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

The association of TMPRSS6 gene polymorphism with iron status in Egyptian children (a pilot study).

BMC pediatrics - 10 Feb 2024

Hamed Hanan M, Bostany Eman El, Motawie Ayat A, Abd Al-Aziz Amany M, Mourad Abbass A, Salama Hassan M, Kamel Solaf, Hassan Eman M, Helmy Neveen A, El-Saeed Gamila S, Elghoroury Eman A

Abstract excerpt

Several studies have shown association of single nucleotide polymorphisms (SNPs) of hepcidin regulatory pathways genes with impaired iron status. The most common is in the TMPRSS6 gene. In Africa, very few studies have been reported. We aimed to investigate the correlation between the common SNPs in the transmembrane protease, serine 6 (TMPRSS6) gene and iron indicators in a sample of Egyptian children for...

Read the complete abstract on PubMed

Topics

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

Share to Anemia, Iron-Deficiency
Share to Egypt

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ferritins

Share to Hepcidins

Share to Peptide Hydrolases

Share to Pilot Projects

Share to Serine

Share to Serine Endopeptidases

Source

Open in PubMed Open full text

Identifiers

PMID: 38341535
DOI: 10.1186/s12887-024-04573-w
PMCID: PMC10858485

Genes

TMPRSS6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The association of TMPRSS6 gene polymorphism with iron status in Egyptian children (a pilot study).PMID 38341535Read ↗

TMPRSS6 gene polymorphisms associated with iron deficiency anaemia among global populationSemantic proximity Read ↗

Genetic analysis of TMPRSS6 gene in Saudi female patients with iron deficiency anemia.Semantic proximity Read ↗

TMPRSS6 Gene Polymorphism and Serum Hepcidin in Iron Deficiency AnemiaSemantic proximity Read ↗

Association of SNPs within TMPRSS6 and BMP2 genes with iron deficiency status in Saudi Arabia.Semantic proximity Read ↗

The role of TMPRSS6 gene polymorphism in iron resistance iron deficiency anaemia (IRIDA): a systematic review.Semantic proximity Read ↗

TMPRSS6 gene mutations in six Saudi families with iron refractory iron deficiency anemia.Semantic proximity Read ↗

The role of TMPRSS6 gene variants in iron-related hematological parameters in Turkish patients with iron deficiency anemia.Semantic proximity Read ↗

Association of the Transmembrane Protease Serine 6 rs855791 Variant and Nongenetic Factors With Iron Deficiency Among Female Medical Students in Yogyakarta: Protocol for a Case-Control Study.Semantic proximity Read ↗

The impact of single nucleotide polymorphisms in human genes that regulate hepcidin and iron on oral iron absorption and the risk of anaemia in AfricansSemantic proximity Read ↗

TMPRSS6, but not TF, TFR2 or BMP2 variants are associated with increased risk of iron-deficiency anemia.Semantic proximity Read ↗

TMPRSS6 as a Therapeutic Target for Disorders of Erythropoiesis and Iron HomeostasisSemantic proximity Read ↗

Association of common TMPRSS6 and TF gene variants with hepcidin and iron status in healthy rural Gambians.Semantic proximity Read ↗

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