Grant: Fellowship: Canada Impact+ Research Training Awards - Postdoctoral
University of British Columbia
$140,000.00
Investigating the molecular basis of platelet function
FY 2025-26
Summary
"Heart attacks and strokes happen because platelets (tiny cells) in the blood are inappropriately activated or triggered to
form blood clots at places that they shouldn’t – a process known as thrombosis. Thrombosis is the cause of 1 in 4 deaths
worldwide. Drugs are used to treat thrombosis. However, a side effect of many anti-thrombotic drugs is that they can also
block normal platelet function and cause bleeding. We will address this important problem by learning exactly how platelets
“read” biochemical signals from the blood and blood vessels. Ideally, we will understand which molecules cause platelets
to react to certain signals, and how we might control these molecules to prevent life-threatening blood clots that cause
heart attacks and strokes. This approach will lead to the development of precision drugs that can target specific platelet
molecules and reduce thrombosis – without interfering with normal platelet function. The goal of this project is to learn
exactly how platelets read the biochemical signals that make them form clots. We will use state-of-the-art laboratory
technology to study platelets and figure out what molecules inside the platelets are “turned on” that makes the platelet
become activated, change shape and stick to other platelets. We will identify those molecules that can make platelets
more “sticky” and likely to form clots. We will also study how platelets control the release of other molecules called “clotting
factors” that can accelerate the formation of clots that cause heart attacks and strokes. Over the long term, this research
will provide insights towards identifying new drug targets that would improve our ability to prevent and treat thrombosis
without increased risk of bleeding."
Department
Program
Fellowship: Canada Impact+ Research Training Awards - Postdoctoral
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
568141
Name
Boyd Emily K
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Prcname2
Canada Impact+ Research Training Awards - Postdoctoral
Projecttitle
Investigating the molecular basis of platelet function
Programtype2
Fellowship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$140,000
Cihrequipment2
$0
Programname2
Fellowship: Canada Impact+ Research Training Awards - Postdoctoral
Keyworddelim
Cell Signalling; Cytoskeleton; Hemostatis; Platelets; Thrombosis
Abstract
"Heart attacks and strokes happen because platelets (tiny cells) in the blood are inappropriately activated or triggered to
form blood clots at places that they shouldn’t – a process known as thrombosis. Thrombosis is the cause of 1 in 4 deaths
worldwide. Drugs are used to treat thrombosis. However, a side effect of many anti-thrombotic drugs is that they can also
block normal platelet function and cause bleeding. We will address this important problem by learning exactly how platelets
“read” biochemical signals from the blood and blood vessels. Ideally, we will understand which molecules cause platelets
to react to certain signals, and how we might control these molecules to prevent life-threatening blood clots that cause
heart attacks and strokes. This approach will lead to the development of precision drugs that can target specific platelet
molecules and reduce thrombosis – without interfering with normal platelet function. The goal of this project is to learn
exactly how platelets read the biochemical signals that make them form clots. We will use state-of-the-art laboratory
technology to study platelets and figure out what molecules inside the platelets are “turned on” that makes the platelet
become activated, change shape and stick to other platelets. We will identify those molecules that can make platelets
more “sticky” and likely to form clots. We will also study how platelets control the release of other molecules called “clotting
factors” that can accelerate the formation of clots that cause heart attacks and strokes. Over the long term, this research
will provide insights towards identifying new drug targets that would improve our ability to prevent and treat thrombosis
without increased risk of bleeding."
Competitiondate
202603
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Boyd, Emily K
Approvedterm
2 ans 0 mois
Cihrcontribution2
~ $140,000~ $0~