Grant: Operating Grant
Centre hospitalier de l'Université de Montréal (CHUM)
$602,314.00
Chemical-genetics approaches using in vivo models of age-dependent neurodegeneration
EF 2013-14
Résumé
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by selective death of motor neurons. Even though recent advances have discovered many of the genetic causes of ALS, it remains an incurable disease. To learn more about disease mechanisms and identify new therapeutic approaches we use the genetic system Caenorhabditis elegans, a nematode worm with powerful and rapid methodologies to model ALS. Using our C. elegans ALS models we have discovered novel mechanisms and FDA approved compounds that alleviate neuronal degeneration caused by mutant human proteins linked to ALS. We propose to further validate these findings in more complex models like mice to set the stage for clinical trials that may open the door to new therapeutics for ALS patients.
Programme
Operating Grant
Emplacement
Quebec, Canada
Type de bénéficiaire
Not-for-profit organization or charity
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
291186
Name
Parker Alex J
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Genetics
Projecttitle
Chemical-genetics approaches using in vivo models of age-dependent neurodegeneration
Programtype2
Operating Grants
Orgnameinp2
Centre hospitalier de l'Université de Montréal (CHUM)
Cihramount2
$602,314
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Amyotrophic Lateral Sclerosis; C. Elegans; Chemical Screen; Genetics; Huntington'S Disease; Neurodegeneration
Abstract
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by selective death of motor neurons. Even though recent advances have discovered many of the genetic causes of ALS, it remains an incurable disease. To learn more about disease mechanisms and identify new therapeutic approaches we use the genetic system Caenorhabditis elegans, a nematode worm with powerful and rapid methodologies to model ALS. Using our C. elegans ALS models we have discovered novel mechanisms and FDA approved compounds that alleviate neuronal degeneration caused by mutant human proteins linked to ALS. We propose to further validate these findings in more complex models like mice to set the stage for clinical trials that may open the door to new therapeutics for ALS patients.
Competitiondate
201309
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Parker, Alex J
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $602,314~ $0~