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 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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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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Saethre–Chotzen mutations cause TWIST protein degradation or impaired nuclear location

By El Ghouzzi Vincent   Legeai-Mallet Laurence   Aresta Sandra   Benoist Catherine   Munnich Arnold   Gunzburg Jean de   Bonaventure Jacky  

Human Molecular Genetics, Vol. 9, Iss. 5, 2000-03 ,pp. : 813-819

Oxford University Press

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Contiguous gene deletion neighboring TWIST1 identified in a patient with Saethre‐Chotzen syndrome associated with neurodevelopmental delay: Possible contribution of HDAC9

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CONGENITAL ANOMALIES, Vol. 58, Iss. 1, 2018-01 ,pp. : 33-35

John Wiley & Sons Inc

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