Gregory B Potter

Summary

Affiliation: University of California
Country: USA

Publications

  1. ncbi Generation of Cre-transgenic mice using Dlx1/Dlx2 enhancers and their characterization in GABAergic interneurons
    Gregory B Potter
    Nina Ireland Laboratory of Developmental Neurobiology, Department of Psychiatry, University of California at San Francisco, San Francisco, CA 94158 2611, USA
    Mol Cell Neurosci 40:167-86. 2009
  2. ncbi Dlx1&2 and Mash1 transcription factors control striatal patterning and differentiation through parallel and overlapping pathways
    Jason E Long
    Department of Psychiatry and the Nina Ireland Laboratory of Developmental Neurobiology, University of California San Francisco, San Francisco, California 94158 2324, USA
    J Comp Neurol 512:556-72. 2009
  3. ncbi Chronic reduction in inhibition reduces receptive field size in mouse auditory cortex
    Bryan A Seybold
    Coleman Memorial Laboratory, Department of Otolaryngology Head and Neck Surgery, University of California, San Francisco, CA 94143, USA
    Proc Natl Acad Sci U S A 109:13829-34. 2012
  4. ncbi Dlx1 and Dlx2 control neuronal versus oligodendroglial cell fate acquisition in the developing forebrain
    Magdalena A Petryniak
    Nina Ireland Laboratory of Developmental Neurobiology, Department of Psychiatry, University of California, San Francisco, San Francisco, CA 94158 2611, USA
    Neuron 55:417-33. 2007
  5. ncbi A time and a place for nkx2-1 in interneuron specification and migration
    Laura A B Elias
    Institute for Regeneration Medicine, University of California San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA
    Neuron 59:679-82. 2008
  6. ncbi CXCR4 and CXCR7 have distinct functions in regulating interneuron migration
    Yanling Wang
    Department of Psychiatry, University of California, San Francisco, CA 94158, USA
    Neuron 69:61-76. 2011
  7. ncbi Myelin restoration: progress and prospects for human cell replacement therapies
    Gregory B Potter
    Department of Pediatrics, UCSF, 513 Parnassus Avenue, San Francisco, CA 94143 0525, USA
    Arch Immunol Ther Exp (Warsz) 59:179-93. 2011

Collaborators

Detail Information

Publications7

  1. ncbi Generation of Cre-transgenic mice using Dlx1/Dlx2 enhancers and their characterization in GABAergic interneurons
    Gregory B Potter
    Nina Ireland Laboratory of Developmental Neurobiology, Department of Psychiatry, University of California at San Francisco, San Francisco, CA 94158 2611, USA
    Mol Cell Neurosci 40:167-86. 2009
    ..Finally, we provide the first in vivo evidence that both I12b and URE2 are direct targets of DLX2 and require Dlx1 and Dlx2 expression for proper activity...
  2. ncbi Dlx1&2 and Mash1 transcription factors control striatal patterning and differentiation through parallel and overlapping pathways
    Jason E Long
    Department of Psychiatry and the Nina Ireland Laboratory of Developmental Neurobiology, University of California San Francisco, San Francisco, California 94158 2324, USA
    J Comp Neurol 512:556-72. 2009
    ..These analyses define core transcriptional components that differentially specify the identity and differentiation of the striatum, nucleus accumbens, and septum...
  3. ncbi Chronic reduction in inhibition reduces receptive field size in mouse auditory cortex
    Bryan A Seybold
    Coleman Memorial Laboratory, Department of Otolaryngology Head and Neck Surgery, University of California, San Francisco, CA 94143, USA
    Proc Natl Acad Sci U S A 109:13829-34. 2012
    ..Our findings suggest chronic conditions that feature changes in inhibitory circuitry are not likely to be well modeled by acute network manipulations, and compensation may be a critical component of chronic neuronal conditions...
  4. ncbi Dlx1 and Dlx2 control neuronal versus oligodendroglial cell fate acquisition in the developing forebrain
    Magdalena A Petryniak
    Nina Ireland Laboratory of Developmental Neurobiology, Department of Psychiatry, University of California, San Francisco, San Francisco, CA 94158 2611, USA
    Neuron 55:417-33. 2007
    ..Our results identify another role for Dlx genes as modulators of neuron versus oligodendrocyte development in the ventral embryonic forebrain...
  5. ncbi A time and a place for nkx2-1 in interneuron specification and migration
    Laura A B Elias
    Institute for Regeneration Medicine, University of California San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA
    Neuron 59:679-82. 2008
    ..demonstrate that postmitotic Nkx2-1 regulates migration and sorting of interneurons to the striatum or cortex by controlling the expression of the guidance receptor, Neuropilin-2...
  6. ncbi CXCR4 and CXCR7 have distinct functions in regulating interneuron migration
    Yanling Wang
    Department of Psychiatry, University of California, San Francisco, CA 94158, USA
    Neuron 69:61-76. 2011
    ..On the other hand, CXCL12 stimulation of CXCR7, but not CXCR4, promoted MAP kinase signaling. Thus, we suggest that CXCR4 and CXCR7 have distinct roles and signal transduction in regulating interneuron movement and laminar positioning...
  7. ncbi Myelin restoration: progress and prospects for human cell replacement therapies
    Gregory B Potter
    Department of Pediatrics, UCSF, 513 Parnassus Avenue, San Francisco, CA 94143 0525, USA
    Arch Immunol Ther Exp (Warsz) 59:179-93. 2011
    ..We summarize studies in which different types of myelin-forming cells have been transplanted into the CNS and highlight the continuing challenges regarding the use of cell-based therapies for human white matter disorders...