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Disease on EC 3.2.1.48 - sucrose alpha-glucosidase

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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Adenocarcinoma
Abundant expression of the intestinal protein villin in Barrett's metaplasia and esophageal adenocarcinomas.
Biomarkers in Barrett's esophagus (review).
Detection of Barrett's adenocarcinoma of the gastric cardia with sucrase isomaltase and p53.
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Gene expression profiling of Caco-2 BBe cells suggests a role for specific signaling pathways during intestinal differentiation.
Sucrase-isomaltase and other brush border glycosidases in colorectal tumors.
Sucrase-isomaltase expression and enterocytic ultrastructure of human colorectal tumors.
Sucrase-isomaltase gene expression in Barrett's esophagus and adenocarcinoma.
Sucrase-isomaltase: a marker associated with the progression of adenomatous polyps to adenocarcinomas.
Adenoma
Brush border hydrolases in normal and neoplastic colonic epithelium.
Sucrase-isomaltase and other brush border glycosidases in colorectal tumors.
Adenomatous Polyps
Sucrase-isomaltase: a marker associated with the progression of adenomatous polyps to adenocarcinomas.
Alkaptonuria
Alcaptonuria and sucrase-isomaltase deficiency in three offspring of a consanguineous marriage.
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2.
alpha,alpha-trehalase deficiency
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
Barrett Esophagus
Sucrase-isomaltase gene expression in Barrett's esophagus and adenocarcinoma.
beta-fructofuranosidase deficiency
Molecular cloning of sucrase-isomaltase cDNA in the house musk shrew Suncus murinus and identification of a mutation responsible for isolated sucrase deficiency.
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
Carcinoma
A and H blood group antigens as markers of sucrase-isomaltase from the enterocyte-like differentiated human colon carcinoma cell lines HT-29 and Caco-2.
A limited upstream region of the human sucrase-isomaltase gene confers glucose-regulated expression on a heterologous gene.
Clonal analysis of sucrase-isomaltase expression in the human colon adenocarcinoma Caco-2 cells.
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Intracellular localization and endocytosis of brush border enzymes in the enterocyte-like cell line Caco-2.
Sucrase-isomaltase: a marker associated with the progression of adenomatous polyps to adenocarcinomas.
Sucrase-isomaltase: a marker of foetal and malignant epithelial cells of the human colon.
The biosynthesis of intestinal sucrase-isomaltase in human embryo is most likely controlled at the level of transcription.
Villin, intestinal brush border hydrolases and keratin polypeptides in intestinal metaplasia and gastric cancer; an immunohistologic study emphasizing the different degrees of intestinal and gastric differentiation in signet ring cell carcinomas.
[Do immunologic markers facilitate differentiation between histologic types of stomach cancer?]
Celiac Disease
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Colic
Sacrosidase therapy for congenital sucrase-isomaltase deficiency.
Colitis, Ulcerative
Prospective evaluation of early morphological changes in pelvic ileal pouches.
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
Sucrase-isomaltase expression in chronic ulcerative colitis and dysplasia.
Colonic Neoplasms
A and H blood group antigens as markers of sucrase-isomaltase from the enterocyte-like differentiated human colon carcinoma cell lines HT-29 and Caco-2.
A potential anti-tumor effect of leukotriene C4 through the induction of 15-hydroxyprostaglandin dehydrogenase expression in colon cancer cells.
Clonal analysis of sucrase-isomaltase expression in the human colon adenocarcinoma Caco-2 cells.
Differentiation-dependent induction of CYP1A1 in cultured rat small intestinal epithelial cells, colonocytes, and human colon carcinoma cells: basement membrane-mediated apoptosis.
Dissection of the asynchronous transport of intestinal microvillar hydrolases to the cell surface.
Endocytosis, recycling, and lysosomal delivery of brush border hydrolases in cultured human intestinal epithelial cells (Caco-2).
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Immunohistological evidence, obtained with monoclonal antibodies, of small intestinal brush border hydrolases in human colon cancers and foetal colons.
Inhibition of laminin alpha 1-chain expression leads to alteration of basement membrane assembly and cell differentiation.
Intrinsically disordered human C/EBP homologous protein regulates biological activity of colon cancer cells during calcium stress.
