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Article

[Can mutation of the AMPD1 gene encoding human deaminase muscle muscle isozyme AMP be a prognostic marker of primary dilated cardiomyopathy?].

Postepy biochemii - 1 Jan 1999

Kaletha K, Chodorowski Z, Nagel-Starczynowska G, Gazda M, Słomińska E

Abstract excerpt

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Share to AMP Deaminase
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10761193

Genes

AMPD1

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

[Can mutation of the AMPD1 gene encoding human deaminase muscle muscle isozyme AMP be a prognostic marker of primary dilated cardiomyopathy?].PMID 10761193Read ↗

Clinical heterogeneity and molecular mechanisms in inborn muscle AMP deaminase deficiencySemantic proximity Read ↗

[AMPD genes and urate metabolism].Semantic proximity Read ↗

Decreased cardiac activity of AMP deaminase in subjects with the AMPD1 mutation--a potential mechanism of protection in heart failure.Semantic proximity Read ↗

[Can myocardial Na+ channel gene mutation be a prognostic factor for sudden death in asymptomatic Brugada syndrome?].Semantic proximity Read ↗

AMP deaminase 1 gene polymorphism and heart disease-a genetic association that highlights new treatment.Semantic proximity Read ↗

AMPD1 C34T mutation selectively affects AMP-deaminase activity in the human heart.Semantic proximity Read ↗

Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 gene.Semantic proximity Read ↗

[AMP deaminase deficiency].Semantic proximity Read ↗

Myoadenylate deaminase deficiency with progressive muscle weakness and atrophy caused by new missense mutations in AMPD1 gene: case report in a Japanese patient.Semantic proximity Read ↗

Clinical significance and neuropathology of primary MADD in C34-T and G468-T mutations of the AMPD1 gene.Semantic proximity Read ↗

[Inherited AMP-deaminase deficiency--molecular basis of the defect].Semantic proximity Read ↗

Molecular biology of AMP deaminase deficiency.Semantic proximity Read ↗

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