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  • Paul D. Rick, Kathleen L Barr, Krishnan Sankaran, Junko Kajimura, Jeffrey S. Rush, Charles J. Waechter
  • Medicine, Biology
  • The Journal of Biological Chemistry
  • 2003 (First Publication: 9 May 2003)
  • The assembly of many bacterial cell surface polysaccharides requires the transbilayer movement of polyisoprenoid-linked saccharide intermediates across the cytoplasmic membrane. It is generallyExpand
  • Xiaohua Wu, Jeffrey S. Rush, +5 authors Hudson H. Freeze
  • Biology, Medicine
  • Human mutation
  • 2003 (First Publication: 1 August 2003)
  • Defects in the assembly of dolichol-linked oligosaccharide or its transfer to proteins result in severe, multi-system human diseases called Type I congenital disorders of glycosylation. We haveExpand
  • Jeffrey S. Rush, Cristina Alaimo, Riccardo Robbiani, Michael A. Wacker, Charles J. Waechter
  • Biology, Medicine
  • The Journal of Biological Chemistry
  • 2009 (First Publication: 18 November 2009)
  • Escherichia coli strain O157 produces an O-antigen with the repeating tetrasaccharide unit α-d-PerNAc-α-l-Fuc-β-d-Glc-α-d-GalNAc, preassembled on undecaprenyl pyrophosphate (Und-P-P). These studiesExpand
  • Amy C Yang, Bobby G. Ng, +7 authors Lakshmi Mehta
  • Medicine, Biology
  • Molecular genetics and metabolism
  • 2013 (First Publication: 1 November 2013)
  • Congenital disorders of glycosylation (CDG) are rare genetic defects mainly in the post-translational modification of proteins via attachment of carbohydrate chains. We describe an infant with theExpand
  • F. Fernández, J. Rush, +7 authors C. J. Waechter
  • Biology, Medicine
  • The Journal of Biological Chemistry
  • 2001 (First Publication: 2 November 2001)
  • Mutations in theCWH8 gene, which encodes an ER transmembrane protein with a phosphate binding pocket in Saccharomyces cerevisiae, result in a deficiency in dolichyl pyrophosphate (Dol-P-P)-linkedExpand
  • Jeffrey S. Rush, Krishnasamy Panneerselvam, Charles J. Waechter, Hudson H. Freeze
  • Biology, Medicine
  • Glycobiology
  • 2000 (First Publication: 1 August 2000)
  • Congenital Disorders of Glycosylation (CDG) are human deficiencies in glycoprotein biosynthesis. Previous studies showed that 1 mM mannose corrects defective protein N-glycosylation in culturedExpand
  • Jeffrey S. Rush, Ningguo Gao, Mark A. Lehrman, Charles J. Waechter
  • Medicine, Biology
  • Journal of Biological Chemistry
  • 2008 (First Publication: 15 February 2008)
  • During protein N-glycosylation, dolichyl pyrophosphate (Dol-P-P) is discharged in the lumenal monolayer of the endoplasmic reticulum (ER). Dol-P-P is then cleaved to Dol-P by Dol-P-P phosphataseExpand
  • Jeffrey S. Rush, Steve K. Cho, Songmin Jiang, Sandra L. Hofmann, Charles J. Waechter
  • Medicine, Biology
  • The Journal of Biological Chemistry
  • 2002 (First Publication: 22 November 2002)
  • The CWH8 gene in Saccharomyces cerevisiae has been shown recently (Fernandez, F., Rush, J. S., Toke, D. A., Han, G., Quinn, J. E., Carman, G. M., Choi, J.-Y., Voelker, D. R., Aebi, M., and Waechter,Expand
  • J. Järnefelt, J. Rush, Y. Li, R. Laine
  • Chemistry, Medicine
  • The Journal of biological chemistry
  • 1978 (First Publication: 25 November 1978)
  • Glycopeptides of molecualr weight range 7,000 to 11,000, unusual in size and structure, have been partially purified from pronase digests of lipid-free human erythrocyte ghosts; we term this fractionExpand