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Reference genes for quantitative, reverse-transcription PCR in Bacillus cereus group strains throughout the bacterial life cycle

https://doi.org/10.1016/j.mimet.2011.05.006
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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/ibd.20966openalex-snapshot
Phylogenetic analysis of inflammatory bowel disease associated Escherichia coli and the fimH virulence determinant
inferredcites →https://doi.org/10.1006/mcpr.2001.0376openalex-snapshot
β-Actin—an unsuitable internal control for RT-PCR
inferredcites →https://doi.org/10.1007/s00018-002-8431-9openalex-snapshot
Bacillus subtilis sporulation and stationary phase gene expression
inferredcites →https://doi.org/10.1007/s00284-006-0099-1openalex-snapshot
A Method for Extracting RNA from Dormant and Germinating Bacillus subtilis Strain 168 Endospores
inferredcites →https://doi.org/10.1016/j.ab.2005.05.022openalex-snapshot
The implications of using an inappropriate reference gene for real-time reverse transcription PCR data normalization
inferredcites →https://doi.org/10.1016/j.anaerobe.2010.06.007openalex-snapshot
Evaluation of candidate reference genes in Clostridium difficile for gene expression normalization
inferredcites →https://doi.org/10.1016/j.meegid.2009.03.009openalex-snapshot
Development of a multilocus sequence typing (MLST) scheme for Mannheimia haemolytica and assessment of the population structure of isolates obtained from cattle and sheep
inferredcites →https://doi.org/10.1016/j.micinf.2007.02.001openalex-snapshot
Bacillus thuringiensis pulmonary infection: critical role for bacterial membrane-damaging toxins and host neutrophils
inferredcites →https://doi.org/10.1016/j.mimet.2004.07.015openalex-snapshot
Comparison of two standardisation methods in real-time quantitative RT-PCR to follow Staphylococcus aureus genes expression during in vitro growth
inferredcites →https://doi.org/10.1016/j.mimet.2007.05.011openalex-snapshot
Identification of suitable internal controls to study expression of a Staphylococcus aureus multidrug resistance system by quantitative real-time PCR
inferredcites →https://doi.org/10.1016/j.mimet.2010.06.013openalex-snapshot
Normalization strategies for real-time expression data in Chlamydia trachomatis
inferredcites →https://doi.org/10.1016/j.mimet.2010.10.016openalex-snapshot
Evaluation of reference genes for real-time quantitative PCR in the marine flavobacterium Zobellia galactanivorans
inferredcites →https://doi.org/10.1016/s0003-2697(02)00311-1openalex-snapshot
Quantitative real-time reverse transcription polymerase chain reaction: normalization to rRNA or single housekeeping genes is inappropriate for human tissue biopsies
inferredcites →https://doi.org/10.1016/s0168-9525(01)02237-5openalex-snapshot
How Bacillus thuringiensis has evolved specific toxins to colonize the insect world
inferredcites →https://doi.org/10.1023/b:bile.0000019559.84305.47openalex-snapshot
Determination of stable housekeeping genes, differentially regulated target genes and sample integrity: BestKeeper – Excel-based tool using pair-wise correlations
inferredcites →https://doi.org/10.1056/nejm199909093411107openalex-snapshot
Anthrax
inferredcites →https://doi.org/10.1074/mcp.m800403-mcp200openalex-snapshot
Identification of Bacillus anthracis Spore Component Antigens Conserved across Diverse Bacillus cereus sensu lato Strains
inferredcites →https://doi.org/10.1093/jxb/ern305openalex-snapshot
Normalization of qRT-PCR data: the necessity of adopting a systematic, experimental conditions-specific, validation of references
inferredcites →https://doi.org/10.1093/nar/29.9.e45openalex-snapshot
A new mathematical model for relative quantification in real-time RT-PCR
