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Article

[Frameshift mutations in the PQBP1 gene prevent its interaction with the splicing factor U5-15kD].

Seikagaku. The Journal of Japanese Biochemical Society - 1 Aug 2015

Mizuguchi Mineyuki

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 26571623

Genes

PQBP1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 9 closest

[Frameshift mutations in the PQBP1 gene prevent its interaction with the splicing factor U5-15kD].PMID 26571623Read ↗

Mutations in the PQBP1 gene prevent its interaction with the spliceosomal protein U5-15 kD.Semantic proximity Read ↗

[Structural study of polyglutamine tract-binding protein 1].Semantic proximity Read ↗

Y65C missense mutation in the WW domain of the Golabi-Ito-Hall syndrome protein PQBP1 affects its binding activity and deregulates pre-mRNA splicing.Semantic proximity Read ↗

Molecular insights into the WW domain of the Golabi-Ito-Hall syndrome protein PQBP1.Semantic proximity Read ↗

A subset of human 35S U5 proteins, including Prp19, function prior to catalytic step 1 of splicingSemantic proximity Read ↗

Common pathological mutations in PQBP1 induce nonsense-mediated mRNA decay and enhance exclusion of the mutant exon.Semantic proximity Read ↗

Studies of point mutants define three essential paired nucleotides in the domain 5 substructure of a group II intron.Semantic proximity Read ↗

[Analysis of the regulatory mechanism for the constitutive splicing using molecular genetics in fission yeast].Semantic proximity Read ↗

The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patients.Semantic proximity Read ↗

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