A role for fibroblast growth factor receptor-2 in the altered osteoblast phenotype induced by Twist haploinsufficiency in the Saethre–Chotzen syndrome

By Guenou Hind   Kaabeche Karim   Mée Sandrine Le   Marie Pierre J.  

Human Molecular Genetics, Vol. 14, Iss. 11, 2005-06 ,pp. : 1429-1439

Oxford University Press

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Translocation Breakpoint Maps 5 kb 3′ from TWIST in a Patient Affected with Saethre-Chotzen Syndrome

By Krebs Inge  

Human Molecular Genetics, Vol. 6, Iss. 7, 1997-01 ,pp. : 1079-1086

Oxford University Press

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The variable expressivity and incomplete penetrance of the twist -null heterozygous mouse phenotype resemble those of human Saethre–Chotzen syndrome

By Bourgeois P.  

Human Molecular Genetics, Vol. 7, Iss. 6, 1998-06 ,pp. : 945-959

Oxford University Press

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Twist haploinsufficiency in Saethre–Chotzen syndrome induces calvarial osteoblast apoptosis due to increased TNFα expression and caspase-2 activation

By Ghouzzi V.E.   Yousfi M.   Lasmoles F.   Marie P.J.  

Human Molecular Genetics, Vol. 11, Iss. 4, 2002-02 ,pp. : 359-369

Oxford University Press

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The Twist Gene, Although Not Disrupted In Saethre-Chotzen Patients With Apparently Balanced Translocations of 7p21, Is Mutated In Familial and Sporadic Cases

By Rose C.S. P.   Patel P.   Reardon W.   Malcolm S.   Winter R. M.  

Human Molecular Genetics, Vol. 6, Iss. 8, 1997-01 ,pp. : 1369-1373

Oxford University Press

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