Lactase and sucrase-isomaltase gene expression during Caco-2 cell differentiation.
Sequence of the complete cDNA and the 5' structure of the human sucrase-isomaltase gene. Possible homology with a yeast glucoamylase.
Sucrase-isomaltase in colon cancers: an example of re-expression of a foetal enzyme with associated blood group antigens.
The processing of asparagine-linked oligosaccharides in HT-29 cells is a function of their state of enterocytic differentiation. An accumulation of Man9,8-GlcNAc2-Asn species is indicative of an impaired N-glycan trimming in undifferentiated cells.
Colorectal Neoplasms
Association between sucrase-isomaltase and p53 expression in colorectal cancer.
Intestinal brush-border-associated enzymes: co-ordinated expression in colorectal cancer.
Sucrase-isomaltase and other brush border glycosidases in colorectal tumors.
Sucrase-isomaltase expression and enterocytic ultrastructure of human colorectal tumors.
Sucrase-isomaltase is an independent prognostic marker for colorectal carcinoma.
Congenital Abnormalities
The multiple roles of sucrase-isomaltase in the intestinal physiology.
Cystic Fibrosis
Anomalous apical plasma membrane phenotype in CK8-deficient mice indicates a novel role for intermediate filaments in the polarization of simple epithelia.
Microvillus inclusion disease: a genetic defect affecting apical membrane protein traffic in intestinal epithelium.
Selected disorders of malabsorption.
Sucrase-isomaltase and cystic fibrosis.
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Transimmortalized mouse intestinal cells (m-ICc12) that maintain a crypt phenotype.
Cytomegalovirus Infections
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Diabetes Complications
MiR-26a and miR-26b downregulate the expression of sucrase-isomaltase enzyme: A new chapter in diabetes treatment.
Diabetes Mellitus
Bioactive compounds in plant materials for the prevention of diabetesand obesity.
Disordered expression of the sucrase-isomaltase complex in the small intestine in Otsuka Long-Evans tokushima fatty rats, a model of non-insulin-dependent diabetes mellitus with insulin resistance.
Morphological changes and increased sucrase and isomaltase activity in small intestines of insulin-deficient and type 2 diabetic rats.
Diabetes Mellitus, Experimental
The intestinal brush border membrane in diabetes. Studies of sucrase-isomaltase metabolism in rats with streptozotocin diabetes.
Diabetes Mellitus, Type 1
Suppressive effect of insulin on the synthesis of sucrase-isomaltase complex in small intestinal epithelial cells, and abnormal increase in the complex under diabetic conditions.
Diabetes Mellitus, Type 2
Bioactive compounds in plant materials for the prevention of diabetesand obesity.
Disordered expression of the sucrase-isomaltase complex in the small intestine in Otsuka Long-Evans tokushima fatty rats, a model of non-insulin-dependent diabetes mellitus with insulin resistance.
Enteritis
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Enterocolitis
Uncommon causes of postoperative chronic diarrhoea mimicking enterocolitis in Hirschsprung's disease: is there a role for digestive endoscopy?
Ganglioneuroma
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
Gastroenteritis
Complex carbohydrate intolerance: diagnostic pitfalls and approach to management.
Gastrointestinal Diseases
Immunoelectrophoretic studies on human small intestinal brush border proteins. A quantitative study of brush border enzymes from single small intestinal biopsies.
Sucrase-Isomaltase Gene Variants in Patients with Abnormal Sucrase Activity and Functional GI Disorders.
The Role of Disaccharidase Deficiencies in Functional Abdominal Pain Disorders-A Narrative Review.
Genetic Diseases, Inborn
Congenital sucrase-isomaltase deficiency: an under-diagnosed disease in Chinese children.
Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.
The patient journey to diagnosis and treatment of congenital sucrase-isomaltase deficiency.
Giardiasis
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Glucose Intolerance
Dietary fructose in the management of intractable diarrhea of infancy.
Hirschsprung Disease
Persistent diarrhea due to sucrase-isomaltase deficiency in a postoperative child with Hirschsprung's disease.
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
Hypercalcemia
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Hyperglycemia
Biological interaction of newly synthesized astaxanthin-s-allyl cysteine biconjugate with Saccharomyces cerevisiae and mammalian ?-glucosidase: In vitro kinetics and in silico docking analysis.
