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

Identification of an unusual deletion within homologous repeats of human reticulocyte beta-spectrin and probable peptide polymorphism.

Gene - 16 Jul 1990

Yoon S H, Kentros C G, Prchal J T

Abstract excerpt

We screened two different human reticulocyte cDNA libraries with beta-spectrin(beta Sp)-specific polyclonal antibodies and with our original radiolabeled human BSP cDNA probe (encoding beta Sp). Of the 20 independent clones, the largest had about a 2.5-kb insert corresponding to the deduced amino acid (aa) sequence of the beta-7 to beta-14 repetitive segments. Among these segments, segment 12 was 7 aa shorter...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Base Sequence
Share to Molecular Sequence Data

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

Share to Mutation

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Share to Polymorphism, Restriction Fragment Length

Share to Restriction Mapping

Source

Identifiers

PMID: 1976574
DOI: 10.1016/0378-1119(90)90104-y

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

Identification of an unusual deletion within homologous repeats of human reticulocyte beta-spectrin and probable peptide polymorphism.PMID 1976574Read ↗

Full-length sequence of the cDNA for human erythroid beta-spectrin.Semantic proximity Read ↗

The complete cDNA and polypeptide sequences of human erythroid alpha-spectrin.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 ↗

Hybrid spectrin type repeats produced by exon-skipping in dystrophin.Semantic proximity Read ↗

Identification of the amino acid mutations associated with human erythrocyte spectrin alpha II domain polymorphisms.Semantic proximity Read ↗

Location and PCR-based detection of three polymorphisms of the human erythrocyte beta-spectrin gene (SPTB).Semantic proximity Read ↗

Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation.Semantic proximity Read ↗

Dinucleotide repeat polymorphism at the human erythroid alpha spectrin (SPTA1) locus.Semantic proximity Read ↗

Dinucleotide repeat polymorphism at the human erythroid alpha-spectrin (SPTA1) mRNA gene detected using PCR.Semantic proximity Read ↗

Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.Semantic proximity Read ↗

Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site.Semantic proximity Read ↗

Characterization of a new β-spectrin gene which is predominantly expressed in brainSemantic proximity Read ↗

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