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

Oxford University Press

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FGF19 is a target for FOXC1 regulation in ciliary body-derived cells

By Tamimi Yahya   Skarie Jonathan M.   Link Brian A.   Walter Michael A.  

Human Molecular Genetics, Vol. 15, Iss. 21, 2006-11 ,pp. : 3229-3240

Oxford University Press

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Truncating mutations in FOXC2 cause multiple lymphedema syndromes

By Finegold D.N.  

Human Molecular Genetics, Vol. 10, Iss. 11, 2001-05 ,pp. : 1185-1189

Oxford University Press

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

By Saleem Ramsey A.  

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

Oxford University Press

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