Pages that link to "Q48350176"

The following pages link to Identification of cryptic nuclear localization signals in the prion protein (Q48350176):

Displaying 29 items.

• Identification of prion protein binding proteins by combined use of far-Western immunoblotting, two dimensional gel electrophoresis and mass spectrometry (Q24295861) (← links)
• Protein microarray analysis identifies human cellular prion protein interactors (Q24312919) (← links)
• Minimotif miner 2nd release: a database and web system for motif search (Q24655431) (← links)
• The prion protein unstructured N‐terminal region is a broad‐spectrum molecular sensor with diverse and contrasting potential functions (Q27022256) (← links)
• Cellular prion protein localizes to the nucleus of endocrine and neuronal cells and interacts with structural chromatin components (Q29347112) (← links)
• The cellular prion protein PrP(c) is involved in the proliferation of epithelial cells and in the distribution of junction-associated proteins (Q33361643) (← links)
• Loss of anti-Bax function in Gerstmann-Sträussler-Scheinker syndrome-associated prion protein mutants (Q33493430) (← links)
• Redox control of prion and disease pathogenesis (Q33830151) (← links)
• The N-terminal, polybasic region is critical for prion protein neuroprotective activity (Q34043470) (← links)
• Prion protein conversion in vitro (Q34304971) (← links)
• Cell-specific metabolism and pathogenesis of transmembrane prion protein (Q34520060) (← links)
• Prion protein promotes kidney iron uptake via its ferrireductase activity. (Q35126635) (← links)
• Opposing roles of prion protein in oxidative stress- and ER stress-induced apoptotic signaling (Q37066530) (← links)
• Cellular prion protein is present in mitochondria of healthy mice (Q37620547) (← links)
• Interactions of prion protein with intracellular proteins: so many partners and no consequences? (Q37664640) (← links)
• Physiological Functions of the Cellular Prion Protein. (Q37739095) (← links)
• Iron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease. (Q38186783) (← links)
• The prion protein is critical for DNA repair and cell survival after genotoxic stress (Q38925522) (← links)
• A nine amino acid domain is essential for mutant prion protein toxicity (Q39486840) (← links)
• Prion protein is required for tumor necrosis factor alpha (TNFα)-triggered nuclear factor kappa B (NF-κB) signaling and cytokine production. (Q40044695) (← links)
• The interaction between cytoplasmic prion protein and the hydrophobic lipid core of membrane correlates with neurotoxicity (Q40305093) (← links)
• Conformational instability of human prion protein upon residue modification: a molecular dynamics simulation study (Q40488310) (← links)
• Genetic mapping of activity determinants within cellular prion proteins: N-terminal modules in PrPC offset pro-apoptotic activity of the Doppel helix B/B' region (Q40508891) (← links)
• Binding of recombinant but not endogenous prion protein to DNA causes DNA internalization and expression in mammalian cells (Q42434578) (← links)
• Goat PRND expression pattern suggests its involvement in early sex differentiation (Q42609100) (← links)
• Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine. (Q45188909) (← links)
• Alterations in the brain interactome of the intrinsically disordered N-terminal domain of the cellular prion protein (PrPC) in Alzheimer's disease. (Q55436167) (← links)
• The C-terminal Globular Domain of the Prion Protein Is Necessary and Sufficient for Import into the Endoplasmic Reticulum (Q60290979) (← links)
• Proteasomal Inhibition Redirects the PrP-Like Shadoo Protein to the Nucleus (Q92299716) (← links)