FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A

By Berry Fred B.   Skarie Jonathan M.   Mirzayans Farideh   Fortin Yannick   Hudson Thomas J.   Raymond Vincent   Link Brian A.   Walter Michael A.  

Human Molecular Genetics, Vol. 17, Iss. 4, 2008-02 ,pp. : 490-505

Oxford University Press

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Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development

By Smith Richard S.  

Human Molecular Genetics, Vol. 9, Iss. 7, 2000-04 ,pp. : 1021-1032

Oxford University Press

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Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesis

By Berry Fred B.   Lines Matthew A.   Footz Tim   Underhill D. Alan   Gage Philip J.   Walter Michael A.  

Human Molecular Genetics, Vol. 15, Iss. 6, 2006-03 ,pp. : 905-919

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Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1

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Human Molecular Genetics, Vol. 12, Iss. 22, 2003-11 ,pp. : 2993-3005

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Protein kinase-A activity in PRKAR1A -mutant cells, and regulation of mitogen-activated protein kinases ERK1/2

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Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1475-1484

Oxford University Press

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