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Grant: Project Grant

University of Toronto

$1,327,276.00

Elucidating the synaptic function of C9orf72

EF 2024-25

Résumé
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are two closely related neurodegenerative diseases, both of which currently lack cures or effective treatments. These conditions involve progressive communication failure between neurons in the brain, a crucial function for maintaining brain health. Understanding the reasons behind this breakdown in neuronal communication in ALS/FTD is vital for developing treatment strategies. The most common genetic cause of ALS/FTD is a mutation in a gene known as C9orf72. Our research has shown that this gene plays a key role in maintaining the brain's neuronal communication system. Our project focuses on understanding how C9orf72 does this. By unravelling how C9orf72 helps maintain brain communication, we hope to pinpoint new treatment targets to pave the way for potential therapies for these devastating diseases.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
524033
Name
Robertson Janice
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Molecular & Cellular Neurosciences - B
Projecttitle
Elucidating the synaptic function of C9orf72
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$1,327,276
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Amyotrophic Lateral Sclerosis; C9orf72; Cofilin; Frontotemporal Dementia; Glua1; Synaptic
Abstract
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are two closely related neurodegenerative diseases, both of which currently lack cures or effective treatments. These conditions involve progressive communication failure between neurons in the brain, a crucial function for maintaining brain health. Understanding the reasons behind this breakdown in neuronal communication in ALS/FTD is vital for developing treatment strategies. The most common genetic cause of ALS/FTD is a mutation in a gene known as C9orf72. Our research has shown that this gene plays a key role in maintaining the brain's neuronal communication system. Our project focuses on understanding how C9orf72 does this. By unravelling how C9orf72 helps maintain brain communication, we hope to pinpoint new treatment targets to pave the way for potential therapies for these devastating diseases.
Competitiondate
202503
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Robertson, Janice
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,327,276~ $0~