On the public citation graph
Bacterial swarming: a model system for studying dynamic self-assembly
0 signed · 442 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known work and none has been retracted — and get a dated CiteStamped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/bies.950170706openalex-snapshot
The significances of bacterial colony patterns
inferredcites →https://doi.org/10.1006/bulm.2002.0287openalex-snapshot
Quantitative Effects of Medium Hardness and Nutrient Availability on the Swarming Motility of Serratia liquefaciens
inferredcites →https://doi.org/10.1007/bf00280011openalex-snapshot
Isolation and characterization of sfp: a gene that functions in the production of the lipopeptide biosurfactant, surfactin, in Bacillus subtilis
inferredcites →https://doi.org/10.1007/s00253-005-0150-3openalex-snapshot
Production of rhamnolipids by Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1007/s00285-005-0345-3openalex-snapshot
A structured-population model of Proteus mirabilis swarm-colony development
inferredcites →https://doi.org/10.1007/s002850050004openalex-snapshot
The interaction of thin-film flow, bacterial swarming and cell differentiation in colonies of Serratia liquefaciens
inferredcites →https://doi.org/10.1007/s002850050100openalex-snapshot
Kinetic model of Proteus mirabilis swarm colony development
inferredcites →https://doi.org/10.1007/s100960050260openalex-snapshot
Ability of Proteus mirabilis to Swarm over Urethral Catheters
inferredcites →https://doi.org/10.1016/0092-8674(88)90197-3openalex-snapshot
Flagellar dynamometer controls swarmer cell differentiation of V. parahaemolyticus
inferredcites →https://doi.org/10.1016/0092-8674(90)90595-6openalex-snapshot
The MotA protein of E. coli is a proton-conducting component of the flagellar motor
inferredcites →https://doi.org/10.1016/0092-8674(94)90313-1openalex-snapshot
Biochemical and genetic characterization of a competence pheromone from B. subtilis
inferredcites →https://doi.org/10.1016/0378-1097(94)00459-5openalex-snapshot
Modular structure of genes encoding multifunctional peptide synthetases required for non-ribosomal peptide synthesis
inferredcites →https://doi.org/10.1016/j.abb.2008.03.027openalex-snapshot
Osteoclast–osteoblast communication
inferredcites →https://doi.org/10.1016/j.femsre.2003.09.004openalex-snapshot
Quorum sensing and swarming migration in bacteria
inferredcites →https://doi.org/10.1016/j.resmic.2005.11.005openalex-snapshot
The role of the Rcs phosphorelay in Enterobacteriaceae
inferredcites →https://doi.org/10.1016/j.tibs.2007.09.014openalex-snapshot
Bacterial chemoreceptors: high-performance signaling in networked arrays
inferredcites →https://doi.org/10.1016/j.tim.2008.07.004openalex-snapshot
Living on a surface: swarming and biofilm formation
inferredcites →https://doi.org/10.1016/s0022-2836(77)80153-8openalex-snapshot
Normal-to-curly flagellar transitions and their role in bacterial tumbling. Stabilization of an alternative quaternary structure by mechanical force
inferredcites →https://doi.org/10.1016/s0074-7696(04)33003-2openalex-snapshot
The Bacterial Flagellar Motor: Structure and Function of a Complex Molecular Machine
inferredcites →https://doi.org/10.1016/s0076-6879(01)36575-8openalex-snapshot
[3] Surface sensing, swarmer cell differentiation, and biofilm development
inferredcites →https://doi.org/10.1016/s0378-4371(00)00085-6openalex-snapshot
Reaction–diffusion modelling of bacterial colony patterns
inferredcites →https://doi.org/10.1016/s0968-0004(00)01770-9openalex-snapshot
Transmembrane signaling in bacterial chemoreceptors
inferredcites →https://doi.org/10.1016/s1369-7021(07)70131-1openalex-snapshot
Fabrication using ‘programmed’ reactions
inferredcites →https://doi.org/10.1021/bi011263oopenalex-snapshot
Conformational Change in the Stator of the Bacterial Flagellar Motor
inferredcites →https://doi.org/10.1021/la001053xopenalex-snapshot
Fabrication and Application of Hydrogel Stampers for Physisorptive Microcontact Printing
inferredcites →https://doi.org/10.1021/la047173copenalex-snapshot
Bacterial Printing Press that Regenerates Its Ink: Contact-Printing Bacteria Using Hydrogel Stamps
inferredcites →https://doi.org/10.1038/211255a0openalex-snapshot
Swarming of Proteus—A Solution to an Old Problem?
inferredcites →https://doi.org/10.1038/239500a0openalex-snapshot
Chemotaxis in Escherichia coli analysed by Three-dimensional Tracking
inferredcites →https://doi.org/10.1038/249073a0openalex-snapshot
Flagellar rotation and the mechanism of bacterial motility
inferredcites →https://doi.org/10.1038/249074a0openalex-snapshot
Change in direction of flagellar rotation is the basis of the chemotactic response in Escherichia coli
inferredcites →https://doi.org/10.1038/278349a0openalex-snapshot
Movement of microorganisms in viscous environments
inferredcites →https://doi.org/10.1038/msb4100050openalex-snapshot
Construction of Escherichia coli K‐12 in‐frame, single‐gene knockout mutants: the Keio collection
inferredcites →https://doi.org/10.1038/nature01830openalex-snapshot
Complete atomic model of the bacterial flagellar filament by electron cryomicroscopy
inferredcites →https://doi.org/10.1038/nmeth.1239openalex-snapshot
eSGA: E. coli synthetic genetic array analysis
inferredcites →https://doi.org/10.1038/nmeth.1240openalex-snapshot
High-throughput, quantitative analyses of genetic interactions in E. coli
inferredcites →https://doi.org/10.1038/nrmicro1616openalex-snapshot
Microfabrication meets microbiology
inferredcites →https://doi.org/10.1038/nrmicro1887openalex-snapshot
Coordinating assembly of a bacterial macromolecular machine
inferredcites →https://doi.org/10.1038/nrmicro1900openalex-snapshot
The surprisingly diverse ways that prokaryotes move
inferredcites →https://doi.org/10.1038/sj.emboj.7600668openalex-snapshot
Sensing wetness: a new role for the bacterial flagellum
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.5021862.xopenalex-snapshot
A motile but non‐swarming mutant of Proteus mirabilis lacks FlgN, a facilitator of flagella filament assembly
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02393.xopenalex-snapshot
A novel feature of the multistep phosphorelay in Escherichia coli: a revised model of the RcsC → YojN → RcsB signalling pathway implicated in capsular synthesis and swarming behaviour
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03584.xopenalex-snapshot
Swarming motility in undomesticated Bacillus subtilis
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03601.xopenalex-snapshot
RcsCDB His‐Asp phosphorelay system negatively regulates the flhDC operon in Escherichia coli
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03815.xopenalex-snapshot
The RcsC sensor kinase is required for normal biofilm formation in Escherichia coli K‐12 and controls the expression of a regulon in response to growth on a solid surface
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03835.xopenalex-snapshot
Evidence that putrescine acts as an extracellular signal required for swarming in Proteus mirabilis
inferredcites →https://doi.org/10.1063/1.2953245openalex-snapshot
Dynamics of pattern formation in bacterial swarms
inferredcites →https://doi.org/10.1073/pnas.060030097openalex-snapshot
Inorganic polyphosphate is needed for swimming, swarming, and twitching motilities of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1073/pnas.1537100100openalex-snapshot
Bacteria–host communication: The language of hormones
inferredcites →https://doi.org/10.1073/pnas.71.4.1239openalex-snapshot
Chemomechanical Coupling without ATP: The Source of Energy for Motility and Chemotaxis in Bacteria
inferredcites →https://doi.org/10.1073/pnas.86.18.6973openalex-snapshot
Migration of bacteria in semisolid agar.
