Please use this identifier to cite or link to this item:
Title: Transcriptome analysis of prion disease animal models
Authors: Barbisin, Maura
Legname, Giuseppe
Keywords: prionprion proteinneurodegenerationgene expressiongenomics
Issue Date: 2014
Publisher: EUT Edizioni Università di Trieste
Source: Maura Barbisin, Giuseppe Legname, Transcriptome analysis of prion disease animal models, in Sabina Passamonti (ed.), The Partners and the Objectives of Trans2Care, an Italy-Slovenia cross-border network of science and healthcare institutions, EUT - Edizioni Università di Trieste, 2014, pp. 35-39
Prion diseases are incurable and fatal neurodegenerative disorders that affect both humans and animals. The causative agent is an infectious protein called prion (PrPSc), which is the pathological form of a normal protein (PrPC) present on the cell membrane. The molecular mechanisms underlying prion replication and subsequent degeneration of the Central Nervous System (CNS) are still poorly understood and therefore innovative approaches are needed to build diagnostic, therapeutic, taxonomic, and disease surveillance tools. We are going to adopt an unbiased genomic approach and conduct whole transcriptome analyses using microarray gene expression methods in brain and/or blood of infected animals versus healthy controls. We hope to identify a set of genes that can be used for early diagnosis and/or as targets for therapeutic strategies. Within the Trans2Care project we intend to promote collaboration and exchange of knowledge to facilitate all partners’ research objectives, and possibly find a common way to accelerate the process aimed at improving our healthcare system.
Type: Book Chapter
ISBN: 978-88-8303-512-8
Appears in Collections:Trans2Care, 2012. The Partnership and the Objectives of Trans2Care, an Italy-Slovenia cross-border network of science

Files in This Item:
File Description SizeFormat
Transcriptome analysis of prion.pdf147.16 kBAdobe PDFThumbnail
Show full item record

CORE Recommender

Page view(s) 50

checked on Sep 27, 2022

Download(s) 50

checked on Sep 27, 2022

Google ScholarTM



This item is licensed under a Creative Commons License Creative Commons