 Myotonin-Protein Kinase
"Myotonin-Protein Kinase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Serine/threonine protein kinase responsible for various SKELETAL MUSCLE functions; HEART CONDUCTION SYSTEM activity; calcium HOMEOSTASIS; calcium uptake by SARCOPLASMIC RETICULUM and SYNAPTIC PLASTICITY. It is encoded by the DMPK gene and its abnormal EXPANDED TRINUCLEOTIDE REPEAT of CTG in the 3'-UTR is associated with MYOTONIC DYSTROPHY 1.
| Descriptor ID |
D065636
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| MeSH Number(s) |
D08.811.913.696.620.682.700.576
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| Concept/Terms |
Myotonin-Protein Kinase- Myotonin-Protein Kinase
- Kinase, Myotonin-Protein
- Myotonin Protein Kinase
- DM-Kinase
- DM Kinase
- Myotonic Dystrophy Protein Kinase
- DMPK Protein
- Protein, DMPK
- MDGP Protein
- Protein, MDGP
- MDPK Protein
- Protein, MDPK
- DM Protein Kinase
- Kinase, DM Protein
- Protein Kinase, DM
- DM1PK Protein
- Protein, DM1PK
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Below are MeSH descriptors whose meaning is more general than "Myotonin-Protein Kinase".
Below are MeSH descriptors whose meaning is more specific than "Myotonin-Protein Kinase".
This graph shows the total number of publications written about "Myotonin-Protein Kinase" by people in this website by year, and whether "Myotonin-Protein Kinase" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Myotonin-Protein Kinase" by people in Profiles.
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Chilton I, Okur V, Vitiello G, Selicorni A, Mariani M, Goldenberg A, Husson T, Campion D, Lichtenbelt KD, van Gassen K, Steinraths M, Rice J, Roeder ER, Littlejohn RO, Srour M, Sebire G, Accogli A, H?ron D, Heide S, Nava C, Depienne C, Larson A, Niyazov D, Azage M, Hoganson G, Burton J, Rush ET, Jenkins JL, Saunders CJ, Thiffault I, Alaimo JT, Fleischer J, Groepper D, Gripp KW, Chung WK. De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype. Am J Med Genet A. 2020 05; 182(5):962-973.
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