inferredcites →https://doi.org/10.1073/pnas.91.18.8631openalex-snapshot
Dimorphic transition in Escherichia coli and Salmonella typhimurium: surface-induced differentiation into hyperflagellate swarmer cells.
inferredcites →https://doi.org/10.1073/pnas.95.11.6436openalex-snapshot
Electrostatic interactions between rotor and stator in the bacterial flagellar motor
inferredcites →https://doi.org/10.1073/pnas.95.5.2568openalex-snapshot
The chemotaxis system, but not chemotaxis, is essential for swarming motility in Escherichia coli
inferredcites →https://doi.org/10.1074/jbc.274.33.22993openalex-snapshot
The Structure of the Colony Migration Factor from PathogenicProteus mirabilis
inferredcites →https://doi.org/10.1074/jbc.r100066200openalex-snapshot
Molecular Information Processing: Lessons from Bacterial Chemotaxis
inferredcites →https://doi.org/10.1089/089277903769013711openalex-snapshot
Swarming of Proteus mirabilis over Ureteral Stents: A Comparative Assessment
inferredcites →https://doi.org/10.1094/mpmi-18-0682openalex-snapshot
Quorum Sensing Regulates Exopolysaccharide Production, Motility, and Virulence in Pseudomonas syringae
inferredcites →https://doi.org/10.1099/00221287-148-6-1785openalex-snapshot
Swarming motility in Bacillus cereus and characterization of a fliY mutant impaired in swarm cell differentiation The EMBL accession number for the sequence reported in this paper is Y08031.
inferredcites →https://doi.org/10.1099/13500872-140-1-49openalex-snapshot
Escherichia coli K12 regains its O antigen
inferredcites →https://doi.org/10.1099/13500872-145-7-1769openalex-snapshot
FliL is a membrane-associated component of the flagellar basal body of Salmonella
inferredcites →https://doi.org/10.1099/mic.0.2006/002576-0openalex-snapshot
Salmonella typhimurium flhE, a conserved flagellar regulon gene required for swarming
inferredcites →https://doi.org/10.1099/mic.0.26154-0openalex-snapshot
rhlA is required for the production of a novel biosurfactant promoting swarming motility in Pseudomonas aeruginosa: 3-(3-hydroxyalkanoyloxy)alkanoic acids (HAAs), the precursors of rhamnolipids
inferredcites →https://doi.org/10.1103/physreve.63.031915openalex-snapshot
Theory of periodic swarming of bacteria: Application to Proteus mirabilis
inferredcites →https://doi.org/10.1103/physreve.71.031908openalex-snapshot
Reaction-diffusion model for pattern formation inE. coliswarming colonies with slime
inferredcites →https://doi.org/10.1103/physrevlett.100.248101openalex-snapshot
Diffusion and Spatial Correlations in Suspensions of Swimming Particles
inferredcites →https://doi.org/10.1103/physrevlett.84.3017openalex-snapshot
Particle Diffusion in a Quasi-Two-Dimensional Bacterial Bath
inferredcites →https://doi.org/10.1103/physrevlett.93.098103openalex-snapshot
Self-Concentration and Large-Scale Coherence in Bacterial Dynamics
inferredcites →https://doi.org/10.1103/physrevlett.95.204501openalex-snapshot
Transport and Collective Dynamics in Suspensions of Confined Swimming Particles
inferredcites →https://doi.org/10.1103/physrevlett.98.158102openalex-snapshot
Concentration Dependence of the Collective Dynamics of Swimming Bacteria
inferredcites →https://doi.org/10.1111/j.1365-2958.1990.tb00678.xopenalex-snapshot
Surface‐induced swarmer cell differentiation of Vibrio parahaemoiyticus
inferredcites →https://doi.org/10.1111/j.1365-2958.1992.tb01451.xopenalex-snapshot
Four homologous domains in the primary structure of GrsB are related to domains in a superfamily of adenylate‐forming enzymes
inferredcites →https://doi.org/10.1111/j.1365-2958.1992.tb01498.xopenalex-snapshot
Four homologous domains in the primary structure of GrsB are related to domains in a superfamily of adenylate‐forming enzymes
inferredcites →https://doi.org/10.1111/j.1365-2958.1993.tb01202.xopenalex-snapshot
Cell differentiation of Proteus mirabilis is initiated by glutamine, a specific chemoattractant for swarming cells
inferredcites →https://doi.org/10.1111/j.1365-2958.1993.tb01629.xopenalex-snapshot
Sequence and analysis of the genetic locus responsible for surfactin synthesis in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.1994.tb00433.xopenalex-snapshot
Bees aren't the only ones: swarming in Gram‐negative bacteria
inferredcites →https://doi.org/10.1111/j.1365-2958.1995.mmi_17061167.xopenalex-snapshot
A cell‐surface polysaccharide that facilitates rapid population migration by differentiated swarm cells of Proteus mirabilis
inferredcites →https://doi.org/10.1111/j.1365-2958.1995.tb02383.xopenalex-snapshot
Requirement for FlhA in flagella assembly and swarm‐cell differentiation by Proteus mirabilis
inferredcites →https://doi.org/10.1111/j.1365-2958.1996.tb02495.xopenalex-snapshot
Involvement of N‐acyl‐ l ‐homoserine lactone autoinducers in controlling the multicellular behaviour of Serratia liquefaciens
inferredcites →https://doi.org/10.1111/j.1365-2958.1996.tb02509.xopenalex-snapshot
The sodium‐driven polar flagellar motor of marine Vibrio as the mechanosensor that regulates lateral flagellar expression
inferredcites →https://doi.org/10.1111/j.1365-2958.2003.03977.xopenalex-snapshot
Gene expression patterns during swarming in Salmonella typhimurium: genes specific to surface growth and putative new motility and pathogenicity genes
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.03996.xopenalex-snapshot
Genes governing swarming in Bacillus subtilis and evidence for a phase variation mechanism controlling surface motility
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04295.xopenalex-snapshot
Metabolic differentiation in actively swarming Salmonella
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05069.xopenalex-snapshot
The PmrA/PmrB and RcsC/YojN/RcsB systems control expression of the Salmonella O‐antigen chain length determinant
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05208.xopenalex-snapshot
A mechanical role for the chemotaxis system in swarming motility
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06170.xopenalex-snapshot
FliL is essential for swarming: motor rotation in absence of FliL fractures the flagellar rod in swarmer cells of Salmonella enterica
inferredcites →https://doi.org/10.1111/j.1462-2920.2007.01396.xopenalex-snapshot
Self‐produced extracellular stimuli modulate the Pseudomonas aeruginosa swarming motility behaviour
inferredcites →https://doi.org/10.1111/j.1574-6968.2006.00403.xopenalex-snapshot
