Improved outcome of N-butyldeoxygalactonojirimycin-mediated substrate reduction therapy in a mouse model of Sandhoff disease.
Sandhoff disease is a severe neurodegenerative glycosphingolipid (GSL) lysosomal storage disorder, currently without treatment options. One therapeutic approach under investigation is substrate reduction therapy (SRT). By partially inhibiting GSL biosynthesis, the impaired rate of GSL catabolism is...
Päätekijät: | Andersson, U, Smith, D, Jeyakumar, M, Butters, T, Borja, M, Dwek, R, Platt, F |
---|---|
Aineistotyyppi: | Journal article |
Kieli: | English |
Julkaistu: |
2004
|
Samankaltaisia teoksia
-
Improved outcome of N-butyldeoxygalactonojirimycin-mediated substrate reduction therapy in a mouse model of Sandhoff disease
Tekijä: Ulrika Andersson, et al.
Julkaistu: (2004-08-01) -
NSAIDs increase survival in the Sandhoff disease mouse: synergy with N-butyldeoxynojirimycin.
Tekijä: Jeyakumar, M, et al.
Julkaistu: (2004) -
N-butyldeoxygalactonojirimycin: a more selective inhibitor of glycosphingolipid biosynthesis than N-butyldeoxynojirimycin, in vitro and in vivo.
Tekijä: Andersson, U, et al.
Julkaistu: (2000) -
N-butyldeoxygalactonojirimycin reduces brain ganglioside and GM2 content in neonatal sandhoff diseased mice
Tekijä: Baek, R, et al.
Julkaistu: (2004) -
N-butyldeoxygalactonojirimycin reduces brain ganglioside and GM2 content in neonatal Sandhoff disease mice.
Tekijä: Baek, R, et al.
Julkaistu: (2008)