inferredcites →https://doi.org/10.1099/mic.0.037341-0openalex-snapshot
Genetic diversity in Italian Lactobacillus sanfranciscensis strains assessed by multilocus sequence typing and pulsed-field gel electrophoresis analyses
inferredcites →https://doi.org/10.1111/j.1365-2672.1974.tb00438.xopenalex-snapshot
A Sporulation Medium for Bacillus anthracis
inferredcites →https://doi.org/10.1111/j.1462-2920.2007.01495.xopenalex-snapshot
Ecological diversification in the Bacillus cereus Group
inferredcites →https://doi.org/10.1111/j.1574-6976.2008.00112.xopenalex-snapshot
From soil to gut: Bacillus cereus and its food poisoning toxins
inferredcites →https://doi.org/10.1128/aem.01736-09openalex-snapshot
Tool for Quantification of Staphylococcal Enterotoxin Gene Expression in Cheese
inferredcites →https://doi.org/10.1128/aem.66.6.2627-2630.2000openalex-snapshot
Bacillus anthracis , Bacillus cereus , and Bacillus thuringiensis —One Species on the Basis of Genetic Evidence
inferredcites →https://doi.org/10.1128/aem.70.1.191-201.2004openalex-snapshot
Multilocus Sequence Typing Scheme for Bacteria of the Bacillus cereus Group
inferredcites →https://doi.org/10.1128/cmr.00073-09openalex-snapshot
Bacillus cereus , a Volatile Human Pathogen
inferredcites →https://doi.org/10.1128/jb.00723-06openalex-snapshot
Transcriptional Profiling of the Bacillus anthracis Life Cycle In Vitro and an Implied Model for Regulation of Spore Formation
inferredcites →https://doi.org/10.1128/jb.01736-06openalex-snapshot
Analysis of Temporal Gene Expression duringBacillus subtilisSpore Germination and Outgrowth
inferredcites →https://doi.org/10.1128/jb.183.24.7094-7101.2001openalex-snapshot
Quantification of Expression of Staphylococcus epidermidis Housekeeping Genes with Taqman Quantitative PCR during In Vitro Growth and under Different Conditions
inferredcites →https://doi.org/10.1128/jb.188.1.169-178.2006openalex-snapshot
Evidence for Clonal Evolution among Highly Polymorphic Genes in Methicillin-Resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1128/jcm.01274-10openalex-snapshot
Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
inferredcites →https://doi.org/10.1128/jcm.02123-09openalex-snapshot
InhA1, NprA, and HlyII as Candidates for Markers To Differentiate Pathogenic from NonpathogenicBacillus cereusStrains
inferredcites →https://doi.org/10.1128/jcm.36.7.2138-2139.1998openalex-snapshot
Bacillus thuringiensis subsp. konkukian (Serotype H34) Superinfection: Case Report and Experimental Evidence of Pathogenicity in Immunosuppressed Mice
inferredcites →https://doi.org/10.1128/mmbr.62.3.775-806.1998openalex-snapshot
Bacillus thuringiensis and Its Pesticidal Crystal Proteins
inferredcites →https://doi.org/10.1136/thorax.57.9.765openalex-snapshot
beta-Actin and GAPDH housekeeping gene expression in asthmatic airways is variable and not suitable for normalising mRNA levels
inferredcites →https://doi.org/10.1146/annurev.micro.091208.073255openalex-snapshot
What Sets Bacillus anthracis Apart from Other Bacillus Species?
inferredcites →https://doi.org/10.1146/annurev.micro.55.1.647openalex-snapshot
Anthrax
inferredcites →https://doi.org/10.1158/0008-5472.can-04-0496openalex-snapshot
Normalization of Real-Time Quantitative Reverse Transcription-PCR Data: A Model-Based Variance Estimation Approach to Identify Genes Suited for Normalization, Applied to Bladder and Colon Cancer Data Sets
inferredcites →https://doi.org/10.1159/000096463openalex-snapshot
Transcriptome Analysis of Temporal Regulation of Carbon Metabolism by CcpA in Bacillus subtilis Reveals Additional Target Genes
inferredcites →https://doi.org/10.1186/1471-2172-11-21openalex-snapshot
Gene expression results in lipopolysaccharide-stimulated monocytes depend significantly on the choice of reference genes.
