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Antibiofilm Properties of Temporin-L on Pseudomonas fluorescens in Static and In-Flow Conditions
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bit.10189openalex-snapshot
Effect of flow regime on the architecture of a Pseudomonas fluorescens biofilm
inferredcites →https://doi.org/10.1007/bf01569983openalex-snapshot
Biofilm formation in laminar flow usingPseudomonas fluorescens EX101
inferredcites →https://doi.org/10.1007/s00449-018-1909-0openalex-snapshot
Turbulence accelerates the growth of drinking water biofilms
inferredcites →https://doi.org/10.1016/j.bbagen.2020.129606openalex-snapshot
The antimicrobial peptide Temporin L impairs E. coli cell division by interacting with FtsZ and the divisome complex
inferredcites →https://doi.org/10.1016/j.bbamem.2015.10.013openalex-snapshot
Antimicrobial peptides and their interaction with biofilms of medically relevant bacteria
inferredcites →https://doi.org/10.1016/j.cbpa.2006.10.016openalex-snapshot
Applications of microfluidics in chemical biology
inferredcites →https://doi.org/10.1016/j.cell.2015.05.005openalex-snapshot
The Mechanical World of Bacteria
inferredcites →https://doi.org/10.1016/j.colsurfb.2020.111047openalex-snapshot
The role of flow in bacterial biofilm morphology and wetting properties
inferredcites →https://doi.org/10.1016/j.peptides.2015.05.012openalex-snapshot
Antimicrobial peptides: Possible anti-infective agents
inferredcites →https://doi.org/10.1038/nmicrobiol.2015.5openalex-snapshot
Local and global consequences of flow on bacterial quorum sensing
inferredcites →https://doi.org/10.1046/j.1365-2672.2001.01244.xopenalex-snapshot
Metabolic response of biofilm to shear stress in fixed-film culture
inferredcites →https://doi.org/10.1074/jbc.m800495200openalex-snapshot
Lipopolysaccharide, a Key Molecule Involved in the Synergism between Temporins in Inhibiting Bacterial Growth and in Endotoxin Neutralization
inferredcites →https://doi.org/10.1080/08927010701368476openalex-snapshot
The effect of hydrodynamic conditions on the phenotype of Pseudomonas fluorescens biofilms
inferredcites →https://doi.org/10.1080/08927010903114603openalex-snapshot
The influence of flow cell geometry related shear stresses on the distribution, structure and susceptibility ofPseudomonas aeruginosa01 biofilms
inferredcites →https://doi.org/10.1080/08927014.2016.1194401openalex-snapshot
Anti-biofilm properties of the antimicrobial peptide temporin 1Tb and its ability, in combination with EDTA, to eradicate Staphylococcus epidermidis biofilms on silicone catheters
inferredcites →https://doi.org/10.1097/00002480-200011000-00037openalex-snapshot
Role of Biofilms in Antimicrobial Resistance
inferredcites →https://doi.org/10.1097/01.blo.0000175714.68624.74openalex-snapshot
Biofilms and Antimicrobial Resistance
inferredcites →https://doi.org/10.1098/rsif.2010.0096openalex-snapshot
Laminar flow around corners triggers the formation of biofilm streamers
inferredcites →https://doi.org/10.1099/00221287-146-10-2395openalex-snapshot
Quantification of biofilm structures by the novel computer program comstat
inferredcites →https://doi.org/10.1111/j.1365-2672.1998.tb05279.xopenalex-snapshot
Influence of hydrodynamics and nutrients on biofilm structure
inferredcites →https://doi.org/10.1124/pr.55.1.2openalex-snapshot
Mechanisms of Antimicrobial Peptide Action and Resistance
inferredcites →https://doi.org/10.1128/aem.00175-11openalex-snapshot
Induction of Attachment-Independent Biofilm Formation and Repression ofhfqExpression by Low-Fluid-Shear Culture of Staphylococcus aureus
inferredcites →https://doi.org/10.1128/aem.01139-12openalex-snapshot
Fluid Flow Induces Biofilm Formation in Staphylococcus epidermidis Polysaccharide Intracellular Adhesin-Positive Clinical Isolates
inferredcites →https://doi.org/10.1128/cmr.00044-14openalex-snapshot
Microbiology, Genomics, and Clinical Significance of the Pseudomonas fluorescens Species Complex, an Unappreciated Colonizer of Humans
inferredcites →https://doi.org/10.1128/iai.00318-08openalex-snapshot
Human Host Defense Peptide LL-37 Prevents Bacterial Biofilm Formation
inferredcites →https://doi.org/10.1128/jb.00118-16openalex-snapshot
Microfluidic Studies of Biofilm Formation in Dynamic Environments
inferredcites →https://doi.org/10.1128/jb.00858-07openalex-snapshot
The EPS Matrix: The “House of Biofilm Cells”
inferredcites →https://doi.org/10.1128/jcm.22.6.996-1006.1985openalex-snapshot
Adherence of coagulase-negative staphylococci to plastic tissue culture plates: a quantitative model for the adherence of staphylococci to medical devices
inferredcites →https://doi.org/10.1128/msphere.00372-19openalex-snapshot
