Pages that link to "Q40766017"
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The following pages link to Prion diseases and neurodegeneration (Q40766017):
Displaying 50 items.
- Regulation of GABA(A) and glutamate receptor expression, synaptic facilitation and long-term potentiation in the hippocampus of prion mutant mice (Q27337373) (← links)
- Normal inhibitory avoidance learning and anxiety, but increased locomotor activity in mice devoid of PrP(C) (Q28145925) (← links)
- Prion protein fragments spanning helix 1 and both strands of beta sheet (residues 125-170) show evidence for predominantly helical propensity by CD and NMR. (Q31979097) (← links)
- Intracerebral administration of interleukin-12 (IL-12) and IL-18 modifies the course of mouse scrapie (Q33267751) (← links)
- E3 Ubiquitin Ligases Neurobiological Mechanisms: Development to Degeneration (Q33705444) (← links)
- Proteomics Approach to Identify the Interacting Partners of Cellular Prion Protein and Characterization of Rab7a Interaction in Neuronal Cells (Q33908948) (← links)
- Bovine spongiform encephalopathy--food safety implications (Q34206657) (← links)
- Amylin deposition in the brain: A second amyloid in Alzheimer disease? (Q34352928) (← links)
- Insights into the evolutionary features of human neurodegenerative diseases (Q34465001) (← links)
- Mapping the prion protein distribution in marsupials: insights from comparing opossum with mouse CNS (Q34500214) (← links)
- Molecular analysis of cases of Italian sheep scrapie and comparison with cases of bovine spongiform encephalopathy (BSE) and experimental BSE in sheep (Q35922310) (← links)
- Glycolipid-anchored proteins in neuroblastoma cells form detergent-resistant complexes without caveolin (Q36235497) (← links)
- Solvent-amino acid interaction energies in three-dimensional-lattice Monte Carlo simulations of a model 27-mer protein: Folding thermodynamics and kinetics (Q36526437) (← links)
- Prion diseases as transmissible zoonotic diseases (Q37105925) (← links)
- Modifications of myelin basic protein in DM20 transgenic mice are similar to those in myelin basic protein from multiple sclerosis (Q37350252) (← links)
- Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform. (Q37593764) (← links)
- Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus (Q37693769) (← links)
- The role of RNA in mammalian prion protein conversion (Q37957794) (← links)
- Microglia and synapse: interactions in health and neurodegeneration (Q38176000) (← links)
- The potential of mesenchymal stem cell in prion research. (Q38213991) (← links)
- A Mutant Prion Protein Displays an Aberrant Membrane Association When Expressed in Cultured Cells (Q38290309) (← links)
- Computational studies on prion proteins: effect of Ala(117)-->Val mutation (Q40207007) (← links)
- Checking the pH-induced conformational transition of prion protein by molecular dynamics simulations: effect of protonation of histidine residues (Q40307214) (← links)
- Alzheimer's disease and prion proteins: a meeting made in muscle. (Q40650636) (← links)
- Impact of SDS surfactant on the interactions of Cu(2 ) ions with the amyloidogenic region of human prion protein. (Q40801758) (← links)
- Prion protein expression in muscle cells and toxicity of a prion protein fragment (Q41055589) (← links)
- Mutant and infectious prion proteins display common biochemical properties in cultured cells. (Q41237869) (← links)
- Prion diseases: transmission from mad cows? (Q41238204) (← links)
- Prion protein and scrapie susceptibility. (Q41607634) (← links)
- Human prion diseases: Possible new directions in prophylaxis and therapy (Q41675646) (← links)
- Y145Stop is sufficient to induce de novo generation prions using protein misfolding cyclic amplification (Q42139323) (← links)
- Channel formation by serum amyloid A: a potential mechanism for amyloid pathogenesis and host defense (Q43986286) (← links)
- Induction of heme oxygenase-1 in the brains of scrapie-infected mice (Q44961362) (← links)
- Intracellular A beta 1-42 aggregates stimulate the accumulation of stable, insoluble amyloidogenic fragments of the amyloid precursor protein in transfected cells. (Q45956646) (← links)
- Thermodynamics of model prions and its implications for the problem of prion protein folding (Q46153921) (← links)
- Histopathological changes in the pituitary glands of female hamsters infected with the 139H strain of scrapie (Q46174449) (← links)
- Prion protein gene polymorphisms in four goat breeds of Pakistan (Q46952556) (← links)
- A Prion Protein Fragment Primes Type 1 Astrocytes to Proliferation Signals from Microglia (Q47834612) (← links)
- Microglial expression of the prion protein (Q47959261) (← links)
- Prion protein peptide neurotoxicity can be mediated by astrocytes (Q48127864) (← links)
- Molecular Alterations in the Cerebellum of Sporadic Creutzfeldt-Jakob Disease Subtypes with DJ-1 as a Key Regulator of Oxidative Stress (Q48395389) (← links)
- Neurocognitive disorders: cluster 1 of the proposed meta-structure for DSM-V and ICD-11. (Q48445053) (← links)
- Prion protein is necessary for latent learning and long-term memory retention (Q48602149) (← links)
- Abnormalities in stress proteins in prion diseases (Q48775242) (← links)
- Familial mutations and the thermodynamic stability of the recombinant human prion protein (Q48784818) (← links)
- Truncated forms of the human prion protein in normal brain and in prion diseases (Q48807964) (← links)
- Development of polarity in cerebellar granule neurons (Q52196570) (← links)
- The role of prion peptide structure and aggregation in toxicity and membrane binding. (Q54029824) (← links)
- Correction of Defective Protein Kinesis of Human P-glycoprotein Mutants by Substrates and Modulators (Q57976939) (← links)
- Prion Protein Aggregation Reverted by Low Temperature in Transfected Cells Carrying a Prion Protein Gene Mutation (Q59505876) (← links)