Tamara J. Stevenson

Normal newt limb regeneration requires matrix metalloproteinase function.

Tissue inhibitor of metalloproteinase 1 regulates matrix metalloproteinase activity during newt limb regeneration.

Cellular electroporation induces dedifferentiation in intact newt limbs.

Human alpha B-crystallin mutation causes oxido-reductive stress and protein aggregation cardiomyopathy in mice.

Identification of a dopaminergic enhancer indicates complexity in vertebrate dopamine neuron phenotype specification.

Hypoxia disruption of vertebrate CNS pathfinding through ephrinB2 Is rescued by magnesium.

Zebrafish foxP2 zinc finger nuclease mutant has normal axon pathfinding.