David A Priestman
University of Oxford
H-index: 28
Europe-United Kingdom
Top articles of David A Priestman
Analysis of glycosphingolipids from cell lines
2024/2/9
David A Priestman
H-Index: 17
Analysis of glycosphingolipids from animal tissues
2024/2/9
David A Priestman
H-Index: 17
Compartmentalisation proteomics revealed endolysosomal protein network changes in a goat model of atrial fibrillation
iScience
2023/3/12
Barry Boland
H-Index: 14
David A Priestman
H-Index: 17
Qianqian Song
H-Index: 2
Antony Galione
H-Index: 35
Rebecca A Capel
H-Index: 8
A mouse systems genetics approach reveals common and uncommon genetic modifiers of hepatic lysosomal enzyme activities and glycosphingolipids
International Journal of Molecular Sciences
2023/3/3
Invariant NKT cells metabolically adapt to the acute myeloid leukaemia environment
Cancer Immunology, Immunotherapy
2023/3
Analysis of glycosphingolipids from human cerebrospinal fluid
2023/2/20
David A Priestman
H-Index: 17
Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patients
Molecular genetics and metabolism
2023/2/1
Glycosphingolipid changes in plasma in Parkinson's disease independent of glucosylceramide levels
Movement Disorders
2022/10
Glucosamine amends CNS pathology in mucopolysaccharidosis IIIC mouse expressing misfolded HGSNAT
Journal of Experimental Medicine
2022/6/15
Glycosphingolipid metabolism and its role in ageing and Parkinson’s disease
2022/2
David A Priestman
H-Index: 17
Identification of genetic modifiers of murine hepatic β-glucocerebrosidase activity
Biochemistry and Biophysics Reports
2021/12/1
A modified density gradient proteomic-based method to analyze endolysosomal proteins in cardiac tissue
Iscience
2021/9/24
Rebecca A Capel
H-Index: 8
David A Priestman
H-Index: 17
Roman Fischer
H-Index: 40
Antony Galione
H-Index: 35
Correction: Molecular basis for a new bovine model of Niemann-Pick type C disease
Plos one
2021/8/31
David A Priestman
H-Index: 17
Oral Glucosamine Ameliorates Aggravated Neurological Phenotype in Mucopolysaccharidosis III Type C Mouse Model Expressing Misfolded HGSNAT Variant
bioRxiv
2021/8/27
An iPSC model of hereditary sensory neuropathy-1 reveals L-serine-responsive deficits in neuronal ganglioside composition and axoglial interactions
Cell Reports Medicine
2021/7/20
Cardiac Atrial Compartmentalisation Proteomics: A Modified Density Gradient Method to Analyse Endo-lysosomal Proteins
bioRxiv
2021/2/22
Correction to: Reduced sphingolipid hydrolase activities, substrate accumulation and ganglioside decline in Parkinson’s disease
Molecular Neurodegeneration
2020/12
David A Priestman
H-Index: 17
Molecular basis for a new bovine model of Niemann-Pick type C disease
Plos one
2020/9/24
David A Priestman
H-Index: 17
Systemic AAV9 gene therapy using the synapsin I promoter rescues a mouse model of neuronopathic Gaucher disease but with limited cross-correction potential to astrocytes
Human Molecular Genetics
2020/1/10
Brain pathology in mucopolysaccharidoses (MPS) patients with neurological forms
Journal of clinical medicine
2020/2/1
David A Priestman
H-Index: 17
Shaukat Khan
H-Index: 23
Co-Authors
