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The Journal of Physiology|January 26, 2008
Temporal changes in the involvement of pyruvate dehydrogenase complex in muscle lactate accumulation during lipopolysaccharide infusion in ratsN Alamdari, D Constantin-Teodosiu, A J Murton, et al.Proceedings of the National Academy of Sciences of the United States of America|August 16, 2000
Inhibition of the ubiquitin-proteasome system in Alzheimer's diseaseY A Lam, C M Pickart, A Alban, et al.Biochemical Society Transactions|October 21, 2004
Structural and functional studies of mutations affecting the UBA domain of SQSTM1 (p62) which cause Paget's disease of boneR Layfield, B Ciani, S H Ralston, et al.Analytical Biochemistry|May 1, 1997
Capillary electrophoresis assay for ubiquitin carboxyl-terminal hydrolases with chemically synthesized ubiquitin-valine as substrateK Franklin, R Layfield, M Landon, et al.Cytogenetics and Cell Genetics|January 1, 1992
Chromosomal location of the human transketolase geneN M Lapsys, R Layfield, E Baker, et al.Journal of Proteome Research|July 3, 2007
Characterization of biomarkers in polycystic ovary syndrome (PCOS) using multiple distinct proteomic platformsB Matharoo-Ball, C Hughes, L Lancashire, et al.Calcified Tissue International|May 13, 2006
Loss of ubiquitin binding is a unifying mechanism by which mutations of SQSTM1 cause Paget's disease of boneJ R Cavey, S H Ralston, P W Sheppard, et al.Analytical Biochemistry|October 21, 1999
Chemically synthesized ubiquitin extension proteins detect distinct catalytic capacities of deubiquitinating enzymesR Layfield, K Franklin, M Landon, et al.American Journal of Physiology. Endocrinology and Metabolism|June 26, 2008
Disassociation between the effects of amino acids and insulin on signaling, ubiquitin ligases, and protein turnover in human muscleP L Greenhaff, L G Karagounis, N Peirce, et al.Bone Reports|November 11, 2017
Second-harmonic generation imaging of collagen in ancient boneB Thomas, D McIntosh, T Fildes, et al.Pageof 5