Autophagy stimulation as a promising approach in treatment of neurodegenerative diseases

K Pierzynowska, L Gaffke, Z Cyske, M Puchalski… - Metabolic Brain …, 2018 - Springer
Autophagy is a process of degradation of macromolecules in the cytoplasm, particularly
proteins of a long half-life, as well as whole organelles, in eukaryotic cells. Lysosomes play …

Effect of transition metals (Mn, Cu, Fe) and deoxycholic acid (DA) on the conversion of PrPC to PrPres

NH Kim, JK Choi, BH Jeong, JI Kim… - The FASEB …, 2005 - Wiley Online Library
The PMCA (protein misfolding cyclic amplification) technique has been shown to drive the
amplification of misfolded prion protein by PrPSc seeds during several cycles of incubation …

[图书][B] Viral encephalitis in humans

J Booss, MM Esiri - 2003 - scholar.archive.org
In 1987 I had the pleasant task of reviewing the precursor of this book, which was called
Viral Encephalitis: Pathology, Diagnosis and Management. The strongly positive tone of that …

Screening a library of potential prion therapeutics against cellular prion proteins and insights into their mode of biological activities by surface plasmon resonance

F Touil, S Pratt, R Mutter, B Chen - Journal of pharmaceutical and …, 2006 - Elsevier
The conversion of cellular prion protein (PrPC) to the protease resistant isoform (PrPSc) is
considered essential for the progression of transmissible spongiform encephalopathies …

Epigenetic control of the notch and Eph signaling pathways by the prion protein: implications for prion diseases

TZ Hirsch, S Martin-Lannerée, F Reine… - Molecular …, 2019 - Springer
Among the ever-growing number of self-replicating proteins involved in neurodegenerative
diseases, the prion protein PrP remains the most infamous for its central role in transmissible …

Psychotropic medications and the treatment of human prion diseases

BS Appleby - CNS & Neurological Disorders-Drug Targets …, 2009 - ingentaconnect.com
Prion diseases are rare, rapidly progressive, fatal neurodegenerative illnesses caused by an
abnormal isoform of the native prion protein. Creutzfeldt-Jakob disease (CJD) is the most …

Sodium valproate does not augment Prpsc in murine neuroblastoma cells

C Legendre, F Casagrande, T Andrieu, D Dormont… - Neurotoxicity …, 2007 - Springer
Sodium valproate (VPA) has been reported to increase the accumulation of the pathologic
isoform of prion protein (PrP sc) in scrapie-infected murine neuroblastoma cells. In this …

Rapidly Progressive Dementia: Human Prion Diseases and an Approach for Evaluating Non-Prion Etiologies

DN Soleimani-Meigooni, MD Geschwind - 2019 - academic.oup.com
Jakob–Creutzfeldt disease (JCD) is a rare prion-mediated disease that causes rapidly
progressive dementia. Prions are pathogenic, misfolded proteins that propagate via an …

[PDF][PDF] Μελέτη της επίδρασης του βαλπροϊκού οξέος στην οργανογένεση και στην κυτταρική απόπτωση του οφθαλμού εμβρύου μυός Balb/C

Κ Μάνθος - 2010 - ikee.lib.auth.gr
Η σύγχρονη ιατρική έχει να παρουσιάσει πολλά επιτεύγματα, που οδήγησαν στη βελτίωση της
ποιότητας της ζωής των ανθρώπων. Η παρασκευή φαρμακευτικών ουσιών που …

Les maladies à prions: risques pour la santé publique et mesures de prévention

A Abdelghani - 2003 - policycommons.net
Les maladies à prions ou encéphalopathies spongiformes subaiguës transmissibles sont
des maladies anciennes qui connaissent un regain de notoriété depuis 1996, avec la crise …