Grant: Emerging Team Grant: From Genes to Proteins, Cells, Tissues and Patients - LOI
University of Ottawa
$0.00
Mechanisms of Motoneuron Degeneration in Spinal Muscular Atrophy and Identification of Therapeutic Targets
FY 2008-09
Summary
Loss of a protein named SMN, for ¿Survival of Motor Neurons¿, causes spinal muscular atrophy, a disease that affects 1 in every 10,000 newborns and is the leading genetic cause of infant death. SMA results in the massive loss of spinal cord motoneurons, which are the cells responsible for voluntary movements. Research in recent years has identified an essential function for the SMN protein, that should be equally important for all cells in the body. Hence, it remains a major challenge in the field to rationalize how loss of SMN can result in a motoneuron-specific disease. Our current research strategy will use novel state-of-the-art approaches to identify the proteins that interact specifically with SMN in motoneurons. Identification of novel components of the SMN complex may provide crucial insights into the function of SMN that is important for motoneurons and to the etiology of SMA. Furthermore, proteins found to be misregulated in SMA cells may constitute new targets for the development of novel strategies for therapeutic intervention.
Department
Program
Emerging Team Grant: From Genes to Proteins, Cells, Tissues and Patients - LOI
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
174400
Name
Jasmin Bernard J
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Not applicable / Specified
Prcname2
Emerging Team Grant: From Genes to Proteins, Cells, Tissues and Patients
Projecttitle
Mechanisms of Motoneuron Degeneration in Spinal Muscular Atrophy and Identification of Therapeutic Targets
Programtype2
Operating Grants
Orgnameinp2
University of Ottawa
Cihramount2
$0
Cihrequipment2
$0
Programname2
Emerging Team Grant: From Genes to Proteins, Cells, Tissues and Patients - LOI
Keyworddelim
Neuromuscular Junction - Mouse Models - Signalling -; Proteomics; Rna Stability - Rna Binding Proteins - Microrna -; Spinal Muscular Atrophy - Motoneurons - Skeletal Muscle -
Abstract
Loss of a protein named SMN, for ¿Survival of Motor Neurons¿, causes spinal muscular atrophy, a disease that affects 1 in every 10,000 newborns and is the leading genetic cause of infant death. SMA results in the massive loss of spinal cord motoneurons, which are the cells responsible for voluntary movements. Research in recent years has identified an essential function for the SMN protein, that should be equally important for all cells in the body. Hence, it remains a major challenge in the field to rationalize how loss of SMN can result in a motoneuron-specific disease. Our current research strategy will use novel state-of-the-art approaches to identify the proteins that interact specifically with SMN in motoneurons. Identification of novel components of the SMN complex may provide crucial insights into the function of SMN that is important for motoneurons and to the etiology of SMA. Furthermore, proteins found to be misregulated in SMA cells may constitute new targets for the development of novel strategies for therapeutic intervention.
Competitiondate
200810
Approvedterm2
1 yr 0 mth
Pinamesdelim
Jasmin, Bernard J; Kothary, Rashmi K
Approvedterm
1 an 0 mois