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

[Physiological function of myotonin protein kinase].

Nihon rinsho. Japanese journal of clinical medicine - 1 Dec 1997

Ishiura S

Abstract excerpt

The mutation underlying myotonic dystrophy is the expansion of polymorphic CTG repeat in the 3'-noncoding region of the myotonin protein kinase (MtPK) gene mapping to chromosome 19q13.3. A full-length cDNA of human MtPK was cloned and expressed in COS-1 cells. We purified native full-length MtPK from rat skeletal muscle. This 70 kDa MtPK is localized in sarcoplasmic reticulum fraction, whereas the previously...

Read the complete abstract on PubMed

Topics

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

Share to Cell Differentiation
Share to Mice
Share to Muscles

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

Share to Mutation

Share to Protein Kinases

Share to Protein Serine-Threonine Kinases

Share to Signal Transduction

Source

Identifiers

PMID: 9436436

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

[Physiological function of myotonin protein kinase].PMID 9436436Read ↗

[Myotonin protein kinase].Semantic proximity Read ↗

[Myotonic dystrophy and myotonin kinase protein gene mutation].Semantic proximity Read ↗

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

A tail-anchored myotonic dystrophy protein kinase isoform induces perinuclear clustering of mitochondria, autophagy, and apoptosis.Semantic proximity Read ↗

Myotonic dystrophy protein kinase phosphorylates phospholamban and regulates calcium uptake in cardiomyocyte sarcoplasmic reticulum.Semantic proximity Read ↗

A novel mechanism of myocyte degeneration involving the Ca2+-permeable growth factor–regulated channelSemantic proximity Read ↗

Identification, Tissue-specific Expression, and Subcellular Localization of the 80- and 71-kDa Forms of Myotonic Dystrophy Kinase ProteinSemantic proximity Read ↗

Improved plasma membrane expression of the trafficking defective P344R mutant of muscle, skeletal, receptor tyrosine kinase (MuSK) causing congenital myasthenic syndrome.Semantic proximity Read ↗

Physiological roles of G-protein-coupled receptor kinases revealed by gene-targeting technology.Semantic proximity Read ↗

Characteristics of myotonic dystrophy in Istria: molecular genetics approach--mutation analysis.Semantic proximity Read ↗

Coiled-coil interactions modulate multimerization, mitochondrial binding and kinase activity of myotonic dystrophy protein kinase splice isoforms.Semantic proximity Read ↗

Modulation of skeletal muscle sodium channels by human myotonin protein kinase.Semantic proximity Read ↗

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