inferredcites →https://doi.org/10.1186/1471-2180-9-227openalex-snapshot
Response of Bacillus cereus ATCC 14579 to challenges with sublethal concentrations of enterocin AS-48
inferredcites →https://doi.org/10.1186/1471-2199-9-18openalex-snapshot
Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus
inferredcites →https://doi.org/10.1186/gb-2002-3-7-research0034openalex-snapshot
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
inferredcites →https://doi.org/10.1373/clinchem.2008.112797openalex-snapshot
The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR Experiments
inferredcites →https://doi.org/10.2144/04371rr03openalex-snapshot
Validation of housekeeping genes for normalizing RNA expression in real-time PCR
inferredcites →https://doi.org/10.5483/bmbrep.2007.40.2.226openalex-snapshot
Identification of Novel Universal Housekeeping Genes by Statistical Analysis of Microarray Data

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.4635542openalex-extracted
Effects of Camellia Saponins on Biofilm Formation and Virulence Factor Genes Of Bacillus Cereus
inferred← citeshttps://doi.org/10.1002/mbo3.109openalex-snapshot
Transcriptomic and phenotypic analysis of paralogous spx gene function in B acillus anthracis Sterne
inferred← citeshttps://doi.org/10.1002/ps.71023openalex-snapshot
RNase III ‐deficient Bacillus thuringiensis enables stable dsRNA production and enhances HD1 activity against Spodoptera frugiperda
inferred← citeshttps://doi.org/10.1007/s00253-014-5729-0openalex-snapshot
Functions of poly-gamma-glutamic acid (γ-PGA) degradation genes in γ-PGA synthesis and cell morphology maintenance
inferred← citeshttps://doi.org/10.1007/s00253-014-6094-8openalex-snapshot
Regulation of sporulation initiation by NprR and its signaling peptide NprRB: molecular recognition and conformational changes
inferred← citeshttps://doi.org/10.1007/s00253-017-8171-2openalex-snapshot
Improvement of levan production in Bacillus amyloliquefaciens through metabolic optimization of regulatory elements
inferred← citeshttps://doi.org/10.1007/s00253-022-11831-3openalex-snapshot
Validation of housekeeping genes as internal controls for gene expression studies on biofilm formation in Bacillus velezensis
inferred← citeshttps://doi.org/10.1007/s00792-019-01109-4openalex-snapshot
Reference genes for real-time RT-PCR expression studies in an Antarctic Pseudomonas exposed to different temperature conditions
inferred← citeshttps://doi.org/10.1007/s10482-015-0524-1openalex-snapshot
Bacterial reference genes for gene expression studies by RT-qPCR: survey and analysis
inferred← citeshttps://doi.org/10.1007/s11274-025-04334-6openalex-snapshot
The role of AbrB from plate to bioreactor: implications of induced expression on physiological and metabolic responses in Bacillus thuringiensis
inferred← citeshttps://doi.org/10.1007/s12033-013-9697-xopenalex-snapshot
Reference Gene Selection in Carnobacterium maltaromaticum, Lactobacillus curvatus, and Listeria innocua Subjected to Temperature and Salt Stress
inferred← citeshttps://doi.org/10.1007/s12275-021-0441-0openalex-snapshot
iTRAQ-facilitated proteomic analysis of Bacillus cereus via degradation of malachite green
inferred← citeshttps://doi.org/10.1016/j.biortech.2024.130499openalex-snapshot
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High lead-tolerant mutant Bacillus tropicus AT31-1 from rhizosphere soil of Pu-erh and its remediation mechanism
inferred← citeshttps://doi.org/10.1016/j.cej.2025.163954openalex-snapshot
Multidimensional engineering and peptidoglycan modulation for surfactin production in Bacillus subtilis
inferred← citeshttps://doi.org/10.1016/j.fm.2026.105166openalex-snapshot
Environmental modulation of cytotoxicity and virulence factor stability in psychrotolerant Bacillus cereus group isolates
inferred← citeshttps://doi.org/10.1016/j.foodcont.2016.02.049openalex-snapshot
Distribution and expression of the enterotoxin genes of Bacillus cereus in food products from Jiangxi Province, China
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2023.110517openalex-snapshot
The potential of lactose to inhibit cereulide biosynthesis of emetic Bacillus cereus in milk
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2013.04.011openalex-snapshot
Evaluation of Clostridium ljungdahlii DSM 13528 reference genes in gene expression studies by qRT-PCR
