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Plos One|October 3, 2012
Molecular characterization of the viaB locus encoding the biosynthetic machinery for Vi capsule formation in Salmonella TyphiMichael Wetter, David Goulding, Derek Pickard, et al.
Current Chemical Biology|April 22, 2016
Novel Citronellyl-Based Photoprobes Designed to Identify ER Proteins Interacting with Dolichyl Phosphate in Yeast and Mammalian CellsJeffrey S Rush, Thangaiah Subramanian, Karunai Leela Subramanian, et al.
The Journal of Biological Chemistry|May 18, 1999
The LPP1 and DPP1 gene products account for most of the isoprenoid phosphate phosphatase activities in Saccharomyces cerevisiaeA Faulkner, X Chen, J Rush, et al.
The Journal of Biological Chemistry|April 8, 1994
Induction of dolichyl-saccharide intermediate biosynthesis corresponds to increased long chain cis-isoprenyltransferase activity during the mitogenic response in mouse B cellsD C Crick, J R Scocca, J S Rush, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 11, 1999
Farnesol is utilized for isoprenoid biosynthesis in plant cells via farnesyl pyrophosphate formed by successive monophosphorylation reactionsL Thai, J S Rush, J E Maul, et al.
Human Mutation|July 23, 2003
Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type IjXiaohua Wu, Jeffrey S Rush, Denise Karaoglu, et al.
The EMBO Journal|May 17, 2011
Nogo-B receptor is necessary for cellular dolichol biosynthesis and protein N-glycosylationKenneth D Harrison, Eon Joo Park, Ningguo Gao, et al.
Molecular Biology of the Cell|February 17, 2001
Requirement of the Lec35 gene for all known classes of monosaccharide-P-dolichol-dependent glycosyltransferase reactions in mammalsM Anand, J S Rush, S Ray, et al.
Carcinogenesis|February 1, 1996
Convergence of three steroid receptor pathways in the mediation of nongenotoxic hepatocarcinogenesisM L O'Brien, S M Rangwala, K W Henry, et al.
Molecular Genetics and Metabolism|July 17, 2013
Congenital disorder of glycosylation due to DPM1 mutations presenting with dystroglycanopathy-type congenital muscular dystrophyAmy C Yang, Bobby G Ng, Steven A Moore, et al.
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