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110Mark M. Stevens, Aurelia R. Honerkamp-Smith and Sarah L. Keller.
Solubility limits of cholesterol, lanosterol, ergosterol, stigmasterol, and β-sitosterol in electroformed lipid vesicles, Soft Matter, 2010, 6, 5882. Yuqin WangAuthors contributed equally., Kyle M. Sousa, Karl Bodin, Spyridon Theofilopoulos, Paola Sacchetti, Martin Hornshaw, Gary Woffendin, Kersti Karu, Jan Sjövall, Ernest Arenas and William J. Griffiths.
Targeted lipidomic analysis of oxysterols in the embryonic central nervous system, Mol. Biosyst., 2009, 5, 529. Youngae Jung, Yun Gyong Ahn, Ho Kyoung Kim, Byeong Cheol Moon, A Yeong Lee, Do Hyun Ryu and Geum-Sook Hwang.
Characterization of dandelion species using 1H NMR- and GC-MS-based metabolite profiling, Analyst, 2011, 136, 4222. Ali Al-Mourabit, Manuel A. Zancanella, Supriya Tilvi and Daniel Romo.
Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids, Nat. Prod. Rep., 2011, 28, 1229. Dean J. Tantillo.
Biosynthesis via carbocations: Theoretical studies on terpene formation, Nat. Prod. Rep., 2011, 28, 1035. Tung-Kung Wu, Yi-Chun Chang, Yuan-Ting Liu, Cheng-Hsiang Chang, Hao-Yu Wen, Wen-Hsuan Li and Wen-Shiang Shie.
Mutation of isoleucine 705 of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae affects lanosterol's C/D-ring cyclization and 17α/β-exocyclic side chain stereochemistry, Org. Biomol. Chem., 2011, 9, 1092. Seiichi P. T. Matsuda, William K. Wilson and Quanbo Xiong.
Mechanistic insights into triterpene synthesis from quantum mechanical calculations. Detection of systematic errors in B3LYP cyclization energies, Org. Biomol. Chem., 2006, 4, 530. Cheng-Hsiang Chang, Hao-Yu Wen, Wen-Shiang Shie, Ching-Ting Lu, Meng-Erh Li, Yuan-Ting Liu, Wen-Hsuan Li and Tung-Kung Wu.
Protein engineering of oxidosqualene-lanosterol cyclase into triterpene monocyclase, Org. Biomol. Chem., 2013, 11, 4214. James Hanson.
Chemistry in the Garden, 2007