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In vitro trans-splicing in Saccharomyces cerevisiae

Proceedings of the National Academy of Sciences - PNAS, 1995-12, Vol.92 (25), p.11461-11464

1995

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Brain homogenates from human tauopathies induce tau inclusions in mouse brain

Proceedings of the National Academy of Sciences - PNAS, 2013-06, Vol.110 (23), p.9535-9540

2013

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Amyloid polymorphisms constitute distinct clouds of conformational variants in different etiological subtypes of Alzheimer’s disease

Proceedings of the National Academy of Sciences - PNAS, 2017-12, Vol.114 (49), p.13018-13023

2017

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Million-fold sensitivity enhancement in proteopathic seed amplification assays for biospecimens by Hofmeister ion comparisons

Proceedings of the National Academy of Sciences - PNAS, 2019-11, Vol.116 (46), p.23029-23039

2019

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Astrocytes contribute to gamma oscillations and recognition memory

Proceedings of the National Academy of Sciences - PNAS, 2014-08, Vol.111 (32), p.E3343-E3352

2014

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Cytosolic Fc receptor TRIM21 inhibits seeded tau aggregation

Proceedings of the National Academy of Sciences - PNAS, 2017-01, Vol.114 (3), p.574-579

2017

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Memory-related hippocampal activation in the sleeping toddler

Proceedings of the National Academy of Sciences - PNAS, 2018-06, Vol.115 (25), p.6500-6505

2018

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Mutation in the Tau Gene in Familial Multiple System Tauopathy with Presenile Dementia

Proceedings of the National Academy of Sciences - PNAS, 1998-06, Vol.95 (13), p.7737-7741

1998

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Accumulation of prion protein in the brain that is not associated with transmissible disease

Proceedings of the National Academy of Sciences - PNAS, 2007-03, Vol.104 (11), p.4712-4717

2007

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Changes in ventromedial prefrontal and insular cortex support the development of metamemory from childhood into adolescence

Proceedings of the National Academy of Sciences - PNAS, 2017-07, Vol.114 (29), p.7582-7587

2017

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Structure of Tau Exon 10 Splicing Regulatory Element RNA and Destabilization by Mutations of Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17

Proceedings of the National Academy of Sciences - PNAS, 1999-07, Vol.96 (14), p.8229-8234

1999

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Bax Deletion Prevents Neuronal Loss but Not Neurological Symptoms in a Transgenic Model of Inherited Prion Disease

Proceedings of the National Academy of Sciences - PNAS, 2005-01, Vol.102 (1), p.238-243

2005

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Genetic Influence on the Structural Variations of the Abnormal Prion Protein

Proceedings of the National Academy of Sciences - PNAS, 2000-08, Vol.97 (18), p.10168-10172

2000

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Presenilin-1 Mutations of Leucine 166 Equally Affect the Generation of the Notch and APP Intracellular Domains Independent of Their Effect on Aβ42Production

Proceedings of the National Academy of Sciences - PNAS, 2002-06, Vol.99 (12), p.8025-8030

2002

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Familial Multiple System Tauopathy with Presenile Dementia: A Disease with Abundant Neuronal and Glial Tau Filaments

Proceedings of the National Academy of Sciences - PNAS, 1997-04, Vol.94 (8), p.4113-4118

1997

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Accumulation of Protease-Resistant Prion Protein (PrP) and Apoptosis of Cerebellar Granule Cells in Transgenic Mice Expressing a PrP Insertional Mutation

Proceedings of the National Academy of Sciences - PNAS, 2000-05, Vol.97 (10), p.5574-5579

2000

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Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's disease

Proceedings of the National Academy of Sciences - PNAS, 1999-12, Vol.96 (26), p.15233-15238

1999

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Vascular Variant of Prion Protein Cerebral Amyloidosis with τ -Positive Neurofibrillary Tangles: The Phenotype of the Stop Codon 145 Mutation in PRNP

