Copper-dependent co-internalization of the prion protein and glypican-1.
about
Glypican-1 mediates both prion protein lipid raft association and disease isoform formationCellular aspects of prion replication in vitroMolecular basis of neurodegeneration and neurodevelopmental defects in Menkes diseaseSuppression of amyloid beta A11 antibody immunoreactivity by vitamin C: possible role of heparan sulfate oligosaccharides derived from glypican-1 by ascorbate-induced, nitric oxide (NO)-catalyzed degradation.Therapeutic approaches for prion and Alzheimer's diseases.Allosteric function and dysfunction of the prion protein.The role of RNA in mammalian prion protein conversion.Heparan sulfate degradation products can associate with oxidized proteins and proteasomes.MEK1 transduces the prion protein N2 fragment antioxidant effects.Hemin interactions and alterations of the subcellular localization of prion protein.The prion protein is embedded in a molecular environment that modulates transforming growth factor β and integrin signaling.
P2860
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P2860
Copper-dependent co-internalization of the prion protein and glypican-1.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Copper-dependent co-internalization of the prion protein and glypican-1.
@en
type
label
Copper-dependent co-internalization of the prion protein and glypican-1.
@en
prefLabel
Copper-dependent co-internalization of the prion protein and glypican-1.
@en
P2093
P2860
P1476
Copper-dependent co-internalization of the prion protein and glypican-1
@en
P2093
David R Brown
Fang Cheng
Josefin Lindqvist
Katrin Mani
P2860
P304
P356
10.1111/J.1471-4159.2006.03981.X
P407
P577
2006-09-01T00:00:00Z