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Grant: Project Grant

Centre hospitalier de l'Université de Montréal (CHUM)

$864,450.00

Simple genetic models of neurodegeneration

FY 2017-18

Summary
The major challenge in human genetics is to use the information on gene variants to help clinical practice. To help address this issue, I have pioneered zebrafish models of genetic disorders of the brain. For example, we developed the first in vivo models of genes in amyotrophic lateral sclerosis (ALS), which led to our discovery of a repurposed drug showing promise in clinical trial. I now seek to develop new models of brain diseases in order to better understand and eventually treat neurological disorders. We have three specific aims. We will characterize new zebrafish models of genes with mutations causing both ALS and a form of dementia by discovering novel protein interactors and studying their synaptic biology and pathobiology; we will also study motoneurons derived from ALS patients and transplanted into chimeric zebrafish embryos to test different drug combinations to treat sporadic ALS.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Not-for-profit organization or charity
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
367985
Name
Drapeau Pierre
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Genetics 2
Projecttitle
Simple genetic models of neurodegeneration
Programtype2
Operating Grants
Orgnameinp2
Centre hospitalier de l'Université de Montréal (CHUM)
Cihramount2
$864,450
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Als; C9orf72; Ftld; Genetics; Motoneuron; Proteomics; Tdp-43; Zebrafish
Abstract
The major challenge in human genetics is to use the information on gene variants to help clinical practice. To help address this issue, I have pioneered zebrafish models of genetic disorders of the brain. For example, we developed the first in vivo models of genes in amyotrophic lateral sclerosis (ALS), which led to our discovery of a repurposed drug showing promise in clinical trial. I now seek to develop new models of brain diseases in order to better understand and eventually treat neurological disorders. We have three specific aims. We will characterize new zebrafish models of genes with mutations causing both ALS and a form of dementia by discovering novel protein interactors and studying their synaptic biology and pathobiology; we will also study motoneurons derived from ALS patients and transplanted into chimeric zebrafish embryos to test different drug combinations to treat sporadic ALS.
Competitiondate
201709
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Drapeau, Pierre
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $864,450~ $0~
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