Items where Author is "Wilson, PJM"

Article

Norman, BP ORCID: 0000-0001-9293-4852, Sutherland, H, Wilson, PJM, Rutland, DA, Milan, AM, Hughes, AT, Davison, AS, Khedr, M, Jarvis, JC ORCID: 0000-0001-8982-6279, Gallagher, JA, Bou-Gharios, G and Ranganath, LR (2024) Hepatobiliary circulation and dominant urinary excretion of homogentisic acid in a mouse model of alkaptonuria. Journal of Inherited Metabolic Disease. ISSN 0141-8955

Norman, BP ORCID: 0000-0001-9293-4852, Davison, AS ORCID: 0000-0001-5501-4475, Hickton, B, Ross, GA, Milan, AM ORCID: 0000-0002-0452-2338, Hughes, AT, Wilson, PJM, Sutherland, H, Hughes, JH ORCID: 0000-0001-6155-4136, Roberts, NB, Bou-Gharios, G ORCID: 0000-0002-9563-9418, Gallagher, JA and Ranganath, LR (2022) Comprehensive Biotransformation Analysis of Phenylalanine-Tyrosine Metabolism Reveals Alternative Routes of Metabolite Clearance in Nitisinone-Treated Alkaptonuria. Metabolites, 12 (10). ISSN 2218-1989

Hughes, JH, Keenan, CM, Sutherland, H, Edwards, HR, Wilson, PJM, Ranganath, LR, Jarvis, JC, Bou-Gharios, G and Gallagher, JA (2020) Anatomical Distribution of Ochronotic Pigment in Alkaptonuric Mice is Associated with Calcified Cartilage Chondrocytes at Osteochondral Interfaces. Calcified Tissue International. ISSN 0171-967X

Hughes, JH, Wilson, PJM, Sutherland, H, Judd, S, Hughes, AT, Milan, AM, Jarvis, JC, Bou-Gharios, G, Ranganath, LR and Gallagher, JA (2020) Dietary restriction of tyrosine and phenylalanine lowers tyrosinaemia associated with nitisinone therapy of alkaptonuria. Journal of Inherited Metabolic Disease. pp. 1-10. ISSN 0141-8955