Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases

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Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases

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im August 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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Characterization of mutations ...... in neurodegenerative diseases

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Characterization of mutations in

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Characterization of mutations ...... in neurodegenerative diseases

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Characterization of mutations in

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Characterization of mutations ...... in neurodegenerative diseases

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Characterization of mutations in

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P1476

Characterization of mutations ...... in neurodegenerative diseases

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P2093

Eva Bagyinszky

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Seong Soo A An

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Vo Van Giau

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P2860

A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure

Differential diagnosis of Alzheimer's disease

Characterizing affinity epitopes between prion protein and β-amyloid using an epitope mapping immunoassay

A novel human disease with abnormal prion protein sensitive to protease

Mutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patients

Solution structure of the E200K variant of human prion protein. Implications for the mechanism of pathogenesis in familial prion diseases

NMR Structure of the Human Prion Protein with the Pathological Q212P Mutation Reveals Unique Structural Features

Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation

Mutations of the prion protein gene phenotypic spectrum

Charge neutralization of the central lysine cluster in prion protein (PrP) promotes PrP(Sc)-like folding of recombinant PrP amyloids.

P304

2067-2085

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scholarly article

P356

10.2147/NDT.S165445

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English

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P50

SangYun Kim

Young Chul Youn

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2018-08-14T00:00:00Z

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P698

30147320

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P921

neurodegeneration

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6097508

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