An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning †

By Brison Nathalie   Debeer Philippe   Fantini Sebastian   Oley Christine   Zappavigna Vincenzo   Luyten Frank P.   Tylzanowski Przemko  

Human Molecular Genetics, Vol. 21, Iss. 11, 2012-06 ,pp. : 2464-2475

Oxford University Press

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A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly

By Johnson K.R.   Sweet H.O.   Donahue L.R.   Ward-Bailey P.   Bronson R.T.   Davisson M.T.  

Human Molecular Genetics, Vol. 7, Iss. 6, 1998-06 ,pp. : 1033-1038

Oxford University Press

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Genomic Structure of HOXD13 Gene: A Nine Polyalanine Duplication Causes Synpolydactyly in Two Unrelated Families

By Akarsu A. Nurten   Stoilov Ivaylo   Yilmaz Engin   Sayli B. Sitki   Sarfarazi Mansoor  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 945-952

Oxford University Press

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The N-terminal domain of the Aurora-A Phe-31 variant encodes an E3 ubiquitin ligase and mediates ubiquitination of IBα

By Briassouli Paraskevi   Chan Florence   Linardopoulos Spiros  

Human Molecular Genetics, Vol. 15, Iss. 22, 2006-11 ,pp. : 3343-3350

Oxford University Press

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Functional capacity of dystrophins carrying deletions in the N-terminal actin-binding domain

By Banks Glen B.   Gregorevic Paul   Allen James M.   Finn Eric E.   Chamberlain Jeffrey S.  

Human Molecular Genetics, Vol. 16, Iss. 17, 2007-09 ,pp. : 2105-2113

Oxford University Press

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