Hyperglycemia induces intestinal sucrase activity in subtotally pancreatectomized rats.
In Vitro and in Vivo Anti-Hyperglycemic Activities of Taxifolin and Its Derivatives Isolated from Pigmented Rice (Oryzae sativa L. cv. Superhongmi).
Morphological changes and increased sucrase and isomaltase activity in small intestines of insulin-deficient and type 2 diabetic rats.
Hyperparathyroidism
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2.
Infections
Alterations in enzymatic activities of the intestinal mucosa during the course of Giardia lamblia infection in mice.
Impairments in enzyme activity and biosynthesis of brush border-associated hydrolases in human intestinal Caco-2/TC7 cells infected by members of the Afa/Dr family of diffusely adhering Escherichia coli.
Small intestinal sucrase activity during experimental infections with Nippostrongylus brasiliensis and/or Eimeria nieschulzi in rats.
Staphylococcus aureus Infection Influences the Function of Intestinal Cells by Altering the Lipid Raft-Dependent Sorting of Sucrase-Isomaltase.
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
Inflammatory Bowel Diseases
Sucrase-isomaltase: a marker associated with the progression of adenomatous polyps to adenocarcinomas.
Uncommon causes of postoperative chronic diarrhoea mimicking enterocolitis in Hirschsprung's disease: is there a role for digestive endoscopy?
Insulin Resistance
Disordered expression of the sucrase-isomaltase complex in the small intestine in Otsuka Long-Evans tokushima fatty rats, a model of non-insulin-dependent diabetes mellitus with insulin resistance.
Intestinal Pseudo-Obstruction
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
Iron Overload
Immunological analysis of beta-thalassemic mouse intestinal proteins reveals up-regulation of sucrase-isomaltase in response to iron overload.
Irritable Bowel Syndrome
Differential Effects of Sucrase-Isomaltase Mutants on Its Trafficking and Function in Irritable Bowel Syndrome: Similarities to Congenital Sucrase-Isomaltase Deficiency.
Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome.
Increased Prevalence of Rare Sucrase-isomaltase (SI) Pathogenic Variants in Irritable Bowel Syndrome Patients.
Rare Hypomorphic Sucrase Isomaltase Variants in Relation to Irritable Bowel Syndrome Risk in UK Biobank.
Sucrase-Isomaltase Deficiency as a Potential Masquerader in Irritable Bowel Syndrome.
Kidney Calculi
Intestinal sucrase-isomaltase deficiency and renal calculi.
lactase deficiency
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Is the assay of disaccharidase activity in small bowel mucosal biopsy relevant for clinical gastroenterologists?
Selected disorders of malabsorption.
The scanning electron microscope: how valuable in the evaluation of small bowel mucosal pathology in chronic childhood diarrhea?
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
[Intestinal disaccharidase and alkaline phosphatase activities of jejunal biopsies in small bowel diseases of children (author's transl)]
[Useful and superfluous measures in the treatment of infant diarrhea]
Lactose Intolerance
Congenital sucrase and isomaltase deficiency with temporary lactose intolerance.
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Evaluation of differential disaccharide excretion in urine for non-invasive investigation of altered intestinal disaccharidase activity caused by alpha-glucosidase inhibition, primary hypolactasia, and coeliac disease.
Selected disorders of malabsorption.
Value of breath hydrogen analysis in management of diarrheal illness in childhood: comparison with duodenal biopsy.
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
Leukemia
Human chromosome 3 and pig chromosome 13 show complete synteny conservation but extensive gene-order differences.
Mapping HSA 3 loci in cattle: additional support for the ancestral synteny of HSA 3 and 21.
Leukemia, Lymphocytic, Chronic, B-Cell
Functional analysis of sucrase-isomaltase mutations from chronic lymphocytic leukemia patients.
Malabsorption Syndromes
A comparative study of lactase and sucrase-isomaltase activities and immunoreactivities in jejunal biopsies of patients suffering from the malabsorption syndrome.
Malnutrition
Effect of pre- & post-weaning protein energy malnutrition on intestinal sucrase & maltase in rats.