Bacterial lateral flagella: an inducible flagella system
inferredcites →https://doi.org/10.1111/j.1574-6976.2007.00071.xopenalex-snapshot
Quorum sensing inSerratia
inferredcites →https://doi.org/10.1126/science.1058758openalex-snapshot
Ordering Genes in a Flagella Pathway by Analysis of Expression Kinetics from Living Bacteria
inferredcites →https://doi.org/10.1126/science.1110329openalex-snapshot
A Self-Organized Vortex Array of Hydrodynamically Entrained Sperm Cells
inferredcites →https://doi.org/10.1126/science.1137223openalex-snapshot
Evidence That Focal Adhesion Complexes Power Bacterial Gliding Motility
inferredcites →https://doi.org/10.1126/science.1140414openalex-snapshot
Long-Lived Giant Number Fluctuations in a Swarming Granular Nematic
inferredcites →https://doi.org/10.1128/.180.23.6126-6139.1998openalex-snapshot
Characterization of Proteus mirabilis Precocious Swarming Mutants: Identification of rsbA , Encoding a Regulator of Swarming Behavior
inferredcites →https://doi.org/10.1128/.180.23.6384-6388.1998openalex-snapshot
N -Acyl- l -Homoserine Lactone Autoinducers Control Production of an Extracellular Lipopeptide Biosurfactant Required for Swarming Motility of Serratia liquefaciens MG1
inferredcites →https://doi.org/10.1128/br.36.4.478-503.1972openalex-snapshot
Bacterial surface translocation: a survey and a classification
inferredcites →https://doi.org/10.1128/iai.72.12.6836-6845.2004openalex-snapshot
Modulation of Swarming and Virulence by Fatty Acids through the RsbA Protein inProteus mirabilis
inferredcites →https://doi.org/10.1128/iai.72.7.3941-3950.2004openalex-snapshot
Ultrastructure of Proteus mirabilis Swarmer Cell Rafts and Role of Swarming in Catheter-Associated Urinary Tract Infection
inferredcites →https://doi.org/10.1128/jb.01109-07openalex-snapshot
The Wetting Agent Required for Swarming in Salmonella enterica Serovar Typhimurium Is Not a Surfactant
inferredcites →https://doi.org/10.1128/jb.01198-07openalex-snapshot
The RcsCDB Signaling System and Swarming Motility inSalmonella entericaSerovar Typhimurium: Dual Regulation of Flagellar and SPI-2 Virulence Genes
inferredcites →https://doi.org/10.1128/jb.01294-06openalex-snapshot
Genome-Wide Screening of Genes Required for Swarming Motility inEscherichia coliK-12
inferredcites →https://doi.org/10.1128/jb.132.1.356-358.1977openalex-snapshot
Motility of flagellated bacteria in viscous environments
inferredcites →https://doi.org/10.1128/jb.154.2.930-937.1983openalex-snapshot
Extracellular slime associated with Proteus mirabilis during swarming
inferredcites →https://doi.org/10.1128/jb.162.3.1111-1119.1985openalex-snapshot
Regulation of capsular polysaccharide synthesis in Escherichia coli K-12: characterization of three regulatory genes
inferredcites →https://doi.org/10.1128/jb.167.1.210-218.1986openalex-snapshot
Regulation of lateral flagella gene transcription in Vibrio parahaemolyticus
inferredcites →https://doi.org/10.1128/jb.171.2.731-736.1989openalex-snapshot
Iron regulation of swarmer cell differentiation of Vibrio parahaemolyticus
inferredcites →https://doi.org/10.1128/jb.171.6.3560-3563.1989openalex-snapshot
Rapid bacterial swimming measured in swarming cells of Thiovulum majus
inferredcites →https://doi.org/10.1128/jb.172.1.334-341.1990openalex-snapshot
Chemotactic control of the two flagellar systems of Vibrio parahaemolyticus
inferredcites →https://doi.org/10.1128/jb.172.8.4322-4328.1990openalex-snapshot
Differentiation of Serratia marcescens 274 into swimmer and swarmer cells
inferredcites →https://doi.org/10.1128/jb.173.19.6279-6288.1991openalex-snapshot
Proteus mirabilis mutants defective in swarmer cell differentiation and multicellular behavior
inferredcites →https://doi.org/10.1128/jb.174.19.6125-6137.1992openalex-snapshot
Mutations that impair swarming motility in Serratia marcescens 274 include but are not limited to those affecting chemotaxis or flagellar function
inferredcites →https://doi.org/10.1128/jb.174.6.1769-1776.1992openalex-snapshot
A novel extracellular cyclic lipopeptide which promotes flagellum-dependent and -independent spreading growth of Serratia marcescens
inferredcites →https://doi.org/10.1128/jb.176.13.4144-4156.1994openalex-snapshot
Structure of the O antigen of Escherichia coli K-12 and the sequence of its rfb gene cluster
inferredcites →https://doi.org/10.1128/jb.176.23.7169-7181.1994openalex-snapshot
Expression of multiple flagellin-encoding genes of Proteus mirabilis
inferredcites →https://doi.org/10.1128/jb.176.8.2308-2311.1994openalex-snapshot
Characterization of the fliL gene in the flagellar regulon of Escherichia coli and Salmonella typhimurium
inferredcites →https://doi.org/10.1128/jb.177.3.823-828.1995openalex-snapshot
Genetic analysis of Proteus mirabilis mutants defective in swarmer cell elongation
inferredcites →https://doi.org/10.1128/jb.177.4.987-991.1995openalex-snapshot
Mutational analysis of flagellum-independent surface spreading of Serratia marcescens 274 on a low-agar medium
inferredcites →https://doi.org/10.1128/jb.178.2.554-559.1996openalex-snapshot
Differentiation of Serratia liquefaciens into swarm cells is controlled by the expression of the flhD master operon
inferredcites →https://doi.org/10.1128/jb.178.22.6525-6538.1996openalex-snapshot
Periodic phenomena in Proteus mirabilis swarm colony development
inferredcites →https://doi.org/10.1128/jb.178.7.1980-1989.1996openalex-snapshot
Patterns of reporter gene expression in the phase diagram of Bacillus subtilis colony forms
inferredcites →https://doi.org/10.1128/jb.179.17.5585-5588.1997openalex-snapshot
Negative feedback from a Proteus class II flagellum export defect to the flhDC master operon controlling cell division and flagellum assembly
inferredcites →https://doi.org/10.1128/jb.180.3.742-745.1998openalex-snapshot
Two Separate Regulatory Systems Participate in Control of Swarming Motility of Serratia liquefaciens MG1
inferredcites →https://doi.org/10.1128/jb.180.5.1009-1022.1998openalex-snapshot
Bacterial Locomotion and Signal Transduction
inferredcites →https://doi.org/10.1128/jb.181.2.600-609.1999openalex-snapshot
Organized Cell Swimming Motions in Bacillus subtilis Colonies: Patterns of Short-Lived Whirls and Jets
inferredcites →https://doi.org/10.1128/jb.181.6.1703-1712.1999openalex-snapshot
Surface Motility of Serratia liquefaciens MG1
