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Publications by Emmanuel A. Asante

Inherited Prion Disease A117V Is Not Simply a Proteinopathy but Produces Prions Transmissible to Transgenic Mice Expressing Homologous Prion Protein

Molecular Biology

English

Expression of Human Full-Length and Minidystrophin in Transgenic MDX Mice: Implications for Gene Therapy of Duchenne Muscular Dystrophy

Human Molecular Genetics

Molecular Biology

English

Related publications

Genesis of Mammalian Prions: From Non-Infectious Amyloid Fibrils to a Transmissible Prion Disease

Molecular Biology

English

Subclinical Bovine Spongiform Encephalopathy Infection in Transgenic Mice Expressing Porcine Prion Protein

Journal of Neuroscience

English

Serial Transmission in Rodents of Neurodegeneration From Transgenic Mice Expressing Mutant Prion Protein.

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Filamentous White Matter Prion Protein Deposition Is a Distinctive Feature of Multiple Inherited Prion Diseases

Acta neuropathologica communications

Forensic Medicine

Molecular Neuroscience

English

The Octarepeat Region of Prion Protein, but Not the TM1 Domain, Is Important for the Antioxidant Effect of Prion Protein

Free Radical Biology and Medicine

English

Human Prion Strain Selection in Transgenic Mice

Annals of Neurology

English

Stability and Cu(II) Binding of Prion Protein Variants Related to Inherited Human Prion Diseases

Biophysical Journal

English

Prion Protein Insertional Mutations Increase Aggregation Propensity but Not Fiber Stability

BMC Biochemistry

Molecular Biology

English

Is Tau a Prion-Like Protein?

Journal of Alzheimer's Disease

Clinical Psychology

English