Available from British Library Document Supply Centre- DSC:DN061286 / BLDSC - British Library Document Supply CentreSIGLEGBUnited Kingdo
SIGLEAvailable from British Library Document Supply Centre-DSC:D200210 / BLDSC - British Library Doc...
Sialidosis is an autosomal recessive disease caused by the genetic deficiency of lysosomal sialidase...
Human lysosomal neuraminidase 1 (hNEU1) is an exo-a-sialidase which cleaves a(2-3) and a(2-6) linked...
The G9 gene, located within the MHC class III region of man and mouse, has been shown to encode a 46...
SIGLEAvailable from British Library Document Supply Centre-DSC:D192259 / BLDSC - British Library Doc...
Mammalian sialidases are important in modulating the sialic acid content of cell-surface and intrace...
SCHAUER R, WEMBER M, Tschesche H. ISOLATION AND CHARACTERIZATION OF AN OLIGOSACCHARIDE-SPECIFIC AND ...
textabstractSince the discovery of the lysosome as a distinct subcellular compartment important for ...
Gangliosides play key roles in cell differentiation, cellcell interactions, and transmembrane signal...
The NEU1 gene is the first identified member of the human sialidases, glycohydrolitic enzymes that r...
textabstractLysosomal neuraminidase initiates the hydrolysis of oligosaccharldes, gangliosides, glyc...
The NEU1 gene is the first identified member of the human sialidases, glycohydrolitic enzymes that r...
Gangliosides play key roles in cell differentiation, cell-cell interactions, and transmembrane signa...
Sialidases or neuramidases are glycoside hydrolases removing terminal sialic acid residues from sial...
Sialidosis is an autosomal recessive lysosomal storage disease caused by mutations in the neuraminid...
SIGLEAvailable from British Library Document Supply Centre-DSC:D200210 / BLDSC - British Library Doc...
Sialidosis is an autosomal recessive disease caused by the genetic deficiency of lysosomal sialidase...
Human lysosomal neuraminidase 1 (hNEU1) is an exo-a-sialidase which cleaves a(2-3) and a(2-6) linked...
The G9 gene, located within the MHC class III region of man and mouse, has been shown to encode a 46...
SIGLEAvailable from British Library Document Supply Centre-DSC:D192259 / BLDSC - British Library Doc...
Mammalian sialidases are important in modulating the sialic acid content of cell-surface and intrace...
SCHAUER R, WEMBER M, Tschesche H. ISOLATION AND CHARACTERIZATION OF AN OLIGOSACCHARIDE-SPECIFIC AND ...
textabstractSince the discovery of the lysosome as a distinct subcellular compartment important for ...
Gangliosides play key roles in cell differentiation, cellcell interactions, and transmembrane signal...
The NEU1 gene is the first identified member of the human sialidases, glycohydrolitic enzymes that r...
textabstractLysosomal neuraminidase initiates the hydrolysis of oligosaccharldes, gangliosides, glyc...
The NEU1 gene is the first identified member of the human sialidases, glycohydrolitic enzymes that r...
Gangliosides play key roles in cell differentiation, cell-cell interactions, and transmembrane signa...
Sialidases or neuramidases are glycoside hydrolases removing terminal sialic acid residues from sial...
Sialidosis is an autosomal recessive lysosomal storage disease caused by mutations in the neuraminid...
SIGLEAvailable from British Library Document Supply Centre-DSC:D200210 / BLDSC - British Library Doc...
Sialidosis is an autosomal recessive disease caused by the genetic deficiency of lysosomal sialidase...
Human lysosomal neuraminidase 1 (hNEU1) is an exo-a-sialidase which cleaves a(2-3) and a(2-6) linked...