The role of chaperones in Parkinson's disease and prion diseases.

Keywords

Disease, Medicine, Neuroscience, Biology, Pathology

References

• Chaperone‐like activity of synucleinsGeorges Cazes — 2000
• Lewy bodies and parkinsonism in families with parkin mutationsMaïlis Labie — 2001
• Quality control in the endoplasmic reticulumGonzález Tomàs, Marc Antoni — 2003
• Parkinson's Disease Mechanisms and ModelsWilliam T. Dauer, Serge Przedborski — 2003
• The Thr183Ala Mutation, Not the Loss of the First Glycosylation Site, Alters the Physical Properties of the Prion ProteinSabina Capellari, Syed I. A. Zaidi, Amy C. Long — 2000
• p185erbB2 binds to GRP94 in vivo. Dissociation of the p185erbB2/GRP94 heterocomplex by benzoquinone ansamycins precedes depletion of p185erbB2.Christine Chavany, Edward G. Mimnaugh, Penny E. Miller — 1996
• Chemical chaperones interfere with the formation of scrapie prion protein.Jörg Tatzelt, Stanley B. Prusiner, William J. Welch — 1996
• Proteasomal inhibition leads to formation of ubiquitin/α‐synuclein‐immunoreactive inclusions in PC12 cellsHardy J. Rideout, Kristin E. Larsen, David Sulzer — 2001
• Synaptic Vesicle Depletion Correlates with Attenuated Synaptic Responses to Prolonged Repetitive Stimulation in Mice Lacking α-SynucleinDeborah E. Cabin, Kazuhiro Shimazu, Diane Murphy — 2002
• A prion protein cycles between the cell surface and an endocytic compartment in cultured neuroblastoma cells.Show‐Ling Shyng, Mary T. Huber, David A. Harris — 1993
• Impairment of the ubiquitin‐proteasome system causes dopaminergic cell death and inclusion body formation in ventral mesencephalic culturesKevin St. P. McNaught, Catherine Mytilineou, Ruth JnoBaptiste — 2002
• Prions: health scare and biological challengeAdriano Aguzzi, Fabio Montrasio, Pascal S. Kaeser — 2001
• Kinetic Stabilization of the α-Synuclein Protofibril by a Dopamine-α-Synuclein AdductKelly A. Conway, Jean‐Christophe Rochet, Robert M. Bieganski — 2001
• Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain.Sabina Capellari, Piero Parchi, Claudio Russo — 2000
• α-Synuclein in Lewy bodiesMaria Grazia Spillantini, Marie L. Schmidt, Virginia M.‐Y. Lee — 1997
• Fine Structure and Biochemical Mechanisms Underlying Nigrostriatal Inclusions and Cell Death after Proteasome InhibitionFrancesco Fornai, Paola Lenzi, Marco Gesi — 2003
• Inhibition of Complex Glycosylation Increases the Formation of PrPscKonstanze F. Winklhofer, Ulrich Heller, Anja Reintjes — 2003
• Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70John M. Warrick, Ho Yin Edwin Chan, Gladys L. Gray-Board — 1999
• Parkin attenuates manganese‐induced dopaminergic cell deathYouichirou Higashi, Masato Asanuma, Ikuko Miyazaki — 2004
• Evidence of Presynaptic Location and Function of the Prion ProteinJochen Herms, Tobias Tings, Stefan Gall — 1999

Cited by

• Human Prion Protein Mutants with Deleted and Inserted Octarepeats Undergo Different Pathways to Trigger Cell ApoptosisJ-P Bertaud, Simon Burrows — 2011
• Molecular Chaperones in Health and DiseaseKlaus Starke, Matthias Gaestel — 2006
• Molecular basis of cerebral neurodegeneration in prion diseasesJörg Tatzelt, Hermann Schätzl — 2007
• Tianma modulates proteins with various neuro-regenerative modalities in differentiated human neuronal SH-SY5Y cells.Umamaheswari Ramachandran, Arulmani Manavalan, Husvinee Sundaramurthi — 2012
• Genome-Scale Modeling of the Protein Secretory Machinery in YeastAmir Feizi, Tobias Österlund, Dina Petranović — 2013
• Aggregopathy in Neurodegenerative Diseases: Mechanisms and Therapeutic ImplicationChristoph P. Dohm, Pawel Kermer, Mathias Bähr — 2008
• Regulatable gene expression systems for gene therapy.Nuria Vilaboa, Richard Voellmy — 2006
• Familial CJD Associated PrP Mutants within Transmembrane Region Induced Ctm-PrP Retention in ER and Triggered Apoptosis by ER Stress in SH-SY5Y CellsXin Wang, Qi Shi, Kun Xu — 2011
• Comparison of the chemical and thermal denaturation of proteins by a two-state transition model.Jayanthi Ramprakash, Victoria Doseeva, Alexander Galkin — 2008
• Stress and prions: Lessons from the yeast modelYury O. Chernoff — 2007
• To be, or not to be — molecular chaperones in protein degradationVerena Arndt, Christian Rogon, Jörg Höhfeld — 2007
• THE DOPAMINERGIC NIGROSTRIATAL SYSTEMAND PARKINSON'S DISEASE: MOLECULAR EVENTSIN DEVELOPMENT, DISEASE, AND CELL DEATH, AND NEW THERAPEUTIC STRATEGIESMojgan Hodaie, Joseph S. Neimat, Andrés M. Lozano — 2007
• Molecular pathways and genetic aspects of Parkinson’s disease: from bench to bedsideMario Di Napoli, Imtiaz M. Shah, David A. Stewart — 2007
• Association of Bcl-2 with misfolded prion protein is linked to the toxic potential of cytosolic PrP.Angelika S. Rambold, Margit Miesbauer, Doron Rapaport — 2006
• Mitochondrial dysfunction in Parkinson's disease.Konstanze F. Winklhofer, Christian Haass — 2010
• Inferring secretory and metabolic pathway activity from omic data with secCellFieHelen O. Masson, Mojtaba Samoudi, Caressa M. Robinson — 2023
• TPPP/p25: A New Unstructured Protein Hallmarking SynucleinopathiesF. Orosz, A. Lehotzky, J. Olah — 2009
• Membrane Changes in BSE and ScrapieC. Ersdal, G. McGovern, M. Jeffrey — 2011
• Prion publications from the NeuroPrion partners - 2008 -S. Colussi, G. Santagada, C. Laurenza — 2006
• ParkinMediatesNeuroprotectionthroughActivationofIB Kinase/NuclearFactor-BSignalingJulia S. Schlehe, Julia E. Schramm — 2007

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