A CRISPR‐Based Selective Gene Inhibition Method Reveals Dynamic Features of a Cell Nucleus Nanobody Related to the Disease Myotonic Dystrophy - Ma - 2018 - Small Methods - Wiley Online Library
DMPK hypermethylation in sperm cells of myotonic dystrophy type 1 patients | European Journal of Human Genetics
Congenital and childhood myotonic dystrophy: Current aspects of disease and future directions
Figure 7 from Epigenetics of the myotonic dystrophy-associated DMPK gene neighborhood | Semantic Scholar
DMPK gene Archives - Baylor College of Medicine Blog Network
What causes Myotonic Dystrophy? - Myotonic Dystrophy Support Group
IJMS | Free Full-Text | Disrupting the Molecular Pathway in Myotonic Dystrophy
Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genes | PNAS
![PDF] Myotonic dystrophy: molecular windows on a complex etiology. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/d07dd371583f4ecb56c757c4f213b2c8f7cb35a2/4-Figure1-1.png "PDF] Myotonic dystrophy: molecular windows on a complex etiology. | Semantic Scholar")
PDF] Myotonic dystrophy: molecular windows on a complex etiology. | Semantic Scholar
Steinert's myotonic dystrophy - Symptoms, diagnosis and treatment
Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1 | Gene Therapy
Specific DMPK-promoter targeting by CRISPRi reverses myotonic dystrophy type 1-associated defects in patient muscle cells: Molecular Therapy - Nucleic Acids
Processing of DMPK and DMAHP genes within normal and DM cells. In the... | Download Scientific Diagram
Myotonic Dystrophy Type 2 - Home
Time-controlled and muscle-specific CRISPR/Cas9-mediated deletion of CTG-repeat expansion in the DMPK gene - ScienceDirect
DM1 pathogenetic mechanisms and therapeutic strategies. The actions of... | Download Scientific Diagram
Kill the messenger where it lives | Nature
Epigenetics of the myotonic dystrophy-associated DMPK gene neighborhood | Epigenomics
Genome Editing of Expanded CTG Repeats within the Human DMPK Gene Reduces Nuclear RNA Foci in the Muscle of DM1 Mice: Molecular Therapy
Mutation analysis of multiple pilomatricomas in a patient with myotonic dystrophy type 1 suggests a DM1-associated hypermutation phenotype | PLOS ONE
Figure 1 from Myotonic Dystrophy Type 1 (DM1): From the Genetics to Molecular Mechanisms | Semantic Scholar
Two hypotheses on interaction of toxic RNA from mutated DMPK gene. I:... | Download Scientific Diagram
Cardiac Involvement and Arrhythmias Associated with Myotonic Dystrophy
