enow.com Web Search

Search results

1. Results from the WOW.Com Content Network

2. α-Galactosidase - Wikipedia

   en.wikipedia.org/wiki/Α-Galactosidase

   α-Galactosidase ( EC 3.2.1.22, α-GAL, α-GAL A; systematic name α-D-galactoside galactohydrolase) is a glycoside hydrolase enzyme that catalyses the following reaction: [1] Hydrolysis of terminal, non-reducing α- D -galactose residues in α- D -galactosides, including galactose oligosaccharides, galactomannans and galactolipids

3. Pegunigalsidase alfa - Wikipedia

   en.wikipedia.org/wiki/Pegunigalsidase_alfa

   Pegunigalsidase alfa, sold under the brand name Elfabrio, is an enzyme replacement therapy for the treatment of Fabry disease. [2] [4] It is a recombinant human α-galactosidase-A. [4] It is a hydrolytic lysosomal neutral glycosphingolipid-specific enzyme. [2] The most common side effects are infusion-related reactions, hypersensitivity and ...

4. Avalglucosidase alfa - Wikipedia

   en.wikipedia.org/wiki/Avalglucosidase_alfa

   Avalglucosidase alfa is composed of the human GAA enzyme that is conjugated with a couple of bis-mannose-6-phosphate (bis-M6P) tetra-mannose glycans. [12] The bis-MGP of avalglucosidase alpha binds to the cation-independent mannose-6-phosphate receptor which is located on the skeletal muscles. [12]

5. Are Dogs Lactose Intolerant? What Experts Advise About ...

   www.aol.com/dogs-lactose-intolerant-experts...

   Not all questions have simple, yes or no answers—including this one. While many dogs are lactose intolerant, many are not! Lactose intolerance develops as a dog grows up, so it can be impossible ...

6. Alglucosidase alfa - Wikipedia

   en.wikipedia.org/wiki/Alglucosidase_alfa

   Alglucosidase alfa, sold under the brand name Myozyme among others, is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II), a rare lysosomal storage disorder (LSD). [6] Chemically, the drug is an analog of the enzyme that is deficient in patients affected by Pompe disease, alpha ...

7. Galactosidases - Wikipedia

   en.wikipedia.org/wiki/Galactosidases

   Galactosidases are enzymes (glycoside hydrolases) that catalyze the hydrolysis of galactosides into monosaccharides.. Galactosides can be classified as either alpha or beta. If the galactoside is classified as an alpha-galactoside, the enzyme is called alpha-galactosidase, and is responsible for catalyzing the hydrolysis of substrates that contain α-galactosidic residues, such as ...