New developments in treating glycosphingolipid storage diseases.
Prif Awduron: | Platt, F, Jeyakumar, M, Andersson, U, Dwek, R, Butters, T |
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Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
2005
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Eitemau Tebyg
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Glycosphingolipid lysosomal storage diseases: therapy and pathogenesis.
gan: Jeyakumar, M, et al.
Cyhoeddwyd: (2002) -
New therapeutics for the treatment of glycosphingolipid lysosomal storage diseases.
gan: Butters, T, et al.
Cyhoeddwyd: (2003) -
Inhibition of glycosphingolipid biosynthesis: application to lysosomal storage disorders.
gan: Butters, T, et al.
Cyhoeddwyd: (2000) -
Substrate deprivation: a new therapeutic approach for the glycosphingolipid lysosomal storage diseases.
gan: Platt, F, et al.
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N-butyldeoxygalactonojirimycin: a more selective inhibitor of glycosphingolipid biosynthesis than N-butyldeoxynojirimycin, in vitro and in vivo.
gan: Andersson, U, et al.
Cyhoeddwyd: (2000)