inferredcites →https://doi.org/10.1128/jb.181.7.2008-2016.1999openalex-snapshot
A Novel Membrane Protein Influencing Cell Shape and Multicellular Swarming of Proteus mirabilis
inferredcites →https://doi.org/10.1128/jb.182.10.2793-2801.2000openalex-snapshot
Real-Time Imaging of Fluorescent Flagellar Filaments
inferredcites →https://doi.org/10.1128/jb.182.21.5990-5996.2000openalex-snapshot
Swarming of Pseudomonas aeruginosa Is Dependent on Cell-to-Cell Signaling and Requires Flagella and Pili
inferredcites →https://doi.org/10.1128/jb.182.22.6308-6321.2000openalex-snapshot
Genetics of Swarming Motility inSalmonella entericaSerovar Typhimurium: Critical Role for Lipopolysaccharide
inferredcites →https://doi.org/10.1128/jb.183.17.5187-5197.2001openalex-snapshot
Quorum Sensing Is a Global Regulatory Mechanism in Enterohemorrhagic Escherichia coli O157:H7
inferredcites →https://doi.org/10.1128/jb.183.20.5848-5854.2001openalex-snapshot
Salmonella enterica Serovar Typhimurium Swarming Mutants with Altered Biofilm-Forming Abilities: Surfactin Inhibits Biofilm Formation
inferredcites →https://doi.org/10.1128/jb.184.21.5946-5954.2002openalex-snapshot
Vibrio parahaemolyticus scrABC , a Novel Operon Affecting Swarming and Capsular Polysaccharide Regulation
inferredcites →https://doi.org/10.1128/jb.186.13.4159-4167.2004openalex-snapshot
Extracellular Proteolytic Activity Plays a Central Role in Swarming Motility inBacillus subtilis
inferredcites →https://doi.org/10.1128/jb.186.4.1158-1164.2004openalex-snapshot
Surface-Associated Flagellum Formation and Swarming Differentiation inBacillus subtilisAre Controlled by theifmLocus
inferredcites →https://doi.org/10.1128/jb.187.19.6789-6803.2005openalex-snapshot
The Ability ofProteus mirabilisTo Sense Surfaces and Regulate Virulence Gene Expression Involves FliL, a Flagellar Basal Body Protein
inferredcites →https://doi.org/10.1128/jb.187.21.7351-7361.2005openalex-snapshot
Rhamnolipids Modulate Swarming Motility Patterns ofPseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.92.1.121-129.1966openalex-snapshot
Effect of Amino Acids and Oxygen on Chemotaxis in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.95.2.732-733.1968openalex-snapshot
Enhancing effect of agar on swarming by Proteus
inferredcites →https://doi.org/10.1128/mmbr.64.4.694-708.2000openalex-snapshot
Coupling of Flagellar Gene Expression to Flagellar Assembly in Salmonella enterica Serovar Typhimurium and Escherichia coli
inferredcites →https://doi.org/10.1139/m66-017openalex-snapshot
CELLULAR CHANGES ACCOMPANYING THE SWARMING OF PROTEUS MIRABILIS: II. OBSERVATIONS OF STAINED ORGANISMS
inferredcites →https://doi.org/10.1143/jpsj.68.1436openalex-snapshot
Periodic Pattern Formation of Bacterial Colonies
inferredcites →https://doi.org/10.1146/annurev.biochem.72.121801.161737openalex-snapshot
The Rotary Motor of Bacterial Flagella
inferredcites →https://doi.org/10.1146/annurev.mi.32.100178.000533openalex-snapshot
Nature of the Swarming Phenomenon in Proteus
inferredcites →https://doi.org/10.1146/annurev.mi.49.100195.002421openalex-snapshot
HOW BACTERIA SENSE AND SWIM
inferredcites →https://doi.org/10.1146/annurev.micro.52.1.81openalex-snapshot
THINKING ABOUT BACTERIAL POPULATIONS AS MULTICELLULAR ORGANISMS
inferredcites →https://doi.org/10.1146/annurev.micro.57.030502.090832openalex-snapshot
How Bacteria Assemble Flagella
inferredcites →https://doi.org/10.1146/annurev.micro.57.030502.091014openalex-snapshot
Bacterial Motility on a Surface: Many Ways to a Common Goal
inferredcites →https://doi.org/10.1146/annurev.micro.59.050405.101230openalex-snapshot
THE RCS PHOSPHORELAY: A Complex Signal Transduction System
inferredcites →https://doi.org/10.1159/000077866openalex-snapshot
Dual Flagellar Systems Enable Motility under Different Circumstances
inferredcites →https://doi.org/10.1161/01.atv.0000218510.04541.5eopenalex-snapshot
The Multiple Languages of Endothelial Cell-to-Cell Communication
inferredcites →https://doi.org/10.3109/10408419309113526openalex-snapshot
Fractal Morphogenesis by a Bacterial Cell Population
inferredcites →https://doi.org/10.7883/yoken1952.38.141openalex-snapshot
PERITRICHOUS FLAGELLA IN MESOPHILIC STRAINS OF AEROMONAS
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781119850809.ch2openalex-snapshot
Control of Micro‐Particles with Liquid Crystals
inferred← citeshttps://doi.org/10.1002/adma.202006237openalex-snapshot
Programmable Design and Performance of Modular Magnetic Microswimmers
inferred← citeshttps://doi.org/10.1002/admt.202200450openalex-snapshot
Propulsion of Magnetic Beads Asymmetrically Covered with DNA Origami Appendages
inferred← citeshttps://doi.org/10.1002/ange.201301386openalex-snapshot
The Rate of Energy Dissipation Determines Probabilities of Non‐equilibrium Assemblies
inferred← citeshttps://doi.org/10.1002/ange.201804599openalex-snapshot
Dynamische Kopplung bei niedriger Reynoldszahl
inferred← citeshttps://doi.org/10.1002/anie.201301386openalex-snapshot
The Rate of Energy Dissipation Determines Probabilities of Non‐equilibrium Assemblies
inferred← citeshttps://doi.org/10.1002/anie.201804599openalex-snapshot
Dynamic Coupling at Low Reynolds Number
inferred← citeshttps://doi.org/10.1002/marc.202200250openalex-snapshot
2D Polymer Nanonets: Controllable Constructions and Functional Applications
inferred← citeshttps://doi.org/10.1002/wnan.70049openalex-snapshot
Living Organs as Micro‐Factories: Material‐Producing Organoids
inferred← citeshttps://doi.org/10.1007/978-1-0716-3060-0_13openalex-snapshot
Swarming Motility Assays in Salmonella
inferred← citeshttps://doi.org/10.1007/978-1-4939-1402-9_10openalex-snapshot
The Role of Biosurfactants in Bacterial Systems
inferred← citeshttps://doi.org/10.1007/978-1-4939-1402-9_4openalex-snapshot
Spatial Structure of Microbes in Nature and the Biophysics of Cell–Cell Communication
inferred← citeshttps://doi.org/10.1007/978-3-319-42913-7_35-1openalex-snapshot
Hydrodynamics in Motile Active Matter
inferred← citeshttps://doi.org/10.1007/978-3-319-44677-6_35openalex-snapshot
Hydrodynamics in Motile Active Matter
inferred← citeshttps://doi.org/10.1007/978-981-92-0108-2_8openalex-snapshot
Components of Biomaterials
inferred← citeshttps://doi.org/10.1007/s00203-020-02159-5openalex-snapshot
Quorum sensing systems, related virulence factors, and biofilm formation in Pseudomonas aeruginosa isolated from fish
