4.6 Article

Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease

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。
Article Biochemistry & Molecular Biology

Dominant-negative effects in prion diseases: insights from molecular dynamics simulations on mouse prion protein chimeras

Xiaojing Cong et al.

JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2013)

Article Virology

Prion Propagation in Cells Expressing PrP Glycosylation Mutants

Muhammad K. Salamat et al.

JOURNAL OF VIROLOGY (2011)

Article Biochemistry & Molecular Biology

Insoluble cellular prion protein and its association with prion and Alzheimer diseases

Wen-Quan Zou et al.

Article Cell Biology

Prions

David W. Colby et al.

COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (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 Biochemistry & Molecular Biology

PrP Conformational Transitions Alter Species Preference of a PrP-specific Antibody

Wen-Quan Zou et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2010)

Article Biochemistry & Molecular Biology

Endogenous Proteolytic Cleavage of Disease-associated Prion Protein to Produce C2 Fragments Is Strongly Cell- and Tissue-dependent

Michel Dron et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2010)

Article Biochemistry & Molecular Biology

Human Prion Protein (PrP) 219K Is Converted to PrPSc but Shows Heterozygous Inhibition in Variant Creutzfeldt-Jakob Disease Infection

Masaki Hizume et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2009)

Article Multidisciplinary Sciences

Species and Strain Glycosylation Patterns of PrPSc

Konstantinos Xanthopoulos et al.

PLOS ONE (2009)

Article Clinical Neurology

A novel human disease with abnormal prion protein sensitive to protease

Pierluigi Gambetti et al.

ANNALS OF NEUROLOGY (2008)

Article Biochemistry & Molecular Biology

Host PrP glycosylation: A major factor determining the outcome of prion infection

Nadia L. Tuzi et al.

PLOS BIOLOGY (2008)

Article Clinical Neurology

A novel phenotype of sporadic Creutzfeldt-Jakob disease

G. Giaccone et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2007)

Article Clinical Neurology

Novel prion protein conformation and glycotype in Creutzfeldt-Jakob disease

Gianluigi Zanusso et al.

ARCHIVES OF NEUROLOGY (2007)

Article Biochemistry & Molecular Biology

The stoichiometry of host PrPC glycoforms modulates the efficiency of PrPSc formation in vitro

Koren A. Nishina et al.

BIOCHEMISTRY (2006)

Article Neurosciences

V180I mutation of the prion protein gene associated with atypical PrPSc glycosylation

Stephanie Chasseigneaux et al.

NEUROSCIENCE LETTERS (2006)

Article Biochemistry & Molecular Biology

Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains

Jue Yuan et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2006)

Article Biochemistry & Molecular Biology

Screening of 145 anti-PrP monoclonal antibodies for their capacity to inhibit PrPSc replication in infected cells

C Féraudet et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2005)

Article Multidisciplinary Sciences

Antibody to DNA detects scrapie but not normal prion protein

WQ Zou et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)

Article Clinical Neurology

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

E Grasbon-Frodl et al.

ACTA NEUROPATHOLOGICA (2004)