Apoptotic Cell Death in Mouse Models of G M2 Gangliosidosis and Observations on Human Tay-Sachs and Sandhoff Diseases

By Huang Jing-Qi  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1879-1885

Oxford University Press

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Molecular pathophysiology in Tay–Sachs and Sandhoff diseases as revealed by gene expression profiling

By Myerowitz R.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1343-1351

Oxford University Press

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Adenoviral gene therapy of the Tay-Sachs disease in hexosaminidase A-deficient knock-out mice

By Guidotti J.E.   Mignon A.   Haase G.   Caillaud C.   McDonell N.   Kahn A.   Poenaru L.  

Human Molecular Genetics, Vol. 8, Iss. 5, 1999-05 ,pp. : 831-838

Oxford University Press

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A direct gene transfer strategy via brain internal capsule reverses the biochemical defect in Tay–Sachs disease

By Martino S.  

Human Molecular Genetics, Vol. 14, Iss. 15, 2005-08 ,pp. : 2113-2123

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Sialidase-mediated depletion of G M2 ganglioside in Tay–Sachs neuroglia cells

By Igdoura Suleiman A.  

Human Molecular Genetics, Vol. 8, Iss. 6, 1999-06 ,pp. : 1111-1116

Oxford University Press

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