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Heightened levels and seasonal inversion of riverine suspended sediment in a tropical biodiversity hot spot due to artisanal gold mining

Proceedings of the National Academy of Sciences - PNAS, 2019-11, Vol.116 (48), p.23936-23941

2019

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Characterization of prion protein (PrP)-derived peptides that discriminate full-length PrPSc from PrPC

Proceedings of the National Academy of Sciences - PNAS, 2007-07, Vol.104 (28), p.11551-11556

2007

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Prions in Skeletal Muscle

Proceedings of the National Academy of Sciences - PNAS, 2002-03, Vol.99 (6), p.3812-3817

2002

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Human Prions and Plasma Lipoproteins

Proceedings of the National Academy of Sciences - PNAS, 2006-07, Vol.103 (30), p.11312-11317

2006

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Species Specificity in the Cell-Free Conversion of Prion Protein to Protease-Resistant Forms: A Model for the Scrapie Species Barrier

Proceedings of the National Academy of Sciences - PNAS, 1995-04, Vol.92 (9), p.3923-3927

1995

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Predicted α-Helical Regions of the Prion Protein when Synthesized as Peptides Form Amyloid

Proceedings of the National Academy of Sciences - PNAS, 1992-11, Vol.89 (22), p.10940-10944

1992

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Circumventing Tolerance to Generate Autologous Monoclonal Antibodies to the Prion Protein

Proceedings of the National Academy of Sciences - PNAS, 1996-07, Vol.93 (14), p.7279-7282

1996

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Acquisition of Protease Resistance by Prion Proteins in Scrapie-Infected Cells does not Require Asparagine-Linked Glycosylation

Proceedings of the National Academy of Sciences - PNAS, 1990-11, Vol.87 (21), p.8262-8266

1990

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Prion Protein (PrP) Synthetic Peptides Induce Cellular PrP to Acquire Properties of the Scrapie Isoform

Proceedings of the National Academy of Sciences - PNAS, 1995-11, Vol.92 (24), p.11160-11164

1995

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Tubulofilaments in Negatively Stained Scrapie-Infected Brains: Relationship to Scrapie-Associated Fibrils

Proceedings of the National Academy of Sciences - PNAS, 1987-11, Vol.84 (21), p.7730-7734

1987

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Evidence that DNA is Present in Abnormal Tubulofilamentous Structures Found in Scrapie

Proceedings of the National Academy of Sciences - PNAS, 1988-05, Vol.85 (10), p.3575-3579

1988

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Primary structure of prion protein may modify scrapie isolate properties

Proceedings of the National Academy of Sciences - PNAS, 1989-10, Vol.86 (19), p.7475-7479

1989

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A 54-kDa Normal Cellular Protein May Be the Precursor of the Scrapie Agent Protease-Resistant Protein

Proceedings of the National Academy of Sciences - PNAS, 1986-04, Vol.83 (7), p.2214-2218

1986

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Astrocyte Gene Expression in Creutzfeldt-Jakob Disease

Proceedings of the National Academy of Sciences - PNAS, 1987-08, Vol.84 (16), p.5937-5941

1987

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Scrapie and Creutzfeldt--Jakob Disease Prion Proteins Share Physical Properties and Antigenic Determinants

Proceedings of the National Academy of Sciences - PNAS, 1985-02, Vol.82 (4), p.997-1001

1985

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Insight into the PrPC → PrPSc conversion from the structures of antibody-bound ovine prion scrapie-susceptibility variants

Proceedings of the National Academy of Sciences - PNAS, 2004-07, Vol.101 (28), p.10254-10259

2004

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Interactions between Heterologous Forms of Prion Protein: Binding, Inhibition of Conversion, and Species Barriers

Proceedings of the National Academy of Sciences - PNAS, 2000-05, Vol.97 (11), p.5836-5841

2000

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Phorbol ester, serum, and Rous sarcoma virus transforming gene product induce similar phosphorylations of ribosomal protein S6

Proceedings of the National Academy of Sciences - PNAS, 1984-10, Vol.81 (20), p.6408-6412

1984

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Phosphorylation and Inactivation of Protein Phosphatase 1 by pp60v-src

Proceedings of the National Academy of Sciences - PNAS, 1986-01, Vol.83 (2), p.207-211

1986

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Heightened levels and seasonal inversion of riverine suspended sediment in a tropical biodiversity hot spot due to artisanal gold mining

Characterization of prion protein (PrP)-derived peptides that discriminate full-length PrPSc from PrPC

Prions in Skeletal Muscle

Human Prions and Plasma Lipoproteins

Species Specificity in the Cell-Free Conversion of Prion Protein to Protease-Resistant Forms: A Model for the Scrapie Species Barrier

Predicted α-Helical Regions of the Prion Protein when Synthesized as Peptides Form Amyloid

Circumventing Tolerance to Generate Autologous Monoclonal Antibodies to the Prion Protein

Acquisition of Protease Resistance by Prion Proteins in Scrapie-Infected Cells does not Require Asparagine-Linked Glycosylation

Prion Protein (PrP) Synthetic Peptides Induce Cellular PrP to Acquire Properties of the Scrapie Isoform

Tubulofilaments in Negatively Stained Scrapie-Infected Brains: Relationship to Scrapie-Associated Fibrils

Evidence that DNA is Present in Abnormal Tubulofilamentous Structures Found in Scrapie

Primary structure of prion protein may modify scrapie isolate properties

A 54-kDa Normal Cellular Protein May Be the Precursor of the Scrapie Agent Protease-Resistant Protein

Astrocyte Gene Expression in Creutzfeldt-Jakob Disease

Scrapie and Creutzfeldt--Jakob Disease Prion Proteins Share Physical Properties and Antigenic Determinants

Insight into the PrPC → PrPSc conversion from the structures of antibody-bound ovine prion scrapie-susceptibility variants

Interactions between Heterologous Forms of Prion Protein: Binding, Inhibition of Conversion, and Species Barriers

Phorbol ester, serum, and Rous sarcoma virus transforming gene product induce similar phosphorylations of ribosomal protein S6

Phosphorylation and Inactivation of Protein Phosphatase 1 by pp60v-src

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