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Vegetative Cell and Spore Proteomes of Clostridioides difficile show finite differences and reveal potential biomarkers.
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/jama.2014.17103openalex-snapshot
Diagnosis and Treatment ofClostridium difficilein Adults
inferredcites →https://doi.org/10.1002/prca.201600069openalex-snapshot
The protein inventory of Clostridium difficile grown in complex and minimal medium
inferredcites →https://doi.org/10.1002/prca.201700169openalex-snapshot
"One‐Pot" Sample Processing Method for Proteome‐Wide Analysis of Microbial Cells and Spores
inferredcites →https://doi.org/10.1002/yea.320080703openalex-snapshot
Effect of benzoic acid on metabolic fluxes in yeasts: A continuous‐culture study on the regulation of respiration and alcoholic fermentation
inferredcites →https://doi.org/10.1007/s00216-007-1486-6openalex-snapshot
Quantitative mass spectrometry in proteomics: a critical review
inferredcites →https://doi.org/10.1007/s00253-009-2063-zopenalex-snapshot
Production of yeastolates for uniform stable isotope labelling in eukaryotic cell culture
inferredcites →https://doi.org/10.1007/s10858-015-9954-3openalex-snapshot
An economic approach to efficient isotope labeling in insect cells using homemade 15N-, 13C- and 2H-labeled yeast extracts
inferredcites →https://doi.org/10.1016/0968-0004(96)30015-7openalex-snapshot
The UBA domain: a sequence motif present in multiple enzyme classes of the ubiquitination pathway
inferredcites →https://doi.org/10.1016/j.chembiol.2015.10.006openalex-snapshot
Quantitative Lipoproteomics in Clostridium difficile Reveals a Role for Lipoproteins in Sporulation
inferredcites →https://doi.org/10.1016/j.jprot.2015.03.035openalex-snapshot
Protein composition of the outermost exosporium-like layer of Clostridium difficile 630 spores
inferredcites →https://doi.org/10.1016/j.pep.2012.06.019openalex-snapshot
Expression and characterization of 15N-labeled human C-reactive protein in Escherichia coli and Pichia pastoris for use in isotope-dilution mass spectrometry
inferredcites →https://doi.org/10.1016/j.tibs.2004.05.007openalex-snapshot
The rocky roots of the acetyl-CoA pathway
inferredcites →https://doi.org/10.1016/j.tim.2014.04.003openalex-snapshot
Clostridium difficile spore biology: sporulation, germination, and spore structural proteins
inferredcites →https://doi.org/10.1016/s0092-8674(02)01132-7openalex-snapshot
CNF1 Exploits the Ubiquitin-Proteasome Machinery to Restrict Rho GTPase Activation for Bacterial Host Cell Invasion
inferredcites →https://doi.org/10.1016/s0143-4160(02)00125-2openalex-snapshot
Expression of a P-type Ca2+-transport ATPase in Bacillus subtilis during sporulation
inferredcites →https://doi.org/10.1021/pr200327topenalex-snapshot
Quantitative Proteomic Analysis of the Heat Stress Response in Clostridium difficile Strain 630
inferredcites →https://doi.org/10.1021/pr3007528openalex-snapshot
Proteomic Comparison of Historic and Recently Emerged Hypervirulent Clostridium difficile Strains
inferredcites →https://doi.org/10.1021/pr4005629openalex-snapshot
In Pursuit of Protein Targets: Proteomic Characterization of Bacterial Spore Outer Layers
inferredcites →https://doi.org/10.1038/nbt.2839openalex-snapshot
ProteomeXchange provides globally coordinated proteomics data submission and dissemination
inferredcites →https://doi.org/10.1038/nprot.2008.211openalex-snapshot
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
inferredcites →https://doi.org/10.1038/nrgastro.2012.156openalex-snapshot
The role of the gut microbiota in nutrition and health
inferredcites →https://doi.org/10.1038/nrmicro1772openalex-snapshot
Control of key metabolic intersections in Bacillus subtilis
inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00663.xopenalex-snapshot
Regulated transcription of Clostridium difficile toxin genes
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.02892.xopenalex-snapshot
Role of rubrerythrin in the oxidative stress response of Porphyromonas gingivalis
