"alpha-Glucosidases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Enzymes that catalyze the exohydrolysis of 1,4-alpha-glucosidic linkages with release of alpha-glucose. Deficiency of alpha-1,4-glucosidase may cause GLYCOGEN STORAGE DISEASE TYPE II.
| Descriptor ID |
D000520
|
| MeSH Number(s) |
D08.811.277.450.420.050
|
| Concept/Terms |
alpha-Glucosidases- alpha-Glucosidases
- alpha Glucosidases
- Maltases
- alpha-Glucosidase
- alpha Glucosidase
- Maltase-Glucoamylase
- Maltase Glucoamylase
|
Below are MeSH descriptors whose meaning is more general than "alpha-Glucosidases".
Below are MeSH descriptors whose meaning is more specific than "alpha-Glucosidases".
This graph shows the total number of publications written about "alpha-Glucosidases" by people in this website by year, and whether "alpha-Glucosidases" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 0 | 2 | 2 |
| 2002 | 1 | 0 | 1 |
| 2003 | 0 | 1 | 1 |
| 2007 | 2 | 0 | 2 |
| 2009 | 1 | 1 | 2 |
| 2013 | 1 | 2 | 3 |
| 2016 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 0 | 2 | 2 |
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Below are the most recent publications written about "alpha-Glucosidases" by people in Profiles.
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Transforming the clinical outcome in CRIM-negative infantile Pompe disease identified via newborn screening: the benefits of early treatment with enzyme replacement therapy and immune tolerance induction. Genet Med. 2021 05; 23(5):845-855.
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Glycogen accumulation in smooth muscle of a Pompe disease mouse model. J Smooth Muscle Res. 2021; 57(0):8-18.
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Conditioning with slowly digestible starch diets in mice reduces jejunal a-glucosidase activity and glucogenesis from a digestible starch feeding. Nutrition. 2020 10; 78:110857.
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The relevance of ANXA5 genetic variants on male fertility. J Assist Reprod Genet. 2019 Jul; 36(7):1355-1359.
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Complementary Starch Feeding of the Young Child: Starch Digestion Consortium Workshop 18. J Pediatr Gastroenterol Nutr. 2018 06; 66 Suppl 3:S1-S3.
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Starch Malabsorption in Infants. J Pediatr Gastroenterol Nutr. 2018 06; 66 Suppl 3:S65-S67.
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Metabolic Impacts of Maltase Deficiencies. J Pediatr Gastroenterol Nutr. 2018 06; 66 Suppl 3:S24-S29.
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Next generation deep sequencing corrects diagnostic pitfalls of traditional molecular approach in a patient with prenatal onset of Pompe disease. Am J Med Genet A. 2017 Sep; 173(9):2500-2504.
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Phenolic compounds increase the transcription of mouse intestinal maltase-glucoamylase and sucrase-isomaltase. Food Funct. 2017 May 24; 8(5):1915-1924.
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Contribution of the Individual Small Intestinal a-Glucosidases to Digestion of Unusual a-Linked Glycemic Disaccharides. J Agric Food Chem. 2016 Aug 24; 64(33):6487-94.