Search Results - "Bateman, Raynard L."

Human Carbonyl Reductase 1 Is an S-Nitrosoglutathione Reductase by Bateman, Raynard L., Rauh, Daniel, Tavshanjian, Brandon, Shokat, Kevan M.

“…Human carbonyl reductase 1 (hCBR1) is an NADPH-dependent short chain dehydrogenase/reductase with broad substrate specificity and is thought to be responsible…”
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Slow-onset inhibition of fumarylacetoacetate hydrolase by phosphinate mimics of the tetrahedral intermediate: kinetics, crystal structure and pharmacokinetics by Bateman, Raynard L, Ashworth, Justin, Witte, John F, Baker, L-J, Bhanumoorthy, Pullooru, Timm, David E, Hurley, Thomas D, Grompe, Markus, McClard, Ronald W

“…FAH (fumarylacetoacetate hydrolase) catalyses the final step of tyrosine catabolism to produce fumarate and acetoacetate. HT1 (hereditary tyrosinaemia type 1)…”
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DNA Replication Is Required To Elicit Cellular Responses to Psoralen-Induced DNA Interstrand Cross-Links by Akkari, Yassmine M. N., Bateman, Raynard L., Reifsteck, Carol A., Olson, Susan B., Grompe, Markus

“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Mechanistic Inferences from the Crystal Structure of Fumarylacetoacetate Hydrolase with a Bound Phosphorus-based Inhibitor by Bateman, Raynard L., Bhanumoorthy, P., Witte, John F., McClard, Ronald W., Grompe, Markus, Timm, David E.

“…Fumarylacetoacetate hydrolase (FAH) catalyzes the hydrolytic cleavage of a carbon–carbon bond in fumarylacetoacetate to yield fumarate and acetoacetate as the…”
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Preclinical Protocol for in Vivo Selection of Hematopoietic Stem Cells Corrected by Gene Therapy in Fanconi Anemia Group C by Noll, Meenakshi, Bateman, Raynard L., D'Andrea, Alan D., Grompe, Markus

“…Fanconi anemia (FA) is an autosomal recessive disorder characterized by birth defects, increased incidence of malignancy, progressive bone marrow failure, and…”
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Human Carbonyl Reductase 1 Is an S-Nitrosoglutathione ReductaseS by Bateman, Raynard L., Rauh, Daniel, Tavshanjian, Brandon, Shokat, Kevan M.

“…Human carbonyl reductase 1 (hCBR1) is an NADPH-dependent short chain dehydrogenase/reductase with broad substrate specificity and is thought to be responsible…”
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The 4N Cell Cycle Delay in Fanconi Anemia Reflects Growth Arrest in Late S Phase by Akkari, Yassmine M.N., Bateman, Raynard L., Reifsteck, Carol A., D'Andrea, Alan D., Olson, Susan B., Grompe, Markus

“…Fanconi anemia (FA) is a human genetic disorder characterized by hypersensitivity to DNA crosslinking agents. Its cellular phenotypes include increased…”
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In vivo selection of wild-type hematopoietic stem cells in a murine model of Fanconi anemia by BATTAILE, K. P, BATEMAN, R. L, MORTIMER, D, MULCAHY, J, RATHBUN, R. K, BAGBY, G, FLEMING, W. H, GROMPE, M

“…Fanconi anemia (FA) is an autosomal recessive disorder characterized by birth defects, increased incidence of malignancy, and progressive bone marrow failure…”
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DNA Replication Is Required To Elicit Cellular Responses to Psoralen-Induced DNA Interstrand Cross-Links by Akkari, Yassmine M. N., Bateman, Raynard L., Reifsteck, Carol A., Olson, Susan B., Grompe, Markus

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In Vivo Selection of Wild-Type Hematopoietic Stem Cells in a Murine Model of Fanconi Anemia by Battaile, Kevin P., Bateman, Raynard L., Mortimer, Derik, Mulcahy, Jean, Rathbun, R. Keaney, Bagby, Grover, Fleming, William H., Grompe, Markus

“…Fanconi anemia (FA) is an autosomal recessive disorder characterized by birth defects, increased incidence of malignancy, and progressive bone marrow failure…”
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