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Article

Structure, function, and molecular genetics of erythroid membrane skeletal protein 4.1 in normal and abnormal red blood cells.

Seminars in hematology - 1 Jan 1993

Conboy J G

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Share to Cytoskeletal Proteins
Share to Elliptocytosis, Hereditary
Share to Erythrocytes
Share to Erythrocytes, Abnormal

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

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Share to Neuropeptides

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Identifiers

PMID: 8434260

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

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Structure, function, and molecular genetics of erythroid membrane skeletal protein 4.1 in normal and abnormal red blood cells.PMID 8434260Read ↗

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Protein 4.1R–deficient mice are viable but have erythroid membrane skeleton abnormalitiesSemantic proximity Read ↗

Band 4.2 abnormalities in human red cells.Semantic proximity Read ↗

The genetic disorders of the red cell skeleton.Semantic proximity Read ↗

Hereditary elliptocytosis: spectrin and protein 4.1R.Semantic proximity Read ↗

Introduction: red blood cell membrane proteins, their genes and mutations.Semantic proximity Read ↗

Red cell membrane disorders: structure meets function.Semantic proximity Read ↗

The red cell skeleton and its genetic disorders.Semantic proximity Read ↗

Erythroid and nonerythroid spectrins.Semantic proximity Read ↗

A large deletion within the protein 4.1 gene associated with a stable truncated mRNA and an unaltered tissue-specific alternative splicing.Semantic proximity Read ↗

The Human Red Blood Cell Proteome and InteractomeSemantic proximity Read ↗

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