| scholarly article | Q13442814 |
| review article | Q7318358 |
| P6179 | Dimensions Publication ID | 1008506899 |
| P356 | DOI | 10.1023/A:1005396420442 |
| P953 | full work available at URL | https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1023%2FA%3A1005396420442 |
| https://onlinelibrary.wiley.com/doi/pdf/10.1023/A%3A1005396420442 | ||
| P698 | PubMed publication ID | 9211188 |
| P2093 | author name string | P. N. Strong | |
| B. S. Brewster | |||
| P2860 | cites work | Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts | Q59242144 |
| Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation | Q60050804 | ||
| Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? | Q62554897 | ||
| Effect of Myotonic Dystrophy Trinucleotide Repeat Expansion on DMPK Transcription and Processing | Q62661555 | ||
| Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy | Q67513917 | ||
| Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member | Q68100373 | ||
| Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscle | Q70720300 | ||
| Origin of the expansion mutation in myotonic dystrophy | Q70765926 | ||
| Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy | Q71167717 | ||
| The myotonin-protein kinase phosphorylates tyrosine residues in normal human skeletal muscle | Q71613287 | ||
| Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene | Q72073093 | ||
| Myotonic dystrophy gene analysis in affected Israeli families | Q72094755 | ||
| Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele | Q72096934 | ||
| Phosphorylation reactions of recombinant human myotonic dystrophy protein kinase and their inhibition | Q72160275 | ||
| Myotonic dystrophy with no trinucleotide repeat expansion | Q72280448 | ||
| Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements | Q72333265 | ||
| Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy | Q72611874 | ||
| Possible role of apamin-sensitive K+ channels in myotonic dystrophy | Q72740803 | ||
| Identification and localization of the myotonic dystrophy gene product in skeletal and cardiac muscles | Q72767097 | ||
| Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene | Q72896182 | ||
| CpG-rich islands and the function of DNA methylation | Q28131800 | ||
| Myotonic dystrophy kinase is a component of neuromuscular junctions | Q28258307 | ||
| Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene | Q28285882 | ||
| Cloning of the essential myotonic dystrophy region and mapping of the putative defect | Q30985550 | ||
| The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy | Q33594634 | ||
| Full-length myotonin protein kinase (72 kDa) displays serine kinase activity | Q34215417 | ||
| Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs | Q34231532 | ||
| Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy | Q34231790 | ||
| Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus. | Q34302066 | ||
| Genomic organization and transcriptional units at the myotonic dystrophy locus | Q34321945 | ||
| Expression of a novel human myotonin protein kinase (MtPK) cDNA clone which encodes a protein with a thymopoietin-like domain in COS cells. | Q34333161 | ||
| Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy | Q34348155 | ||
| An unstable triplet repeat in a gene related to myotonic muscular dystrophy | Q34355359 | ||
| Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy. | Q34363062 | ||
| A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat | Q34374463 | ||
| Control of the sperm–oocyte switch in Caenorhabditis elegans hermaphrodites by the fem-3 3′ untranslated region | Q34572336 | ||
| Negative regulatory sequences in the lin-14 3'-untranslated region are necessary to generate a temporal switch during Caenorhabditis elegans development | Q34927780 | ||
| Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy | Q35194656 | ||
| Anticipation in myotonic dystrophy: new light on an old problem | Q35196194 | ||
| Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues | Q36235446 | ||
| Pausing of DNA synthesis in vitro at specific loci in CTG and CGG triplet repeats from human hereditary disease genes. | Q38289363 | ||
| Myotonic dystrophy reviewed: back to the future? | Q40742525 | ||
| Overexpression of myotonic dystrophy kinase in BC3H1 cells induces the skeletal muscle phenotype | Q41240489 | ||
| Identification, Tissue-specific Expression, and Subcellular Localization of the 80- and 71-kDa Forms of Myotonic Dystrophy Kinase Protein | Q41302208 | ||
| Somatic instability of CTG repeat in myotonic dystrophy | Q41510869 | ||
| A novel serine/threonine kinase binding the Ras-related RhoA GTPase which translocates the kinase to peripheral membranes | Q42819347 | ||
| The Drosophila tumor suppressor gene warts encodes a homolog of human myotonic dystrophy kinase and is required for the control of cell shape and proliferation | Q46192247 | ||
| Decreased myotonin-protein kinase in the skeletal and cardiac muscles in myotonic dystrophy | Q48089445 | ||
| Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy | Q48134264 | ||
| Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes | Q48196688 | ||
| Identification of a protein product of the myotonic dystrophy gene using peptide specific antibodies | Q48232490 | ||
| Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice. | Q52200997 | ||
| Characterization of myotonic dystrophy kinase (DMK) protein in human and rodent muscle and central nervous tissue | Q52537879 | ||
| Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy | Q55670526 | ||
| (CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients | Q58194111 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | myotonic dystrophy | Q1860507 |
| trinucleotide repeats | Q71240613 | ||
| P304 | page(s) | 159-170 | |
| P577 | publication date | 1997-06-01 | |
| P1433 | published in | Journal of Inherited Metabolic Disease | Q6295359 |
| P1476 | title | Myotonic dystrophy: molecular and cellular consequences of expanded DNA repeats are elusive | |
| Myotonic dystrophy: Molecular and cellular consequences of expanded DNA repeats are elusive | |||
| P478 | volume | 20 |
| Q77912145 | Expansion and deletion of triplet repeat sequences in Escherichia coli occur on the leading strand of DNA replication |
| Q36840564 | RNA in brain disease: no longer just "the messenger in the middle". |
| Q33903996 | The 3' untranslated region of messenger RNA: A molecular 'hotspot' for pathology? |
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