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Division of Pediatric Neurology,
Department of Pediatrics,
Division of Pediatric Neurology, Department of Pediatrics
Tamara J. Stevenson has not added Biography.
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Normal newt limb regeneration requires matrix metalloproteinase function.
Developmental biology Mar, 2005 | Pubmed ID: 15708560
Tissue inhibitor of metalloproteinase 1 regulates matrix metalloproteinase activity during newt limb regeneration.
Developmental dynamics : an official publication of the American Association of Anatomists Mar, 2006 | Pubmed ID: 16372340
Cellular electroporation induces dedifferentiation in intact newt limbs.
Developmental biology Nov, 2006 | Pubmed ID: 16949563
Human alpha B-crystallin mutation causes oxido-reductive stress and protein aggregation cardiomyopathy in mice.
Cell Aug, 2007 | Pubmed ID: 17693254
Identification of a dopaminergic enhancer indicates complexity in vertebrate dopamine neuron phenotype specification.
Developmental biology Apr, 2011 | Pubmed ID: 21276790
Hypoxia disruption of vertebrate CNS pathfinding through ephrinB2 Is rescued by magnesium.
PLoS genetics , 2012 | Pubmed ID: 22511881
Zebrafish foxP2 zinc finger nuclease mutant has normal axon pathfinding.
PloS one , 2012 | Pubmed ID: 22937139
University of Utah School of Medicine
Lingyan Xing1,2,3,
Tyler S. Quist1,
Tamara J. Stevenson1,
Timothy J. Dahlem4,
Joshua L. Bonkowsky1,2,3,5
1Division of Pediatric Neurology, Department of Pediatrics, University of Utah School of Medicine,
2Department of Neurobiology and Anatomy, University of Utah School of Medicine,
3Interdepartmental Program in Neurosciences, University of Utah School of Medicine,
4Mutation Generation and Detection Core, HSC Core Research Facility, University of Utah School of Medicine,
5Department of Neurology, University of Utah School of Medicine
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