Jonathan Ewbank

Antifungal Innate Immunity in C. elegans: PKCdelta Links G Protein Signaling and a Conserved p38 MAPK Cascade.

Neuroimmune regulation of antimicrobial peptide expression by a noncanonical TGF-beta signaling pathway in Caenorhabditis elegans epidermis.

Negative regulation of Caenorhabditis elegans epidermal damage responses by death-associated protein kinase.

Anti-fungal innate immunity in C. elegans is enhanced by evolutionary diversification of antimicrobial peptides.

Pathogenomics: an updated European Research Agenda.

Distinct Innate Immune Responses to Infection and Wounding in the C. elegans Epidermis.

The genetics of pathogen avoidance in Caenorhabditis elegans.

A model of bacterial intestinal infections in Drosophila melanogaster.

Detection and avoidance of a natural product from the pathogenic bacterium Serratia marcescens by Caenorhabditis elegans.

Infection in a dish: high-throughput analyses of bacterial pathogenesis.

Genome-wide investigation reveals pathogen-specific and shared signatures in the response of Caenorhabditis elegans to infection.

A semi-automated high-throughput approach to the generation of transposon insertion mutants in the nematode Caenorhabditis elegans.

A generalized transducing phage (phiIF3) for the genomically sequenced Serratia marcescens strain Db11: a tool for functional genomics of an opportunistic human pathogen.

Signaling in the immune response.

'TaiLoRing' the response of dendritic cells to pathogens.

XNP-1/ATR-X acts with RB, HP1 and the NuRD complex during larval development in C. elegans.

Diversity and specificity in the interaction between Caenorhabditis elegans and the pathogen Serratia marcescens.

TLR-independent control of innate immunity in Caenorhabditis elegans by the TIR domain adaptor protein TIR-1, an ortholog of human SARM.

Evolution of the innate immune system: the worm perspective.

Immunity in Caenorhabditis elegans.

Genetic models in pathogenesis.

[A worm's life]

Q & A. Jonathan Ewbank.

Caenorhabditis elegans: an emerging genetic model for the study of innate immunity.

Virulence factors of the human opportunistic pathogen Serratia marcescens identified by in vivo screening.

[The nematode Caenorhabditis elegans as a model for the study of host-pathogen interactions]

Diverse bacteria are pathogens of Caenorhabditis elegans.

Inducible antibacterial defense system in C. elegans.

Tackling both sides of the host-pathogen equation with Caenorhabditis elegans.

A reverse genetic analysis of components of the Toll signaling pathway in Caenorhabditis elegans.

The Caenorhabditis elegans unc-32 gene encodes alternative forms of a vacuolar ATPase a subunit.

Comment on Lee M. Silver's article 'Reprogenetics: third millenium speculation' in EMBO reports, November 2000.

Caenorhabditis elegans is a model host for Salmonella typhimurium.

The homeodomain protein CePHOX2/CEH-17 controls antero-posterior axonal growth in C. elegans.

Caenorhabditis elegans for the study of host-pathogen interactions.

Biotech companies must get back to basics to weigh up risks.

Characterization of xnp-1, a Caenorhabditis elegans gene similar to the human XNP/ATR-X gene.

CLK-1 controls respiration, behavior and aging in the nematode Caenorhabditis elegans.

Problems of germline therapy.

Molecular genetics of life span in C. elegans: how much does it teach us?

Structural and functional conservation of the Caenorhabditis elegans timing gene clk-1.

What is the molten globule?

Conformation of GroEL-bound alpha-lactalbumin probed by mass spectrometry.

Conformational specificity of the chaperonin GroEL for the compact folding intermediates of alpha-lactalbumin.

Disulfide-rearranged molten globule state of alpha-lactalbumin.

Pathway of disulfide-coupled unfolding and refolding of bovine alpha-lactalbumin.

Structural characterization of the disulfide folding intermediates of bovine alpha-lactalbumin.

Protein folding by stages.

The molten globule protein conformation probed by disulphide bonds.

Embryo research.

Large scale high-performance liquid chromatography of urogastrone produced by recombinant DNA technology.