inferred← citeshttps://doi.org/10.1007/s00294-021-01225-9openalex-snapshot
Genome-wide analysis reveals a rhamnolipid-dependent modulation of flagellar genes in Pseudomonas aeruginosa PAO1
inferred← citeshttps://doi.org/10.1007/s00354-020-00089-wopenalex-snapshot
Designing Dynamical Molecular Systems with the PEN Toolbox
inferred← citeshttps://doi.org/10.1007/s10404-012-1060-1openalex-snapshot
Fluidic assembly at the microscale: progress and prospects
inferred← citeshttps://doi.org/10.1007/s10867-019-09524-6openalex-snapshot
Active fluid with Acidithiobacillus ferrooxidans: correlations between swimming and the oxidation route
inferred← citeshttps://doi.org/10.1007/s11274-022-03238-zopenalex-snapshot
Genome analysis of Pseudomonas sp. 14A reveals metabolic capabilities to support epiphytic behavior
inferred← citeshttps://doi.org/10.1007/s12650-013-0159-0openalex-snapshot
Live-cell imaging of swarming bacteria in a fluidic biofilm formed on a soft agar gel substrate
inferred← citeshttps://doi.org/10.1007/s40484-015-0057-7openalex-snapshot
Collective motion of bacteria in two dimensions
inferred← citeshttps://doi.org/10.1007/s40843-017-9058-8openalex-snapshot
Collective motion of bacteria and their dynamic assembly behavior
inferred← citeshttps://doi.org/10.1016/b978-0-32-342993-1.00002-1openalex-snapshot
Motivation for microbiorobotics
inferred← citeshttps://doi.org/10.1016/b978-0-32-342993-1.00009-4openalex-snapshot
Development of active controllable tumor targeting bacteriobot
inferred← citeshttps://doi.org/10.1016/b978-1-4557-7891-1.00010-4openalex-snapshot
Bacteria-Powered Microrobots
inferred← citeshttps://doi.org/10.1016/b978-1-4557-7891-1.00014-1openalex-snapshot
Motivation for Microbiorobotics
inferred← citeshttps://doi.org/10.1016/bs.abl.2025.07.002openalex-snapshot
Recent advances in computational modeling of the effects of micro/nanoparticle interactions on vesicle morphology
inferred← citeshttps://doi.org/10.1016/j.bpj.2010.01.053openalex-snapshot
Dynamics of Bacterial Swarming
inferred← citeshttps://doi.org/10.1016/j.bpj.2011.07.019openalex-snapshot
Collective Motion of Surfactant-Producing Bacteria Imparts Superdiffusivity to Their Upper Surface
inferred← citeshttps://doi.org/10.1016/j.bpj.2016.05.043openalex-snapshot
Anomalous Fluctuations in the Orientation and Velocity of Swarming Bacteria
inferred← citeshttps://doi.org/10.1016/j.bpj.2019.06.005openalex-snapshot
Orbiting of Flagellated Bacteria within a Thin Fluid Film around Micrometer-Sized Particles
inferred← citeshttps://doi.org/10.1016/j.bpj.2021.02.021openalex-snapshot
Collective motion enhances chemotaxis in a two-dimensional bacterial swarm
inferred← citeshttps://doi.org/10.1016/j.bpj.2023.11.3279openalex-snapshot
Swarming bacterial fronts: Dynamics and morphology of active swarm interfaces propagating through passive frictional domains
inferred← citeshttps://doi.org/10.1016/j.bpj.2026.06.007openalex-snapshot
Motion-refined machine learning enables characterization of bacterial swarming dynamics
inferred← citeshttps://doi.org/10.1016/j.chaos.2022.112411openalex-snapshot
Ratchet transport of particles in the obstacle lattices with topographical gradients
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.129153openalex-snapshot
Resistance risk induced by quorum sensing inhibitors and their combined use with antibiotics: Mechanism and its relationship with toxicity
inferred← citeshttps://doi.org/10.1016/j.fbio.2026.110000openalex-snapshot
Synergistic antibacterial activities of ε-polylysine hydrochloride and sodium diacetate against Salmonella Typhimurium
inferred← citeshttps://doi.org/10.1016/j.hermed.2023.100688openalex-snapshot
Antibiofilm activity of Equisetum hyemale: interference with quorum sensing
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.132550openalex-snapshot
Cyclic olefin copolymer (COC) as a promising biomaterial for affecting bacterial colonization: investigation on Vibrio campbellii
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2019.118575openalex-snapshot
Hybrid Ofloxacin/eugenol co-loaded solid lipid nanoparticles with enhanced and targetable antimicrobial properties
inferred← citeshttps://doi.org/10.1016/j.isci.2019.09.007openalex-snapshot
Entrainment of the Circadian Clock of the Enteric Bacterium Klebsiella aerogenes by Temperature Cycles
inferred← citeshttps://doi.org/10.1016/j.isci.2019.11.012openalex-snapshot
Single Nanoparticle Tracking Reveals Efficient Long-Distance Undercurrent Transport in Upper Fluid of Bacterial Swarms
inferred← citeshttps://doi.org/10.1016/j.jde.2026.114127openalex-snapshot
Dynamics of an on-off self-propelled particle in a cellular flow
inferred← citeshttps://doi.org/10.1016/j.jelechem.2020.114472openalex-snapshot
Bifurcations induced by the electrode surface area during the electrochemical oxidation of bisulfite
inferred← citeshttps://doi.org/10.1016/j.jnnfm.2024.105245openalex-snapshot
Numerical study of collective motion of microswimmers in Giesekus viscoelastic fluids
inferred← citeshttps://doi.org/10.1016/j.micron.2012.01.014openalex-snapshot
Atomic force microscopy: A powerful tool for studying bacterial swarming motility
inferred← citeshttps://doi.org/10.1016/j.msec.2020.111267openalex-snapshot
Magnetic nanoparticles coated with carbohydrates for 3D culture of bacteria
inferred← citeshttps://doi.org/10.1016/j.physa.2015.01.080openalex-snapshot
Effective strategies of collective evacuation from an enclosed space
inferred← citeshttps://doi.org/10.1016/j.physa.2025.130897openalex-snapshot
From flocking to condensation: Collective dynamics in binary chiral active matter
inferred← citeshttps://doi.org/10.1016/j.physleta.2025.130626openalex-snapshot
Pseudo transitions in the finite-size Blume-capel model
inferred← citeshttps://doi.org/10.1016/j.snb.2013.08.040openalex-snapshot
Mixing of solutions by coordinated ciliary motion in Vorticella convallaria and patterning method for microfluidic applications
inferred← citeshttps://doi.org/10.1016/j.surfcoat.2016.12.076openalex-snapshot
The development of a Zr-Cu-Al-Ag-N thin film metallic glass coating in pursuit of improved mechanical, corrosion, and antimicrobial property for bio-medical application
inferred← citeshttps://doi.org/10.1016/j.surfcoat.2019.05.041openalex-snapshot
Antimicrobial properties of Cu-based bulk metallic glass composites after surface modification
inferred← citeshttps://doi.org/10.1016/j.tsf.2013.08.028openalex-snapshot
