Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification.


Journal

Laboratory investigation; a journal of technical methods and pathology
ISSN: 1530-0307
Titre abrégé: Lab Invest
Pays: United States
ID NLM: 0376617

Informations de publication

Date de publication:
11 2019
Historique:
received: 18 02 2019
accepted: 28 05 2019
revised: 11 05 2019
pubmed: 30 6 2019
medline: 7 7 2020
entrez: 29 6 2019
Statut: ppublish

Résumé

Prion diseases are transmissible neurological disorders associated with the presence of abnormal, disease-related prion protein (PrP

Identifiants

pubmed: 31249376
doi: 10.1038/s41374-019-0282-1
pii: S0023-6837(22)00571-2
doi:

Substances chimiques

PrPC Proteins 0
Prion Proteins 0
Prions 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1741-1748

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS052319
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS088604
Pays : United States
Organisme : NIAID NIH HHS
ID : P01 AI106705
Pays : United States

Auteurs

Manuel V Camacho (MV)

Department of Pathology, Case Western Reserve University, Cleveland, OH, USA.

Glenn Telling (G)

Prion Research Center, Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.

Qingzhong Kong (Q)

Department of Pathology, Case Western Reserve University, Cleveland, OH, USA.
Department of Neurology, Case Western Reserve University, Cleveland, OH, USA.

Pierluigi Gambetti (P)

Department of Pathology, Case Western Reserve University, Cleveland, OH, USA.

Silvio Notari (S)

Department of Pathology, Case Western Reserve University, Cleveland, OH, USA. silvio.notari@gmail.com.

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Classifications MeSH