/10.1016/j.cej.2024.152765openalex-snapshot
Accelerating cell division of Shewanella oneidensis to promote extracellular electron transfer rate for efficient pollution treatment
inferred← citeshttps://doi.org/10.1016/j.copbio.2020.05.004openalex-snapshot
Engineering microbial cell morphology and membrane homeostasis toward industrial applications
inferred← citeshttps://doi.org/10.1016/j.cub.2017.10.005openalex-snapshot
Bacterial Size: Tuning In to a Clearer Connection
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2019.11.015openalex-snapshot
Efficient modification of the Pseudomonas aeruginosa toxin 2-heptyl-1-hydroxyquinolin-4-one by three Bacillus glycosyltransferases with broad substrate ranges
inferred← citeshttps://doi.org/10.1016/j.mib.2021.01.011openalex-snapshot
Recent progress in our understanding of peptidoglycan assembly in Firmicutes
inferred← citeshttps://doi.org/10.1016/j.mib.2023.102326openalex-snapshot
Bacterial growth — from physical principles to autolysins
inferred← citeshttps://doi.org/10.1016/j.tim.2018.04.008openalex-snapshot
Surface Area to Volume Ratio: A Natural Variable for Bacterial Morphogenesis
inferred← citeshttps://doi.org/10.1016/j.vetmic.2021.109102openalex-snapshot
The phosphorylation of phosphoglucosamine mutase GlmM by Ser/Thr kinase STK mediates cell wall synthesis and virulence in Streptococcus suis serotype 2
inferred← citeshttps://doi.org/10.1021/acssuschemeng.5c02138openalex-snapshot
Increasing Cell Width and Volume to Boost Extracellular Electron Transfer Rate for Enhanced Bioelectricity Harvest and Pollution Treatment
inferred← citeshttps://doi.org/10.1038/nrmicro.2017.79openalex-snapshot
Sizing up the bacterial cell cycle
inferred← citeshttps://doi.org/10.1038/s42003-021-01918-4openalex-snapshot
The metabolic network of the last bacterial common ancestor
inferred← citeshttps://doi.org/10.1038/s42003-025-08849-4openalex-snapshot
Carbon metabolism shapes FtsZ levels and cell division in the cyanobacterium Anabaena PCC 7120
inferred← citeshttps://doi.org/10.1073/pnas.1816018116openalex-snapshot
Movement dynamics of divisome proteins and PBP2x:FtsW in cells of Streptococcus pneumoniae
inferred← citeshttps://doi.org/10.1073/pnas.2510285122openalex-snapshot
Dysregulation of a nucleotidyltransferase induces division and surface glycan defects in Escherichia coli by altering related metabolite levels
inferred← citeshttps://doi.org/10.1091/mbc.e26-03-0129openalex-snapshot
The phosphoenolpyruvate phosphotransferase system regulates cell length and width through semi-independent pathways
inferred← citeshttps://doi.org/10.1093/femsle/fny029openalex-snapshot
Beyond nitrogen metabolism: nitric oxide, cyclic-di-GMP and bacterial biofilms
inferred← citeshttps://doi.org/10.1093/femsml/uqad031openalex-snapshot
(p)ppGpp and moonlighting RNases influence the first step of lipopolysaccharide biosynthesis in Escherichia coli
inferred← citeshttps://doi.org/10.1101/2020.06.18.160713openalex-snapshot
Disruption of the MreB elongasome is overcome by mutations in the TCA cycle
inferred← citeshttps://doi.org/10.1101/2020.07.20.213264openalex-snapshot
Cell biological studies of ethanologenic bacterium Zymomonas mobilis
inferred← citeshttps://doi.org/10.1101/2025.05.26.656067openalex-snapshot
Carbon metabolism shapes FtsZ levels and cell division in a cyanobacterium
inferred← citeshttps://doi.org/10.1101/2025.11.05.686802openalex-snapshot
Staying in the loop to make ends meet: roles and regulation of GlmR in Bacillus subtilis
inferred← citeshttps://doi.org/10.1107/s2053230x24005831openalex-snapshot
Preliminary X-ray diffraction and ligand-binding analyses of the N-terminal domain of hypothetical protein Rv1421 from Mycobacterium tuberculosis H37Rv
inferred← citeshttps://doi.org/10.1111/1751-7915.14109openalex-snapshot
Rational engineering of natural polyhydroxyalkanoates producing microorganisms for improved synthesis and recovery
inferred← citeshttps://doi.org/10.1111/mmi.14193openalex-snapshot
LiaR‐independent pathways to daptomycin resistance in Enterococcus faecalis reveal a multilayer defense against cell envelope antibiotics
inferred← citeshttps://doi.org/10.1128/aem.00210-26openalex-snapshot
A multi-tetracycline responsive induction system for gene expression in Bacillus subtilis
inferred← citeshttps://doi.org/10.1128/aem.02441-20openalex-snapshot
The Ethanologenic Bacterium Zymomonas mobilis Divides Asymmetrically and Exhibits Heterogeneity in DNA Content
