WebNeuronal dystonin isoforms are giant cytoskeletal cross-linking proteins capable of interacting with actin and microtubule networks, protein complexes, membrane-bound … WebJun 1, 1998 · A central role for the Schwann cell cytoskeleton in the process of peripheral nerve myelination has long been suggested. However, there is no genetic or biological evidence as yet to support this assumption. Here we show that dystonia musculorum (dt) mice, which carry mutations in dystonin, a cytoskeletal crosslinker protein, have …
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WebDec 21, 2011 · This result indicates that phenotypic onset correlates closely with severe degeneration of DRG sensory neurons. We then sought to determine which neuronal isoform of dystonin was critical to maintaining cell viability in sensory neurons. dt Tg4 transgenic mice are null for dystonin-a1 and dystonin-a2 but express dystonin-a3 … WebJun 27, 2024 · Dystonia musculorum (dt) is a hereditary neurodegenerative disease in mice that leads to sensory ataxia (see ANIMAL MODEL). Brown et al. (1995) cloned a candidate gene for mouse dt, called dystonin, that was predominantly expressed in the dorsal root ganglia and other sites of neurodegeneration in dt mice. They showed that the dystonin … WebImmunocytochemistry/ Immunofluorescence: Dystonin Antibody (1B10) [H00000667-M01] - Analysis of monoclonal antibody to DST on HeLa cell . Antibody concentration 10 ug/ml. … small office copier machines