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Sucrase-isomaltase deficiency, congenital

Known as: Congenital Sucrose-Isomaltose Malabsorption, deficiency of isomaltase, CSID 
An autosomal recessive genetic disorder caused by mutations in the SI gene, encoding sucrase-isomaltase, intestinal. The condition is characterized… Expand
National Institutes of Health

Papers overview

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Highly Cited
2001
Highly Cited
2001
Attachment of the cationic sugar 4-amino-4-deoxy-l-arabinose (l-Ara4N) to lipid A is required for the maintenance of polymyxin… Expand
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Review
2000
Review
2000
The disaccharide trehalose is widely distributed in nature and can be found in many organisms, including bacteria, fungi, plants… Expand
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Highly Cited
1996
Highly Cited
1996
Chitin, the second most abundant polysaccharide on earth, is degraded by chitinases and chitobiases. The structure of Serratia… Expand
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Highly Cited
1993
Highly Cited
1993
The process of wound repair in monolayers of the intestinal epithelial cell line, Caco-2BBe, was analyzed by a combination of… Expand
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Highly Cited
1993
Highly Cited
1993
Human anti-pig antibodies were obtained by perfusing pig hearts (n = 4) and kidneys (n = 8) with human AB or O plasma followed by… Expand
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Highly Cited
1986
Highly Cited
1986
The complete primary structure (1827 amino acids) of rabbit intestinal pro-sucrase-isomaltase (pro-SI) was deduced from the… Expand
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Highly Cited
1985
Highly Cited
1985
A panel of monoclonal antibodies was produced against purified microvillus membranes of human small intestinal enterocytes. By… Expand
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Highly Cited
1982
Highly Cited
1982
A differentiated population of cells with metachromatically staining granules and surface IgE receptors was obtained from mouse… Expand
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Highly Cited
1975
Highly Cited
1975
Pulmonary H2 excretion was used to quantitate the small bowel transit time in man. This technique is based on the observation… Expand
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Highly Cited
1968
Highly Cited
1968
Abstract 1. An enzyme, "chondroitinase-ABC," has been purified to apparent homogeneity from extracts of Proteus vulgaris, NCTC… Expand
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