(Q45823963)

16 December 2017

title

The diversities of PrP(Sc) distributions and pathologic changes in various brain regions from a Chinese patient with G114V genetic CJD. (English)

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16 December 2017

1

Qi Shi

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16 December 2017

Xiao-Ping Dong

8

object named as

Xiao-Ping Dong

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16 December 2017

author name string

Bao-Yun Zhang

2

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16 December 2017

Chen Gao

3

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16 December 2017

Jun Han

4

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16 December 2017

Gui-Rong Wang

5

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16 December 2017

Cao Chen

6

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16 December 2017

Chan Tian

7

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16 December 2017

publication date

7 July 2011

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16 December 2017

published in

Neuropathology

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16 December 2017

volume

32

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16 December 2017

issue

1

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16 December 2017

page(s)

51-59

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16 December 2017

Molecular neurology of prion disease

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Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.

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Molecular pathology of human prion diseases

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Prion diseases: from protein to cell pathology

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Evidence for a pathogenic role of different mutations at codon 188 of PRNP

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Human prion disease with a G114V mutation and epidemiological studies in a Chinese family: a case series

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A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease

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Fatal familial insomnia: a new Austrian family

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Proteomic and transcriptomic analysis of rice mature seed-derived callus differentiation.

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Accelerated prion disease in the absence of interleukin-10.

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Novel molecular method for detection of bovine-specific central nervous system tissues as bovine spongiform encephalopathy risk material in meat and meat products

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Formation of native prions from minimal components in vitro

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Fatal familial insomnia: clinical, neuropathological, and genetic description of a Spanish family.

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Induction of glial fibrillary acidic protein expression in astrocytes by nitric oxide

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Accelerated prion replication in, but prolonged survival times of, prion-infected CXCR3-/- mice

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Subcellular localization of disease-associated prion protein in the human brain

21 January 2018

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Chemical and biophysical insights into the propagation of prion strains.

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Biochemical fingerprints of prion infection: accumulations of aberrant full-length and N-terminally truncated PrP species are common features in mouse prion disease

21 January 2018

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Heterogeneity of normal prion protein in two- dimensional immunoblot: presence of various glycosylated and truncated forms.

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Genetic influence on the structural variations of the abnormal prion protein

21 January 2018

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Selective processing and metabolism of disease-causing mutant prion proteins

21 January 2018

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Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family

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21 January 2018

Identifiers

DOI

1 reference

16 December 2017

1 reference

16 December 2017