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

Myotonic dystrophy: molecular windows on a complex etiology.

Nucleic acids research - 15 Mar 1998

Korade-Mirnics Z, Babitzke P, Hoffman E

Abstract excerpt

Myotonic dystrophy (DM) is the most common form of adult onset muscular dystrophy, with an incidence of approximately 1 in 8500 adults. DM is caused by an expanded number of trinucleotide repeats in the 3'-untranslated region (UTR) of a cAMP-dependent protein kinase (DM protein kinase, DMPK). Although a large number of transgenic animals have been generated with different gene constructions and knock-outs, none...

Read the complete abstract on PubMed

Topics

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

Share to Disease Models, Animal
Share to Genes, Dominant
Share to Homeodomain Proteins

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

Share to Mice, Transgenic

Share to Phenotype

Share to Protein Serine-Threonine Kinases

Source

Open in PubMed Open full text

Identifiers

PMID: 9490778
DOI: 10.1093/nar/26.6.1363
PMCID: PMC147423

Genes

DMPK

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

Myotonic dystrophy: molecular windows on a complex etiology.PMID 9490778Read ↗

Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular MechanismSemantic proximity Read ↗

Clinical and molecular aspects of the myotonic dystrophies: A reviewSemantic proximity Read ↗

Myotonic dystrophy: RNA pathogenesis comes into focus.Semantic proximity Read ↗

Myotonic dystrophy, when simple repeats reveal complex pathogenic entities: new findings and future challengesSemantic proximity Read ↗

Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2.Semantic proximity Read ↗

Clinical aspects, molecular pathomechanisms and management of myotonic dystrophies.Semantic proximity Read ↗

[Myotonic dystrophy - a new insight into a well-known disease].Semantic proximity Read ↗

Myotonic dystrophy 1 in the nervous system: From the clinic to molecular mechanismsSemantic proximity Read ↗

Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.Semantic proximity Read ↗

Myotonic dystrophy: molecular and cellular consequences of expanded DNA repeats are elusive.Semantic proximity Read ↗

Myotonic dystrophySemantic proximity Read ↗

Myotonic dystrophy: Emerging mechanisms for DM1 and DM2Semantic proximity Read ↗

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