Pages that link to "Q37557193"
Jump to navigation
Jump to search
The following pages link to Compound loss of muscleblind-like function in myotonic dystrophy (Q37557193):
Displaying 50 items.
- The splicing regulators Esrp1 and Esrp2 direct an epithelial splicing program essential for mammalian development (Q28588736) (← links)
- Disease Phenotypes in a Mouse Model of RNA Toxicity Are Independent of Protein Kinase Cα and Protein Kinase Cβ (Q30275866) (← links)
- NKX2-5, a modifier of skeletal muscle pathology due to RNA toxicity. (Q30361778) (← links)
- Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy (Q30653577) (← links)
- Muscleblind-like 1 is required for normal heart valve development in vivo. (Q30668792) (← links)
- Mechanistic determinants of MBNL activity (Q30830825) (← links)
- Autoregulation of MBNL1 function by exon 1 exclusion from MBNL1 transcript (Q33557647) (← links)
- Lomofungin and dilomofungin: inhibitors of MBNL1-CUG RNA binding with distinct cellular effects (Q33698593) (← links)
- Muscleblind-like 1 (Mbnl1) regulates pre-mRNA alternative splicing during terminal erythropoiesis (Q33948731) (← links)
- RNA-protein interactions in unstable microsatellite diseases. (Q34243144) (← links)
- MBNL proteins and their target RNAs, interaction and splicing regulation. (Q34248811) (← links)
- Loss of muscleblind-like 1 results in cardiac pathology and persistence of embryonic splice isoforms (Q34466715) (← links)
- Loss of MBNL leads to disruption of developmentally regulated alternative polyadenylation in RNA-mediated disease. (Q34473863) (← links)
- Repeat associated non-ATG (RAN) translation: new starts in microsatellite expansion disorders (Q34543709) (← links)
- Identification of Targets of CUG-BP, Elav-Like Family Member 1 (CELF1) Regulation in Embryonic Heart Muscle (Q35920624) (← links)
- Therapeutic impact of systemic AAV-mediated RNA interference in a mouse model of myotonic dystrophy. (Q35924075) (← links)
- MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain (Q35984230) (← links)
- Muscleblind-Like 1 and Muscleblind-Like 3 Depletion Synergistically Enhances Myotonia by Altering Clc-1 RNA Translation (Q36106234) (← links)
- Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I. (Q36151477) (← links)
- A flow cytometry-based screen identifies MBNL1 modulators that rescue splicing defects in myotonic dystrophy type I. (Q36378612) (← links)
- MBNL1-mediated regulation of differentiation RNAs promotes myofibroblast transformation and the fibrotic response (Q36437997) (← links)
- Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy. (Q36796408) (← links)
- Determination of a Comprehensive Alternative Splicing Regulatory Network and Combinatorial Regulation by Key Factors during the Epithelial-to-Mesenchymal Transition (Q37122584) (← links)
- Derepressing muscleblind expression by miRNA sponges ameliorates myotonic dystrophy-like phenotypes in Drosophila. (Q37386187) (← links)
- Progressive Cl- channel defects reveal disrupted skeletal muscle maturation in R6/2 Huntington's mice (Q37565636) (← links)
- Circles reshaping the RNA world: from waste to treasure (Q37692556) (← links)
- Sponging of cellular proteins by viral RNAs (Q38252264) (← links)
- Developmental insights into the pathology of and therapeutic strategies for DM1: Back to the basics (Q38287631) (← links)
- Elimination of Toxic Microsatellite Repeat Expansion RNA by RNA-Targeting Cas9. (Q38695021) (← links)
- Roles for RNA-binding proteins in development and disease (Q38772987) (← links)
- Monocyte Chemoattractant Protein-Induced Protein 1 Overexpression Modulates Transcriptome, Including MicroRNA, in Human Neuroblastoma Cells. (Q38840679) (← links)
- Myotonic dystrophy: approach to therapy (Q38855524) (← links)
- Muscleblind-like 3 deficit results in a spectrum of age-associated pathologies observed in myotonic dystrophy (Q39533050) (← links)
- Optical Mapping Approaches on Muscleblind-Like Compound Knockout Mice for Understanding Mechanistic Insights Into Ventricular Arrhythmias in Myotonic Dystrophy (Q41166103) (← links)
- Dmpk gene deletion or antisense knockdown does not compromise cardiac or skeletal muscle function in mice (Q41643458) (← links)
- Erythroid mRNA processing: a "splice of life". (Q42129313) (← links)
- Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy. (Q47154610) (← links)
- RNA-binding proteins in neurodegeneration: mechanisms in aggregate (Q47569012) (← links)
- MBNL expression in autoregulatory feedback loops. (Q47741773) (← links)
- Detection of expanded RNA repeats using thermostable group II intron reverse transcriptase (Q49819843) (← links)
- Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome. (Q49905433) (← links)
- Daunorubicin reduces MBNL1 sequestration caused by CUG-repeat expansion and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy. (Q54967674) (← links)
- rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences. (Q55087601) (← links)
- miR-23b and miR-218 silencing increase Muscleblind-like expression and alleviate myotonic dystrophy phenotypes in mammalian models. (Q55418837) (← links)
- Simplified in vitro engineering of neuromuscular junctions between rat embryonic motoneurons and immortalized human skeletal muscle cells (Q64227851) (← links)
- (CTG)n repeat-mediated dysregulation of MBNL1 and MBNL2 expression during myogenesis in DM1 occurs already at the myoblast stage. (Q64900419) (← links)
- Modeling of Myotonic Dystrophy Cardiac Phenotypes in Drosophila. (Q64980454) (← links)
- Of Mice and Men: Advances in the Understanding of Neuromuscular Aspects of Myotonic Dystrophy. (Q64989527) (← links)
- Myotonic dystrophy (Q87411199) (← links)
- Myotonic Dystrophy and Developmental Regulation of RNA Processing (Q88453318) (← links)