Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Genetics of sucrose metabolism disorders in different population groups].

Voprosy pitaniia - 1 Jan 2024

Kozlov A I, Malyarchuk B A

Abstract excerpt

The study of the genetic determinants of the disaccharidase activity opens up new prospects for improving diagnostics and choosing medical tactics in gastroenterology. The aim of the study was to systematize the data on the role of the sucrase-isomaltase gene (SI) in regulating sucrose metabolism and the contribution of SI mutations to the prevalence of sucrose malabsorption disorders (sucrase-isomaltase...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Carbohydrate Metabolism, Inborn Errors
Share to Malabsorption Syndromes
Share to Mutation

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Sucrose

Source

Identifiers

PMID: 38809799
DOI: 10.33029/0042-8833-2024-93-2-52-62

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Genetics of sucrose metabolism disorders in different population groups].PMID 38809799Read ↗

Genetic and acquired sucrase‐isomaltase deficiency: A clinical reviewSemantic proximity Read ↗

Congenital sucrase-isomaltase deficiency in Türkiye; a single center experience.Semantic proximity Read ↗

Genetic Loss of Sucrase-Isomaltase Function: Mechanisms, Implications, and Future PerspectivesSemantic proximity Read ↗

Rare Hypomorphic Sucrase Isomaltase Variants in Relation to Irritable Bowel Syndrome Risk in UK BiobankSemantic proximity Read ↗

Increased Prevalence of Rare Sucrase-isomaltase Pathogenic Variants in Irritable Bowel Syndrome Patients.Semantic proximity Read ↗

Exploring genetic variants in congenital monosaccharide-disaccharide metabolism: Carrier ratios and phenotypic insights.Semantic proximity Read ↗

Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption.Semantic proximity Read ↗

Dietary effect on glucose homeostasis is modulated by a loss-of-function variant in the sucrase-isomaltase gene: a randomised, dietary crossover intervention in Inuit.Semantic proximity Read ↗

Genetic sucrase-isomaltase deficiency: epidemiology, clinical spectrum, and diagnostic challenge.Semantic proximity Read ↗

A mutation map for human glycoside hydrolase genes.Semantic proximity Read ↗

Heterozygotes Are a Potential New Entity among Homozygotes and Compound Heterozygotes in Congenital Sucrase-Isomaltase DeficiencySemantic proximity Read ↗

Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.