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  1. Faculty Opinions recommendation of Loss of function of glucocerebrosidase GBA2 is...

    http://iris.ucl.ac.uk/iris/publication/1704255/13

  2. Inhibition of GBA2 may influence the neuronal response to oxidative stress: Implications...

    http://iris.ucl.ac.uk/iris/publication/1770107/3

  3. Lysosomal beta-glucosidase (GBA1) and non-lysosomal beta-glucosidase (GBA2): Potential...

    http://iris.ucl.ac.uk/iris/publication/1019395/3

  4. β-Glucosidase 2 (GBA2) activity and imino sugar pharmacology.

    β-Glucosidase 2 (GBA2) is an enzyme that cleaves the membrane lipid glucosylceramide into glucose and ceramide. The GBA2 gene is mutated in genetic neurological diseases (hereditary spastic paraplegia and cerebellar ataxia). Pharmacologically, GBA2

    http://iris.ucl.ac.uk/iris/publication/889441/2

  5. Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity.

    Autosomal-recessive cerebellar ataxia (ARCA) comprises a large and heterogeneous group of neurodegenerative disorders with more than 20 different forms currently recognized, many of which are also associated with increased tone and some of which

    http://iris.ucl.ac.uk/iris/publication/845990/2

  6. Interplay between Glucocerebrosidase 1 and Glucocerebrosidase 2; potential implications...

    Gaucher disease (GD) is a lysosomal storage disorder with wide clinical heterogeneity, caused by mutations in the GBA gene leading to low or deficient levels of the lysosomal enzyme Glucocerebrosidase (GBA1). Mutations in GBA1 are also the single

    http://iris.ucl.ac.uk/iris/publication/1415051/1

  7. Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in...

    Lysosomal glucocerebrosidase (GBA1) deficiency is causative for Gaucher disease. Not all individuals with GBA1 mutations develop neurological involvement raising the possibility that other factors may provide compensatory protection. One factor may

    http://iris.ucl.ac.uk/iris/publication/832175/2

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