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Article

The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced

1 Feb 1995

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

Identifiers

PMID: 7719347
DOI: 10.1038/ng0295-184

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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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Research trail→

Click a neighbor to travelStep 1 · 12 closest

The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally splicedPMID 7719347Read ↗

Sequence differences in introns flanking exon 48 of the dystrophin gene.Semantic proximity Read ↗

Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion.Semantic proximity Read ↗

When Size <em>R</em><em>eally</em> Matters: The Eccentricities of Dystrophin Transcription and the Hazards of Quantifying mRNA from Very Long GenesSemantic proximity Read ↗

Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and miceSemantic proximity Read ↗

The structural and functional diversity of dystrophin.Semantic proximity Read ↗

A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions.Semantic proximity Read ↗

Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression.Semantic proximity Read ↗

Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues.Semantic proximity Read ↗

Intronic Alternative Polyadenylation in the Middle of the DMD Gene Produces Half-Size N-Terminal Dystrophin with a Potential Implication of ECG Abnormalities of DMD Patients.Semantic proximity Read ↗

Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transferSemantic proximity Read ↗

Analysis of splicing parameters in the dystrophin gene: relevance for physiological and pathogenetic splicing mechanisms.Semantic proximity Read ↗

A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy.Semantic proximity Read ↗

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