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Human Genetics, Vol. 120, Iss. 4, 2006-11 ,pp. : 581-588

Springer Publishing Company

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Genomic Imprinting of Human p57 KIP2 and Its Reduced Expression in Wilms' Tumors

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Transgenic Research, Vol. 15, Iss. 5, 2006-10 ,pp. : 647-653

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Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse

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Interaction between parkin and mutant glucocerebrosidase variants: a possible link between Parkinson disease and Gaucher disease

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