Antimicrobial properties of Zr–Cu–Al–Ag thin film metallic glass
inferred← citeshttps://doi.org/10.1017/9781316796047openalex-snapshot
The Fluid Dynamics of Cell Motility
inferred← citeshttps://doi.org/10.1017/9781316796047.004openalex-snapshot
The Fluid Dynamics of Microscopic Locomotion
inferred← citeshttps://doi.org/10.1017/9781316796047.008openalex-snapshot
Flagella and the Physics of Viscous Propulsion
inferred← citeshttps://doi.org/10.1017/9781316796047.009openalex-snapshot
Hydrodynamics of Slender Filaments
inferred← citeshttps://doi.org/10.1017/9781316796047.010openalex-snapshot
Waving of Eukaryotic Flagella
inferred← citeshttps://doi.org/10.1017/9781316796047.011openalex-snapshot
Rotation of Bacterial Flagellar Filaments
inferred← citeshttps://doi.org/10.1017/9781316796047.012openalex-snapshot
Flows and Stresses Induced by Cells
inferred← citeshttps://doi.org/10.1017/9781316796047.015openalex-snapshot
Self-Propulsion and Surfaces
inferred← citeshttps://doi.org/10.1017/9781316796047.016openalex-snapshot
Hydrodynamic Synchronisation
inferred← citeshttps://doi.org/10.1017/9781316796047.017openalex-snapshot
Diffusion and Noisy Swimming
inferred← citeshttps://doi.org/10.1017/9781316796047.018openalex-snapshot
Hydrodynamics of Collective Locomotion
inferred← citeshttps://doi.org/10.1017/9781316796047.019openalex-snapshot
Locomotion and Transport in Complex Fluids
inferred← citeshttps://doi.org/10.1017/jfm.2025.138openalex-snapshot
A regularised force-doublet framework for self-propelled microswimmers
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00389openalex-snapshot
Bicomponent Supramolecular Architectures at the Vacuum–Solid Interface
inferred← citeshttps://doi.org/10.1021/acs.jctc.4c00912openalex-snapshot
Dynamics and Collective Behavior of Chemically Propelled Janus Sphere Dimers in Complex Solvents
inferred← citeshttps://doi.org/10.1021/acs.langmuir.0c00516openalex-snapshot
Clustering and Phase Separation in Mixtures of Dipolar and Active Particles in an External Field
inferred← citeshttps://doi.org/10.1021/acs.langmuir.4c03395openalex-snapshot
Mucin Promotes Bacterial Swarming by Making the Agar Surface More Slippery
inferred← citeshttps://doi.org/10.1021/acsmaterialslett.6c00557openalex-snapshot
Bacterial Swarming-Guided Biomineralization Enables Pattern Formation in Engineered Living Materials
inferred← citeshttps://doi.org/10.1021/acsomega.6b00541openalex-snapshot
Template-Free Assembly in Living Bacterial Suspension under an External Electric Field
inferred← citeshttps://doi.org/10.1021/acsphotonics.3c00890openalex-snapshot
Emergence of Directional Rotation in an Optothermally Activated Colloidal System
inferred← citeshttps://doi.org/10.1038/ismej.2011.27openalex-snapshot
IS 5 inserts upstream of the master motility operon flhDC in a quasi-Lamarckian way
inferred← citeshttps://doi.org/10.1038/ncomms9396openalex-snapshot
Swarming bacteria migrate by Lévy Walk
inferred← citeshttps://doi.org/10.1038/s41396-020-00764-2openalex-snapshot
To hunt or to rest: prey depletion induces a novel starvation survival strategy in bacterial predators
inferred← citeshttps://doi.org/10.1038/s41396-021-01124-4openalex-snapshot
Kin discrimination drives territorial exclusion during Bacillus subtilis swarming and restrains exploitation of surfactin
inferred← citeshttps://doi.org/10.1038/s41467-019-09818-2openalex-snapshot
Self-organization of swimmers drives long-range fluid transport in bacterial colonies
inferred← citeshttps://doi.org/10.1038/s41467-019-12153-1openalex-snapshot
Surface association sensitizes Pseudomonas aeruginosa to quorum sensing
inferred← citeshttps://doi.org/10.1038/s41564-026-02505-1openalex-snapshot
Bacteria regulate collective behaviour by mechanosensing cell–cell collisions
inferred← citeshttps://doi.org/10.1038/s41579-021-00626-4openalex-snapshot
Bacterial motility: machinery and mechanisms
inferred← citeshttps://doi.org/10.1038/s41598-018-34192-2openalex-snapshot
The 3D architecture of a bacterial swarm has implications for antibiotic tolerance
inferred← citeshttps://doi.org/10.1038/s42005-022-00820-7openalex-snapshot
Emergence of active turbulence in microswimmer suspensions due to active hydrodynamic stress and volume exclusion
inferred← citeshttps://doi.org/10.1038/s42005-025-01996-4openalex-snapshot
Immobility of isolated swarmer cells due to local liquid depletion
inferred← citeshttps://doi.org/10.1038/s42005-025-02479-2openalex-snapshot
Variational approach to open quantum systems with long-range competing interactions
inferred← citeshttps://doi.org/10.1038/s42254-023-00593-0openalex-snapshot
Proliferating active matter
inferred← citeshttps://doi.org/10.1038/srep36702openalex-snapshot
Intermediate scattering function of an anisotropic active Brownian particle
inferred← citeshttps://doi.org/10.1039/9781839169465-00354openalex-snapshot
Computational Physics of Active Matter
inferred← citeshttps://doi.org/10.1039/c000463dopenalex-snapshot
Motility enhancement of bacteria actuated microstructures using selective bacteria adhesion
inferred← citeshttps://doi.org/10.1039/c0py00024hopenalex-snapshot
Dynamic supramacromolecular self-assembly: deformable polymer fabricated nanostructures through a host-controlled approach
inferred← citeshttps://doi.org/10.1039/c0sm00164copenalex-snapshot
Swimmer-tracer scattering at low Reynolds number
inferred← citeshttps://doi.org/10.1039/c0sm01106aopenalex-snapshot
Understanding energy dissipation and thermodynamics in biomotor-driven nanocomposite assemblies
inferred← citeshttps://doi.org/10.1039/c1cc14705fopenalex-snapshot
Polyacrylamide hydrogels as substrates for studying bacteria
inferred← citeshttps://doi.org/10.1039/c1sm06002copenalex-snapshot
Surface tension gradient control of bacterial swarming in colonies of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1039/c2sm26460aopenalex-snapshot
Flow-controlled densification and anomalous dispersion of E. coli through a constriction
inferred← citeshttps://doi.org/10.1039/c3ib40130hopenalex-snapshot
From swimming to swarming: Escherichia coli cell motility in two-dimensions
inferred← citeshttps://doi.org/10.1039/c3sm52120fopenalex-snapshot
Dynamics of self-organized rotating spiral-coils in bacterial swarms
inferred← citeshttps://doi.org/10.1039/c5sm01412copenalex-snapshot
Virial pressure in systems of spherical active Brownian particles
