Pages that link to "Q44184139"
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The following pages link to Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol (Q44184139):
Displaying 50 items.
- Protein microarray analysis identifies human cellular prion protein interactors (Q24312919) (← links)
- Anchorless 23-230 PrPC interactomics for elucidation of PrPC protective role (Q24317448) (← links)
- Protein folding by the effects of macromolecular crowding (Q24645313) (← links)
- Prion-induced neurotoxicity: Possible role for cell cycle activity and DNA damage response (Q26797972) (← links)
- The delicate balance between secreted protein folding and endoplasmic reticulum-associated degradation in human physiology (Q27015793) (← links)
- Neuronal death induced by misfolded prion protein is due to NAD+ depletion and can be relieved in vitro and in vivo by NAD+ replenishment (Q27303843) (← links)
- Endoplasmic Reticulum Stress Is a Determinant of Retrovirus-Induced Spongiform Neurodegeneration (Q27487568) (← links)
- PrP knock-out and PrP transgenic mice in prion research (Q28206331) (← links)
- Proposed pathogenetic cascade of inclusion-body myositis: importance of amyloid-β, misfolded proteins, predisposing genes, and aging (Q28211446) (← links)
- Protein aggregation and neurodegenerative disease (Q28273600) (← links)
- The state of the prion (Q28288758) (← links)
- Expression of mutant or cytosolic PrP in transgenic mice and cells is not associated with endoplasmic reticulum stress or proteasome dysfunction (Q28477995) (← links)
- Solvent microenvironments and copper binding alters the conformation and toxicity of a prion fragment (Q28538070) (← links)
- Recognition of 27-class protein folds by adding the interaction of segments and motif information. (Q30365842) (← links)
- Changes in protein structure and distribution observed at pre-clinical stages of scrapie pathogenesis. (Q30370633) (← links)
- The recognition of multi-class protein folds by adding average chemical shifts of secondary structure elements (Q30385700) (← links)
- Lethal recessive myelin toxicity of prion protein lacking its central domain (Q30478899) (← links)
- Heat shock factor 1 regulates lifespan as distinct from disease onset in prion disease (Q30483457) (← links)
- Cytoplasmic prion protein induces forebrain neurotoxicity (Q30488090) (← links)
- Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions (Q30492360) (← links)
- Molecular interaction of TPPP with PrP antagonized the CytoPrP-induced disruption of microtubule structures and cytotoxicity (Q31029724) (← links)
- Intrabody applications in neurological disorders: progress and future prospects (Q33217378) (← links)
- The expanding universe of prion diseases (Q33239695) (← links)
- Clearance and prevention of prion infection in cell culture by anti-PrP antibodies. (Q33248701) (← links)
- Substrate-specific translocational attenuation during ER stress defines a pre-emptive quality control pathway (Q33264756) (← links)
- Functional depletion of mahogunin by cytosolically exposed prion protein contributes to neurodegeneration (Q33289413) (← links)
- In vitro and in vivo neurotoxicity of prion protein oligomers. (Q33296885) (← links)
- Molecular distinction between pathogenic and infectious properties of the prion protein (Q33338476) (← links)
- Endoplasmic reticulum stress, PrP trafficking, and neurodegeneration (Q33346044) (← links)
- Pathologic prion protein infects cells by lipid-raft dependent macropinocytosis (Q33434501) (← links)
- Prion strain discrimination based on rapid in vivo amplification and analysis by the cell panel assay (Q33455591) (← links)
- Persistent hijacking of brain proteasomes in HIV-associated dementia (Q33520783) (← links)
- The efficiency of protein compartmentalization into the secretory pathway (Q33564834) (← links)
- Perturbation of endoplasmic reticulum homeostasis facilitates prion replication. (Q33581647) (← links)
- Context dependent neuroprotective properties of prion protein (PrP). (Q33595425) (← links)
- Signal sequence insufficiency contributes to neurodegeneration caused by transmembrane prion protein (Q33689595) (← links)
- Cell type-specific neuroprotective activity of untranslocated prion protein (Q33742065) (← links)
- Redox control of prion and disease pathogenesis (Q33830151) (← links)
- Biological characteristics of Chinese hamster ovary cells transfected with bovine Prnp (Q33860922) (← links)
- Cytosolic PrP can participate in prion-mediated toxicity (Q33900238) (← links)
- Protein aggregation and aggregate toxicity: new insights into protein folding, misfolding diseases and biological evolution (Q34225700) (← links)
- Direct observation of multiple misfolding pathways in a single prion protein molecule (Q34261701) (← links)
- Transmissible spongiform encephalopathies. (Q34289917) (← links)
- Compartment-restricted biotinylation reveals novel features of prion protein metabolism in vivo (Q34408461) (← links)
- Cell-specific metabolism and pathogenesis of transmembrane prion protein (Q34520060) (← links)
- Prion protein in Caenorhabditis elegans: Distinct models of anti-BAX and neuropathology (Q34570047) (← links)
- Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion disease (Q34576746) (← links)
- Selective re-routing of prion protein to proteasomes and alteration of its vesicular secretion prevent PrP(Sc) formation (Q34633462) (← links)
- The intricate mechanisms of neurodegeneration in prion diseases. (Q34664576) (← links)
- High titers of transmissible spongiform encephalopathy infectivity associated with extremely low levels of PrPSc in vivo. (Q34699610) (← links)