Novel reference genes for quantifying transcriptional responses of Escherichia coli to protein overexpression by quantitative PCR - Wikidata - wikimedia - TriplyDB

Novel reference genes for quantifying transcriptional responses of Escherichia coli to protein overexpression by quantitative PCR

Novel reference genes for quantifying transcriptional responses of Escherichia coli to protein overexpression by quantitative PCR

http://www.wikidata.org/entity/Q33879869

about

Genome-wide mapping of furfural tolerance genes in Escherichia coli Investigation of Proposed Ladderane Biosynthetic Genes from Anammox Bacteria by Heterologous Expression in E. coli Programming mRNA decay to modulate synthetic circuit resource allocation Development of a native Escherichia coli induction system for ionic liquid tolerance.Metabolite profiling identified methylerythritol cyclodiphosphate efflux as a limiting step in microbial isoprenoid production.Overexpression of fetA (ybbL) and fetB (ybbM), Encoding an Iron Exporter, Enhances Resistance to Oxidative Stress in Escherichia coli.Comparison of genome-wide selection strategies to identify furfural tolerance genes in Escherichia coli.Overexpression of the Lactobacillus plantarum peptidoglycan biosynthesis murA2 gene increases the tolerance of Escherichia coli to alcohols and enhances ethanol production.Engineering of bacterial methyl ketone synthesis for biofuels De novo design of heat-repressible RNA thermosensors in E. coli.P1 Ref Endonuclease: A Molecular Mechanism for Phage-Enhanced Antibiotic Lethality.A highly precise and portable genome engineering method allows comparison of mutational effects across bacterial species Chlamydia trachomatis Type III Secretion Proteins Regulate Transcription.Balancing gene expression without library construction via a reusable sRNA pool.Programmable control of bacterial gene expression with the combined CRISPR and antisense RNA system.Selection of new appropriate reference genes for RT-qPCR analysis via transcriptome sequencing of cynomolgus monkeys (Macaca fascicularis)Selection and Validation of Reference Genes for Quantitative Real-time PCR in Gentiana macrophylla.Combining genotype improvement and statistical media optimization for isoprenoid production in E. coli Physiological Response of Escherichia coli O157:H7 Sakai to Dynamic Changes in Temperature and Water Activity as Experienced during Carcass Chilling.Bacterial reference genes for gene expression studies by RT-qPCR: survey and analysis.Effects of Stress, Reactive Oxygen Species, and the SOS Response on De Novo Acquisition of Antibiotic Resistance in Escherichia coli.Fitness of Salmonella mutants resistant to antimicrobial peptides.Copy number variability of expression plasmids determined by cell sorting and Droplet Digital PCR Movement protein of Apple chlorotic leaf spot virus is genetically unstable and negatively regulated by Ribonuclease E in E. coli.Stoichiometry and deletion analyses of subunits in the heterotrimeric F-ATP synthase c ring from the acetogenic bacterium Acetobacterium woodii.Integrating artificial with natural cells to translate chemical messages that direct E. coli behaviour The Shigella ProU system is required for osmotic tolerance and virulence.An engineered small RNA-mediated genetic switch based on a ribozyme expression platform.A particular silent codon exchange in a recombinant gene greatly influences host cell metabolic activity.RNA-sequence data normalization through in silico prediction of reference genes: the bacterial response to DNA damage as case study.Broad-Host-Range Expression Reveals Native and Host Regulatory Elements That Influence Heterologous Antibiotic Production in Gram-Negative Bacteria Deacetylation of topoisomerase I is an important physiological function of E. coli CobB.In vivo evolution of a catalytic RNA couples trans-splicing to translation.3'-UTR engineering to improve soluble expression and fine-tuning of activity of cascade enzymes in Escherichia coli.Three-dimensional, sharp-tipped electrodes concentrate applied fields to enable direct electrical release of intact biomarkers from cells.In silico profiling of Escherichia coli and Saccharomyces cerevisiae as terpenoid factories.Toward a semisynthetic stress response system to engineer microbial solvent tolerance The CTX-M-14 plasmid pHK01 encodes novel small RNAs and influences host growth and motility.Transcriptional engineering of Escherichia coli K4 for fructosylated chondroitin production.Microcystin-LR does not induce alterations to transcriptomic or metabolomic profiles of a model heterotrophic bacterium.

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Novel reference genes for quantifying transcriptional responses of Escherichia coli to protein overexpression by quantitative PCR

http://www.wikidata.org/entity/Q33879869

description

2011 nî lūn-bûn

@nan

2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Novel reference genes for quan ...... expression by quantitative PCR

@ast

Novel reference genes for quan ...... expression by quantitative PCR

@en

type

label

Novel reference genes for quan ...... expression by quantitative PCR

@ast

Novel reference genes for quan ...... expression by quantitative PCR

@en

prefLabel

Novel reference genes for quan ...... expression by quantitative PCR

@ast

Novel reference genes for quan ...... expression by quantitative PCR

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1471-2199-12-18

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BMC Molecular Biology

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Novel reference genes for quan ...... expression by quantitative PCR

@en

P2093

Gregory Stephanopoulos

http://www.w3.org/2001/XMLSchema#string

Heng-Phon Too

http://www.w3.org/2001/XMLSchema#string

Kang Zhou

http://www.w3.org/2001/XMLSchema#string

Lihan Zhou

http://www.w3.org/2001/XMLSchema#string

Qing 'En Lim

http://www.w3.org/2001/XMLSchema#string

Ruiyang Zou

http://www.w3.org/2001/XMLSchema#string

P2860

Sequence analysis of the GntII (subsidiary) system for gluconate metabolism reveals a novel pathway for L-idonic acid catabolism in Escherichia coli.

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

Isoprenoid pathway optimization for Taxol precursor overproduction in Escherichia coli

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

Pitfalls in the normalization of real-time polymerase chain reaction data.

Metabolic engineering of the nonmevalonate isopentenyl diphosphate synthesis pathway in Escherichia coli enhances lycopene production.

Normalization with genes encoding ribosomal proteins but not GAPDH provides an accurate quantification of gene expressions in neuronal differentiation of PC12 cells.

Molecular structure and enzymatic function of lycopene cyclase from the cyanobacterium Synechococcus sp strain PCC7942.

Multiple high-throughput analyses monitor the response of E. coli to perturbations.

Many Microbe Microarrays Database: uniformly normalized Affymetrix compendia with structured experimental metadata

P2888

1471-2199-12-18

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18

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scholarly article

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10.1186/1471-2199-12-18

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12

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2011-04-23T00:00:00Z

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51070626

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1048912473

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21513543

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P921

Escherichia coli

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3110127

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