W Todd Lowther
Affiliations: | Biochemistry and Molecular Biology | Wake Forest University, Winston-Salem, NC, United States |
Area:
BiochemistryGoogle:
"W Lowther"Parents
Sign in to add mentor| Ben M. Dunn | grad student | University of Florida College of Medicine (Microtree) | |
| Brian W. Matthews | post-doc | University of Oregon (Chemistry Tree) |
Children
Sign in to add trainee| Charles W. Pemble | grad student | 2008 | Wake Forest |
| Travis J. Riedel | grad student | 2012 | Wake Forest |
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Publications
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| Forshaw TE, Reisz JA, Nelson KJ, et al. (2021) Specificity of Human Sulfiredoxin for Reductant and Peroxiredoxin Oligomeric State. Antioxidants (Basel, Switzerland). 10 |
| Buchalski B, Wood KD, Challa A, et al. (2019) The effects of the inactivation of Hydroxyproline dehydrogenase on urinary oxalate and glycolate excretion in mouse models of primary hyperoxaluria. Biochimica Et Biophysica Acta. Molecular Basis of Disease. 165633 |
| Randall LM, Rizza JD, Parsonage D, et al. (2019) Unraveling the effects of peroxiredoxin 2 nitration; role of C-terminal tyrosine 193. Free Radical Biology & Medicine |
| Loberg MA, Hurtig JE, Graff AH, et al. (2019) Aromatic Residues at the Dimer-Dimer Interface in the Peroxiredoxin Tsa1 Facilitate Decamer Formation and Biological Function. Chemical Research in Toxicology |
| Akter S, Fu L, Jung Y, et al. (2018) Chemical proteomics reveals new targets of cysteine sulfinic acid reductase. Nature Chemical Biology |
| Bolduc JA, Nelson KJ, Haynes AC, et al. (2018) Novel hyperoxidation resistance motifs in 2-Cys peroxiredoxins. The Journal of Biological Chemistry |
| Fargue S, Milliner DS, Knight J, et al. (2018) Hydroxyproline Metabolism and Oxalate Synthesis in Primary Hyperoxaluria. Journal of the American Society of Nephrology : Jasn |
| Chen X, Wu H, Park CM, et al. (2017) Discovery of Heteroaromatic Sulfones As A New Class of Biologically Compatible Thiol-Selective Reagents. Acs Chemical Biology |
| Hill TK, Davis AL, Wheeler FB, et al. (2016) Development of a Self-Assembled Nanoparticle Formulation of Orlistat, Nano-ORL, with Increased Cytotoxicity against Human Tumor Cell Lines. Molecular Pharmaceutics |
| Ritchie MK, Johnson LC, Clodfelter JE, et al. (2015) Crystal Structure and Substrate Specificity of Human Thioesterase 2: Insights into the Molecular Basis for the Modulation of Fatty Acid Synthase. The Journal of Biological Chemistry |