Defective survival of proliferating Sertoli cells and androgen receptor function in a mouse model of the ATR-X syndrome

By Bagheri-Fam Stefan   Argentaro Anthony   Svingen Terje   Combes Alexander N.   Sinclair Andrew H.   Koopman Peter   Harley Vincent R.  

Human Molecular Genetics, Vol. 20, Iss. 11, 2011-06 ,pp. : 2213-2224

Oxford University Press

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A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects

By Johnstone Karen A.   DuBose Amanda J.   Futtner Christopher R.   Elmore Michael D.   Brannan Camilynn I.   Resnick James L.  

Human Molecular Genetics, Vol. 15, Iss. 3, 2006-02 ,pp. : 393-404

Oxford University Press

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Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome

By Nuber Ulrike A.  

Human Molecular Genetics, Vol. 14, Iss. 15, 2005-08 ,pp. : 2247-2256

Oxford University Press

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Pharmacological interference with the glucocorticoid system influences symptoms and lifespan in a mouse model of Rett syndrome

By Braun Sebastian   Kottwitz Denise   Nuber Ulrike A.  

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1673-1680

Oxford University Press

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Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund–Thomson syndrome

By Mann Michael B.  

Human Molecular Genetics, Vol. 14, Iss. 6, 2005-03 ,pp. : 813-825

Oxford University Press

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