Stability and Cu(II) Binding of Prion Protein Variants Related to Inherited Human Prion Diseases

Biophysical Journal - United States
doi 10.1016/s0006-3495(03)75007-3
Full Text
Abstract

Available in full text

Categories
Biophysics
Date
Authors
Publisher

Elsevier BV

Related search

Filamentous White Matter Prion Protein Deposition Is a Distinctive Feature of Multiple Inherited Prion Diseases

Acta neuropathologica communications
Forensic MedicineMolecular NeurosciencePathologyNeurologyCellular
2013English

Prion Diseases

Seminars in Neurology
Neurology
2013English

Insoluble Cellular Prion Protein and Its Association With Prion and Alzheimer Diseases

Prion
BiochemistryMolecular NeuroscienceInfectious DiseasesCell BiologyCellular
2011English

18. Transmission of Prion and Prion-Like Proteins in Prion Diseases and Neurodegenerative Diseases

Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine
Medicine
2019English

Lack of TAR-DNA Binding Protein-43 (TDP-43) Pathology in Human Prion Diseases

Neuropathology and Applied Neurobiology
Forensic MedicinePathologyNeurologyHistologyPhysiology
2008English

Animal Prion Diseases: The Risks to Human Health

Brain Pathology
Forensic MedicineNeurosciencePathologyNeurology
2019English

Copper Binding to the Octarepeats of the Prion Protein

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2002English

Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay

PLoS ONE
Multidisciplinary
2013English

Peculiarities of Prion Diseases

PLoS Pathogens
ImmunologyMolecular BiologyVirologyMicrobiologyParasitologyGenetics
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy