4.6 Article

Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Clinical Neurology

Environmental and host factors that contribute to prion strain evolution

Jason C. Bartz

Summary: Prions are novel pathogens composed of PrPSc, with strain distribution influenced by both environmental and host factors. The host amino acid sequence and post-translational modifications of PrP(C) play a critical role in dictating the repertoire of prion strains, and interference between prion strains may impact the emergence of dominant strains.

ACTA NEUROPATHOLOGICA (2021)

Article Neurosciences

A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease

Satish K. Nemani et al.

ACTA NEUROPATHOLOGICA COMMUNICATIONS (2020)

Letter Neurosciences

Clinicopathological features of the rare form of Creutzfeldt-Jakob disease in R208H-V129V PRNP carrier

Dorina Tiple et al.

ACTA NEUROPATHOLOGICA COMMUNICATIONS (2019)

Article Clinical Neurology

A Novel Eight Octapeptide Repeat Insertion in PRNP Causing Prion Disease in a Danish Family

Ausrine Areskeviciute et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2019)

Article Clinical Neurology

Age at onset in genetic prion disease and the design of preventive clinical trials

Eric Vallabh Minikel et al.

NEUROLOGY (2019)

Review Genetics & Heredity

Genetic Factors in Mammalian Prion Diseases

Simon Mead et al.

ANNUAL REVIEW OF GENETICS, VOL 53 (2019)

Article Clinical Neurology

Two distinct prions in fatal familial insomnia and its sporadic form

Atsuko Takeuchi et al.

BRAIN COMMUNICATIONS (2019)

Article Clinical Neurology

Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges

Samir Abu-Rumeileh et al.

ANNALS OF NEUROLOGY (2018)

Article Cell Biology

Quantifying prion disease penetrance using large population control cohorts

Eric Vallabh Minikel et al.

SCIENCE TRANSLATIONAL MEDICINE (2016)

Review Clinical Neurology

The influence of PRNP polymorphisms on human prion disease susceptibility: an update

Atsushi Kobayashi et al.

ACTA NEUROPATHOLOGICA (2015)

Article Microbiology

Evidence That Bank Vole PrP Is a Universal Acceptor for Prions

Joel C. Watts et al.

PLOS PATHOGENS (2014)

Review Neurosciences

Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems

Atsushi Kobayashi et al.

ACTA NEUROPATHOLOGICA COMMUNICATIONS (2014)

Article Immunology

Transmission Characteristics of Variably Protease-Sensitive Prionopathy

Silvio Notari et al.

EMERGING INFECTIOUS DISEASES (2014)

Article Biochemistry & Molecular Biology

Post-translational changes to PrP alter transmissible spongiform encephalopathy strain properties

Enrico Cancellotti et al.

EMBO JOURNAL (2013)

Article Biochemistry & Molecular Biology

Analyses of Protease Resistance and Aggregation State of Abnormal Prion Protein across the Spectrum of Human Prions

Daniela Saverioni et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2013)

Article Clinical Neurology

Intraneuronal Immunoreactivity for the Prion Protein Distinguishes a Subset of E200K Genetic From Sporadic Creutzfeldt-Jakob Disease

Gabor G. Kovacs et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2012)

Article Pathology

Co-Occurrence of Types 1 and 2 PrPres in Sporadic Creutzfeldt-Jakob Disease MM1

Atsushi Kobayashi et al.

AMERICAN JOURNAL OF PATHOLOGY (2011)

Article Clinical Neurology

Comprehensive Neuropathologic Analysis of Genetic Prion Disease Associated With the E196K Mutation in PRNP Reveals Phenotypic Heterogeneity

Sabina Eigenbrod et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2011)

Article Clinical Neurology

Variably Protease-Sensitive Prionopathy: A New Sporadic Disease of the Prion Protein

Wen-Quan Zou et al.

ANNALS OF NEUROLOGY (2010)

Article Virology

Experimental Verification of a Traceback Phenomenon in Prion Infection

Atsushi Kobayashi et al.

JOURNAL OF VIROLOGY (2010)

Article Multidisciplinary Sciences

Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties

Matthew T. Bishop et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Article Biotechnology & Applied Microbiology

Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins

Emmanuel A. Asante et al.

JOURNAL OF GENERAL VIROLOGY (2009)

Article Multidisciplinary Sciences

Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP

Sigrun Roeber et al.

PLOS ONE (2008)

Article Medicine, Research & Experimental

A refined method for molecular typing reveals that co-occurrence of PrPSc types in Creutzfeldt-Jakob disease is not the rule

Silvio Notari et al.

LABORATORY INVESTIGATION (2007)

Article Biochemistry & Molecular Biology

Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain

Atsushi Kobayashi et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2007)

Review Cell Biology

Mechanisms of disease - Insights into prion strains and neurotoxicity

Adriano Aguzzi et al.

NATURE REVIEWS MOLECULAR CELL BIOLOGY (2007)

Article Clinical Neurology

Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease

M Polymenidou et al.

LANCET NEUROLOGY (2005)

Article Genetics & Heredity

Genetic prion disease:: the EUROCJD experience

GG Kovács et al.

HUMAN GENETICS (2005)

Article Clinical Neurology

Loss of glycosylation associated with the T183A mutation in human prion disease

E Grasbon-Frodl et al.

ACTA NEUROPATHOLOGICA (2004)

Article Multidisciplinary Sciences

Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene

C Korth et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)

Article Medicine, General & Internal

TSE strain variation

ME Bruce

BRITISH MEDICAL BULLETIN (2003)

Article Multidisciplinary Sciences

Genetic influence on the structural variations of the abnormal prion protein

P Parchi et al.

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