Cited by 239

Widespread Disruption of Repressor Element-1 Silencing Transcription Factor/Neuron-Restrictive Silencer Factor Occupancy at Its Target Genes in Huntington's Disease

Zuccato, C., Belyaev, N., Conforti, P., Ooi, L., Tartari, M., Papadimou, E., MacDonald, M., Fossale, E. +3 more·2007·Journal of Neuroscience

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Integrity signals

Registry

Crossref · 10.1523/jneurosci.4278-06.2007

Cites

2 of 2 references verified0 citation errors · 0 not checkable

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  • REST is mislocalized in brains of patients with Huntington's disease, with increased nuclear localization and occupancy at RE1 sites compared to healthy controls.

    “The transcriptional repressor REST is mislocalized in brains of patients with HD, with increased nuclear localization and occupancy at RE1 sites compared to healthy controls (Zuccato et al., 2003 ; Zuccato et al., 2007).”
  • One putative mechanism underlying the transcriptional changes in Huntington's disease is aberrant cellular distribution of the transcriptional repressor REST.

    “One putative mechanism underlying the transcriptional changes is aberrant cellular distribution of the transcriptional repressor RE1-silencing transcription factor (REST, also known as neuronal restrictive silencing factor, NRSF) (Lunyak et al., 2002; Zuccato et al., 2003 ; Zuccato et al., 2007).”

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Research works printed but not linked: 1

  1. Van Raamsdonk JM, Pearson J, Rogers DA, Bissada N, Vogl AW, Hayden MR, Leavitt BR (2005) Loss of wild-type huntingtin influences motor dys- function and survival in the YAC128 mouse model of Huntington disease. Hum Mol Genet 14:1379 -1392.

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Authors
Zuccato, C., Belyaev, N., Conforti, P., Ooi, L., Tartari, M., Papadimou, E., MacDonald, M., Fossale, E., Zeitlin, S., Buckley, N., & Cattaneo, E.
Venue
Journal of Neuroscience
Published
2007-06-27
Volume
27
Issue
26
Pages
6972-6983
ISSN
  • 0270-6474
  • 1529-2401
Cited by
239
References
2
Language
en

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