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Publications by Lilla Reiniger
Filamentous White Matter Prion Protein Deposition Is a Distinctive Feature of Multiple Inherited Prion Diseases
Acta neuropathologica communications
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
Differentially Expressed miRNAs Influence Metabolic Processes in Pituitary Oncocytoma
Neurochemical Research
Medicine
Biochemistry
Cellular
Molecular Neuroscience
Related publications
Stability and Cu(II) Binding of Prion Protein Variants Related to Inherited Human Prion Diseases
Biophysical Journal
Biophysics
Prion Diseases
Seminars in Neurology
Neurology
Inherited Prion Disease A117V Is Not Simply a Proteinopathy but Produces Prions Transmissible to Transgenic Mice Expressing Homologous Prion Protein
PLoS Pathogens
Immunology
Molecular Biology
Virology
Microbiology
Parasitology
Genetics
Is Tau a Prion-Like Protein?
Journal of Alzheimer's Disease
Gerontology
Clinical Psychology
Mental Health
Psychiatry
Geriatrics
Medicine
Neuroscience
18. Transmission of Prion and Prion-Like Proteins in Prion Diseases and Neurodegenerative Diseases
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine
Medicine
Insoluble Cellular Prion Protein and Its Association With Prion and Alzheimer Diseases
Prion
Biochemistry
Molecular Neuroscience
Infectious Diseases
Cell Biology
Cellular
Peculiarities of Prion Diseases
PLoS Pathogens
Immunology
Molecular Biology
Virology
Microbiology
Parasitology
Genetics
Prion Neurotoxicity: Insights From Prion Protein Mutants
Current Issues in Molecular Biology
Medicine
Microbiology
Molecular Biology
Cytosolic Prion Protein Is the Predominant Anti-Bax Prion Protein Form: Exclusion of Transmembrane and Secreted Prion Protein Forms in the Anti-Bax Function
Biochimica et Biophysica Acta - Molecular Cell Research
Cell Biology
Molecular Biology
