Grant: Operating Grant
Ottawa Hospital Research Institute
$753,790.00
The molecular pathogenesis of spinal muscular atrophy
EF 2012-13
Résumé
Spinal muscular atrophy (SMA) is the number one genetic killer of young children. It is a group of inherited and often fatal diseases that destroys the nerves controlling voluntary muscle movement, with the result that activities like crawling, walking, head and neck control, and even swallowing are affected. At present there is no cure for this devastating disorder. Fortunately, there has been great success at the development of appropriate mouse models for the severe and intermediate forms of the disease. These mice are helping us to get a better understanding of the pathological steps in the progression of the disease, and serve as pre-clinical models for the development and testing of novel therapeutics. Indeed, our work has shown that both motor neurons and skeletal muscle have intrinsic defects, and that both cell types need to be targeted for effective therapy.
Programme
Operating Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
278744
Name
Kothary Rashmi K
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Genetics
Projecttitle
The molecular pathogenesis of spinal muscular atrophy
Programtype2
Operating Grants
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$753,790
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Mouse Models; Myogenesis; Neuromuscular Junction; Rho-Kinase Inhibitors; Spinal Muscular Atrophy; Synaptosomes; Therapeutics
Abstract
Spinal muscular atrophy (SMA) is the number one genetic killer of young children. It is a group of inherited and often fatal diseases that destroys the nerves controlling voluntary muscle movement, with the result that activities like crawling, walking, head and neck control, and even swallowing are affected. At present there is no cure for this devastating disorder. Fortunately, there has been great success at the development of appropriate mouse models for the severe and intermediate forms of the disease. These mice are helping us to get a better understanding of the pathological steps in the progression of the disease, and serve as pre-clinical models for the development and testing of novel therapeutics. Indeed, our work has shown that both motor neurons and skeletal muscle have intrinsic defects, and that both cell types need to be targeted for effective therapy.
Competitiondate
201303
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Kothary, Rashmi K
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $753,790~ $0~