Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins (Q46155239)

From Wikidata

Jump to navigation Jump to search

scientific article published in January 1994

Language	Label	Description	Also known as
English	Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins	scientific article published in January 1994

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

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

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

prion protein family

0 references

1 reference

based on heuristic

inferred from title

Stanley B. Prusiner

9

object named as

Prusiner SB

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

Stephen J DeArmond

2

object named as

DeArmond SJ

0 references

author name string

Westaway D

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

DeArmond SJ

2

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

Cayetano-Canlas J

3

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

Groth D

4

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

Foster D

5

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

Yang SL

6

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

Torchia M

7

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

Carlson GA

8

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

language of work or name

0 references

publication date

1 January 1994

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

76

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

117-129

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Unraveling prion diseases through molecular genetics

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Nearly ubiquitous tissue distribution of the scrapie agent precursor protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Demyelinating peripheral neuropathy in Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

The skeletal muscle of sheep affected with scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Germ-line transformation of mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

The MRL +/+ mouse: a new model of tubular aggregates which are gender- and age-related.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Genetic complementation reveals a novel regulatory role for 3' untranslated regions in growth and differentiation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Myopathy in sheep; its relationship to scrapie and to dermatomyositis and muscular dystrophy

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Chemistry and biology of prions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

The prion protein gene: a role in mouse embryogenesis?

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Cellular isoform of the scrapie agent protein participates in lymphocyte activation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

DEGENERATION OF THE CEREBELLAR AND HYPOTHALAMONEUROHYPOPHYSIAL SYSTEMS IN SHEEP WITH SCRAPIE; AND ITS RELATIONSHIP TO HUMAN SYSTEM DEGENERATIONS

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Paradoxical shortening of scrapie incubation times by expression of prion protein transgenes derived from long incubation period mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: a mouse model of amyotrophic lateral sclerosis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Neurotoxicity of a prion protein fragment

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

ARIA, a protein that stimulates acetylcholine receptor synthesis, is a member of the neu ligand family

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Glycosylinositol phospholipid anchors of the scrapie and cellular prion proteins contain sialic acid

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Spontaneous neurodegeneration in transgenic mice with mutant prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Molecular biology of prion diseases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Familial neurological disease associated with spongiform encephalopathy

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Predicted secondary structure and membrane topology of the scrapie prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0092-8674(94)90177-5

Identifiers

10.1016/0092-8674(94)90177-5

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/8287472

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q46155239&oldid=2095239419"