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Molecular Pathology of Fatal Familial Insomnia

Brain pathology (Zurich, Switzerland), 1998-07, Vol.8 (3), p.539-548

1998

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Ubiquitin is Associated with Abnormal Cytoplasmic Filaments Characteristic of Neurodegenerative Diseases

Proceedings of the National Academy of Sciences - PNAS, 1988-06, Vol.85 (12), p.4501-4505

1988

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Paired Helical Filaments from Alzheimer Disease Patients Contain Cytoskeletal Components

Proceedings of the National Academy of Sciences - PNAS, 1985-06, Vol.82 (11), p.3916-3920

1985

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Ultrastructural Localization of β-Amyloid, τ, and Ubiquitin Epitopes in Extracellular Neurofibrillary Tangles

Proceedings of the National Academy of Sciences - PNAS, 1991-03, Vol.88 (6), p.2098-2102

1991

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Role of amyloid precursor protein (APP): Study with antisense transfection of human neuroblastoma cells

Journal of neuroscience research, 1992-04, Vol.31 (4), p.635-645

1992

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Analysis of the prion protein gene in thalamic dementia

Neurology, 1992-10, Vol.42 (10), p.1859-1859

1992

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Experimental diabetic neuropathy: impairment of slow transport with changes in axon cross-sectional area

Proceedings of the National Academy of Sciences - PNAS, 1985-11, Vol.82 (22), p.7716-7720

1985

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Experimental diabetic neuropathy: similar changes of slow axonal transport and axonal size in different animal models

The Journal of neuroscience, 1988-05, Vol.8 (5), p.1814-1821

1988

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Truncated Forms of the Human Prion Protein in Normal Brain and in Prion Diseases

The Journal of biological chemistry, 1995-08, Vol.270 (32), p.19173-19180

1995

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Aluminium effect on slow axonal transport: a novel impairment of neurofilament transport

The Journal of neuroscience, 1984-03, Vol.4 (3), p.722-731

1984

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Bodian's Silver Method Stains Neurofilament Polypeptides

Science (American Association for the Advancement of Science), 1981-09, Vol.213 (4515), p.1521-1522

1981

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Giant Axonal Neuropathy: Acceleration of Neurofilament Transport in Optic Axons

Proceedings of the National Academy of Sciences - PNAS, 1985-02, Vol.82 (3), p.920-924

1985

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Amyloid precursor protein and ubiquitin immunoreactivity in dystrophic axons is not unique to Alzheimer's disease

The American journal of pathology, 1991-09, Vol.139 (3), p.485-489

1991

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Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17

Neurology, 1995-06, Vol.45 (6), p.1062-1067

1995

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Reorganization of Axoplasmic Organelles Following β,β′-Iminodipropionitrile Administration

The Journal of cell biology, 1981-12, Vol.91 (3), p.866-871

1981

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Regional distribution of protease-resistant prion protein in fatal familial insomnia

Annals of neurology, 1995-07, Vol.38 (1), p.21-29

1995

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Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene

The New England journal of medicine, 1992-02, Vol.326 (7), p.444-449

1992

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Differential APP gene expression in rat cerebral cortex, meninges, and primary astroglial, microglial and neuronal cultures

FEBS letters, 1991-11, Vol.292 (1), p.171-178

1991

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Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Different Prion Proteins Determined by a DNA Polymorphism

Proceedings of the National Academy of Sciences - PNAS, 1994-03, Vol.91 (7), p.2839-2842

1994

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Selective presence of ubiquitin in intracellular inclusions

The American journal of pathology, 1989-03, Vol.134 (3), p.505-513

1989

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Fatal familial insomnia and the widening spectrum of prion diseases

British medical bulletin, 1993-10, Vol.49 (4), p.980-994

1993

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Ubiquitin is present on the cytokeratin intermediate filaments and Mallory bodies of hepatocytes

Laboratory investigation, 1988-12, Vol.59 (6), p.848

1988

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Allelic origin of the abnormal prion protein isoform in familial prion diseases

Nature medicine, 1997-09, Vol.3 (9), p.1009-1015

1997

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Immunocytochemical properties of Alzheimer straight filaments

The Journal of neuroscience, 1987-11, Vol.7 (11), p.3736-3738

1987

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Axonal transport of neurofilament is accelerated in peripheral nerve during 2,5-hexanedione intoxication

Brain research, 1989-07, Vol.491 (2), p.328-334

1989

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Molecular Pathology of Fatal Familial Insomnia

Ubiquitin is Associated with Abnormal Cytoplasmic Filaments Characteristic of Neurodegenerative Diseases

Paired Helical Filaments from Alzheimer Disease Patients Contain Cytoskeletal Components

Ultrastructural Localization of β-Amyloid, τ, and Ubiquitin Epitopes in Extracellular Neurofibrillary Tangles

Role of amyloid precursor protein (APP): Study with antisense transfection of human neuroblastoma cells

Analysis of the prion protein gene in thalamic dementia

Experimental diabetic neuropathy: impairment of slow transport with changes in axon cross-sectional area

Experimental diabetic neuropathy: similar changes of slow axonal transport and axonal size in different animal models

Truncated Forms of the Human Prion Protein in Normal Brain and in Prion Diseases

Aluminium effect on slow axonal transport: a novel impairment of neurofilament transport

Bodian's Silver Method Stains Neurofilament Polypeptides

Giant Axonal Neuropathy: Acceleration of Neurofilament Transport in Optic Axons

Amyloid precursor protein and ubiquitin immunoreactivity in dystrophic axons is not unique to Alzheimer's disease

Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17

Reorganization of Axoplasmic Organelles Following β,β′-Iminodipropionitrile Administration

Regional distribution of protease-resistant prion protein in fatal familial insomnia

Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene

Differential APP gene expression in rat cerebral cortex, meninges, and primary astroglial, microglial and neuronal cultures

Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Different Prion Proteins Determined by a DNA Polymorphism

Selective presence of ubiquitin in intracellular inclusions

Fatal familial insomnia and the widening spectrum of prion diseases

Ubiquitin is present on the cytokeratin intermediate filaments and Mallory bodies of hepatocytes

Allelic origin of the abnormal prion protein isoform in familial prion diseases

Immunocytochemical properties of Alzheimer straight filaments

Axonal transport of neurofilament is accelerated in peripheral nerve during 2,5-hexanedione intoxication

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