Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes

By Pauws Erwin   Hoshino Aya   Bentley Lucy   Prajapati Suresh   Keller Charles   Hammond Peter   Martinez-Barbera Juan-Pedro   Moore Gudrun E.   Stanier Philip  

Human Molecular Genetics, Vol. 19, Iss. 15, 2010-08 ,pp. : 3103-3103

Oxford University Press

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Tbx22 null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes

By Pauws Erwin   Hoshino Aya   Bentley Lucy   Prajapati Suresh   Keller Charles   Hammond Peter   Martinez-Barbera Juan-Pedro   Moore Gudrun E.   Stanier Philip  

Human Molecular Genetics, Vol. 18, Iss. 21, 2009-11 ,pp. : 4171-4179

Oxford University Press

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Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick

By Roberts Catherine   Ivins Sarah   Cook Andrew C.   Baldini Antonio   Scambler Peter J.  

Human Molecular Genetics, Vol. 15, Iss. 23, 2006-12 ,pp. : 3394-3410

Oxford University Press

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Cre-mediated generation of a VCAM-1 null allele in transgenic mice

By Terry R.W.  

Transgenic Research, Vol. 6, Iss. 5, 1997-01 ,pp. : 349-356

Springer Publishing Company

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Mkks-null mice have a phenotype resembling Bardet–Biedl syndrome

By Fath Melissa A.  

Human Molecular Genetics, Vol. 14, Iss. 9, 2005-05 ,pp. : 1109-1118

Oxford University Press

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