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

Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis.

European journal of human genetics : EJHG - 1 Jul 2011

Mądry Edyta, Fidler Ewa, Sobczyńska-Tomaszewska Agnieszka, Lisowska Aleksandra, Krzyżanowska Patrycja, Pogorzelski Andrzej, Minarowski Łukasz, Oralewska Beata, Mojs Ewa, Sapiejka Ewa, Marciniak Ryszard, Sands Dorota, Korzon-Burakowska Anna, Kwiecień Jarosław, Walkowiak Jarosław

Abstract excerpt

Taking into account the reported incidence of hypolactasia in cystic fibrosis (CF) and the possible impact of milk products on nutritional status we aimed to assess the genetic predisposition to adult-type hypolactasia (ATH) and its incidence in CF. Single nucleotide polymorphism upstream of the lactase gene (LCT) was assessed in 289 CF patients. In subject with -13910C/C genotype (C/C) predisposing to ATH,...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Cystic Fibrosis

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

Share to Adolescent

Share to Cystic Fibrosis Transmembrane Conductance Regulator

Share to Gene Frequency

Share to Lactase

Share to Lactose Intolerance

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 21407263
DOI: 10.1038/ejhg.2011.36
PMCID: PMC3137504

Genes

CFTR
LCT

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

Mild CFTR mutations and genetic predisposition to lactase persistence in cystic fibrosis.PMID 21407263Read ↗

Adult-type hypolactasia and lactose malabsorption in Poland.Semantic proximity Read ↗

Prevalence of adult-type hypolactasia as diagnosed with genetic and lactose hydrogen breath tests in Hungarians.Semantic proximity Read ↗

Genetic testing for adult-type hypolactasia in Italian families.Semantic proximity Read ↗

Molecular genetics of adult-type hypolactasia.Semantic proximity Read ↗

Lactose malabsorption is a risk factor for decreased bone mineral density in pancreatic insufficient cystic fibrosis patients.Semantic proximity Read ↗

Lactase non-persistent genotype distribution in Italy.Semantic proximity Read ↗

A genetic test which can be used to diagnose adult-type hypolactasia in children.Semantic proximity Read ↗

Genetic test for lactase non-persistence and hydrogen breath test: is genotype better than phenotype to diagnose lactose malabsorption?Semantic proximity Read ↗

Use of genetic testing for hypolactasia trait in the North Denmark Region.Semantic proximity Read ↗

The C/C(-13910) and G/G(-22018) genotypes for adult-type hypolactasia are not associated with inflammatory bowel disease.Semantic proximity Read ↗

Correlation between lactose absorption and the C/T-13910 and G/A-22018 mutations of the lactase-phlorizin hydrolase (LCT) gene in adult-type hypolactasia.Semantic proximity Read ↗

Molecularly defined adult-type hypolactasia in school-aged children with a previous history of cow's milk allergy.Semantic proximity Read ↗

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