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

[Fasting hyperglycaemia and polymorphism in glucokinase promoter (rs1799884)].

Anales de pediatria (Barcelona, Spain : 2003) - 1 Oct 2011

Bahíllo Curieses P, Hermoso López F, Garrote Molpeceres R, Zurita Muñoz O, Campos Barros A

Abstract excerpt

Glucokinase is one of the most important regulators of fasting glucose levels. There are several mutations in the glucokinase gene (GCK) which are linked with monogenic diabetes. Recently, a polymorphism in its promoter has been described, which is associated with impaired fasting glucose levels....

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Fasting
Share to GCK gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucokinase

Share to Hyperglycemia

Share to Mutation

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 21697023
DOI: 10.1016/j.anpedi.2011.05.009

Genes

GCK

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21697023-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Fasting hyperglycaemia and polymorphism in glucokinase promoter (rs1799884)].PMID 21697023Read ↗

[Diabetes mellitus caused by a mutation of glucokinase gene. Report of an affected family].Semantic proximity Read ↗

[Glucokinase gene mutation as a causative factor of permanent neonatal diabetes mellitus].Semantic proximity Read ↗

Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia.Semantic proximity Read ↗

Impact of Type 2 diabetes on Glucokinase diabetes (GCK-MODY) phenotype in a Roma (Gypsy) family - case report.Semantic proximity Read ↗

[Glucokinase gene abnormalities in maturity-onset diabetes of the young (MODY) and late-onset NIDDM].Semantic proximity Read ↗

Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy.Semantic proximity Read ↗

[A three-year follow-up observation of a pedigree of maturity onset diabetes of the young caused by a novel mutation of glucokinase and literature review].Semantic proximity Read ↗

[A rare cause of diabetes mellitus].Semantic proximity Read ↗

Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families.Semantic proximity Read ↗

[Monogenic forms of diabetes mellitus].Semantic proximity Read ↗

[Diabetes caused by glucokinase mutation].Semantic proximity Read ↗

Opposite clinical phenotypes of glucokinase disease: Description of a novel activating mutation and contiguous inactivating mutations in human glucokinase (GCK) gene.Semantic proximity Read ↗

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