inferred← citeshttps://doi.org/10.1016/j.jip.2015.11.009openalex-snapshot
High instability of a nematicidal Cry toxin plasmid in Bacillus thuringiensis
inferred← citeshttps://doi.org/10.1016/j.jprot.2016.08.019openalex-snapshot
iTRAQ-based proteomic analysis of LI-F type peptides produced by Paenibacillus polymyxa JSa-9 mode of action against Bacillus cereus
inferred← citeshttps://doi.org/10.1016/j.lwt.2024.116023openalex-snapshot
Effects of camellia saponins on biofilm formation and virulence factor genes of Bacillus cereus
inferred← citeshttps://doi.org/10.1016/j.mimet.2012.07.005openalex-snapshot
Identification and validation of reference genes to study the gene expression in Gluconacetobacter diazotrophicus grown in different carbon sources using RT-qPCR
inferred← citeshttps://doi.org/10.1016/j.mimet.2016.10.004openalex-snapshot
Validation of reference genes for RT-qPCR analysis in Burkholderia pyrrocinia JK-SH007
inferred← citeshttps://doi.org/10.1016/j.mimet.2024.106987openalex-snapshot
Interrelationship among substrate utilization, metabolic productions, and housekeeping-related gene expression levels in Mortierella alpine CBS 754.68
inferred← citeshttps://doi.org/10.1016/j.pestbp.2020.104599openalex-snapshot
For: Pesticide biochemistry and physiology recG is involved with the resistance of Bt to UV
inferred← citeshttps://doi.org/10.1016/j.resmic.2021.103850openalex-snapshot
CdgL is a degenerate nucleotide cyclase domain protein affecting flagellin synthesis and motility in Bacillus thuringiensis
inferred← citeshttps://doi.org/10.1016/j.syapm.2020.126075openalex-snapshot
Chitinolytic activity of phylogenetically diverse Bacillus cereus sensu lato from natural environments
inferred← citeshttps://doi.org/10.1016/j.tcsw.2019.100032openalex-snapshot
Bacillus thuringiensis CbpA is a collagen binding cell surface protein under c-di-GMP control
inferred← citeshttps://doi.org/10.1038/s41396-020-0623-5openalex-snapshot
The CRISPR-Cas systems were selectively inactivated during evolution of Bacillus cereus group for adaptation to diverse environments
inferred← citeshttps://doi.org/10.1038/s41522-022-00292-1openalex-snapshot
Adaptation and phenotypic diversification of Bacillus thuringiensis biofilm are accompanied by fuzzy spreader morphotypes
inferred← citeshttps://doi.org/10.1038/s41598-022-23804-7openalex-snapshot
Evaluation of candidate reference genes stability for gene expression analysis by reverse transcription qPCR in Clostridium perfringens
inferred← citeshttps://doi.org/10.1038/srep14129openalex-snapshot
Genomic and transcriptomic insights into the efficient entomopathogenicity of Bacillus thuringiensis
inferred← citeshttps://doi.org/10.1039/c5ra15766hopenalex-snapshot
Identification and characterization of a Bacillus methylotrophicus strain with high flocculating activity
inferred← citeshttps://doi.org/10.1080/08927014.2019.1586889openalex-snapshot
Bacillus cereus biofilm formation on central venous catheters of hospitalised cardiac patients
inferred← citeshttps://doi.org/10.1080/09583157.2022.2085662openalex-snapshot
Molecular and biochemical characterisation of antagonistic mechanisms of the biocontrol agent Bacillus cereus B25 inhibiting the growth of the phytopathogen Fusarium verticillioides P03 during their direct interaction in vitro
inferred← citeshttps://doi.org/10.1093/femsle/fnaf128openalex-snapshot
The mhqPOD gene cluster in lignin-degrading Paenibacillus sp. B2 encodes a pathway for the degradation of lignin-derived 5,5’-di(dehydrovanillic acid) (DDVA)
inferred← citeshttps://doi.org/10.1093/femsle/fnv079openalex-snapshot
Construction of a Bacillus amyloliquefaciens strain for high purity levan production
inferred← citeshttps://doi.org/10.1111/1574-6968.12503openalex-snapshot
Comparative analysis of quantitative reverse transcription real-time PCR and commercial enzyme imunoassays for detection of enterotoxigenicBacillus thuringiensisisolates
inferred← citeshttps://doi.org/10.1111/1758-2229.12305openalex-snapshot
The worldwide distribution of genetically and phylogenetically diverse B acillus cereus isolates harbouring B acillus anthracis ‐like plasmids
inferred← citeshttps://doi.org/10.1111/jam.12096openalex-snapshot
Small Bacillus cereus ATCC 14579 subpopulations are responsible for cytotoxin K production
