Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10 Dom mouse model of Hirschsprung disease

By Cantrell V. Ashley   Owens Sarah E.   Bradley Kevin M.   Smith Jeffrey R.   Southard-Smith E. Michelle  

Human Molecular Genetics, Vol. 13, Iss. 19, 2004-10 ,pp. : 2289-2301

Oxford University Press

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Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10 Dom model of Hirschsprung disease

By Owens Sarah E.  

Human Molecular Genetics, Vol. 14, Iss. 11, 2005-06 ,pp. : 1549-1558

Oxford University Press

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Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10 Dom model of Hirschsprung disease

By Walters Lauren C.   Cantrell V. Ashley   Weller Kevin P.   Mosher Jack T.   Southard-Smith E. Michelle  

Human Molecular Genetics, Vol. 19, Iss. 22, 2010-11 ,pp. : 4353-4372

Oxford University Press

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Sox10 haploinsufficiency affects maintenance of progenitor cells in a mouse model of Hirschsprung disease

By Paratore C.   Eichenberger C.   Suter U.   Sommer L.  

Human Molecular Genetics, Vol. 11, Iss. 24, 2002-09 ,pp. : 3075-3085

Oxford University Press

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Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg–Shah (WS4) syndrome

By Antonellis Anthony   Bennett William R.   Prasad Arjun B.   Lee-Lin Shih-Queen   Green Eric D.   Paisley Derek   Kelsh Robert N.   Pavan William J.   Ward Andrew  

Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 259-271

Oxford University Press

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