SOX10 structurefunction analysis in the chicken neural tube reveals important insights into its role in human neurocristopathies

By Cossais Franois   Wahlbuhl Mandy   Kriesch Jana   Wegner Michael  

Human Molecular Genetics, Vol. 19, Iss. 12, 2010-06 ,pp. : 2409-2420

Oxford University Press

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Translation of SOX10 3 untranslated region causes a complex severe neurocristopathy by generation of a deleterious functional domain

By Inoue Ken   Ohyama Tomoko   Sakuragi Yosuke   Yamamoto Ryoko   Inoue Naoko A.   Li-Hua Yu   Goto Yu-ichi   Wegner Michael   Lupski James R.  

Human Molecular Genetics, Vol. 16, Iss. 24, 2007-12 ,pp. : 3037-3046

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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Interaction among SOX10 , PAX3 and MITF , three genes altered in Waardenburg syndrome

By Bondurand Nadege   Pingault Veronique   Goerich DerkE.   Lemort Nicole   Sock Elisabeth   Caignec Cedric Le   Wegner Michael   Goossens Michel  

Human Molecular Genetics, Vol. 9, Iss. 13, 2000-08 ,pp. : 1907-1917

Oxford University Press

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Sox10 gain-of-function causes XX sex reversal in mice: implications for human 22q-linked disorders of sex development

By Polanco Juan Carlos   Wilhelm Dagmar   Davidson Tara-Lynne   Knight Deon   Koopman Peter  

Human Molecular Genetics, Vol. 19, Iss. 3, 2010-02 ,pp. : 506-516

Oxford University Press

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