inferred← citeshttps://doi.org/10.1111/jam.14792openalex-snapshot
Comparison of the antibiotic resistance between genetically diverse and toxigenic Bacillus cereus sensu lato from milk, pepper and natural habitats
inferred← citeshttps://doi.org/10.1111/lam.13590openalex-snapshot
Characterization of CwlC, an autolysin, and its role in mother cell lysis of Bacillus thuringiensis subsp. israelensis
inferred← citeshttps://doi.org/10.1111/mmi.12798openalex-snapshot
spxA2 , encoding a regulator of stress resistance in B acillus anthracis, is controlled by SaiR , a new member of the Rrf2 protein family
inferred← citeshttps://doi.org/10.1111/mmi.13405openalex-snapshot
Cyclic diguanylate regulation of Bacillus cereus group biofilm formation
inferred← citeshttps://doi.org/10.1111/pce.15278openalex-snapshot
Metabolism Interaction Between Bacillus cereus SESY and Brassica napus Contributes to Enhance Host Selenium Absorption and Accumulation
inferred← citeshttps://doi.org/10.1128/aac.01302-25openalex-snapshot
Differences in β-lactamase activity and carbapenem resistance among the Bacillus cereus group
inferred← citeshttps://doi.org/10.1128/aem.02245-17openalex-snapshot
CerR, a Single-Domain Regulatory Protein of the LuxR Family, Promotes Cerecidin Production and Immunity in Bacillus cereus
inferred← citeshttps://doi.org/10.1128/aem.03032-19openalex-snapshot
Potential Enterotoxicity of Phylogenetically Diverse Bacillus cereus Sensu Lato Soil Isolates from Different Geographical Locations
inferred← citeshttps://doi.org/10.1128/aem.03096-14openalex-snapshot
Decreasing Global Transcript Levels over Time Suggest that Phytoplasma Cells Enter Stationary Phase during Plant and Insect Colonization
inferred← citeshttps://doi.org/10.1128/iai.00765-18openalex-snapshot
Porcine Gastric Mucin Triggers Toxin Production of Enteropathogenic Bacillus cereus
inferred← citeshttps://doi.org/10.1128/jb.05309-11openalex-snapshot
Evolutionary History and Functional Characterization of Three Large Genes Involved in Sporulation in Bacillus cereus Group Bacteria
inferred← citeshttps://doi.org/10.1128/mbio.01602-17openalex-snapshot
In Vivo Behavior of the Tandem Glycine Riboswitch in Bacillus subtilis
inferred← citeshttps://doi.org/10.1128/msystems.00291-21openalex-snapshot
Direct Regulons of AtxA, the Master Virulence Regulator of Bacillus anthracis
inferred← citeshttps://doi.org/10.1128/spectrum.00604-21openalex-snapshot
Tandem Mass Tag-Based Quantitative Proteomics and Virulence Phenotype of Hemolymph-Treated Bacillus thuringiensis kurstaki Cells Reveal New Insights on Bacterial Pathogenesis in Insects
inferred← citeshttps://doi.org/10.1155/2020/8926120openalex-snapshot
Selection of Suitable Reference Genes for qPCR Gene Expression Analysis of HepG2 and L02 in Four Different Liver Cell Injured Models
inferred← citeshttps://doi.org/10.1186/s12934-017-0704-yopenalex-snapshot
Enhancing poly-γ-glutamic acid production in Bacillus amyloliquefaciens by introducing the glutamate synthesis features from Corynebacterium glutamicum
inferred← citeshttps://doi.org/10.1186/s12934-019-1121-1openalex-snapshot
Enhanced production of antifungal lipopeptide iturin A by Bacillus amyloliquefaciens LL3 through metabolic engineering and culture conditions optimization
inferred← citeshttps://doi.org/10.1186/s12934-020-01485-zopenalex-snapshot
Engineering of a genome-reduced strain Bacillus amyloliquefaciens for enhancing surfactin production
inferred← citeshttps://doi.org/10.1186/s13068-026-02791-1openalex-snapshot
Genome-level insights into coordinated ethanol production and chaperone-driven stress tolerance in Bacillus cereus strain GRJBSBT-1 isolated from petroleum refinery sludge
inferred← citeshttps://doi.org/10.1261/rna.065011.117openalex-snapshot
Fitness advantages conferred by the L20-interacting RNAcis-regulator of ribosomal protein synthesis inBacillus subtilis
inferred← citeshttps://doi.org/10.1371/journal.pone.0036720openalex-snapshot
BC4707 Is a Major Facilitator Superfamily Multidrug Resistance Transport Protein from Bacillus cereus Implicated in Fluoroquinolone Tolerance
inferred← citeshttps://doi.org/10.1371/journal.pone.0080175openalex-snapshot
Eco-Genetic Structure of Bacillus cereus sensu lato Populations from Different Environments in Northeastern Poland
inferred← citeshttps://doi.org/10.1371/journal.ppat.1014017openalex-snapshot
