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Project

Study of the molecular pathogenesis of forkhead transcription factors in human developmental disorders.

Output en outcomes

Code

01SB1409

Looptijd

01-01-2009 → 31-10-2011

Financiering

Regional and community funding: Special Research Fund

Promotor

Anne De Paepe

Onderzoeksdisciplines

Natural sciences
- Genetics
- Systems biology
Medical and health sciences
- Molecular and cell biology
- Molecular and cell biology

Trefwoorden

FOXL2 forkhead transcriptiefactor humane ontwikkelingsaandoening BPES

Projectomschrijving

A first aim is the development of a functional assay for intragenic FOXL2 mutations, for predictive testing for ovarian dysfunction in BPES. A second aim is the identification of the genetic defect in BPES patients without an intragenic mutation, gene deletion or large long-range genetic defect, and functional studies of potential regulators of FOXL2 transcription.

English

Dutch

English

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