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Identification and functional analysis of imprinted genes
Reference
BBS/E/B/21976602
Principal Investigator / Supervisor
Dr Gavin Kelsey
Co-Investigators /
Co-Supervisors
Institution
Babraham Institute
Department
Babraham Institute Department
Funding type
Research
Value (£)
18,234
Status
Completed
Type
Institute Project
Start date
01/04/1997
End date
30/09/2000
Duration
42 months
Abstract
We inherit a set of genes from our mother and from our father. For most genes, both copies are equally active irrespective of their parentage. A few genes defy this expectation: only one copy of an theirimprintedthat gene is normally expressed. Consequently, developmental processes in which imprinted genes function are especially susceptible to the effect of mutation. For example, problems in imprinting give rise to disturbances in fetal growth which, in addition to immediate clinical implications, may predispose to diseases in later life, such as hypertension and diabetes. It is not known how many of our genes are controlled by imprinting. We are using a molecular landmark to identify all the imprinted genes present in mammals. This work will create important diagnostic markers for growth and other disorders in which imprinting is suspected to be a factor, and pave the way for new therapeutic strategies with which to treat them.
Summary
unavailable
Committee
Closed Committee - Genes & Developmental Biology (GDB)
Research Topics
X – not assigned to a current Research Topic
Research Priority
X – Research Priority information not available
Research Initiative
X - not in an Initiative
Funding Scheme
X – not Funded via a specific Funding Scheme
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