Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Gregory C Leo"'
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0198156 (2018)
Roux-en-Y gastric bypass (RYGB) is an effective way to lose weight and reverse type 2 diabetes. We profiled the metabolome of 18 obese patients (nine euglycemic and nine diabetics) that underwent RYGB surgery and seven lean subjects. Plasma samples f
Externí odkaz:
https://doaj.org/article/4ede0c57c7344c15a45d43f607679995
Autor:
Fang Liu-Walsh, John A. Masucci, James E. Hauschild, Gregory C Leo, Kimberly A. Capone, Allison Rush, Neena K. Tierney
Publikováno v:
Clinical, Cosmetic and Investigational Dermatology
Fang Liu-Walsh,1 Neena K Tierney,1 James Hauschild,2 Allison K Rush,1 John Masucci,3 Gregory C Leo,3 Kimberly A Capone1 1Johnson & Johnson Consumer Inc., Skillman, NJ, USA; 2Johnson & Johnson Microbiological Quality & Sterility Assurance, Johnson & J
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0198156 (2018)
PLoS ONE
PLoS ONE
Roux-en-Y gastric bypass (RYGB) is an effective way to lose weight and reverse type 2 diabetes. We profiled the metabolome of 18 obese patients (nine euglycemic and nine diabetics) that underwent RYGB surgery and seven lean subjects. Plasma samples f
Roux-en-Y gastric bypass (RYGB) is an effective way to lose weight and reverse type 2 diabetes. We profiled the metabolome of 18 obese patients (nine euglycemic and nine diabetics) that underwent RYGB surgery and seven lean subjects. Plasma samples f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eff28fc83944d1140946623cd7a503d8
Autor:
Gregory C. Leo, Gary W. Caldwell
Publikováno v:
Current Topics in Medicinal Chemistry. 17
Untargeted metabolomics is a promising approach for reducing the significant attrition rate for discovering and developing drugs in the pharmaceutical industry. This review aims to highlight the practical decision-making value of untargeted metabolom
Autor:
James Lenhard, Gregory C. Leo, Matthew Jennis, Cassandre R. Cavanaugh, Pamela J. Hornby, John R. Mabus
Publikováno v:
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society. 30(2)
Background The diet and microbiome contribute to metabolic disease in part due to increased intestinal inflammation and permeability. Dietary tryptophan is metabolized by both mammalian and bacterial enzymes. Using in vitro, in vivo models, and clini
Autor:
Shawn Branum, Fawzy Nagy E, Christopher A. Teleha, Luc Van Der Steen, Mark J. Wall, Derek A. Beauchamp, Michael Reuman, Marc Verbeek, Michael Kolpak, Zhihua Sui, Chaozhong Cai, Gregory C. Leo, Ronald K. Russell, Yongzheng Zhang, Fu-An Kang, Hilde Vanbaelen
Publikováno v:
Organic Process Research & Development. 18:1622-1629
The preparation of a novel chemokine receptor type 2 (CCR-2) antagonist is described on a 135 g scale. The synthesis of an all-carbon bicyclic core was accomplished using a radical cyclization strategy using chiral precursors, wherein elaboration led
Autor:
Ronald K. Russell, Yongzheng Zhang, Marc Verbeek, Michael Reuman, Zhihua Sui, Hilde Vanbaelen, Christopher A. Teleha, Shawn Branum, James C. Lanter, Fawzy Nagy E, Fu-An Kang, Luc Van Der Steen, Michael Kolpak, Michael P. Winters, Derek A. Beauchamp, Gregory C. Leo
Publikováno v:
Organic Process Research & Development. 18:1630-1640
The preparation of a chemokine receptor type 2 (CCR-2) antagonist bearing a cyclopenta[b]furan core is described on a 600 g scale. Compared to our previously reported synthesis of the all-carbon core CCR-2 antagonist with a similar peripheral 3-metho
Autor:
Gregory C. Leo, Andrew L. Darrow
Publikováno v:
Magnetic Resonance in Chemistry. 47:S20-S25
NMR-based metabolomics of mouse urine was used in conjunction with the traditional staining and imaging of aortas for the characterization of disease advancement, that is, plaque formation in untreated and drug-treated apolipoprotein-E (apoE) knockou
Publikováno v:
Drug Metabolism and Disposition. 35:21-29
Comparative metabolite profiling of geldanamycin and 17-allylamino-17-demethoxygeldanamycin (17AAG) using human liver microsomes in normoxia and hypoxia was conducted to understand their differential metabolic fates. Geldanamycin bearing a 17-methoxy