inferredcites →https://doi.org/10.1073/pnas.97.24.13027openalex-snapshot
A nucleolar protein related to ribosomal protein L7 is required for an early step in large ribosomal subunit biogenesis
inferredcites →https://doi.org/10.1074/jbc.m005619200openalex-snapshot
A Simplifed Functional Version of the Escherichia coli Sulfite Reductase
inferredcites →https://doi.org/10.1074/jbc.m008470200openalex-snapshot
A Novel Type of Iron Hydrogenase in the Green AlgaScenedesmus obliquus Is Linked to the Photosynthetic Electron Transport Chain
inferredcites →https://doi.org/10.1074/jbc.m111.259150openalex-snapshot
Clostridium difficile Has an Original Peptidoglycan Structure with a High Level of N-Acetylglucosamine Deacetylation and Mainly 3-3 Cross-links
inferredcites →https://doi.org/10.1074/jbc.ra118.004273openalex-snapshot
N-Deacetylases required for muramic-δ-lactam production are involved in Clostridium difficile sporulation, germination, and heat resistance
inferredcites →https://doi.org/10.1093/infdis/jir112openalex-snapshot
Clostridium difficile Transcriptome Analysis Using Pig Ligated Loop Model Reveals Modulation of Pathways Not Modulated In Vitro
inferredcites →https://doi.org/10.1093/jaoac/94.2.618openalex-snapshot
Clospore: A Liquid Medium for Producing High Titers of Semi-purified Spores of Clostridium difficile
inferredcites →https://doi.org/10.1093/nar/gkl334openalex-snapshot
The Pathway Tools cellular overview diagram and Omics Viewer
inferredcites →https://doi.org/10.1097/mco.0b013e3283619e63openalex-snapshot
Carbohydrates and the human gut microbiota
inferredcites →https://doi.org/10.1099/jmm.0.070409-0openalex-snapshot
Comparative proteomic analysis of Clostridium difficile isolates of varying virulence
inferredcites →https://doi.org/10.1099/mic.0.032771-0openalex-snapshot
The surprising diversity of clostridial hydrogenases: a comparative genomic perspective
inferredcites →https://doi.org/10.1105/tpc.106.044891openalex-snapshot
The Senescence-Induced Staygreen Protein Regulates Chlorophyll Degradation
inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05906.xopenalex-snapshot
Repression of Clostridium difficile toxin gene expression by CodY
inferredcites →https://doi.org/10.1111/j.1462-2920.2012.02841.xopenalex-snapshot
Genomic determinants of sporulation in Bacilli and Clostridia : towards the minimal set of sporulation‐specific genes
inferredcites →https://doi.org/10.1111/mmi.13121openalex-snapshot
The C lostridium difficile cell wall protein CwpV confers phase‐variable phage resistance
inferredcites →https://doi.org/10.1111/mmi.13457openalex-snapshot
GerM is required to assemble the basal platform of the SpoIIIA–SpoIIQ transenvelope complex during sporulation in Bacillus subtilis
inferredcites →https://doi.org/10.1128/aem.03410-15openalex-snapshot
Ultrastructural Variability of the Exosporium Layer of Clostridium difficile Spores
inferredcites →https://doi.org/10.1128/cmr.18.2.247-263.2005openalex-snapshot
Clostridium difficile Toxins: Mechanism of Action and Role in Disease
inferredcites →https://doi.org/10.1128/iai.00121-16openalex-snapshot
Control of Clostridium difficile Physiopathology in Response to Cysteine Availability
inferredcites →https://doi.org/10.1128/iai.00515-13openalex-snapshot
Adaptive Strategies and Pathogenesis of Clostridium difficile fromIn VivoTranscriptomics
inferredcites →https://doi.org/10.1128/iai.68.9.5269-5276.2000openalex-snapshot
Evidence for Contribution of Tripartite Hemolysin BL, Phosphatidylcholine-Preferring Phospholipase C, and Collagenase to Virulence of Bacillus cereus Endophthalmitis
inferredcites →https://doi.org/10.1128/jb.00321-13openalex-snapshot
Effect of an Oxygen-Tolerant Bifurcating Butyryl Coenzyme A Dehydrogenase/Electron-Transferring Flavoprotein Complex from Clostridium difficile on Butyrate Production in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.00341-10openalex-snapshot
Integration of Metabolism and Virulence by Clostridium difficile CodY
