To find a new biomarker of Tay-Sachs disease and Sandhoff disease. The lyso-GM2 ganglioside (lyso-GM2) levels in the brain and plasma in Sandhoff mice were measured by means of high performance liquid chromatography and the effect of a modified hexosaminidase (Hex) B exhibiting Hex A-like activity was examined. Then, the lyso-GM2 concentrations in human plasma samples were determined. The lyso-GM2 levels in the brain and plasma in Sandhoff mice were apparently increased compared with those in wild-type mice, and they decreased on intracerebroventricular administration of the modified Hex B. The lyso-GM2 levels in plasma of patients with Tay-Sachs disease and Sandhoff disease were increased, and the increase in lyso-GM2 was associated with a...
Tay–Sachs and Sandhoff diseases are autosomal recessive neurodegenerative diseases resulting from th...
Drug-induced phospholipidosis (DIPL) is characterized by an increase in the phospholipid content of ...
The therapeutic potential of bone marrow-derived stromal cells for the therapy of Tay-Sachs disease ...
To find a new biomarker of Tay-Sachs disease and Sandhoff disease. The lyso-GM2 ganglioside (lyso-GM...
Tay-Sachs and Sandhoff diseases are autosomal recessive disorders of GM2 ganglioside catabolism resu...
β-hexosaminidase is an enzyme responsible for the degradation of gangliosides, glycans, and other gl...
Sandhoff disease is a devastating autosomal recessive GM2 gangliosidosis in which a deficiency of β-...
β-N-acetylhexosaminidase B, or just β-hexosaminidase, is an enzyme responsible for the degradation o...
Sandhoff disease (SD) is a lysosomal disease caused by mutations in the gene coding for the β subuni...
<p>Lyso-GM2 levels in brain tissues (<b>A</b>) and plasma (B). Wild-type mice (W,♦), untreated Sandh...
<div><p>Tay-Sachs and Sandhoff diseases are lethal inborn errors of acid β-N-acetylhexosaminidase ac...
Tay-Sachs disease is an autosomal recessive lysosomal storage disease caused by beta-hexosaminidase ...
Gangliosides are found at high levels in neuronal tissues where they play a variety of important fun...
Sandhoff disease involves the CNS accumulation of ganglioside GM2 and asialo-GM2 (GA2) due to inheri...
Gangliosides are found at high levels in neuronal tissues where they play a variety of important fun...
Tay–Sachs and Sandhoff diseases are autosomal recessive neurodegenerative diseases resulting from th...
Drug-induced phospholipidosis (DIPL) is characterized by an increase in the phospholipid content of ...
The therapeutic potential of bone marrow-derived stromal cells for the therapy of Tay-Sachs disease ...
To find a new biomarker of Tay-Sachs disease and Sandhoff disease. The lyso-GM2 ganglioside (lyso-GM...
Tay-Sachs and Sandhoff diseases are autosomal recessive disorders of GM2 ganglioside catabolism resu...
β-hexosaminidase is an enzyme responsible for the degradation of gangliosides, glycans, and other gl...
Sandhoff disease is a devastating autosomal recessive GM2 gangliosidosis in which a deficiency of β-...
β-N-acetylhexosaminidase B, or just β-hexosaminidase, is an enzyme responsible for the degradation o...
Sandhoff disease (SD) is a lysosomal disease caused by mutations in the gene coding for the β subuni...
<p>Lyso-GM2 levels in brain tissues (<b>A</b>) and plasma (B). Wild-type mice (W,♦), untreated Sandh...
<div><p>Tay-Sachs and Sandhoff diseases are lethal inborn errors of acid β-N-acetylhexosaminidase ac...
Tay-Sachs disease is an autosomal recessive lysosomal storage disease caused by beta-hexosaminidase ...
Gangliosides are found at high levels in neuronal tissues where they play a variety of important fun...
Sandhoff disease involves the CNS accumulation of ganglioside GM2 and asialo-GM2 (GA2) due to inheri...
Gangliosides are found at high levels in neuronal tissues where they play a variety of important fun...
Tay–Sachs and Sandhoff diseases are autosomal recessive neurodegenerative diseases resulting from th...
Drug-induced phospholipidosis (DIPL) is characterized by an increase in the phospholipid content of ...
The therapeutic potential of bone marrow-derived stromal cells for the therapy of Tay-Sachs disease ...