Regulation of lactase and sucrase-isomaltase gene expression in the duodenum during childhood.
Muscle Cramp
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency.
Neoplasm Metastasis
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Neoplasms
A and H blood group antigens as markers of sucrase-isomaltase from the enterocyte-like differentiated human colon carcinoma cell lines HT-29 and Caco-2.
Bioactive compounds in plant materials for the prevention of diabetesand obesity.
Brush border hydrolases in normal and neoplastic colonic epithelium.
Control of gene expression in intestinal epithelial cells.
Detection and characterization of sucrase-isomaltase in adult human colon and in colonic polyps.
Enterocytic columnar non-goblet cells of Barrett's esophagus--an immunohistochemical demonstration of association with malignant evolution.
Expression of enzymatically active sucrase-isomaltase is a ubiquitous property of colon adenocarcinomas.
Intestinal brush-border-associated enzymes: co-ordinated expression in colorectal cancer.
Posttranslational regulation of sucrase-isomaltase expression in intestinal crypt and villus cells.
Sucrase-isomaltase expression and enterocytic ultrastructure of human colorectal tumors.
Sucrase-isomaltase: a marker of foetal and malignant epithelial cells of the human colon.
Use of a monoclonal antibody to sucrase-isomaltase for evaluation of the columnar cuff after stapled restorative proctocolectomy.
[Do immunologic markers facilitate differentiation between histologic types of stomach cancer?]
Nephrocalcinosis
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
oligo-1,6-glucosidase deficiency
Adult onset sucrase-isomaltase deficiency with secondary disaccharidase deficiency resulting from severe dietary carbohydrate restriction.
Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency.
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
[Intestinal disaccharidase and alkaline phosphatase activities of jejunal biopsies in small bowel diseases of children (author's transl)]
Pneumonia, Staphylococcal
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
Pouchitis
Mucosal characteristics of pelvic ileal pouches.
Protein-Energy Malnutrition
Effect of pre- & post-weaning protein energy malnutrition on intestinal sucrase & maltase in rats.
Rotavirus Infections
Rotavirus infection reduces sucrase-isomaltase expression in human intestinal epithelial cells by perturbing protein targeting and organization of microvillar cytoskeleton.
Shwachman-Diamond Syndrome
Selected disorders of malabsorption.
Staphylococcal Infections
Staphylococcus aureus Infection Influences the Function of Intestinal Cells by Altering the Lipid Raft-Dependent Sorting of Sucrase-Isomaltase.
Starvation
Effect of fasting on the structure and function of the gastrointestinal tract of house sparrows (Passer domesticus).
Precocious and reversible expression of sucrase-isomaltase unrelated to intestinal cell turnover.
sucrose alpha-glucosidase deficiency
13C-breath tests for sucrose digestion in congenital sucrase isomaltase-deficient and sacrosidase-supplemented patients.
13C-Labeled-Starch Breath Test in Congenital Sucrase-isomaltase Deficiency.
50 years of progress since congenital sucrase-isomaltase deficiency recognition.
A glutamine to proline exchange at amino acid residue 1098 in sucrase causes a temperature-sensitive arrest of sucrase-isomaltase in the endoplasmic reticulum and cis-Golgi.
A mutation in a highly conserved region in brush-border sucrase-isomaltase and lysosomal alpha-glucosidase results in Golgi retention.
A Mutation Map for Human Glycoside Hydrolase Genes.
A phenylalanine-based folding determinant in intestinal sucrase-isomaltase that functions in the context of a quality control mechanism beyond the endoplasmic reticulum.
A study of the molecular pathology of sucrase-isomaltase deficiency. A defect in the intracellular processing of the enzyme.
Adult onset sucrase-isomaltase deficiency with secondary disaccharidase deficiency resulting from severe dietary carbohydrate restriction.
Alcaptonuria and sucrase-isomaltase deficiency in three offspring of a consanguineous marriage.
Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency.
Breath hydrogen test and sucrase isomaltase deficiency.
Catalytically inactive sucrase antigen of rabbit small intestine: the enzyme precursor.
Clinical and Histopathologic Predictors of Disaccharidase Deficiency in Duodenal Biopsy Specimens.
Clinical aspects and treatment of congenital sucrase-isomaltase deficiency.
