scholarly article | Q13442814 |
P50 | author | Alessandra Carbone | Q27559542 |
P2860 | cites work | Experimental Determination and System Level Analysis of Essential Genes in Escherichia coli MG1655 | Q22065459 |
The Minimal Gene Complement of Mycoplasma genitalium | Q22065573 | ||
The genome of M. acetivorans reveals extensive metabolic and physiological diversity | Q22065756 | ||
Genome sequence of Streptococcus mutans UA159, a cariogenic dental pathogen | Q22066245 | ||
Essential genes of a minimal bacterium | Q22066349 | ||
Reductive genome evolution in Buchnera aphidicola | Q22066374 | ||
Genome sequence of the endocellular obligate symbiont of tsetse flies, Wigglesworthia glossinidia | Q22122040 | ||
The codon Adaptation Index--a measure of directional synonymous codon usage bias, and its potential applications | Q24498207 | ||
A genome-scale analysis for identification of genes required for growth or survival of Haemophilus influenzae | Q24530777 | ||
Extreme genome reduction in Buchnera spp.: toward the minimal genome needed for symbiotic life | Q24536091 | ||
From genetic footprinting to antimicrobial drug targets: examples in cofactor biosynthetic pathways | Q24539226 | ||
Synonymous codon usage is subject to selection in thermophilic bacteria | Q24540514 | ||
Generating a synthetic genome by whole genome assembly: phiX174 bacteriophage from synthetic oligonucleotides | Q24618245 | ||
A phylogenomic approach to bacterial phylogeny: evidence of a core of genes sharing a common history | Q24671811 | ||
Essential Bacillus subtilis genes | Q24681292 | ||
Variation in the strength of selected codon usage bias among bacteria | Q24792094 | ||
From gene trees to organismal phylogeny in prokaryotes: the case of the gamma-Proteobacteria | Q24795892 | ||
Functional profiling of the Saccharomyces cerevisiae genome | Q27860544 | ||
Whole-genome random sequencing and assembly of Haemophilus influenzae Rd | Q27860765 | ||
Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis | Q27860815 | ||
Systematic functional analysis of the Caenorhabditis elegans genome using RNAi | Q27860839 | ||
Correlation between protein and mRNA abundance in yeast | Q28137554 | ||
A minimal gene set for cellular life derived by comparison of complete bacterial genomes | Q29616790 | ||
Global transposon mutagenesis and a minimal Mycoplasma genome | Q29617096 | ||
Universal trees based on large combined protein sequence data sets. | Q30655328 | ||
Comparative genomics of the Archaea (Euryarchaeota): evolution of conserved protein families, the stable core, and the variable shell. | Q30738900 | ||
Insights on the evolution of metabolic networks of unicellular translationally biased organisms from transcriptomic data and sequence analysis | Q31007446 | ||
How many genes can make a cell: the minimal-gene-set concept | Q31029180 | ||
Global transposon mutagenesis and essential gene analysis of Helicobacter pylori | Q31129026 | ||
Comparative genomics, minimal gene-sets and the last universal common ancestor | Q33199916 | ||
Identification of critical staphylococcal genes using conditional phenotypes generated by antisense RNA. | Q33954835 | ||
Computing prokaryotic gene ubiquity: rescuing the core from extinction | Q33983466 | ||
DNA microarray analysis of the hyperthermophilic archaeon Pyrococcus furiosus: evidence for anNew type of sulfur-reducing enzyme complex | Q33997164 | ||
Codon catalog usage and the genome hypothesis | Q34056686 | ||
A genome-wide strategy for the identification of essential genes in Staphylococcus aureus | Q34123679 | ||
Identification of 113 conserved essential genes using a high-throughput gene disruption system in Streptococcus pneumoniae | Q34140737 | ||
The genetic core of the universal ancestor | Q34181411 | ||
An integrated analysis of the genome of the hyperthermophilic archaeon Pyrococcus abyssi | Q34182074 | ||
How essential are nonessential genes? | Q34433664 | ||
Comparison of archaeal and bacterial genomes: computer analysis of protein sequences predicts novel functions and suggests a chimeric origin for the archaea | Q34447405 | ||
Massive parallelism, randomness and genomic advances | Q35074868 | ||
Identification of thermophilic species by the amino acid compositions deduced from their genomes | Q35082445 | ||
Metabolic interdependence of obligate intracellular bacteria and their insect hosts | Q35980170 | ||
Studies of the processing of the protease which initiates degradation of small, acid-soluble proteins during germination of spores of Bacillus species | Q36107428 | ||
Purification and characterization of the alanine aminotransferase from the hyperthermophilic Archaeon pyrococcus furiosus and its role in alanine production | Q39587425 | ||
Over-representation of repeats in stress response genes: a strategy to increase versatility under stressful conditions? | Q39600777 | ||
DNA sequence and complementation analysis of a mutation in the rplX gene from Escherichia coli leading to loss of ribosomal protein L24. | Q39981188 | ||
Enzymes of hydrogen metabolism in Pyrococcus furiosus | Q42636458 | ||
Defining the core of nontransferable prokaryotic genes: the euryarchaeal core | Q42662262 | ||
Codon bias signatures, organization of microorganisms in codon space, and lifestyle | Q43016695 | ||
Amino acid composition of genomes, lifestyles of organisms, and evolutionary trends: a global picture with correspondence analysis | Q43031540 | ||
An estimation of minimal genome size required for life | Q47355702 | ||
Cell size and nucleoid organization of engineered Escherichia coli cells with a reduced genome. | Q47397444 | ||
Codon adaptation index as a measure of dominating codon bias. | Q52641347 | ||
Genomics. Tinker, tailor: can Venter stitch together a genome from scratch? | Q57143516 | ||
P433 | issue | 6 | |
P304 | page(s) | 733-746 | |
P577 | publication date | 2006-11-10 | |
P1433 | published in | Journal of Molecular Evolution | Q6295595 |
P1476 | title | Computational prediction of genomic functional cores specific to different microbes. | |
P478 | volume | 63 |
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