The coding and noncoding architecture of the Caulobacter crescentus genome - Wikidata - awgldk - TriplyDB

The coding and noncoding architecture of the Caulobacter crescentus genome

The coding and noncoding architecture of the Caulobacter crescentus genome

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The use of duplex-specific nuclease in ribosome profiling and a user-friendly software package for Ribo-seq data analysis.Comparative genomic analysis of translation initiation mechanisms for genes lacking the Shine-Dalgarno sequence in prokaryotes.The global regulatory architecture of transcription during the Caulobacter cell cycle Nutritional Control of DNA Replication Initiation through the Proteolysis and Regulated Translation of DnaA.CspC regulates the expression of the glyoxylate cycle genes at stationary phase in Caulobacter.Leaderless Transcripts and Small Proteins Are Common Features of the Mycobacterial Translational Landscape.Transcriptomic analysis of the stationary phase response regulator SpdR in Caulobacter crescentus.Structured and Dynamic Disordered Domains Regulate the Activity of a Multifunctional Anti-σ Factor.The bacterial cell cycle regulator GcrA is a σ70 cofactor that drives gene expression from a subset of methylated promoters.CauloBrowser: A systems biology resource for Caulobacter crescentus The dynamic transcriptional and translational landscape of the model antibiotic producer Streptomyces coelicolor A3(2)Cell cycle progression in Caulobacter requires a nucleoid-associated protein with high AT sequence recognition.Dynamic translation regulation in Caulobacter cell cycle control.Depletion of Shine-Dalgarno Sequences within Bacterial Coding Regions Is Expression Dependent.Two outer membrane proteins contribute to cellular fitness in Caulobacter crescentus by preventing intracellular S-layer protein accumulation.Leveraging genome-wide datasets to quantify the functional role of the anti-Shine-Dalgarno sequence in regulating translation efficiency.Contact-dependent killing by Caulobacter crescentus via cell surface-associated, glycine zipper proteins.Identification of Unannotated Small Genes in Salmonella.Shapeshifting to Survive: Shape Determination and Regulation in Caulobacter crescentus.Conservation of the Essential Genome Among Caulobacter and Brevundimonas Species.A comparative genomics study on the effect of individual amino acids on ribosome stalling.Release of nonstop ribosomes is essential.Association of the Cold Shock DEAD-Box RNA Helicase RhlE to the RNA Degradosome in Caulobacter crescentus.Allosteric control of a bacterial stress response system by an anti-σ factor.Molecular recognition of RhlB and RNase D in the Caulobacter crescentus RNA degradosome.Cyclic di-GMP differentially tunes a bacterial flagellar motor through a novel class of CheY-like regulators.Diversity of translation initiation mechanisms across bacterial species is driven by environmental conditions and growth demands.Translation efficiency is maintained at elevated temperature in E. coli.Role and regulation of ferritin-like proteins in iron homeostasis and oxidative stress survival of Caulobacter crescentus.GWIPS-viz: 2018 update.Cytoskeletal Proteins in Caulobacter crescentus: Spatial Orchestrators of Cell Cycle Progression, Development, and Cell Shape.Exopolysaccharide production in Caulobacter crescentus: A resource allocation trade-off between protection and proliferation.An essential regulatory function of the DnaK chaperone dictates the decision between proliferation and maintenance in Caulobacter crescentus.Replication fork passage drives asymmetric dynamics of a critical nucleoid-associated protein in Caulobacter.A conserved coiled-coil protein pair focuses the cytokinetic Z-ring in Caulobacter crescentus.Gene network analysis identifies a central post-transcriptional regulator of cellular stress survival.Non-coding RNAs Potentially Controlling Cell Cycle in the Model Caulobacter crescentus: A Bioinformatic Approach.Control of proline utilization by the Lrp-like regulator PutR in Caulobacter crescentus Exposed to Sublethal Levels of Hydrogen Peroxide Mounts a Complex Transcriptional Response Iron Deficiency Generates Oxidative Stress and Activation of the SOS Response in

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The coding and noncoding architecture of the Caulobacter crescentus genome

http://www.wikidata.org/entity/Q28655054

description

2014 nî lūn-bûn

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2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2014 թվականի հուլիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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name

The coding and noncoding architecture of the Caulobacter crescentus genome

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The coding and noncoding architecture of the Caulobacter crescentus genome

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The coding and noncoding architecture of the Caulobacter crescentus genome

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type

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The coding and noncoding architecture of the Caulobacter crescentus genome

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The coding and noncoding architecture of the Caulobacter crescentus genome

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The coding and noncoding architecture of the Caulobacter crescentus genome

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prefLabel

The coding and noncoding architecture of the Caulobacter crescentus genome

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The coding and noncoding architecture of the Caulobacter crescentus genome

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The coding and noncoding architecture of the Caulobacter crescentus genome

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The coding and noncoding architecture of the Caulobacter crescentus genome

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Brandon Williams

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Gene-Wei Li

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Keren Lasker

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Tao Long

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W Seth Childers

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Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

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Operons in Escherichia coli: genomic analyses and predictions

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How ribosomes select initiator regions in mRNA: base pair formation between the 3' terminus of 16S rRNA and the mRNA during initiation of protein synthesis in Escherichia coli

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Jared M Schrader

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