Observations of Shear Stress Effects on Staphylococcus aureus Biofilm Formation
inferredcites →https://doi.org/10.1146/annurev-biophys-051013-022916openalex-snapshot
Microfluidics Expanding the Frontiers of Microbial Ecology
inferredcites →https://doi.org/10.1146/annurev.micro.56.012302.160705openalex-snapshot
Biofilms as Complex Differentiated Communities
inferredcites →https://doi.org/10.1371/journal.pone.0175197openalex-snapshot
Bacterial biofilm under flow: First a physical struggle to stay, then a matter of breathing
inferredcites →https://doi.org/10.3389/fmicb.2011.00128openalex-snapshot
Susceptibility of Pseudomonas aeruginosa Biofilm to Alpha-Helical Peptides: D-enantiomer of LL-37
inferredcites →https://doi.org/10.3390/biom10040652openalex-snapshot
Antimicrobial and Antibiofilm Peptides
inferredcites →https://doi.org/10.3390/ma11122468openalex-snapshot
Action of Antimicrobial Peptides against Bacterial Biofilms
inferredcites →https://doi.org/10.3748/wjg.v19.i7.1056openalex-snapshot
Pseudomonas fluorescens-like bacteria from the stomach: A microbiological and molecular study
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.4641673openalex-extracted
The Role of Air Relative Humidity on the Wettability of Pseudomonas Fluorescens AR11 Biofilms
inferred← citeshttps://doi.org/10.1002/9781394299188.ch12openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10989-025-10687-1openalex-snapshot
Antimicrobial and Antibiofilm Activity of Analogous Synthetic Peptides from Anoplin, Temporin, and Aurein
inferred← citeshttps://doi.org/10.1007/s11756-024-01703-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-91160-3.00007-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-95756-4.00009-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-13288-9.00001-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106440openalex-snapshot
Introduction of a β-leucine residue instead of leucine9 and glycine10 residues in Temporin L for improved cell selectivity, stability and activity against planktonic and biofilm of methicillin resistant S. aureus
inferred← citeshttps://doi.org/10.1016/j.fbio.2025.106864openalex-snapshot
Promising eco-friendly agents targeting Pseudomonas fluorescens biofilms
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.1c01033openalex-snapshot
First-in-Class Cyclic Temporin L Analogue: Design, Synthesis, and Antimicrobial Assessment
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c01984openalex-snapshot
Probing Guanidino Pendant or Bridged Groups in Cyclic Antimicrobial Peptides Derived from Temporin L: A Strategy to Improve Efficacy against Gram-Negative Bacteria
inferred← citeshttps://doi.org/10.1021/acs.langmuir.3c00179openalex-snapshot
Forced Wetting Properties of Bacteria-Laden Droplets Experiencing Initial Evaporation
inferred← citeshttps://doi.org/10.1038/s41598-024-60601-wopenalex-snapshot
Vesicle protrusion induced by antimicrobial peptides suggests common carpet mechanism for short antimicrobial peptides
inferred← citeshttps://doi.org/10.1080/08927014.2026.2630941openalex-snapshot
Sequential attachment and Listeria predominance under turbulent flow
inferred← citeshttps://doi.org/10.1088/1748-605x/ad6549openalex-snapshot
Se-functionalized ZIF-8 nanoparticles: synthesis, characterization and disruption of biofilms and quorum sensing in Serratia marcescens
inferred← citeshttps://doi.org/10.1088/1757-899x/1265/1/012003openalex-snapshot
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inferred← citeshttps://doi.org/10.1155/bri/8058282openalex-snapshot
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inferred← citeshttps://doi.org/10.11606/t.46.2023.tde-11122023-182928openalex-snapshot
How do antimicrobial peptides destroy membranes? A Molecular Dynamics perspective
inferred← citeshttps://doi.org/10.1186/s40643-025-00988-0openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/biom12060759openalex-snapshot
Discovery of a Novel Antimicrobial Peptide, Temporin-PKE, from the Skin Secretion of Pelophylax kl. esculentus, and Evaluation of Its Structure-Activity Relationships
inferred← citeshttps://doi.org/10.3390/coatings11030294openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/foods11182809openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms222111401openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms232112732openalex-snapshot
Antimicrobial Peptides Mediate Apoptosis by Changing Mitochondrial Membrane Permeability
inferred← citeshttps://doi.org/10.3390/ijms24065426openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microorganisms11030621openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules27092675openalex-snapshot
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