Prion disease with 144 base pair insertion in a Japanese family line. (Q48076727)

8 February 2018

title

Prion disease with 144 base pair insertion in a Japanese family line. (English)

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8 February 2018

author name string

T Oda

1

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8 February 2018

T Kitamoto

2

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8 February 2018

J Tateishi

3

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8 February 2018

T Mitsuhashi

4

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8 February 2018

K Iwabuchi

5

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8 February 2018

C Haga

6

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8 February 2018

E Oguni

7

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8 February 2018

Y Kato

8

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8 February 2018

I Tominaga

9

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8 February 2018

K Yanai

10

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8 February 2018

publication date

1 January 1995

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8 February 2018

published in

Acta Neuropathologica

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8 February 2018

volume

90

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8 February 2018

issue

1

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8 February 2018

page(s)

80-86

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8 February 2018

https://scigraph.springernature.com/pub.10.1007/bf00294463

exact match

0 references

cites work

N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Sträussler syndrome.

1 reference

12 December 2020

The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system

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12 December 2020

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease

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12 December 2020

A dementing illness associated with a novel insertion in the prion protein gene

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12 December 2020

Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features.

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12 December 2020

Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies

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12 December 2020

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

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12 December 2020

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

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12 December 2020

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

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12 December 2020

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

1 reference

12 December 2020

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

12 December 2020

An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease

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12 December 2020

Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene

1 reference

12 December 2020

Human prion diseases with variant prion protein

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12 December 2020

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome

1 reference

12 December 2020

A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob disease

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00294463

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8 February 2018

PubMed ID

7572084

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8 February 2018