R. S. Stewart

发表

Facility Configuration Study of the High Temperature Gas-Cooled Reactor Component Test Facility

S. L. Austad, L. E. Guillen, D. S. Ferguson, 2008 .

The virion host shutoff protein of herpes simplex virus type 1: messenger ribonucleolytic activity in vitro

R. S. Stewart, B. Zelus, J. Ross, 1996, Journal of virology.

A transmembrane form of the prion protein contains an uncleaved signal peptide and is retained in the endoplasmic Reticulum.

R. S. Stewart, D. Harris, B. Drisaldi, 2001, Molecular biology of the cell.

A Transmembrane Form of the Prion Protein Is Localized in the Golgi Apparatus of Neurons*

R. S. Stewart, D. Harris, 2005, Journal of Biological Chemistry.

Cytosolic Prion Protein (PrP) Is Not Toxic in N2a Cells and Primary Neurons Expressing Pathogenic PrP Mutations*

R. S. Stewart, G. Forloni, D. Harris, 2005, Journal of Biological Chemistry.

The Role of a Novel Topological Form of the Prion Protein in Prion Disease

R. S. Stewart, 2008 .

Award Number: DAMD17-03-1-0531 TITLE: The Role of a Novel Topological Form of the Prion Protein in Prion Disease PRINCIPLE INVESTIGATOR:

R. S. Stewart, 2006 .

Neurodegenerative Illness in Transgenic Mice Expressing a Transmembrane Form of the Prion Protein

R. S. Stewart, B. Ghetti, D. Harris, 2005, The Journal of Neuroscience.

The neurotoxicity of prion protein (PrP) peptide 106–126 is independent of the expression level of PrP and is not mediated by abnormal PrP species

R. S. Stewart, G. Forloni, D. Harris, 2005, Molecular and Cellular Neuroscience.

Effects of Storage Conditions on the Morphology and Titer of Lentiviral Vectors

R. S. Stewart, Josephine Taylor, B. Clack, 2013 .

“Late” macroendosomes and acidic endosomes in vertebrate motor nerve terminals

R. S. Stewart, R. S. Wilkinson, H. Teng, 2012, The Journal of comparative neurology.

Most Pathogenic Mutations Do Not Alter the Membrane Topology of the Prion Protein*

R. S. Stewart, D. Harris, D A Harris, 2001, The Journal of Biological Chemistry.

Mutational Analysis of Topological Determinants in Prion Protein (PrP) and Measurement of Transmembrane and Cytosolic PrP during Prion Infection*

R. S. Stewart, D. Harris, 2003, Journal of Biological Chemistry.

Mutant PrP Is Delayed in Its Exit from the Endoplasmic Reticulum, but Neither Wild-type nor Mutant PrP Undergoes Retrotranslocation Prior to Proteasomal Degradation*

R. S. Stewart, D. Harris, R. Chiesa, 2003, Journal of Biological Chemistry.

A Novel, Drug-based, Cellular Assay for the Activity of Neurotoxic Mutants of the Prion Protein*

R. S. Stewart, I. Solomon, D. Harris, 2009, The Journal of Biological Chemistry.

A Transmembrane Form of the Prion Protein Is Localized in the Golgi Apparatus of Neurons*

R. S. Stewart, D. Harris, 2005, Journal of Biological Chemistry.

A transmembrane form of the prion protein contains an uncleaved signal peptide and is retained in the endoplasmic Reticulum.

R. S. Stewart, D. Harris, B. Drisaldi, 2001, Molecular biology of the cell.