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Publications by D. E. Britton
Gaucher Disease: Isolation and Comparison of Normal and Mutant Glucocerebrosidase From Human Spleen Tissue.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
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Glucocerebrosidase Deficiency Dramatically Impairs Human Bone Marrow Haematopoiesis in an in Vitro Model of Gaucher Disease
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Mechanism of Glucocerebrosidase Activation and Dysfunction in Gaucher Disease Unraveled by Molecular Dynamics and Deep Learning
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Unfolded Protein Response in Gaucher Disease: From Human to Drosophila
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Isolation of Multiple TT Virus Genotypes From Spleen Biopsy Tissue From a Hodgkin's Disease Patient: Genome Reorganization and Diversity in the Hypervariable Region
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Identification of Three Additional Genes Contiguous to the Glucocerebrosidase Locus on Chromosome 1q21: Implications for Gaucher Disease
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Isofagomine- And 2, 5-Anhydro-2, 5-Imino-D-Glucitol-Based Glucocerebrosidase Pharmacological Chaperones for Gaucher Disease Intervention
