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

[Band 3 deficiency as a cause of hereditary spherocytosis].

[Rinsho ketsueki] The Japanese journal of clinical hematology - 1 Jul 2015

Wada Hideho, Suemori Shin-Ichiro, Nakanishi Hidekazu, Sugihara Takashi

Abstract excerpt

Band 3 protein accounts for the largest percentage of whole erythrocyte membrane proteins. Abnormalities in this protein are closely associated with pathologies including hereditary spherocytosis (HS), Southeast Asian ovalocytosis and distant renal tubular acidosis. Currently, EMA binding capacity measurement in erythrocytes is the most useful screening test for diagnosing HS. We have also demonstrated reduced...

Read the complete abstract on PubMed

Topics

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

Share to Anion Exchange Protein 1, Erythrocyte
Share to Ankyrins

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

Share to Erythrocyte Membrane

Share to Mutation

Share to Protein Binding

Share to Spherocytosis, Hereditary

Source

Identifiers

PMID: 26251147
DOI: 10.11406/rinketsu.56.837

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

[Band 3 deficiency as a cause of hereditary spherocytosis].PMID 26251147Read ↗

Molecular Defect of the Band 3 Protein in Southeast Asian OvalocytosisSemantic proximity Read ↗

Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects.Semantic proximity Read ↗

Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patientsSemantic proximity Read ↗

Hereditary red cell membrane defects: diagnostic and clinical aspects.Semantic proximity Read ↗

[Hereditary red cell membrane disorders in Japan: comparison with other countries].Semantic proximity Read ↗

Hereditary spherocytosis.Semantic proximity Read ↗

Band 3 and its alterations in health and disease.Semantic proximity Read ↗

[Molecular mechanism of hereditary spherocytosis].Semantic proximity Read ↗

Band 3 Tuscaloosa: Pro327----Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2.Semantic proximity Read ↗

Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.Semantic proximity Read ↗

The structure and function of band 3 (AE1): Recent developments (Review)Semantic proximity Read ↗

Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis.Semantic proximity Read ↗

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