HPRT-APRT-deficient Mice Are Not a Model for Lesch-Nyhan Syndrome

By Engle Sandra J.   Womer Daniel E.   Davies Philip M.   Boivin Greg   Sahota Amrik   Simmonds H. Anne   Stambrook Peter J.   Tischfield Jay A.  

Human Molecular Genetics, Vol. 5, Iss. 10, 1996-10 ,pp. : 1607-1610

Oxford University Press

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Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesis

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Human Molecular Genetics, Vol. 18, Iss. 13, 2009-07 ,pp. : 2317-2327

Oxford University Press

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MicroRNA-mediated dysregulation of neural developmental genes in HPRT deficiency: clues for Lesch–Nyhan disease?

By Guibinga Ghiabe-Henri   Hrustanovic Gorjan   Bouic Kathryn   Jinnah Hyder A.   Friedmann Theodore  

Human Molecular Genetics, Vol. 21, Iss. 3, 2012-02 ,pp. : 609-622

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Human neural stem cells: a model system for the study of LeschNyhan disease neurological aspects

By Cristini Silvia   Navone Stefania   Canzi Laura   Acerbi Francesco   Ciusani Emilio   Hladnik Uros   de Gemmis Paola   Alessandri Giulio   Colombo Augusto   Parati Eugenio   Invernici Gloria  

Human Molecular Genetics, Vol. 19, Iss. 10, 2010-05 ,pp. : 1939-1950

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Animal models for muscular dystrophy: valuable tools for the development of therapies

By Allamand Valérie   Campbell KevinP.  

Human Molecular Genetics, Vol. 9, Iss. 16, 2000-10 ,pp. : 2459-2467

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