AGL gene

Known as: amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase, AMYLO-1,6-GLUCOSIDASE, 4-ALPHA-GLUCANOTRANSFERASE, glycogen storage disease type III 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1967-2018
010203019672018

Papers overview

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2013
2013
UNLABELLED Two determinants of infectivity have been identified in the hepatitis B virus (HBV) envelope proteins: a pre-S1… (More)
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2009
2009
The hepatitis B virus (HBV) particles bear a receptor-binding site located in the pre-S1 domain of the large HBV envelope protein… (More)
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2009
2009
BACKGROUND Fragmented QRS complexes (fQRS) on a 12-lead ECG are a marker of myocardial scar in patients with coronary artery… (More)
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2007
2007
Cori's disease is a glycogen storage disorder characterized by a deficiency in the glycogen debranching enzyme, amylo-1,6… (More)
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Highly Cited
2002
Highly Cited
2002
Lipodystrophies are characterized by selective but variable loss of body fat and metabolic complications of insulin resistance… (More)
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2002
2002
Consistency-based diagnosis is the most widely used approach to model-based diagnosis within the Artificial Intelligence… (More)
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2000
2000
Deficiency of glycogen debranching enzyme (AGL) activity causes glycogen storage disease type III (GSD-III). Generalized loss of… (More)
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1996
1996
Glycogen debranching enzyme (gene symbol, AGL) is a multifunctional enzyme acting as 1,4-alpha-D-glucan:1,4-alpha-D-glucan 4… (More)
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1996
1996
Glycogen storage disease type HI (GSD-III), an autosomal recessive disease, is caused by deficient glycogen debranching enzyme… (More)
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Highly Cited
1991
Highly Cited
1991
The predicted products of floral homeotic genes, AGAMOUS (AG) from Arabidopsis thaliana and DEFICIENS A (DEF A) from Antirrhinum… (More)
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