inferred← citeshttps://doi.org/10.1039/c5sm02965aopenalex-snapshot
Dynamics of flexible active Brownian dumbbells in the absence and the presence of shear flow
inferred← citeshttps://doi.org/10.1039/c5tb01880copenalex-snapshot
Impact of confining 3-D polymer networks on dynamics of bacterial ingress and self-organisation
inferred← citeshttps://doi.org/10.1039/c6sm01424kopenalex-snapshot
Modeling a spheroidal microswimmer and cooperative swimming in a narrow slit
inferred← citeshttps://doi.org/10.1039/c6sm01532hopenalex-snapshot
Bacterial swarmer cells in confinement: a mesoscale hydrodynamic simulation study
inferred← citeshttps://doi.org/10.1039/c7sm02301dopenalex-snapshot
Maximum in density heterogeneities of active swimmers
inferred← citeshttps://doi.org/10.1039/c8sm01366gopenalex-snapshot
Clustering and phase separation of circle swimmers dispersed in a monolayer
inferred← citeshttps://doi.org/10.1039/c8sm01390jopenalex-snapshot
Clustering of microswimmers: interplay of shape and hydrodynamics
inferred← citeshttps://doi.org/10.1039/c9sm00144aopenalex-snapshot
Flow and clogging of particles in shaking random obstacles
inferred← citeshttps://doi.org/10.1039/c9sm00159jopenalex-snapshot
Collective oscillation in dense suspension of self-propelled chiral rods
inferred← citeshttps://doi.org/10.1039/c9sm00391fopenalex-snapshot
Active Brownian filaments with hydrodynamic interactions: conformations and dynamics
inferred← citeshttps://doi.org/10.1039/c9sm02311aopenalex-snapshot
Clustering and phase separation in mixtures of dipolar and active particles
inferred← citeshttps://doi.org/10.1039/d0sm00571aopenalex-snapshot
Wall entrapment of peritrichous bacteria: a mesoscale hydrodynamics simulation study
inferred← citeshttps://doi.org/10.1039/d0sm00719fopenalex-snapshot
Light-powered active colloids from monodisperse and highly tunable microspheres with a thin TiO 2 shell
inferred← citeshttps://doi.org/10.1039/d1sm00311aopenalex-snapshot
Mechanistic underpinning of cell aspect ratio-dependent emergent collective motions in swarming bacteria
inferred← citeshttps://doi.org/10.1039/d1sm01065dopenalex-snapshot
Morphologies and dynamics of the interfaces between active and passive phases
inferred← citeshttps://doi.org/10.1039/d3sm00572kopenalex-snapshot
Self-buckling and self-writhing of semi-flexible microorganisms
inferred← citeshttps://doi.org/10.1039/d5sm00192gopenalex-snapshot
Turbulent-like flows in quasi two-dimensional dense suspensions of motile colloids
inferred← citeshttps://doi.org/10.1042/bst20200972openalex-snapshot
Biofilm and swarming emergent behaviours controlled through the aid of biophysical understanding and tools
inferred← citeshttps://doi.org/10.1063/1.4774041openalex-snapshot
Mechanics of swimming of multi-body bacterial swarmers using non-labeled cell tracking algorithm
inferred← citeshttps://doi.org/10.1063/1.4918978openalex-snapshot
Hydrodynamics of a self-actuated bacterial carpet using microscale particle image velocimetry
inferred← citeshttps://doi.org/10.1063/1.5049719openalex-snapshot
Transport of particles driven by the traveling obstacle arrays
inferred← citeshttps://doi.org/10.1063/1.5085755openalex-snapshot
Hydrodynamic interactions dominate the structure of active swimmers’ pair distribution functions
inferred← citeshttps://doi.org/10.1063/5.0005013openalex-snapshot
Rectification and separation of mixtures of active and passive particles driven by temperature difference
inferred← citeshttps://doi.org/10.1063/5.0011466openalex-snapshot
The physics of active polymers and filaments
inferred← citeshttps://doi.org/10.1063/5.0062290openalex-snapshot
Effective medium model for a suspension of active swimmers
inferred← citeshttps://doi.org/10.1063/5.0096955openalex-snapshot
Designing, synthesizing, and modeling active fluids
inferred← citeshttps://doi.org/10.1073/pnas.1001651107openalex-snapshot
Collective motion and density fluctuations in bacterial colonies
inferred← citeshttps://doi.org/10.1073/pnas.1016693108openalex-snapshot
Microbubbles reveal chiral fluid flows in bacterial swarms
inferred← citeshttps://doi.org/10.1073/pnas.1019079108openalex-snapshot
Fluid dynamics and noise in bacterial cell–cell and cell–surface scattering
inferred← citeshttps://doi.org/10.1073/pnas.1118238109openalex-snapshot
Water reservoir maintained by cell growth fuels the spreading of a bacterial swarm
inferred← citeshttps://doi.org/10.1073/pnas.1202032109openalex-snapshot
Meso-scale turbulence in living fluids
inferred← citeshttps://doi.org/10.1073/pnas.1613007114openalex-snapshot
Cell morphology drives spatial patterning in microbial communities
inferred← citeshttps://doi.org/10.1073/pnas.1811722116openalex-snapshot
Learning the space-time phase diagram of bacterial swarm expansion
inferred← citeshttps://doi.org/10.1073/pnas.1917789117openalex-snapshot
Dynamic motility selection drives population segregation in a bacterial swarm
inferred← citeshttps://doi.org/10.1073/pnas.2220033120openalex-snapshot
Decoding the hydrodynamic properties of microscale helical propellers from Brownian fluctuations
inferred← citeshttps://doi.org/10.1073/pnas.2534573123openalex-snapshot
Initiation of swarming in Bacillus subtilis as a resolution for the sorites paradox in bacteria
inferred← citeshttps://doi.org/10.1080/08927014.2012.725130openalex-snapshot
Tannin derived materials can block swarming motility and enhance biofilm formation inPseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1088/0034-4885/78/5/056601openalex-snapshot
Physics of microswimmers—single particle motion and collective behavior: a review
inferred← citeshttps://doi.org/10.1088/0953-8984/24/46/464130openalex-snapshot
Emergent states in dense systems of active rods: from swarming to turbulence
inferred← citeshttps://doi.org/10.1088/1361-648x/aa5a40openalex-snapshot
Lattice Boltzmann simulations of the bead-spring microswimmer with a responsive stroke—from an individual to swarms
inferred← citeshttps://doi.org/10.1088/1361-648x/ae4933openalex-snapshot
Confined floating active carpets generate coherent vortical flows that enhance transport
inferred← citeshttps://doi.org/10.1088/1361-6633/ad3e11openalex-snapshot
Non-equilibrium structural and dynamic behaviors of active polymers in complex and crowded environments
inferred← citeshttps://doi.org/10.1088/1367-2630/aa8ed7openalex-snapshot
How many dissenters does it take to disorder a flock?
