Canada Spends Logo

Explore our Budget 2026 analysis

Grant: Operating Grant

University of British Columbia

$100,000.00

The function of TBX22 in orofacial clefting

FY 2008-09

Summary
Every year 500-600 infants are born in Canada with cleft lip and/or cleft palate. These serious birth defects require a number of surgeries beginning in infancy and carrying on until adulthood. In addition there are major dental challenges such as the need to replace missing teeth and correct jaw misalignments. The main reason clefts occur is that growth is insufficient to allow contact between neighbouring facial prominences in the early embryo. In this grant we focus on a genes that causes human clefting, TBX22 and determine the mechanisms by which this gene inhibits outgrowth using the chicken embryo model. The significance is that we will arrive at a better understanding of the genes and molecules that control facial development. The long term goal is to reduce the severity of and to prevent orofacial clefting.
Program
Operating Grant
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
183806
Name
Richman Joy M
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Dental Sciences
Projecttitle
The function of TBX22 in orofacial clefting
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$100,000
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Craniofacial Development; Growth Factors; Molecular Biology; Orofacial Clefting; Skeletal Development; Transcription Factors
Abstract
Every year 500-600 infants are born in Canada with cleft lip and/or cleft palate. These serious birth defects require a number of surgeries beginning in infancy and carrying on until adulthood. In addition there are major dental challenges such as the need to replace missing teeth and correct jaw misalignments. The main reason clefts occur is that growth is insufficient to allow contact between neighbouring facial prominences in the early embryo. In this grant we focus on a genes that causes human clefting, TBX22 and determine the mechanisms by which this gene inhibits outgrowth using the chicken embryo model. The significance is that we will arrive at a better understanding of the genes and molecules that control facial development. The long term goal is to reduce the severity of and to prevent orofacial clefting.
Competitiondate
200810
Approvedterm2
1 yr 0 mth
Pinamesdelim
Richman, Joy M
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $100,000~ $0~