4.0 Article

Binding of bovine T194A PrPC by PrPSc-specific antibodies Potential implications for immunotherapy of familial prion diseases

Related references

Note: Only part of the references are listed.
Review Clinical Neurology

Immunotherapy in prion disease

Yvonne Roettger et al.

NATURE REVIEWS NEUROLOGY (2013)

Review Immunology

Prion-like spread of protein aggregates in neurodegeneration

Magdalini Polymenidou et al.

JOURNAL OF EXPERIMENTAL MEDICINE (2012)

Article Neurosciences

Targeting of Monomer/Misfolded SOD1 as a Therapeutic Strategy for Amyotrophic Lateral Sclerosis

Hsueh-Ning Liu et al.

JOURNAL OF NEUROSCIENCE (2012)

Article Biochemistry & Molecular Biology

Induction of ligand-specific PrPC signaling in human neuronal cells

Ryan J. Arsenault et al.

PRION (2012)

Article Biochemistry & Molecular Biology

Nanopore analysis An emerging technique for studying the folding and misfolding of proteins

Claudia Madampage et al.

PRION (2012)

Editorial Material Multidisciplinary Sciences

A Unifying Role for Prions in Neurodegenerative Diseases

Stanley B. Prusiner

SCIENCE (2012)

Article Multidisciplinary Sciences

Intermolecular transmission of superoxide dismutase 1 misfolding in living cells

Leslie I. Grad et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)

Article Neurosciences

Antibody Therapy in Neurodegenerative Disease

Amber L Southwell et al.

REVIEWS IN THE NEUROSCIENCES (2011)

Article Biochemical Research Methods

Nanopore detection of antibody prion interactions

Claudia Avis Madampage et al.

ANALYTICAL BIOCHEMISTRY (2010)

Article Biochemistry & Molecular Biology

Divalent cations induce a compaction of intrinsically disordered myelin basic protein

Christian Baran et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2010)

Article Biochemistry & Molecular Biology

Nanopore analysis of the interaction of metal ions with prion proteins and peptides

Radu I. Stefureac et al.

BIOCHEMISTRY AND CELL BIOLOGY (2010)

Article Biochemistry & Molecular Biology

Pathogenic Mutations in the Hydrophobic Core of the Human Prion Protein Can Promote Structural Instability and Misfolding

Marc W. van der Kamp et al.

JOURNAL OF MOLECULAR BIOLOGY (2010)

Article Biochemistry & Molecular Biology

Nanopore analysis of tethered peptides

Howard Meng et al.

JOURNAL OF PEPTIDE SCIENCE (2010)

Article Chemistry, Physical

The Conversion of Helix H2 to β-Sheet Is Accelerated in the Monomer and Dimer of the Prion Protein upon T183A Mutation

Yassmine Chebaro et al.

JOURNAL OF PHYSICAL CHEMISTRY B (2009)

News Item Multidisciplinary Sciences

NEURODEGENERATION Could They All Be Prion Diseases?

Greg Miller

SCIENCE (2009)

Article Chemistry, Multidisciplinary

Nanopore analysis of a small 86-residue protein

Radu Stefureac et al.

SMALL (2008)

Article Immunology

Atypical bovine spongiform encephalopathies, France, 2001-2007

Anne-Gaaeile Biacabe et al.

EMERGING INFECTIOUS DISEASES (2008)

Review Biochemistry & Molecular Biology

Chronic wasting disease

Christina J. Sigurdson et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2007)

Article Biochemistry & Molecular Biology

An immunological epitope selective for pathological monomer-misfolded SOD1 in ALS

Rishi Rakhit et al.

NATURE MEDICINE (2007)

Article Physics, Multidisciplinary

Unfolding of proteins and long transient conformations detected by single nanopore recording

G. Oukhaled et al.

PHYSICAL REVIEW LETTERS (2007)

Article Biochemistry & Molecular Biology

Transport of α-helical peptides through α-hemolysin and aerolysin pores

Radu Stefureac et al.

BIOCHEMISTRY (2006)

Letter Medicine, General & Internal

Origin of bovine spongiform encephalopathy

T Baron et al.

LANCET (2006)

Review Biochemistry & Molecular Biology

Prion diseases of humans and farm animals: epidemiology, genetics, and pathogenesis

Adriano Aguzzi

JOURNAL OF NEUROCHEMISTRY (2006)

Article Immunology

Generation of antibodies against bovine recombinant prion protein in various strains of mice

O Andrievskaia et al.

CLINICAL AND VACCINE IMMUNOLOGY (2006)

Review Pathology

Chronic wasting disease

ES Williams

VETERINARY PATHOLOGY (2005)

Article Multidisciplinary Sciences

Cross-linking cellular prion protein triggers neuronal apoptosis in vivo

L Solforosi et al.

SCIENCE (2004)

Article Chemistry, Multidisciplinary

Structure of peptides investigated by nanopore analysis

TC Sutherland et al.

NANO LETTERS (2004)

Article Biochemistry & Molecular Biology

A prion protein epitope selective for the pathologically misfolded conformation

E Paramithiotis et al.

NATURE MEDICINE (2003)

Review Clinical Neurology

Mutations of the prion protein gene -: Phenotypic spectrum

GG Kovács et al.

JOURNAL OF NEUROLOGY (2002)

Article Biochemistry & Molecular Biology

Pathway complexity of prion protein assembly into amyloid

IV Baskakov et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2002)

Review Neurosciences

Prion diseases of humans and animals: Their causes and molecular basis

J Collinge

ANNUAL REVIEW OF NEUROSCIENCE (2001)

Article Multidisciplinary Sciences

Signal transduction through prion protein

S Mouillet-Richard et al.

SCIENCE (2000)

Article Multidisciplinary Sciences

NMR structure of the bovine prion protein

FL Garcia et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)