Regulatory diversity in Bacillus thuringiensis cry genes reveals flexible evolutionary strategies for in vivo toxin expression
inferred← citeshttps://doi.org/10.1515/jvetres-2016-0060openalex-snapshot
Chlamydia psittaci reference genes for normalisation of expression data differ depending on the culture conditions and selected time points during the chlamydial replication cycle
inferred← citeshttps://doi.org/10.18502/ijm.v14i2.9188openalex-snapshot
Validation of reference genes for the normalization of RT-qPCR gene expression in Bacillus siamensis 1021 grown in different culture media
inferred← citeshttps://doi.org/10.21161/mjm.230003openalex-snapshot
The effect of simulated copper stress on genes associated with the metabolism of polyphosphates and polyhydroxyalkanoates in Bacillus thuringiensis Y1
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1108435/v1openalex-snapshot
Evaluation of Candidate Reference Genes Stability for Gene Expression Analysis by Reverse Transcription QPCR in Clostridium Perfringens
inferred← citeshttps://doi.org/10.21203/rs.3.rs-8551494/v1openalex-snapshot
Disruption of Protein BA_3317 Affects Asymmetric Division as an Exporter of Sporulation Signal Molecules in Bacillus anthracis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-8659215/v1openalex-snapshot
Soil Moisture Modulates Rhizosphere Microbiota and Suppresses Root Rot in Organic Panax ginseng Cultivated Under Pine Forests
inferred← citeshttps://doi.org/10.2139/ssrn.5477421openalex-snapshot
The mhqPOD gene cluster in lignin-degrading Paenibacillus sp. encodes a pathway for degradation of lignin-derived 5,5’-di(dehydrovanillic acid) (DDVA)
inferred← citeshttps://doi.org/10.2217/fmb.15.130openalex-snapshot
Surface Lipoproteome of Mycoplasma Hominis PG21 and Differential Expression After Contact with Human Dendritic Cells
inferred← citeshttps://doi.org/10.2903/j.efsa.2016.4524openalex-snapshot
Risks for public health related to the presence of Bacillus cereus and other Bacillus spp. including Bacillus thuringiensis in foodstuffs
inferred← citeshttps://doi.org/10.3389/fmicb.2020.00879openalex-snapshot
GTP-Dependent FlhF Homodimer Supports Secretion of a Hemolysin in Bacillus cereus
inferred← citeshttps://doi.org/10.3389/fmicb.2020.610650openalex-snapshot
MogR Is a Ubiquitous Transcriptional Repressor Affecting Motility, Biofilm Formation and Virulence in Bacillus thuringiensis
inferred← citeshttps://doi.org/10.3389/fmicb.2022.897836openalex-snapshot
A Flagella Hook Coding Gene flgE Positively Affects Biofilm Formation and Cereulide Production in Emetic Bacillus cereus
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1250542openalex-snapshot
Characterization of a novel cell wall hydrolase CwlE involved in Bacillus thuringiensis subsp. israelensis mother cell lysis
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1519202openalex-snapshot
Effect of environmental stress factors on the expression of virulence genes and pathogenicity of lethal Bacillus cereus of bovine origin
inferred← citeshttps://doi.org/10.3390/biology12050645openalex-snapshot
Genome Sequence and Phenotypic Analysis of a Protein Lysis-Negative, Attenuated Anthrax Vaccine Strain
inferred← citeshttps://doi.org/10.3390/ijms252413528openalex-snapshot
Organic vs. Conventional Milk: Uncovering the Link to Antibiotic Resistance in Bacillus cereus sensu lato
inferred← citeshttps://doi.org/10.3390/microorganisms12051024openalex-snapshot
Reference Genes for Expression Analyses by qRT-PCR in Enterobacter cancerogenus
inferred← citeshttps://doi.org/10.3390/microorganisms8121896openalex-snapshot
Comparative Analysis of the Global Transcriptomic Response to Oxidative Stress of Bacillus anthracis htrA-Disrupted and Parental Wild Type Strains
inferred← citeshttps://doi.org/10.3390/toxins17020058openalex-snapshot
Establishing Reference Genes for Accurate Gene Expression Profiling in Toxigenic Bacillus cereus
inferred← citeshttps://doi.org/10.6084/m9.figshare.13346287openalex-snapshot
Additional file 1 of Engineering of a genome-reduced strain Bacillus amyloliquefaciens for enhancing surfactin production
inferred← citeshttps://doi.org/10.70675/c4213ca7z6456z4babz80a2z0ed4ae19d641openalex-snapshot
Contamination risks control of food products by B. cereus group.
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