inferredcites →https://doi.org/10.1128/jb.00597-09openalex-snapshot
Proteomic and Genomic Characterization of Highly Infectious Clostridium difficile 630 Spores
inferredcites →https://doi.org/10.1128/jb.00980-10openalex-snapshot
Mapping Interactions between Germinants and Clostridium difficile Spores
inferredcites →https://doi.org/10.1128/jb.01469-14openalex-snapshot
Identification and Characterization of Glycoproteins on the Spore Surface of Clostridium difficile
inferredcites →https://doi.org/10.1128/jb.01582-08openalex-snapshot
The Iron-Hydrogenase of Thermotoga maritima Utilizes Ferredoxin and NADH Synergistically: a New Perspective on Anaerobic Hydrogen Production
inferredcites →https://doi.org/10.1128/jb.01778-12openalex-snapshot
Gene Conservation among Endospore-Forming Bacteria Reveals Additional Sporulation Genes in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.02575-14openalex-snapshot
Spore Cortex Hydrolysis Precedes Dipicolinic Acid Release during Clostridium difficile Spore Germination
inferredcites →https://doi.org/10.1128/jb.05182-11openalex-snapshot
Surface Layers of Clostridium difficile Endospores
inferredcites →https://doi.org/10.1128/jb.182.12.3482-3489.2000openalex-snapshot
The Brucella abortus CcrM DNA Methyltransferase Is Essential for Viability, and Its Overexpression Attenuates Intracellular Replication in Murine Macrophages
inferredcites →https://doi.org/10.1128/jb.184.11.2906-2913.2002openalex-snapshot
Plasmid-Encoded asp Operon Confers a Proton Motive Metabolic Cycle Catalyzed by an Aspartate-Alanine Exchange Reaction
inferredcites →https://doi.org/10.1128/jb.186.1.164-178.2004openalex-snapshot
Formation and Composition of the Bacillus anthracis Endospore
inferredcites →https://doi.org/10.1128/microbiolspec.ei10-0007-2015openalex-snapshot
Clostridium difficile Infection
inferredcites →https://doi.org/10.1146/annurev-micro-090816-093458openalex-snapshot
Clostridium difficile Toxin Biology
inferredcites →https://doi.org/10.1186/s12918-014-0117-zopenalex-snapshot
A curated C. difficile strain 630 metabolic network: prediction of essential targets and inhibitors
inferredcites →https://doi.org/10.1371/journal.pgen.1003756openalex-snapshot
Genome-Wide Analysis of Cell Type-Specific Gene Transcription during Spore Formation in Clostridium difficile
inferredcites →https://doi.org/10.1371/journal.pone.0042410openalex-snapshot
Comparative Transcriptional Analysis of Clinically Relevant Heat Stress Response in Clostridium difficile Strain 630
inferredcites →https://doi.org/10.1371/journal.pone.0062157openalex-snapshot
Clostridium difficile Is an Autotrophic Bacterial Pathogen
inferredcites →https://doi.org/10.1371/journal.pone.0064011openalex-snapshot
Transcriptional Analysis of Temporal Gene Expression in Germinating Clostridium difficile 630 Endospores
inferredcites →https://doi.org/10.1371/journal.pone.0088960openalex-snapshot
Semiquantitative Analysis of Clinical Heat Stress in Clostridium difficile Strain 630 Using a GeLC/MS Workflow with emPAI Quantitation
inferredcites →https://doi.org/10.1371/journal.ppat.1002024openalex-snapshot
The Clostridium difficile Cell Wall Protein CwpV is Antigenically Variable between Strains, but Exhibits Conserved Aggregation-Promoting Function
inferredcites →https://doi.org/10.1371/journal.ppat.1003356openalex-snapshot
Bile Acid Recognition by the Clostridium difficile Germinant Receptor, CspC, Is Important for Establishing Infection
inferredcites →https://doi.org/10.1371/journal.ppat.1006443openalex-snapshot
Intestinal calcium and bile salts facilitate germination of Clostridium difficile spores
inferredcites →https://doi.org/10.3389/fmicb.2018.02371openalex-snapshot
A Metabolic Labeling Strategy for Relative Protein Quantification in Clostridioides difficile
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1579161openalex-snapshot
UV-C and hydration state drive pulsed light-induced proteome damage in Bacillus pumilus spores
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