Inhibition of ICE slows ALS in mice
Robert M. Friedlander,
Robert H. Brown,
Valeria Gagliardini,
Joy Wang and
Junying Yuan ()
Additional contact information
Robert M. Friedlander: Neurosurgical Service, Massachusetts General Hospital, Harvard Medical School
Robert H. Brown: Day Neuromuscular Research Laboratory, Massachusetts General Hospital
Valeria Gagliardini: Cardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School
Joy Wang: Cardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School
Junying Yuan: Cardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School
Nature, 1997, vol. 388, issue 6637, 31-31
Abstract:
Abstract Amyotrophic lateral sclerosis (ALS) is a progressive age-dependent disease involving degeneration of motor neurons in the brain, brainstem and spinal cord. ALS is universally fatal, with the median survival of patients being five years from diagnosis. In a transgenic mouse model of ALS, we now show that a dominant negative inhibitor of a cell-death gene, the interleukin-1β-converting enzyme (ICE), significantly slows the symptomatic progression of ALS.
Date: 1997
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DOI: 10.1038/40299
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