Proceedings of the National Academy of Sciences - PNAS, 1996-01, Vol.93 (2), p.744-748

1996

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Astrocytes contribute to gamma oscillations and recognition memory

Proceedings of the National Academy of Sciences - PNAS, 2014-08, Vol.111 (32), p.11583-11583

2014

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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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Synthetic Peptides Homologous to Prion Protein Residues 106-147 Form Amyloid-Like Fibrils in vitro

Proceedings of the National Academy of Sciences - PNAS, 1993-10, Vol.90 (20), p.9678-9682

1993

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Regional variability of imaging biomarkers in autosomal dominant Alzheimer's disease

Proceedings of the National Academy of Sciences - PNAS, 2013-11, Vol.110 (47), p.18751-18751

2013

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Prion Protein Preamyloid and Amyloid Deposits in Gerstmann-Straussler- Scheinker Disease, Indiana Kindred

Proceedings of the National Academy of Sciences - PNAS, 1992-10, Vol.89 (19), p.9349-9353

1992

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Selective Vulnerability of Late-Generated Dopaminergic Neurons of the Substantia Nigra in Weaver Mutant Mice

Proceedings of the National Academy of Sciences - PNAS, 1995-09, Vol.92 (20), p.9137-9140

1995

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Transplantation of Ventral Mesencephalic Anlagen to Hosts with Genetic Nigrostriatal Dopamine Deficiency

Proceedings of the National Academy of Sciences - PNAS, 1986-11, Vol.83 (22), p.8789-8793

1986

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In vitro trans-splicing in Saccharomyces cerevisiae

Brain homogenates from human tauopathies induce tau inclusions in mouse brain

Amyloid polymorphisms constitute distinct clouds of conformational variants in different etiological subtypes of Alzheimer’s disease

Million-fold sensitivity enhancement in proteopathic seed amplification assays for biospecimens by Hofmeister ion comparisons

Astrocytes contribute to gamma oscillations and recognition memory

Cytosolic Fc receptor TRIM21 inhibits seeded tau aggregation

Memory-related hippocampal activation in the sleeping toddler

Mutation in the Tau Gene in Familial Multiple System Tauopathy with Presenile Dementia

Accumulation of prion protein in the brain that is not associated with transmissible disease

Changes in ventromedial prefrontal and insular cortex support the development of metamemory from childhood into adolescence

Structure of Tau Exon 10 Splicing Regulatory Element RNA and Destabilization by Mutations of Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17

Bax Deletion Prevents Neuronal Loss but Not Neurological Symptoms in a Transgenic Model of Inherited Prion Disease

Genetic Influence on the Structural Variations of the Abnormal Prion Protein

Presenilin-1 Mutations of Leucine 166 Equally Affect the Generation of the Notch and APP Intracellular Domains Independent of Their Effect on Aβ42Production

Familial Multiple System Tauopathy with Presenile Dementia: A Disease with Abundant Neuronal and Glial Tau Filaments

Accumulation of Protease-Resistant Prion Protein (PrP) and Apoptosis of Cerebellar Granule Cells in Transgenic Mice Expressing a PrP Insertional Mutation

Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's disease

Vascular Variant of Prion Protein Cerebral Amyloidosis with τ -Positive Neurofibrillary Tangles: The Phenotype of the Stop Codon 145 Mutation in PRNP

Astrocytes contribute to gamma oscillations and recognition memory

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

Synthetic Peptides Homologous to Prion Protein Residues 106-147 Form Amyloid-Like Fibrils in vitro

Regional variability of imaging biomarkers in autosomal dominant Alzheimer's disease

Prion Protein Preamyloid and Amyloid Deposits in Gerstmann-Straussler- Scheinker Disease, Indiana Kindred

Selective Vulnerability of Late-Generated Dopaminergic Neurons of the Substantia Nigra in Weaver Mutant Mice

Transplantation of Ventral Mesencephalic Anlagen to Hosts with Genetic Nigrostriatal Dopamine Deficiency

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