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ALS (Lou Gehrig's diseae) |
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Amyotrophic lateral
sclerosis (ALS) is one of the most devastating neurological disorders in adults.
It is characterized by progressive motor neuron degeneration and inevitably
leads to death within 3 to 5 years of onset. Despite decades of research, the
etiology of ALS is still unknown. Some of the suggested pathogenic factors are
glutamate toxicity, oxidative stress, neurofilament accumulation, exogenous
factors (toxins, viruses) and neuroinflammation. All of these hypotheses are not
mutually exclusive and may individually or together cause motor neuron disease
through a common final pathway. The majority of ALS cases are sporadic (~90%),
but in the inherited form of the disease (familial ALS) about 10 to 20% of the
cases are associated with mutations in the superoxide dismutase 1 (mtSOD1) gene.
Our labs studies the role of
neuroinflammation in
ALS as well as the molecular mechanisms regulating
microRNA
expression in this disease.
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Send mail to: moeller@u.washington.edu
Last modified: 7/16/2008 4:36 PM |
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