Alzheimer's and prion diseases: PDK1 at the crossroads.

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Manipulating the Prion Protein Gene Sequence and Expression Levels with CRISPR/Cas9.

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Alzheimer's and prion diseases: PDK1 at the crossroads.

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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name

Alzheimer's and prion diseases: PDK1 at the crossroads.

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Alzheimer's and prion diseases: PDK1 at the crossroads.

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Alzheimer's and prion diseases: PDK1 at the crossroads.

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Alzheimer's and prion diseases: PDK1 at the crossroads.

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Alzheimer's and prion diseases: PDK1 at the crossroads.

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Alzheimer's and prion diseases: PDK1 at the crossroads.

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P1476

Alzheimer's and prion diseases: PDK1 at the crossroads.

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P2093

Frédéric Checler

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P2860

Reversing EphB2 depletion rescues cognitive functions in Alzheimer model

Alzheimer amyloid-β oligomer bound to postsynaptic prion protein activates Fyn to impair neurons.

Abeta-generating enzymes: recent advances in beta- and gamma-secretase research.

Alzheimer's and prion diseases: distinct pathologies, common proteolytic denominators.

The extracellular regulated kinase-1 (ERK1) controls regulated alpha-secretase-mediated processing, promoter transactivation, and mRNA levels of the cellular prion protein.

A naturally occurring C-terminal fragment of the prion protein (PrP) delays disease and acts as a dominant-negative inhibitor of PrPSc formation.

α-Secretase-derived fragment of cellular prion, N1, protects against monomeric and oligomeric amyloid β (Aβ)-associated cell death.

The molecular pathology of Alzheimer's disease.

An N-terminal fragment of the prion protein binds to amyloid-β oligomers and inhibits their neurotoxicity in vivo

α-Secretase in Alzheimer's disease and beyond: mechanistic, regulation and function in the shedding of membrane proteins.

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nm.3332

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1088-1090

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scholarly article

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10.1038/NM.3332

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English

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2013-09-01T00:00:00Z

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24013743

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Prion protein family

Alzheimer's and prion diseases: PDK1 at the crossroads.

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P2860

P2860

Alzheimer's and prion diseases: PDK1 at the crossroads.

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