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Grant: Project Grant

Research Institute of the McGill University Health Centre

$615,060.00

Midface hypoplasia caused by cartilage calcification: A mechanistic study with translational implications

EF 2018-19

Résumé
Genetic defects may cause congenital disfigurements of the face which may have profound effects on the appearance of the person leading to psychological complications. More importantly, these anomalies have serious effects on vital body functions, such as feeding and breathing. Our group has studied a form of abnormal facial development caused by mutations in matrix Gla protein (MGP) gene. MGP is produced in the cartilage and its absence leads to cartilage calcification. More specifically, we observe abnormal calcification of the nasal cartilage and cartilaginous joints in the head of mice lacking MGP. In the current study, we will examine the structural features in MGP, which are necessary for its function and use gene therapy to correct the head and face problems in MGP-deficient mice. This knowledge will be very useful to prevent some forms of facial abnormalities in humans with genetic defects causing abnormal cartilage calcification.
Programme
Project Grant
Emplacement
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
402216
Name
Murshed Monzur
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Musculoskeletal Health and Arthritis
Theme2
Biomedical
Prcname2
Clinical Investigation - B: Arthritis, Bone, Skin and Cartilage
Projecttitle
Midface hypoplasia caused by cartilage calcification: A mechanistic study with translational implications
Programtype2
Operating Grants
Orgnameinp2
Research Institute of the McGill University Health Centre
Cihramount2
$615,060
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Ectopic Calcification; Midface Hypoplasia; Nasal Septum Calcification; Skeletal Development
Abstract
Genetic defects may cause congenital disfigurements of the face which may have profound effects on the appearance of the person leading to psychological complications. More importantly, these anomalies have serious effects on vital body functions, such as feeding and breathing. Our group has studied a form of abnormal facial development caused by mutations in matrix Gla protein (MGP) gene. MGP is produced in the cartilage and its absence leads to cartilage calcification. More specifically, we observe abnormal calcification of the nasal cartilage and cartilaginous joints in the head of mice lacking MGP. In the current study, we will examine the structural features in MGP, which are necessary for its function and use gene therapy to correct the head and face problems in MGP-deficient mice. This knowledge will be very useful to prevent some forms of facial abnormalities in humans with genetic defects causing abnormal cartilage calcification.
Competitiondate
201903
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Murshed, Monzur
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $615,060~ $0~