K D Micheva

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. ncbi Retrograde regulation of synaptic vesicle endocytosis and recycling
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, California 94305, USA
    Nat Neurosci 6:925-32. 2003
  2. ncbi Array tomography: a new tool for imaging the molecular architecture and ultrastructure of neural circuits
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA
    Neuron 55:25-36. 2007
  3. ncbi Pregabalin reduces the release of synaptic vesicles from cultured hippocampal neurons
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA
    Mol Pharmacol 70:467-76. 2006
  4. ncbi The gain in brain: novel imaging techniques and multiplexed proteomic imaging of brain tissue ultrastructure
    Kristina D Micheva
    Stanford University School of Medicine, Department of Molecular and Cellular Physiology, Stanford, CA 94305, USA
    Curr Opin Neurobiol 22:94-100. 2012
  5. ncbi Single-synapse analysis of a diverse synapse population: proteomic imaging methods and markers
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA
    Neuron 68:639-53. 2010
  6. ncbi Strong effects of subphysiological temperature on the function and plasticity of mammalian presynaptic terminals
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, California 94305, USA
    J Neurosci 25:7481-8. 2005
  7. ncbi Regulation of presynaptic phosphatidylinositol 4,5-biphosphate by neuronal activity
    K D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA
    J Cell Biol 154:355-68. 2001
  8. ncbi Detection of glutamate release from neurons by genetically encoded surface-displayed FRET nanosensors
    Sakiko Okumoto
    Department of Plant Biology, Carnegie Institution of Washington, 260 Panama Street, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 102:8740-5. 2005
  9. ncbi Visualizing the distribution of synapses from individual neurons in the mouse brain
    Ling Li
    Howard Hughes Medical Institute, Department of Biology, Stanford University, Stanford, California, United States of America
    PLoS ONE 5:e11503. 2010
  10. ncbi Classical MHCI molecules regulate retinogeniculate refinement and limit ocular dominance plasticity
    Akash Datwani
    Departments of Biology, James H Clark Center, Stanford University, Stanford, CA 94305, USA
    Neuron 64:463-70. 2009

Collaborators

Detail Information

Publications11

  1. ncbi Retrograde regulation of synaptic vesicle endocytosis and recycling
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, California 94305, USA
    Nat Neurosci 6:925-32. 2003
    ....
  2. ncbi Array tomography: a new tool for imaging the molecular architecture and ultrastructure of neural circuits
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA
    Neuron 55:25-36. 2007
    ..The application of array tomography can reveal important but previously unseen features of brain molecular architecture...
  3. ncbi Pregabalin reduces the release of synaptic vesicles from cultured hippocampal neurons
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA
    Mol Pharmacol 70:467-76. 2006
    ..Finally, the action of pregabalin on dye release is most apparent before and early during a train of electrical stimuli when vesicle release preferentially involves the readily releasable pool...
  4. ncbi The gain in brain: novel imaging techniques and multiplexed proteomic imaging of brain tissue ultrastructure
    Kristina D Micheva
    Stanford University School of Medicine, Department of Molecular and Cellular Physiology, Stanford, CA 94305, USA
    Curr Opin Neurobiol 22:94-100. 2012
    ....
  5. ncbi Single-synapse analysis of a diverse synapse population: proteomic imaging methods and markers
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA
    Neuron 68:639-53. 2010
    ..These results establish a means for the high-throughput acquisition of proteomic data from individual cortical synapses in situ...
  6. ncbi Strong effects of subphysiological temperature on the function and plasticity of mammalian presynaptic terminals
    Kristina D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, California 94305, USA
    J Neurosci 25:7481-8. 2005
    ....
  7. ncbi Regulation of presynaptic phosphatidylinositol 4,5-biphosphate by neuronal activity
    K D Micheva
    Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA
    J Cell Biol 154:355-68. 2001
    ..Thus, PIP2 in the presynaptic terminal appears to be regulated by postsynaptic activity via a retrograde action of NO...
  8. ncbi Detection of glutamate release from neurons by genetically encoded surface-displayed FRET nanosensors
    Sakiko Okumoto
    Department of Plant Biology, Carnegie Institution of Washington, 260 Panama Street, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 102:8740-5. 2005
    ..The results demonstrate that FLIPE sensors can be used for real-time monitoring of glutamate metabolism in living cells, in tissues, or in intact organisms, providing tools for studying metabolism or for drug discovery...
  9. ncbi Visualizing the distribution of synapses from individual neurons in the mouse brain
    Ling Li
    Howard Hughes Medical Institute, Department of Biology, Stanford University, Stanford, California, United States of America
    PLoS ONE 5:e11503. 2010
    ..To understand how complex neural circuits function, it is crucial to precisely describe neuronal connectivity and the distributions of synapses to and from individual neurons...
  10. ncbi Classical MHCI molecules regulate retinogeniculate refinement and limit ocular dominance plasticity
    Akash Datwani
    Departments of Biology, James H Clark Center, Stanford University, Stanford, CA 94305, USA
    Neuron 64:463-70. 2009
    ..H2-K(b) and H2-D(b) ligands, signaling via neuronal MHCI receptors, may enable activity-dependent remodeling of brain circuits during developmental critical periods...
  11. ncbi Fragmentation of the Golgi apparatus induced by the overexpression of wild-type and mutant human tau forms in neurons
    Dalinda Liazoghli
    Departement de pathologie et biologie cellulaire, Universite de Montreal, 2900, Boulevard Edouard Montpetit, Montreal, Quebec, Canada, H3T 1J4
    Am J Pathol 166:1499-514. 2005
    ..The pre-sent results implicate tau in GA fragmentation and show that this event occurs before the formation of neurofibrillary tangles...