Raquel Conde-Alvarez

Synthesis of phosphatidylcholine, a typical eukaryotic phospholipid, is necessary for full virulence of the intracellular bacterial parasite Brucella abortus.

Brucellosis vaccines: assessment of Brucella melitensis lipopolysaccharide rough mutants defective in core and O-polysaccharide synthesis and export.

The differential interaction of Brucella and ochrobactrum with innate immunity reveals traits related to the evolution of stealthy pathogens.

Brucella abortus ornithine lipids are dispensable outer membrane components devoid of a marked pathogen-associated molecular pattern.

Identification and functional analysis of the cyclopropane fatty acid synthase of Brucella abortus.

The lipopolysaccharide core of Brucella abortus acts as a shield against innate immunity recognition.

Lipopolysaccharide as a target for brucellosis vaccine design.

Specific inhibition of diverse pathogens in human cells by synthetic microRNA-like oligonucleotides inferred from RNAi screens.

The identification of wadB, a new glycosyltransferase gene, confirms the branched structure and the role in virulence of the lipopolysaccharide core of Brucella abortus.

Brucella abortus depends on pyruvate phosphate dikinase and malic enzyme but not on Fbp and GlpX fructose-1,6-bisphosphatases for full virulence in laboratory models.

Mutants in the lipopolysaccharide of Brucella ovis are attenuated and protect against B. ovis infection in mice.

Brucella, nitrogen and virulence.

Simultaneous analysis of large-scale RNAi screens for pathogen entry.

gespeR: a statistical model for deconvoluting off-target-confounded RNA interference screens.

Erratum to: gespeR: a statistical model for deconvoluting off-target-confounded RNA interference screens.

Structural Studies of Lipopolysaccharide-defective Mutants from Brucella melitensis Identify a Core Oligosaccharide Critical in Virulence.

A review of the basis of the immunological diagnosis of ruminant brucellosis.