ALPHA-D-GALACTOSIDASE ENZYME

Known as: alpha Galactosidases, ALPHA-GALACTOSIDASE, alpha-Galactosidase A 
An enzyme that catalyzes the hydrolysis of terminal, non-reducing alpha-D-galactose residues in alpha-galactosides including galactose… (More)
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
Fabry disease, an inherited deficiency of the lysosomal enzyme alpha-galactosidase A, causes progressive intralysosomal… (More)
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Highly Cited
2004
Highly Cited
2004
Fabry disease is an X-linked lysosomal storage disease afflicting 1 in 40,000 males with chronic pain, vascular degeneration… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Fabry's disease, lysosomal alpha-galactosidase A deficiency, results from the progressive accumulation of… (More)
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Highly Cited
2001
Highly Cited
2001
CONTEXT Fabry disease is a metabolic disorder without a specific treatment, caused by a deficiency of the lysosomal enzyme alpha… (More)
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Highly Cited
2001
Highly Cited
2001
Preclinical studies of enzyme-replacement therapy for Fabry disease (deficient alpha-galactosidase A [alpha-Gal A] activity) were… (More)
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Highly Cited
2001
Highly Cited
2001
Fabry disease results from deficient alpha-galactosidase A (alpha-Gal A) activity and the pathologic accumulation of the… (More)
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Highly Cited
2000
Highly Cited
2000
Fabry disease is a lysosomal storage disorder caused by a deficiency of the lysosomal enzyme alpha-galactosidase A (alpha-gal A… (More)
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Highly Cited
1997
Highly Cited
1997
Fabry disease is an X-linked inherited metabolic disorder that is caused by a deficiency of alpha-galactosidase A (alpha-Gal A… (More)
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Highly Cited
1981
Highly Cited
1981
A simple and sensitive fluorometric method has been described for the differential determination of the activity of lysosomal… (More)
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Highly Cited
1970
Highly Cited
1970
The leukocytes of male patients with Fabry's disease are deficient in alpha-galactosidase. The alpha-galactosidase activity in… (More)
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