Sucrase-Isomaltase Complex
"Sucrase-Isomaltase Complex" 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.
An enzyme complex found in the brush border membranes of the small intestine. It is believed to be an enzyme complex with different catalytic sites. Its absence is manifested by an inherited disease called sucrase-isomaltase deficiency.
| Descriptor ID |
D013394
|
| MeSH Number(s) |
D05.500.562.875 D08.811.277.450.329.738.700 D08.811.277.450.770.800 D08.811.600.850
|
| Concept/Terms |
Sucrase-Isomaltase Complex- Sucrase-Isomaltase Complex
- Complex, Sucrase-Isomaltase
- Sucrase Isomaltase Complex
- Complex, Sucrase Isomaltase
- Isomaltase Complex, Sucrase
|
Below are MeSH descriptors whose meaning is more general than "Sucrase-Isomaltase Complex".
Below are MeSH descriptors whose meaning is more specific than "Sucrase-Isomaltase Complex".
This graph shows the total number of publications written about "Sucrase-Isomaltase Complex" by people in this website by year, and whether "Sucrase-Isomaltase Complex" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2012 | 4 | 0 | 4 |
| 2013 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Sucrase-Isomaltase Complex" by people in Profiles.
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Hypomorphic SI genetic variants are associated with childhood chronic loose stools. PLoS One. 2020; 15(5):e0231891.
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Loss of MYO5B Leads to Reductions in Na+ Absorption With Maintenance of CFTR-Dependent Cl- Secretion in Enterocytes. Gastroenterology. 2018 12; 155(6):1883-1897.e10.
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13C-Labeled-Starch Breath Test in Congenital Sucrase-isomaltase Deficiency. J Pediatr Gastroenterol Nutr. 2018 Jun; 66 Suppl 3:S61-S64.
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Improved Starch Digestion of Sucrase-deficient Shrews Treated With Oral Glucoamylase Enzyme Supplements. J Pediatr Gastroenterol Nutr. 2017 08; 65(2):e35-e42.
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Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome. Gut. 2018 02; 67(2):263-270.
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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.
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Maltase-glucoamylase modulates gluconeogenesis and sucrase-isomaltase dominates starch digestion glucogenesis. J Pediatr Gastroenterol Nutr. 2013 Dec; 57(6):704-12.
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Starch digestion and patients with congenital sucrase-isomaltase deficiency. J Pediatr Gastroenterol Nutr. 2012 Nov; 55 Suppl 2:S24-8.
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Inhibition of maltase-glucoamylase activity to hydrolyze a-1,4 linkages by the presence of undigested sucrose. J Pediatr Gastroenterol Nutr. 2012 Nov; 55 Suppl 2:S45-7.
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Congenital sucrase-isomaltase deficiency: summary of an evaluation in one family. J Pediatr Gastroenterol Nutr. 2012 Nov; 55 Suppl 2:S36.