Pages that link to "Q28585854"
Jump to navigation
Jump to search
The following pages link to Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease (Q28585854):
Displaying 27 items.
- Hexosaminidase A (Q21984075) (← links)
- I-SceI-induced gene replacement at a natural locus in embryonic stem cells (Q24522393) (← links)
- Pathology of GM2 Gangliosidosis in Jacob Sheep (Q28299661) (← links)
- Apoptotic Cell Death in Mouse Models of GM2 Gangliosidosis and Observations on Human Tay-Sachs and Sandhoff Diseases (Q28585898) (← links)
- Targeted disruption of otog results in deafness and severe imbalance (Q28592378) (← links)
- Specificity of mouse GM2 activator protein and beta-N-acetylhexosaminidases A and B. Similarities and differences with their human counterparts in the catabolism of GM2 (Q28594978) (← links)
- Future perspectives for Tay-Sachs disease (Q34094763) (← links)
- Glycosphingolipid lysosomal storage diseases: therapy and pathogenesis (Q34941895) (← links)
- Substrate reduction therapy in mouse models of the glycosphingolipidoses (Q35153239) (← links)
- Mouse models for neurological disease (Q35172443) (← links)
- Gene therapy for lysosomal storage diseases (LSDs) in large animal models (Q35923476) (← links)
- Neuraminidase-1 contributes significantly to the degradation of neuronal B-series gangliosides but not to the bypass of the catabolic block in Tay-Sachs mouse models (Q36571614) (← links)
- Animal models for mucopolysaccharidosis disorders and their clinical relevance (Q36772983) (← links)
- Animal models of lysosomal disease: an overview (Q38578684) (← links)
- 5. The Contribution of the Mouse to Advances in Human Genetics (Q41625119) (← links)
- Biology and potential strategies for the treatment of GM2 gangliosidoses (Q41757590) (← links)
- Cloning of the cDNA and Gene Encoding Mouse Lysosomal Sialidase and Correction of Sialidase Deficiency in Human Sialidosis and Mouse SM/J Fibroblasts (Q42546301) (← links)
- Structural organization and expression of the gene for the mouse GM2 activator protein (Q42803938) (← links)
- GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: a potential model for Tay Sachs disease (Q48241353) (← links)
- lacZ sequences prevent regulated expression of housekeeping genes (Q50515297) (← links)
- Lysosomal storage results in impaired survival but normal neurite outgrowth in dorsal root ganglion neurones from a mouse model of Sandhoff disease. (Q52123748) (← links)
- Catabolism of asialo-GM2 in man and mouse. Specificity of human/mouse chimeric GM2 activator proteins. (Q52536453) (← links)
- The beta-hexosaminidase story in Toronto: from enzyme structure to gene mutation. (Q53471675) (← links)
- New Approaches to Tay-Sachs Disease Therapy (Q59792086) (← links)
- Quantification of mRNAs encoding proteins of the glycosphingolipid catabolism in mouse models of GM2 gangliosidoses and sphingolipid activator protein precursor (prosaposin) deficiency (Q73163848) (← links)
- Glycosphingolipid degradation and animal models of GM2-gangliosidoses (Q77202738) (← links)
- Efficacy of a Bicistronic Vector for Correction of Sandhoff Disease in a Mouse Model (Q90387987) (← links)