(Q48479400)

11 February 2018

title

Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions. (English)

1 reference

11 February 2018

author

Jürgen Götz

6

1 reference

11 February 2018

Christian von Mering

10

1 reference

11 February 2018

Adriano Aguzzi

12

1 reference

11 February 2018

Sebastian Brandner

1 reference

ORCID Public Data File 2021

author name string

Shmerling D

1

1 reference

11 February 2018

Hegyi I

2

1 reference

11 February 2018

Fischer M

3

1 reference

11 February 2018

Blättler T

4

1 reference

11 February 2018

Brandner S

5

1 reference

11 February 2018

Rülicke T

7

1 reference

11 February 2018

Flechsig E

8

1 reference

11 February 2018

Cozzio A

9

1 reference

11 February 2018

Hangartner C

11

1 reference

11 February 2018

Weissmann C

13

1 reference

11 February 2018

language of work or name

English

0 references

publication date

1 April 1998

1 reference

11 February 2018

published in

Cell

1 reference

11 February 2018

volume

93

1 reference

11 February 2018

page(s)

203-214

1 reference

11 February 2018

issue

2

1 reference

11 February 2018

Nearly ubiquitous tissue distribution of the scrapie agent precursor protein.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Normal host prion protein necessary for scrapie-induced neurotoxicity.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Factors affecting the efficiency of introducing foreign DNA into mice by microinjecting eggs

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

B lymphocytes and neuroinvasion

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Truncated forms of the human prion protein in normal brain and in prion diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Hippocampal slices from prion protein null mice: disrupted Ca(2+)-activated K+ currents.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Prion protein is necessary for normal synaptic function.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Various rat adult tissues express only one major mRNA species from the glyceraldehyde-3-phosphate-dehydrogenase multigenic family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Processing of a cellular prion protein: identification of N- and C-terminal cleavage sites.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Patch-clamp analysis of synaptic transmission to cerebellar purkinje cells of prion protein knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Complementary hydropathy identifies a cellular prion protein receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Targeting of transforming growth factor-alpha expression to pituitary lactotrophs in transgenic mice results in selective lactotroph proliferation and adenomas

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Metal-chelate affinity chromatography

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Novel proteinaceous infectious particles cause scrapie

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Altered circadian activity rhythms and sleep in mice devoid of prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

PrP effects clarified

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Genetic manipulation of mammals and its application in reproductive biology

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Identification of candidate proteins binding to prion protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981572-X

7 January 2021

10.1016/S0092-8674(00)81572-X

Identifiers

DOI

1 reference

11 February 2018

PubMed ID

9568713

1 reference

11 February 2018