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

Functional analysis of mutant SLCO2A1 transporters found in patients with chronic enteropathy associated with SLCO2A1.

Journal of gastroenterology and hepatology - 1 Sept 2022

Seki Satowa, Tanaka Gen, Kimura Toru, Hayashida Mari, Miyoshi Jun, Matsuura Minoru, Sakurai Hiroyuki, Hisamatsu Tadakazu

Abstract excerpt

BACKGROUND AND AIM: Chronic enteropathy associated with the solute carrier organic anion transporter family member 2A1 (SLCO2A1), or CEAS, causes anemia and hypoalbuminemia in young people. Dysfunction of the SLCO2A1 transporter protein is thought to involve genetic mutation, but mutant proteins have not been functionally characterized. We examined the prostaglandin E2 (PGE2 ) transport ability of recombinant...

Read the complete abstract on PubMed

Topics

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

Share to Dinoprostone
Share to Inflammatory Bowel Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Organic Anion Transporters

Source

Identifiers

PMID: 35877192
DOI: 10.1111/jgh.15968

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Functional analysis of mutant SLCO2A1 transporters found in patients with chronic enteropathy associated with SLCO2A1.PMID 35877192Read ↗

A novel mutation in the SLCO2A1 gene, encoding a prostaglandin transporter, induces chronic enteropathy.Semantic proximity Read ↗

A novel variant in the SLCO2A1 gene in a Chinese patient with chronic gastroenteropathy and primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

Clinical and genetic characteristics of Chinese patients diagnosed with chronic enteropathy associated with SLCO2A1 gene.Semantic proximity Read ↗

A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter.Semantic proximity Read ↗

Four Variants of SLCO2A1 Identified in Three Chinese Patients with Chronic Enteropathy Associated with the SLCO2A1 Gene.Semantic proximity Read ↗

Genotype and phenotype characterization of primary hypertrophic osteoarthropathy type 2 and chronic enteropathy associated with SLCO2A1: Report of two cases and literature review.Semantic proximity Read ↗

Inherited epithelial transporter disorders--an overview.Semantic proximity Read ↗

Chronic Enteropathy Associated with SLCO2A1-Associated Primary Hypertrophic Osteoarthropathy in Female Patients: A Case Report and Literature ReviewSemantic proximity Read ↗

Severe Chronic Enteropathy Associated with SLCO2A1 Mutation in a Male Child Complicated by Extensive Jejunal Strictures and Perforation: A Case ReportSemantic proximity Read ↗

Chronic Enteropathy Associated with SLCO2A1 with Pachydermoperiostosis.Semantic proximity Read ↗

Clinical and Genetic Characteristics of Korean Patients Diagnosed with Chronic Enteropathy Associated with SLCO2A1 Gene: A KASID Multicenter Study.Semantic proximity Read ↗

Mutations in the SLCO2A1 gene and primary hypertrophic osteoarthropathy: a clinical and biochemical characterization.Semantic proximity Read ↗

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