Pages that link to "Q21984075"
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The following pages link to Hexosaminidase A (Q21984075):
Displaying 19 items.
- Hexa (Q18251181) (← links)
- Mouse model of G M2 activator deficiency manifests cerebellar pathology and motor impairment (Q28504760) (← links)
- Prevention of lysosomal storage in Tay-Sachs mice treated with N-butyldeoxynojirimycin (Q28505993) (← links)
- Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases (Q28506454) (← links)
- Mice deficient in all forms of lysosomal beta-hexosaminidase show mucopolysaccharidosis-like pathology (Q28507414) (← links)
- II. Characterization and development of the regional- and cellular-specific abnormalities in the epididymis of mice with beta-hexosaminidase A deficiency (Q28510054) (← links)
- A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorder (Q28511052) (← links)
- Characterization of the testis and epididymis in mouse models of human Tay Sachs and Sandhoff diseases and partial determination of accumulated gangliosides (Q28585326) (← links)
- Dynamics of major histocompatibility complex class II compartments during B cell receptor-mediated cell activation (Q28585845) (← links)
- Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease (Q28585854) (← links)
- Apoptotic Cell Death in Mouse Models of GM2 Gangliosidosis and Observations on Human Tay-Sachs and Sandhoff Diseases (Q28585898) (← links)
- Targeted disruption of the Hexa gene results in mice with biochemical and pathologic features of Tay-Sachs disease (Q28592824) (← links)
- TGF-β/Smad2/3 signaling directly regulates several miRNAs in mouse ES cells and early embryos (Q28593016) (← links)
- Late onset Tay-Sachs disease in mice with targeted disruption of the Hexa gene: behavioral changes and pathology of the central nervous system (Q28593569) (← links)
- Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis (Q28594483) (← links)
- Adenoviral gene therapy of the Tay-Sachs disease in hexosaminidase A-deficient knock-out mice (Q28594525) (← 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)
- Beta-hexosaminidase A complex (Q107602702) (← links)
- Beta-hexosaminidase S complex (Q107602706) (← links)