Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain
the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in
Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles
and JavaScript.
T cells genetically modified to express a peptide–MHC complex, normally involved in the induction of autoimmunity, can kill pathogenic T cells and inhibit autoimmune disease.
The recently determined high-resolution crystal structure of the bacterial multidrug resistance transporter AcrB brings us one step closer to the design of more effective therapeutic agents.
The Plasmodium falciparum genome sequence will facilitate the identification of novel classes of antimalarials and new vaccine candidates that bring the control of malaria in humans one step closer.
Two reports on immortalized neural precursor cells, seeded in a biodegradable polymer scaffold or directly injected in the injured brain, offer insights into the repair of damage from stroke and Parkinson's disease.
Characterization of novel multifunctional proteins involved in assembly of the enediyne natural products C-1027 and calicheamicin furthers the potential of combinatorial biosynthesis.
By combining a refined Agrobacterium tumefaciens–mediated transformation protocol with stringent selection, researchers have succeeded in isolating gene-targeted rice plants with surprisingly high efficiency.
Cloned cattle engineered to carry an artificial chromosome encoding human immunoglobulin genes are a significant leap toward the production of safer and more potent therapeutic antibodies.
Growing human embryonic stem cells in an environment free of mouse feeder cells lowers the risk of cross-species infection but does little to clarify what makes stem cells “tick.”
By the imprinting of a molecular memory in their core, dendrimers can be tailored to bind to defined molecular targets in a selective and reversible fashion.