نتایج جستجو برای: aspartoacylase deficiency

تعداد نتایج: 137211  

Journal: :Human gene therapy 2002
Christopher Janson Scott McPhee Larissa Bilaniuk John Haselgrove Mark Testaiuti Andrew Freese Dah-Jyuu Wang David Shera Peter Hurh Joan Rupin Elizabeth Saslow Olga Goldfarb Michael Goldberg Ghassem Larijani William Sharrar Larisa Liouterman Angelique Camp Edwin Kolodny Jude Samulski Paola Leone

This clinical protocol describes virus-based gene transfer for Canavan disease, a childhood leukodystrophy. Canavan disease, also known as Van Bogaert-Bertrand disease, is a monogeneic, autosomal recessive disease in which the gene coding for the enzyme aspartoacylase (ASPA) is defective. The lack of functional enzyme leads to an increase in the central nervous system of the substrate molecule,...

Journal: :Proceedings for Annual Meeting of The Japanese Pharmacological Society 2019

Journal: :Proceedings of the National Academy of Sciences 2006

Journal: :Current opinion in molecular therapeutics 1999
P Leone C G Janson S J McPhee M J During

The neurogenetic prototypic disease on which we chose to test our gene therapy strategy is Canavan disease (CD). CD is an autosomal recessive leukodystrophy associated with spongiform degeneration of the brain. At present the disease is uniformly fatal in affected probands. CD is characterized by mutations in the aspartoacylase (ASPA) gene, resulting in loss of enzyme activity. In this review, ...

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