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Gene Therapy|December 5, 2014
Widespread correction of central nervous system disease after intracranial gene therapy in a feline model of Sandhoff diseaseV J McCurdy, H E Rockwell, J R Arthur, et al.
Nature Communications|November 24, 2023
Genetic separation of Brca1 functions reveal mutation-dependent Polθ vulnerabilitiesJohn J Krais, David J Glass, Ilse Chudoba, et al.
Neuroscience|November 7, 2016
AAV-mediated gene delivery attenuates neuroinflammation in feline Sandhoff diseaseAllison M Bradbury, Tiffany A Peterson, Amanda L Gross, et al.
The Journal of Clinical Investigation|August 11, 2020
Krabbe disease successfully treated via monotherapy of intrathecal gene therapyAllison M Bradbury, Jessica H Bagel, Duc Nguyen, et al.
The Journal of Biological Chemistry|January 28, 2015
Receptor tyrosine kinase EphA5 is a functional molecular target in human lung cancerFernanda I Staquicini, Ming D Qian, Ahmad Salameh, et al.
Annals of Neurology|August 1, 2023
Life-Limiting Peripheral Organ Dysfunction in Feline Sandhoff Disease Emerges after Effective CNS Gene TherapyAime K Johnson, Victoria J McCurdy, Heather L Gray-Edwards, et al.
Molecular Genetics and Metabolism|May 15, 2015
Mucopolysaccharidosis-like phenotype in feline Sandhoff disease and partial correction after AAV gene therapyHeather L Gray-Edwards, Brandon L Brunson, Merrilee Holland, et al.
Experimental Neurology|October 7, 2014
Biomarkers for disease progression and AAV therapeutic efficacy in feline Sandhoff diseaseAllison M Bradbury, Heather L Gray-Edwards, Jamie L Shirley, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 22, 2013
Therapeutic response in feline sandhoff disease despite immunity to intracranial gene therapyAllison M Bradbury, J Nicholas Cochran, Victoria J McCurdy, et al.
Mabs|February 28, 2018
When monoclonal antibodies are not monospecific: Hybridomas frequently express additional functional variable regionsAndrew R M Bradbury, Nathan D Trinklein, Holger Thie, et al.
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