Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase

By Benayoun Bérénice A.   Georges Adrien B.   L'Hôte David   Andersson Noora   Dipietromaria Aurélie   Todeschini Anne-Laure   Caburet Sandrine   Bazin Claude   Anttonen Mikko   Veitia Reiner A.  

Human Molecular Genetics, Vol. 20, Iss. 9, 2011-05 ,pp. : 1673-1686

Oxford University Press

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Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development

By Moumn Lara   Dipietromaria Aurlie   Batista Frank   Kocer Ayhan   Fellous Marc   Pailhoux Eric   Veitia Reiner A.  

Human Molecular Genetics, Vol. 17, Iss. 7, 2007-12 ,pp. : 1010-1019

Oxford University Press

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Transcription factor MEF2A mutations in patients with coronary artery disease

By Bhagavatula M.R. Krishna  

Human Molecular Genetics, Vol. 13, Iss. 24, 2004-12 ,pp. : 3181-3188

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Disease-causing mutations within the lysosomal integral membrane protein type 2 (LIMP-2) reveal the nature of binding to its ligand -glucocerebrosidase

By Blanz Judith   Groth Johann   Zachos Christina   Wehling Christina   Saftig Paul   Schwake Michael  

Human Molecular Genetics, Vol. 19, Iss. 4, 2010-02 ,pp. : 563-572

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Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation

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Human Molecular Genetics, Vol. 14, Iss. 23, 2005-12 ,pp. : 3557-3564

Oxford University Press

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