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Nature Genetics|October 1, 1995
Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolismK Sango, S Yamanaka, A Hoffmann, et al.
Human Molecular Genetics|April 18, 2000
Alleviation of neuronal ganglioside storage does not improve the clinical course of the Niemann-Pick C disease mouseY Liu, Y P Wu, R Wada, et al.
The Journal of Biological Chemistry|January 3, 2001
Mice expressing only monosialoganglioside GM3 exhibit lethal audiogenic seizuresH Kawai, M L Allende, R Wada, et al.
Nature Genetics|November 1, 1996
Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosisK Sango, M P McDonald, J N Crawley, et al.
The Journal of Clinical Investigation|February 18, 1999
A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorderY Liu, R Wada, H Kawai, et al.
The Journal of Clinical Investigation|October 18, 2000
Edg-1, the G protein-coupled receptor for sphingosine-1-phosphate, is essential for vascular maturationY Liu, R Wada, T Yamashita, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 30, 2004
Immune cell regulation and cardiovascular effects of sphingosine 1-phosphate receptor agonists in rodents are mediated via distinct receptor subtypesM Forrest, S-Y Sun, R Hajdu, et al.
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