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Etiology and pathogenesis of prion diseases.The nosology of Creutzfeldt-Jakob disease and conditions related to the accumulation of PrPCJD in the nervous system.Prion protein transgenes and the neuropathology in prion diseases.Phospholipase A2 inhibitors or platelet-activating factor antagonists prevent prion replication.Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathyActivation effects of a prion protein fragment [PrP-(106-126)] on human leucocytes.The neurodegeneration sequence in prion diseases: evidence from functional, morphological and ultrastructural studies of the GABAergic system.Detection of prion epitopes on PrP and PrP of transmissible spongiform encephalopathies using specific monoclonal antibodies to PrP.
P2860
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P2860
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
The neurochemistry of prion diseases.
@en
type
label
The neurochemistry of prion diseases.
@en
prefLabel
The neurochemistry of prion diseases.
@en
P2860
P1476
The neurochemistry of prion diseases.
@en
P2860
P304
P356
10.1111/J.1471-4159.1993.TB09792.X
P407
P577
1993-11-01T00:00:00Z