Clinical Characteristics of Disaccharidase Deficiencies Among Children Undergoing Upper Endoscopy.
Clinical heterogeneity in congenital sucrase-isomaltase deficiency.
Combined assessment of intestinal disaccharidases in congenital asucrasia by differential urinary disaccharide excretion.
Complex carbohydrate intolerance: diagnostic pitfalls and approach to management.
Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency.
Congenital and Putatively Acquired Forms of Sucrase-isomaltase Deficiency in Infancy: Effects of Sacrosidase Therapy.
Congenital Lactase Deficiency: Mutations, Functional and Biochemical Implications, and Future Perspectives.
Congenital sucrase and isomaltase deficiency with temporary lactose intolerance.
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.
Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum.
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
Congenital sucrase-isomaltase deficiency.
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
Congenital sucrase-isomaltase deficiency. Observations over a period of 6 years.
Congenital Sucrase-isomaltase Deficiency: A Novel Compound Heterozygous Mutation Causing Aberrant Protein Localization.
Congenital sucrase-isomaltase deficiency: an under-diagnosed disease in Chinese children.
Congenital sucrase-isomaltase deficiency: diagnostic challenges and response to enzyme replacement therapy.
Congenital sucrase-isomaltase deficiency: diet assessment and education guidelines.
Congenital sucrase-isomaltase deficiency: heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex.
Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.
Congenital sucrase-isomaltase deficiency: summary of an evaluation in one family.
Deletion of enzyme protein from the brush border membrane in sucrase-isomaltase deficiency.
Demonstration of an inactive enzyme antigen in sucrase-isomaltase deficiency.
Detection of primary and secondary sucrose malabsorption in children by means of the breath hydrogen technique.
Diagnostic value of sucrose tolerance test in children evaluated by breath hydrogen measurement.
Diarrhoea due to sucrase and isomaltase deficiency.
Diet and intestinal enzyme adaptation: implications for gastrointestinal disorders.
Dietary fructose in the management of intractable diarrhea of infancy.
Dietary stimulation of sucrase in a patient with sucrase-isomaltase deficiency.
Differential Effects of Sucrase-Isomaltase Mutants on Its Trafficking and Function in Irritable Bowel Syndrome: Similarities to Congenital Sucrase-Isomaltase Deficiency.
Disaccharide digestion and maldigestion.
Editorial: Sucrase-isomaltase deficiency.
Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency.
Ethnic differences in intestinal disaccharidase values in children in Finland.
Evaluation of liquid yeast-derived sucrase enzyme replacement in patients with sucrase-isomaltase deficiency.
Failure of the hydrogen breath test to detect pulmonary sugar malabsorption.
Food Intolerances.
Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome.
Glucose polymer as a cause of protracted diarrhea in infants with unsuspected congenital sucrase-isomaltase deficiency.
Heterozygotes Are a Potential New Entity among Homozygotes and Compound Heterozygotes in Congenital Sucrase-Isomaltase Deficiency.
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2.
Hypomorphic SI genetic variants are associated with childhood chronic loose stools.
Improved Starch Digestion of Sucrase Deficient Shrews Treated with Oral Glucoamylase Enzyme Supplements.
Index of suspicion. Case 3. Congenital sucrase-isomaltase deficiency.
Interaction of antipsychotic drugs with sucrase; kinetics and structural study.
Interaction of methocarbamol and yeast sucrase induces enzyme inhibition.
Intestinal disaccharidase activities in relation to age, race, and mucosal damage.
Intestinal disaccharidases in Greenland Eskimos.
Intestinal sucrase and isomaltase deficiency in two siblings.
Intestinal sucrase deficiency presenting as sucrose intolerance in adult life.
Intestinal sucrase deficiency.
Intestinal sucrase-isomaltase deficiency and renal calculi.
Letter: Gene frequency of sucrase-isomaltase deficiency.
Letter: Sucrase-isomaltase deficiency.
Maltase-glucoamylase and residual isomaltase in sucrose intolerant patients.
Molecular aspects of disaccharidase deficiencies.
Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder.
Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.
Mosaic pattern of sucrase isomaltase deficiency in two brothers.
