Dystonin Is Essential for Maintaining Neuronal Cytoskeleton Organization
- 1 April 1998
- journal article
- Published by Elsevier in Molecular and Cellular Neuroscience
- Vol. 10 (5-6) , 243-257
- https://doi.org/10.1006/mcne.1997.0660
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Developmental Expression of BPAG1-n: Insights into the Spastic Ataxia and Gross Neurologic Degeneration inDystonia MusculorumMiceDevelopmental Biology, 1997
- Cloning and Characterization of Mouse ACF7, a Novel Member of the Dystonin Subfamily of Actin Binding ProteinsGenomics, 1996
- Dystonin Expression in the Developing Nervous System Predominates in the Neurons That Degenerate indystonia musculorumMutant MiceMolecular and Cellular Neuroscience, 1995
- Cloning and Characterization of the Neural Isoforms of Human DystoninGenomics, 1995
- The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1Nature Genetics, 1995
- The Genomic Structure of an Insertional Mutation in the Dystonia Musculorum LocusGenomics, 1994
- Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: A mouse model of amyotrophic lateral sclerosisCell, 1993
- An intrinsic neuronal defect operates in dystonia musculorum: A study of dt/dt↔+/+ chimerasNeuron, 1992
- Aluminum effect on slow axonal transport: a novel impairment of neurofilament transportJournal of Neuroscience, 1984
- Association of microtubule-associated protein 2 (MAP 2) with microtubules and intermediate filaments in cultured brain cells.The Journal of cell biology, 1983