Pages that link to "Q40508891"

The following pages link to 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):

Displaying 33 items.

• The Cellular Prion Protein: A Player in Immunological Quiescence (Q26782895) (← links)
• Mutant PrP suppresses glutamatergic neurotransmission in cerebellar granule neurons by impairing membrane delivery of VGCC α(2)δ-1 Subunit (Q28508384) (← links)
• Mammalian prion protein suppresses Bax-induced cell death in yeast (Q28594938) (← links)
• The prion protein modulates A-type K+ currents mediated by Kv4.2 complexes through dipeptidyl aminopeptidase-like protein 6 (Q28771518) (← links)
• Amyloid β (Aβ) peptide directly activates amylin-3 receptor subtype by triggering multiple intracellular signaling pathways (Q30175699) (← links)
• Frequent missense and insertion/deletion polymorphisms in the ovine Shadoo gene parallel species-specific variation in PrP. (Q33490984) (← links)
• Functionally relevant domains of the prion protein identified in vivo (Q33501189) (← links)
• Context dependent neuroprotective properties of prion protein (PrP). (Q33595425) (← links)
• A novel, drug-based, cellular assay for the activity of neurotoxic mutants of the prion protein. (Q33748230) (← links)
• Copper binding extrinsic to the octarepeat region in the prion protein (Q33999707) (← links)
• Differential responses of neuronal and spermatogenic cells to the doppel cytotoxicity (Q35067708) (← links)
• Establishment and characterization of Prnp knockdown neuroblastoma cells using dual microRNA-mediated RNA interference (Q35194917) (← links)
• The cellular prion protein (PrP(C)): its physiological function and role in disease (Q36003019) (← links)
• Integrity of helix 2-helix 3 domain of the PrP protein is not mandatory for prion replication (Q36003628) (← links)
• Copper and the prion protein: methods, structures, function, and disease (Q36640347) (← links)
• Molecular basis of cerebral neurodegeneration in prion diseases. (Q36731464) (← links)
• Prion neurotoxicity: insights from prion protein mutants (Q36767231) (← links)
• Helix 3 is necessary and sufficient for prion protein's anti-Bax function (Q37262632) (← links)
• Prion proteins with pathogenic and protective mutations show similar structure and dynamics (Q37388684) (← links)
• Prion disease tempo determined by host-dependent substrate reduction (Q37524308) (← links)
• Endoproteolytic processing of the mammalian prion glycoprotein family (Q39052720) (← links)
• A nine amino acid domain is essential for mutant prion protein toxicity (Q39486840) (← links)
• TMZ-induced PrPc/par-4 interaction promotes the survival of human glioma cells (Q39590618) (← links)
• The CNS glycoprotein Shadoo has PrP(C)-like protective properties and displays reduced levels in prion infections (Q40093030) (← links)
• Dominant-negative effects of the N-terminal half of prion protein on neurotoxicity of prion protein-like protein/doppel in mice (Q40451562) (← links)
• A Drug-Based Cellular Assay (DBCA) for studying cytotoxic and cytoprotective activities of the prion protein: A practical guide (Q41907406) (← links)
• The role of the octarepeat region in neuroprotective function of the cellular prion protein (Q42080796) (← links)
• The alpha-secretase-derived N-terminal product of cellular prion, N1, displays neuroprotective function in vitro and in vivo (Q42151993) (← links)
• The octarepeat domain of the prion protein binds Cu(II) with three distinct coordination modes at pH 7.4. (Q42703327) (← links)
• The affinity of copper binding to the prion protein octarepeat domain: evidence for negative cooperativity (Q42731475) (← links)
• Prion protein lacks robust cytoprotective activity in cultured cells (Q42745830) (← links)
• Neonatal lethality in transgenic mice expressing prion protein with a deletion of residues 105-125. (Q42976640) (← links)
• Purkinje-cell degeneration in prion protein-deficient mice is associated with a cerebellum-specific Doppel protein species signature (Q48908089) (← links)