Naturally occurring mutations in intestinal sucrase-isomaltase provide evidence for the existence of an intracellular sorting signal in the isomaltase subunit.
Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption.
Nutrient absorption.
Onset of sucrase-isomaltase deficiency in late adulthood.
Persistent diarrhea due to sucrase-isomaltase deficiency in a postoperative child with Hirschsprung's disease.
Primary combined saccharase and isomaltase deficiency. Report of two adult siblings of consanguineous parentage.
Primary sucrase-isomaltase deficiency: importance of clinical judgment.
Protein traffic in intestinal epithelial cells.
Protracted diarrhoea in infancy. Analysis of 82 cases with particular reference to diagnosis and management.
Ranitidine induces inhibition and structural changes in sucrase.
Relationships among Dietary Intakes and Persistent Gastrointestinal Symptoms in Patients Receiving Enzyme Treatment for Genetic Sucrase-Isomaltase Deficiency.
Research progress reported at the 50th Anniversary of the Discovery of Congenital Sucrase-Isomaltase Deficiency Workshop.
Sacrosidase therapy for congenital sucrase-isomaltase deficiency.
Selected disorders of malabsorption.
Starch digestion and patients with congenital sucrase-isomaltase deficiency.
Subcellular fractionation studies of the intestinal mucosa in congenital sucrase--isomaltase deficiency.
Sucrase-Isomaltase Deficiency as a Potential Masquerader in Irritable Bowel Syndrome.
Sucrase-Isomaltase Deficiency Causing Persistent Bloating and Diarrhea in an Adult Female.
Sucrase-isomaltase deficiency in 2 siblings.
Sucrase-isomaltase deficiency in humans. Different mutations disrupt intracellular transport, processing, and function of an intestinal brush border enzyme.
Sucrase-isomaltase deficiency. A follow-up report.
Sucrase-isomaltase deficiency. Absence of an inactive enzyme variant.
Sucrase-isomaltase deficiency: changing pattern over two decades.
Sucrase-isomaltase deficiency: difficulties in diagnosis.
Sucrase-Isomaltase Gene Variants in Patients with Abnormal Sucrase Activity and Functional GI Disorders.
Sucrose malabsorption in children: noninvasive diagnosis by interval breath hydrogen determination.
The brush border membrane in hereditary sucrase-isomaltase deficiency: abnormal protein pattern and presence of immunoreactive enzyme.
The clinical consequences of sucrase-isomaltase deficiency.
The glucose-regulated protein GRP94 interacts avidly in the endoplasmic reticulum with sucrase-isomaltase isoforms that are associated with congenital sucrase-isomaltase deficiency.
The History of Maltose-active Disaccharidases.
The multiple roles of sucrase-isomaltase in the intestinal physiology.
The patient journey to diagnosis and treatment of congenital sucrase-isomaltase deficiency.
The Role of Disaccharidase Deficiencies in Functional Abdominal Pain Disorders-A Narrative Review.
Transport to cell surface of intestinal sucrase-isomaltase is blocked in the Golgi apparatus in a patient with congenital sucrase-isomaltase deficiency.
Uncommon causes of postoperative chronic diarrhoea mimicking enterocolitis in Hirschsprung's disease: is there a role for digestive endoscopy?
Value of breath hydrogen analysis in management of diarrheal illness in childhood: comparison with duodenal biopsy.
[Congenital primary saccharase and isomaltase deficiency of the small intestine]
[Congenital saccharase-isomaltase defect--diagnostic difficulties]
[Congenital sucrase-isomaltase deficiency: a rare cause of chronic or recurrent diarrhea in children]
[Intestinal disaccharidase and alkaline phosphatase activities of jejunal biopsies in small bowel diseases of children (author's transl)]
[Peripheral gangrene in a congenital sucrase isomaltase deficiency (author's transl)]
[Primary saccharose-isomaltose deficit: a 20-year case load]
[Sucrase-isomaltase deficiency as a cause of chronic diarrhoea in adults (author's transl)]
[Sucrase-isomaltase deficiency. Value of the hydrogen respiratory test]
[Useful and superfluous measures in the treatment of infant diarrhea]
Vesicular Stomatitis
A novel type of detergent-resistant membranes may contribute to an early protein sorting event in epithelial cells.