A novel approach to analyze lysosomal dysfunctions through subcellular proteomics and lipidomics: the case of NPC1 deficiency
2017 · Scientific Reports · 121 citations
https://doi.org/10.1038/srep41408
D
David A. Priestman
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David A. Priestman is an academic researcher from University of Oxford. The author has contributed to research in topics: Lysosomal Storage Disorders Research & Glycosylation and Glycoproteins Research & Cellular transport and secretion. The author has an h-index of 30, co-authored 75 publications.
ORCID: 0000-0002-0030-0148Papers by this author
worksInhibition of β-Glucocerebrosidase Activity Preserves Motor Unit Integrity in a Mouse Model of Amyotrophic Lateral Sclerosis
2017 · Scientific Reports · 48 citations
https://doi.org/10.1038/s41598-017-05313-0
An iPSC model of hereditary sensory neuropathy-1 reveals L-serine-responsive deficits in neuronal ganglioside composition and axoglial interactions
2021 · Cell Reports Medicine · 33 citations
https://doi.org/10.1016/j.xcrm.2021.100345
Glucosamine amends CNS pathology in mucopolysaccharidosis IIIC mouse expressing misfolded HGSNAT
2022 · The Journal of Experimental Medicine · 32 citations
https://doi.org/10.1084/jem.20211860
A modified density gradient proteomic-based method to analyze endolysosomal proteins in cardiac tissue
2021 · iScience · 7 citations
https://doi.org/10.1016/j.isci.2021.102949
Identification of genetic modifiers of murine hepatic β-glucocerebrosidase activity
2021 · Biochemistry and Biophysics Reports · 5 citations
https://doi.org/10.1016/j.bbrep.2021.101105
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