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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Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased α7 integrin, utrophin and associated glycoproteins

By Voit T.  

Human Molecular Genetics, Vol. 12, Iss. 19, 2003-10 ,pp. : 2467-2479

Oxford University Press

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Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)

By Willems P.  

Human Molecular Genetics, Vol. 10, Iss. 5, 2001-03 ,pp. : 537-543

Oxford University Press

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Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks

By Kerzendorfer Claudia   Whibley Annabel   Carpenter Gillian   Outwin Emily   Chiang Shih-Chieh   Turner Gillian   Schwartz Charles   El-Khamisy Sherif   Raymond F. Lucy   O'Driscoll Mark  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1324-1334

Oxford University Press

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Increased SK3 expression in DM1 lens cells leads to impaired growth through a greater calcium-induced fragility

By Rhodes Jeremy D.   Monckton Darren G.   McAbney John P.   Prescott Alan R.   Duncan George  

Human Molecular Genetics, Vol. 15, Iss. 24, 2006-12 ,pp. : 3559-3568

Oxford University Press

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