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You searched for: Author/Creator Watabe, Kazuhiko

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1. A Japanese patient with familial ALS and a p.K510M mutation in the gene for FUS (FUS) resulting in the totally locked‐in state. Issue 5 (19th May 2014)

2. A low amyloidogenic E61K transthyretin mutation may cause familial amyloid polyneuropathy. Issue 6 (20th September 2020)

3. A spontaneously immortalized Schwann cell line from aldose reductase‐deficient mice as a useful tool for studying polyol pathway and aldehyde metabolism. Issue 6 (16th January 2018)

4. Adenoviral expression of TDP‐43 and FUS genes and shRNAs for protein degradation pathways in rodent motoneurons in vitro and in vivo. Issue 1 (12th August 2013)

5. Astrocytes release glutamate via cystine/glutamate antiporter upregulated in response to increased oxidative stress related to sporadic amyotrophic lateral sclerosis. Issue 6 (10th December 2020)

8. Involvement of oxidative stress and impaired lysosomal degradation in amiodarone‐induced schwannopathy. (7th June 2016)

9. L-leucine and SPNS1 coordinately ameliorate dysfunction of autophagy in mouse and human Niemann-Pick type C disease. Issue 1 (December 2017)