Pages that link to "Q39605681"

The following pages link to Prion Propagation in Cells Expressing PrP Glycosylation Mutants (Q39605681):

Displaying 16 items.

• Prions in variably protease-sensitive prionopathy: an update (Q27014886) (← links)
• Small changes huge impact: the role of protein posttranslational modifications in cellular homeostasis and disease (Q28396109) (← links)
• Mammalian prions: tolerance to sequence changes-how far? (Q30424667) (← links)
• N-glycans and glycosylphosphatidylinositol-anchor act on polarized sorting of mouse PrP(C) in Madin-Darby canine kidney cells. (Q34023780) (← links)
• Propagation of RML prions in mice expressing PrP devoid of GPI anchor leads to formation of a novel, stable prion strain (Q34299382) (← links)
• Glycoform-selective prion formation in sporadic and familial forms of prion disease (Q34634279) (← links)
• Integrity of helix 2-helix 3 domain of the PrP protein is not mandatory for prion replication (Q36003628) (← links)
• Generating Bona Fide Mammalian Prions with Internal Deletions (Q37093469) (← links)
• N-glycoprotein macroheterogeneity: biological implications and proteomic characterization. (Q38659790) (← links)
• Cell Biology Approaches to Studying Prion Diseases (Q40061707) (← links)
• Glycoform-independent prion conversion by highly efficient, cell-based, protein misfolding cyclic amplification. (Q40623141) (← links)
• Establishment of a Madin-Darby bovine kidney cell line expressing anchorless bovine prion protein. (Q52331784) (← links)
• Spermine increases acetylation of tubulins and facilitates autophagic degradation of prion aggregates. (Q55564490) (← links)
• Glycosylation Significantly Inhibits the Aggregation of Human Prion Protein and Decreases Its Cytotoxicity (Q58722021) (← links)
• Full restoration of specific infectivity and strain properties from pure mammalian prion protein (Q64056734) (← links)
• Transient multimers modulate conformer abundances of prion protein monomer through conformational selection (Q92757387) (← links)