Identity and function of a large gene network underlying mutagenic repair of DNA breaks. - Wikidata - wikimedia - TriplyDB

Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

http://www.wikidata.org/entity/Q42969505

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SOS response and its regulation on the fluoroquinolone resistance.Atypical Role for PhoU in Mutagenic Break Repair under Stress in Escherichia coli Markovian language model of the DNA and its information content Multiple Osmotic Stress Responses in Acidihalobacter prosperus Result in Tolerance to Chloride Ions.Development of a 3-hydroxypropionate resistant Escherichia coli strain PortEco: a resource for exploring bacterial biology through high-throughput data and analysis tools.A Network Biology Approach to Decipher Stress Response in Bacteria Using Escherichia coli As a Model.Antibiotics trigger initiation of SCCmec transfer by inducing SOS responses.Ancient genes establish stress-induced mutation as a hallmark of cancer The road not taken: Could stress-specific mutations lead to different evolutionary paths?Was low CO2 a driving force of C4 evolution: Arabidopsis responses to long-term low CO2 stress.Medicine. Combating evolution to fight disease.Different tradeoffs result from alternate genetic adaptations to a common environment Escherichia coli genes and pathways involved in surviving extreme exposure to ionizing radiation.Environmentally responsive genome-wide accumulation of de novo Arabidopsis thaliana mutations and epimutations Prediction and redesign of protein-protein interactions Mutations in global regulators lead to metabolic selection during adaptation to complex environments.Selection-driven accumulation of suppressor mutants in bacillus subtilis: the apparent high mutation frequency of the cryptic gudB gene and the rapid clonal expansion of gudB(+) suppressors are due to growth under selection.Emergence of antibiotic resistance from multinucleated bacterial filaments Engineered proteins detect spontaneous DNA breakage in human and bacterial cells.Multilayered genetic safeguards limit growth of microorganisms to defined environments Antimicrobials, stress and mutagenesis Structures of RNA complexes with the Escherichia coli RNA pyrophosphohydrolase RppH unveil the basis for specific 5'-end-dependent mRNA decay.Targets for Combating the Evolution of Acquired Antibiotic Resistance Development of a stress-induced mutagenesis module for autonomous adaptive evolution of Escherichia coli to improve its stress tolerance Cancer as a mitochondrial metabolic disease.An ultra-dense library resource for rapid deconvolution of mutations that cause phenotypes in Escherichia coli.Establishment of a multi-species biofilm model and metatranscriptomic analysis of biofilm and planktonic cell communities.Bacteriophage GIL01 gp7 interacts with host LexA repressor to enhance DNA binding and inhibit RecA-mediated auto-cleavage.Roles of Nucleoid-Associated Proteins in Stress-Induced Mutagenic Break Repair in Starving Escherichia coli.A shifting mutational landscape in 6 nutritional states: Stress-induced mutagenesis as a series of distinct stress input-mutation output relationships.Staying in Shape: the Impact of Cell Shape on Bacterial Survival in Diverse Environments R-loops and nicks initiate DNA breakage and genome instability in non-growing Escherichia coli.Systematically Altering Bacterial SOS Activity under Stress Reveals Therapeutic Strategies for Potentiating Antibiotics Macrophage adaptation leads to parallel evolution of genetically diverse Escherichia coli small-colony variants with increased fitness in vivo and antibiotic collateral sensitivity.Hypermutability and error catastrophe due to defects in ribonucleotide reductase.Role of yqiC in the Pathogenicity of Salmonella and Innate Immune Responses of Human Intestinal Epithelium.Structural insight into LexA-RecA* interaction.Holliday junction trap shows how cells use recombination and a junction-guardian role of RecQ helicase.Cancer as a metabolic disease: implications for novel therapeutics.

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P2860

Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

http://www.wikidata.org/entity/Q42969505

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

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Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

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type

label

Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

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Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

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Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

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Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

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Identity and function of a large gene network underlying mutagenic repair of DNA breaks.

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Abu Amar M Al Mamun

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Andreas M Lisewski

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Caleb Gonzalez

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Chandan Shee

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Claude Saint-Ruf

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Dongxu Lin

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Janet L Gibson

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Mary-Jane Lombardo

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P J Hastings

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Ralf B Nehring

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P2860

Inhibition of mutation and combating the evolution of antibiotic resistance

Escherichia coli K-12: a cooperatively developed annotation snapshot--2005

The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored

Mutational processes molding the genomes of 21 breast cancers

The role of UbiX in Escherichia coli coenzyme Q biosynthesis

Lipoic acid metabolism in Escherichia coli: isolation of null mutants defective in lipoic acid biosynthesis, molecular cloning and characterization of the E. coli lip locus, and identification of the lipoylated protein of the glycine cleavage system

Adaptive amplification and point mutation are independent mechanisms: evidence for various stress-inducible mutation mechanisms

The complete genome sequence of Escherichia coli K-12

One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products

Stochastic gene expression in a single cell

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6112

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338

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Olivier Lichtarge

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