inferred← citeshttps://doi.org/10.1128/jb.00202-23openalex-snapshot
Bacillus subtilis YisK possesses oxaloacetate decarboxylase activity and exhibits Mbl-dependent localization
inferred← citeshttps://doi.org/10.1128/jb.00535-17openalex-snapshot
Suppression of a Thermosensitive zipA Cell Division Mutant by Altering Amino Acid Metabolism
inferred← citeshttps://doi.org/10.1128/mbio.02047-17openalex-snapshot
Peptide Uptake Is Essential for Borrelia burgdorferi Viability and Involves Structural and Regulatory Complexity of its Oligopeptide Transporter
inferred← citeshttps://doi.org/10.1186/s12934-019-1165-2openalex-snapshot
Generation of an E. coli platform strain for improved sucrose utilization using adaptive laboratory evolution
inferred← citeshttps://doi.org/10.1186/s40170-023-00326-yopenalex-snapshot
Cone photoreceptor phosphodiesterase PDE6H inhibition regulates cancer cell growth and metabolism, replicating the dark retina response
inferred← citeshttps://doi.org/10.1242/dev.200506openalex-snapshot
Approaches to investigating metabolism in human neurodevelopment using organoids: insights from intestinal and cancer studies
inferred← citeshttps://doi.org/10.12688/f1000research.12663.1openalex-snapshot
Recent advances in understanding how rod-like bacteria stably maintain their cell shapes
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006978openalex-snapshot
Crosstalk between the tricarboxylic acid cycle and peptidoglycan synthesis in Caulobacter crescentus through the homeostatic control of α-ketoglutarate
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008591openalex-snapshot
The conserved transcriptional regulator CdnL is required for metabolic homeostasis and morphogenesis in Caulobacter
inferred← citeshttps://doi.org/10.1371/journal.pgen.1012096openalex-snapshot
Post-translational modifications of GlmR integrate metabolic and stress signals to maintain cell envelope homeostasis in Bacillus subtilis
inferred← citeshttps://doi.org/10.1371/journal.ppat.1007030openalex-snapshot
A global regulatory system links virulence and antibiotic resistance to envelope homeostasis in Acinetobacter baumannii
inferred← citeshttps://doi.org/10.18388/abp.2018_2798openalex-snapshot
When size matters – coordination of growth and cell cycle in bacteria
inferred← citeshttps://doi.org/10.3389/fcimb.2024.1482919openalex-snapshot
DegS regulates the aerobic metabolism of Vibrio cholerae via the ArcA-isocitrate dehydrogenase pathway for growth and intestinal colonization
inferred← citeshttps://doi.org/10.3389/fmicb.2017.01352openalex-snapshot
Xanthomonas citri MinC Oscillates from Pole to Pole to Ensure Proper Cell Division and Shape
inferred← citeshttps://doi.org/10.3389/fmicb.2021.697930openalex-snapshot
Metabolic Control of Cell Elongation and Cell Division in Bacillus subtilis
inferred← citeshttps://doi.org/10.3389/fmicb.2022.858440openalex-snapshot
RdsA Is a Global Regulator That Controls Cell Shape and Division in Rhizobium etli
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1141775openalex-snapshot
Pleiotropic effects of PipX, PipY, or RelQ overexpression on growth, cell size, photosynthesis, and polyphosphate accumulation in the cyanobacterium Synechococcus elongatus PCC7942
inferred← citeshttps://doi.org/10.3390/medsci10030040openalex-snapshot
Polyamine and Ethanolamine Metabolism in Bacteria as an Important Component of Nitrogen Assimilation for Survival and Pathogenicity
inferred← citeshttps://doi.org/10.3390/metabo9050094openalex-snapshot
Improved Algal Toxicity Test System for Robust Omics-Driven Mode-of-Action Discovery in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.3390/microorganisms12081571openalex-snapshot
Role of Carbon, Nitrogen, Phosphate and Sulfur Metabolism in Secondary Metabolism Precursor Supply in Streptomyces spp.
inferred← citeshttps://doi.org/10.70675/e0ec12ffz9d8dz44f9za2b5z52b754613d42openalex-snapshot
Cell cycle regulation by non-coding RNAs in Caulobacter crescentus
inferred← citeshttps://doi.org/10.70675/e7dac5e6zfa10z4c08za678z2990ea345143openalex-snapshot
Influence du microenvironnement sur la virulence et la formation de biofilm de Cutibacterium acnes.
inferred← citeshttps://doi.org/10.7717/peerj.7959openalex-snapshot
Exploration of the effects of a degS mutant on the growth of Vibrio cholerae and the global regulatory function of degS by RNA sequencing
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.