inferred← citeshttps://doi.org/10.1088/1478-3975/8/5/055003openalex-snapshot
Self-organization in bacterial swarming: lessons from myxobacteria
inferred← citeshttps://doi.org/10.1088/1757-899x/577/1/012046openalex-snapshot
Rotational dynamics of Bacillus subtilis in an optical trap
inferred← citeshttps://doi.org/10.1088/2632-072x/ad9b63openalex-snapshot
Swarming network inference with importance clustering of relative interactions
inferred← citeshttps://doi.org/10.1089/ast.2014.1162openalex-snapshot
Drying Bacterial Biosaline Patterns Capable of Vital Reanimation upon Rehydration: Novel Hibernating Biomineralogical Life Formations
inferred← citeshttps://doi.org/10.1098/rsif.2009.0223openalex-snapshot
Suspension biomechanics of swimming microbes
inferred← citeshttps://doi.org/10.1098/rsif.2018.0960openalex-snapshot
Quenching active swarms: effects of light exposure on collective motility in swarming Serratia marcescens
inferred← citeshttps://doi.org/10.1098/rsif.2020.0147openalex-snapshot
Bacterial surface motility is modulated by colony-scale flow and granular jamming
inferred← citeshttps://doi.org/10.1098/rstb.2017.0106openalex-snapshot
Emergence of evolutionary driving forces in pattern-forming microbial populations
inferred← citeshttps://doi.org/10.1099/mic.0.000426openalex-snapshot
Environment-directed activation of the Escherichia coli flhDC operon by transposons
inferred← citeshttps://doi.org/10.1101/331801openalex-snapshot
Quenching an active swarm: Effects of light exposure on collective motility in swarming Serratia marcescens colonies
inferred← citeshttps://doi.org/10.1101/657353openalex-snapshot
Single Nanoparticle Tracking Reveals Efficient Long-Distance Undercurrent Transport above Swarming Bacteria
inferred← citeshttps://doi.org/10.1101/719245openalex-snapshot
Physical factors contributing to regulation of bacterial surface motility
inferred← citeshttps://doi.org/10.1103/9tdw-3y1bopenalex-snapshot
Redirecting countermoving swarms through collision
inferred← citeshttps://doi.org/10.1103/gqf6-nbl4openalex-snapshot
Attraction-induced cluster fragmentation and local alignment in active particle systems
inferred← citeshttps://doi.org/10.1103/physreve.100.042603openalex-snapshot
Transport coefficients of self-propelled particles: Reverse perturbations and transverse current correlations
inferred← citeshttps://doi.org/10.1103/physreve.101.052612openalex-snapshot
Hydrodynamics of polymers in an active bath
inferred← citeshttps://doi.org/10.1103/physreve.103.032413openalex-snapshot
Heterogeneous bacterial swarms with mixed lengths
inferred← citeshttps://doi.org/10.1103/physreve.108.034303openalex-snapshot
Phase transitions on a multiplex of swarmalators
inferred← citeshttps://doi.org/10.1103/physreve.109.064402openalex-snapshot
Run-and-tumble kinematics of Enterobacter Sp. SM3
inferred← citeshttps://doi.org/10.1103/physreve.111.054128openalex-snapshot
Geometric properties of the additional third-order transitions in the two-dimensional Potts model
inferred← citeshttps://doi.org/10.1103/physreve.80.021903openalex-snapshot
Noisy swimming at low Reynolds numbers
inferred← citeshttps://doi.org/10.1103/physreve.83.061907openalex-snapshot
Dynamics of swimming bacteria: Transition to directional order at high concentration
inferred← citeshttps://doi.org/10.1103/physreve.84.011914openalex-snapshot
Motor-driven dynamics of cytoskeletal filaments in motility assays
inferred← citeshttps://doi.org/10.1103/physreve.85.041913openalex-snapshot
Modeling the role of water inBacillus subtiliscolonies
inferred← citeshttps://doi.org/10.1103/physreve.87.032712openalex-snapshot
Vortex arrays as emergent collective phenomena for circle swimmers
inferred← citeshttps://doi.org/10.1103/physreve.92.062706openalex-snapshot
Nontoxic colloidal particles impede antibiotic resistance of swarming bacteria by disrupting collective motion and speed
inferred← citeshttps://doi.org/10.1103/physreve.94.022406openalex-snapshot
Front structure and dynamics in dense colonies of motile bacteria: Role of active turbulence
inferred← citeshttps://doi.org/10.1103/physreve.96.022407openalex-snapshot
Role of tumbling in bacterial swarming
inferred← citeshttps://doi.org/10.1103/physreve.96.050601openalex-snapshot
Discontinuous fluidization transition in time-correlated assemblies of actively deforming particles
inferred← citeshttps://doi.org/10.1103/physreve.97.020401openalex-snapshot
Self-organization in a bimotility mixture of model microswimmers
inferred← citeshttps://doi.org/10.1103/physreve.98.032415openalex-snapshot
Collective dynamics of two-dimensional swimming bacteria: Experiments and models
inferred← citeshttps://doi.org/10.1103/physrevfluids.1.043202openalex-snapshot
Flagellar flows around bacterial swarms
inferred← citeshttps://doi.org/10.1103/physrevlett.108.098102openalex-snapshot
Collective Motion and Nonequilibrium Cluster Formation in Colonies of Gliding Bacteria
inferred← citeshttps://doi.org/10.1103/physrevlett.109.248109openalex-snapshot
Physical Properties of Collective Motion in Suspensions of Bacteria
inferred← citeshttps://doi.org/10.1103/physrevlett.110.228102openalex-snapshot
Fluid Dynamics of Bacterial Turbulence
inferred← citeshttps://doi.org/10.1103/physrevlett.111.208101openalex-snapshot
Loss of Collective Motion in Swarming Bacteria Undergoing Stress
inferred← citeshttps://doi.org/10.1103/physrevlett.113.138101openalex-snapshot
Tangling of Tethered Swimmers: Interactions between Two Nematodes
inferred← citeshttps://doi.org/10.1103/physrevlett.113.218101openalex-snapshot
Trapping of Swimming Microorganisms at Lower Surfaces by Increasing Buoyancy
inferred← citeshttps://doi.org/10.1103/physrevlett.114.018105openalex-snapshot
Antibiotic-Induced Anomalous Statistics of Collective Bacterial Swarming
inferred← citeshttps://doi.org/10.1103/physrevlett.118.158002openalex-snapshot
Effect of Cell Aspect Ratio on Swarming Bacteria
showing the first 200 of 286 · page through all 286
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.