sphingolipidosis

navigate by keyword : 1r46 acid agalsidase alpha amino atoms cause ceramide dimer dimeric diseas disease enzyme fabri fabry gal galactose galactosidase glycolipid glycoprotein hydrolase lysosomal lysosome molecule pdb peptide polymer polypeptide protein replacement sphingolipidosis storage structure therapy

Glucocerebrosidase (beta-glucosidase) enzyme molecule. Royalty Free Stock Photo

Alpha-galactosidase (Agalsidase) enzyme. Royalty Free Stock Photo

Brain neurons in Tay-Sachs disease, 3D illustration Royalty Free Stock Photo

$Alpha-galactosidase (Agalsidase) enzyme. Cause of Fabry\'s disease. Administered as enzyme replacement therapy Royalty Free Stock Photo$

Molecule of Ganglioside GM2 Royalty Free Stock Photo

Tay-Sachs disease, 3D illustration Royalty Free Stock Photo

Alpha-galactosidase (Agalsidase) enzyme. Cause of Fabry's diseas Royalty Free Stock Photo

$Alpha-galactosidase (Agalsidase) enzyme. Cause of Fabry\'s disease. Administered as enzyme replacement therapy Royalty Free Stock Photo$

Molecule of beta-hexosaminidase A Royalty Free Stock Photo

$Glucocerebrosidase (beta-glucosidase) enzyme molecule. Deficient in Gaucher\'s disease. Recombinant analog used as drug in Gaucher Royalty Free Stock Photo$

$Alpha-galactosidase (Agalsidase) enzyme. Cause of Fabry\'s disease. Administered as enzyme replacement therapy Royalty Free Stock Photo$

Alpha-galactosidase (Agalsidase) enzyme. Cause of Fabry's disease. Administered as enzyme replacement therapy. Cartoon & wire representation. Chain gradient coloring.