Latest papers

AtTFC B is involved in control of cell division.

Theoretical methods for identifying important functional genes in bacterial genomes.

Drosophila liquid facets-Related encodes Golgi epsin and is an essential gene required for cell proliferation, growth, and patterning.

The complementation of yeast with human or Plasmodium falciparum Hsp90 confers differential inhibitor sensitivities.

Methylene tetrahydrofolate dehydrogenase/cyclohydrolase and the synthesis of 10-CHO-THF are essential in Leishmania major

Predicting genetic interactions with random walks on biological networks.

Comprehensive identification of essential Staphylococcus aureus genes using Transposon-Mediated Differential Hybridisation (TMDH)

Hipk is an essential protein that promotes Notch signal transduction in the Drosophila eye by inhibition of the global co-repressor Groucho

DEG 5.0, a database of essential genes in both prokaryotes and eukaryotes.

Ssd1 is required for thermotolerance and Hsp104-mediated protein disaggregation in Saccharomyces cerevisiae.

Genome-scale analysis to the impact of gene deletion on the metabolism of E. coli: constraint-based simulation approach

Selection of suitable housekeeping genes for expression analysis in glioblastoma using quantitative RT-PCR.

Constraint-based analysis of metabolic capacity of Salmonella typhimurium during host-pathogen interaction.

Genome-wide deletion mutant analysis reveals genes required for respiratory growth, mitochondrial genome maintenance and mitochondrial protein synthesis in Saccharomyces cerevisiae

Plasma membrane microdomains regulate turnover of transport proteins in yeast.

In vitro and in vivo validation of ligA and tarI as essential targets in Staphylococcus aureus.

ScrB (Cg2927) is a sucrose-6-phosphate hydrolase essential for sucrose utilization by Corynebacterium glutamicum.

The essential and non-essential genes of Bovine herpesvirus 1.

Involvement of an essential gene, mviN, in murein synthesis in Escherichia coli.

Recovery of infectious virus by transfection of in vitro-generated RNA from tulane calicivirus cDNA.