Publications by authors named "Matthew W Carson"

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Branched-chain α-ketoacids are preferentially reaminated and activate protein synthesis in the heart.
Jacquelyn M Walejko, Bridgette A Christopher, Scott B Crown, Guo-Fang Zhang, Adrian Pickar-Oliver, Matthew W Carson

Nat Commun· March 2021

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Muscle-Liver Trafficking of BCAA-Derived Nitrogen Underlies Obesity-Related Glycine Depletion.
Phillip J White, Amanda L Lapworth, Robert W McGarrah, Lydia Coulter Kwee, Scott B Crown, Matthew W Carson

Cell Rep· November 2020

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Indole Glucocorticoid Receptor Antagonists Active in a Model of Dyslipidemia Act via a Unique Association with an Agonist Binding Site.
John G Luz, Matthew W Carson, Bradley Condon, David Clawson, Anna Pustilnik

J Med Chem· August 2015

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HDX reveals unique fragment ligands for the vitamin D receptor.
Matthew W Carson, Jun Zhang, Michael J Chalmers, Wayne P Bocchinfuso, Karol D Holifield

Bioorg Med Chem Lett· August 2014

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Glucocorticoid receptor modulators informed by crystallography lead to a new rationale for receptor selectivity, function, and implications for structure-based design.
Matthew W Carson, John G Luz, Chen Suen, Chahrzad Montrose, Richard Zink

J Med Chem· February 2014

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An intra/intermolecular suzuki sequence to benzopyridyloxepines containing geometrically pure exocyclic tetrasubstituted alkenes.
Matthew W Carson, Matthew W Giese, Michael J Coghlan

Org Lett· July 2008

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Cyclocarbopalladation of alkynes: a stereoselective method for preparing dibenzoxapine containing tetrasubstituted exocyclic alkenes.
Hannah Yu, Rachel N Richey, Matthew W Carson, Michael J Coghlan

Org Lett· April 2006

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Concise Stereoselective Routes to Advanced Intermediates Related to Natural and Unnatural Pinnaic Acid This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154), M.F.H. (5T32 CA62948-05), and D.T. (Schering Research Foundation, Berlin). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses.
Matthew W. Carson, Guncheol Kim, Martin F. Hentemann, Dirk Trauner, Samuel J. Danishefsky

Angew Chem Int Ed Engl· December 2001

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Total Synthesis and Proof of Stereochemistry of Natural and Unnatural Pinnaic Acids: A Remarkable Long-Range Stereochemical Effect in the Reduction of 17-Oxo Precursors of the Pinnaic Acids This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses. We would like to thank professor Nakanishi for his supportive interest in the project.
Matthew W. Carson, Guncheol Kim, Samuel J. Danishefsky

Angew Chem Int Ed Engl· December 2001

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