Histone deacetylase inhibitors as therapeutics for polyglutamine disorders
R Butler, GP Bates - Nature Reviews Neuroscience, 2006 - nature.com
During the past 5 years, gene expression studies in cell culture, animal models and in the
brains of patients have shown that the perturbation of transcription frequently results in …
brains of patients have shown that the perturbation of transcription frequently results in …
[HTML][HTML] A protein–protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration
Many human inherited neurodegenerative disorders are characterized by loss of balance
due to cerebellar Purkinje cell (PC) degeneration. Although the disease-causing mutations …
due to cerebellar Purkinje cell (PC) degeneration. Although the disease-causing mutations …
TOR-mediated cell-cycle activation causes neurodegeneration in a Drosophila tauopathy model
V Khurana, Y Lu, ML Steinhilb, S Oldham, JM Shulman… - Current Biology, 2006 - cell.com
Background Previous studies have demonstrated reexpression of cell-cycle markers within
postmitotic neurons in neurodegenerative tauopathies, including Alzheimer's disease (AD) …
postmitotic neurons in neurodegenerative tauopathies, including Alzheimer's disease (AD) …
A Drosophila ortholog of the human MRJ modulates polyglutamine toxicity and aggregation
Z Fayazi, S Ghosh, S Marion, X Bao, M Shero… - Neurobiology of …, 2006 - Elsevier
In the Drosophila eye, proteins with an expanded polyglutamine (polyQ) tract form nuclear
and cytoplasmic inclusions and produce cytotoxicity, demonstrated as loss of eye …
and cytoplasmic inclusions and produce cytotoxicity, demonstrated as loss of eye …
Protein-protein interaction networks in the spinocerebellar ataxias
DC Rubinsztein - Genome Biology, 2006 - Springer
A large yeast two-hybrid study investigating whether the proteins mutated in different forms
of spinocerebellar ataxia have interacting protein partners in common suggests that some …
of spinocerebellar ataxia have interacting protein partners in common suggests that some …
Delayed spinocerebellar ataxia in transgenic mice expressing mutant ubiquitin
M Tsirigotis, MY Tang, M Beyers… - Neuropathology and …, 2006 - Wiley Online Library
Spinocerebellar ataxia type 1 (SCA1) is an incurable neurodegenerative disease resulting
from loss of Purkinje neurones within the cerebellum. The ubiquitin proteasome pathway …
from loss of Purkinje neurones within the cerebellum. The ubiquitin proteasome pathway …
[图书][B] Mitogenic signaling and cell-cycle activation mediate neurodegeneration in Drosophila
V Khurana - 2006 - search.proquest.com
Background. Previous studies have demonstrated re-expression of cell-cycle markers within
postmitotic neurons in neurodegenerative tauopathies, including Alzheimer's disease (AD) …
postmitotic neurons in neurodegenerative tauopathies, including Alzheimer's disease (AD) …