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Brain and Nerve, ISSN 1881-6096, 01/2017, Volume 69, Issue 1, pp. 61 - 69
Journal Article
NATURE CELL BIOLOGY, ISSN 1465-7392, 12/2005, Volume 7, Issue 12, pp. 1240 - 1247
We show that localized expression of the integrin alpha(3) protein is regulated at the level of RNA localization by the human homologue of Drosophila... 
ORGANIZATION | MIGRATION | CELLS | LAMININ-5 | IN-VIVO | MBNL | ACTIN MESSENGER-RNA | DROSOPHILA | EXPANDED-REPEAT TRANSCRIPTS | CELL BIOLOGY
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 04/2018, Volume 112, pp. 35 - 48
Myotonic dystrophy (DM) is a progressive, multisystem disorder affecting skeletal muscle, heart, and central nervous system. In both DM1 and DM2,... 
Myotonic dystrophy | flavoprotein | Corpus callosum | MBNL | Microsatellite repeats | ACTIVATION | BLOOD-FLOW | NEUROSCIENCES | GLUTAMATE RECEPTORS | INHIBITION | CORTEX | CONNECTIVITY | CORPUS-CALLOSUM | NITRIC-OXIDE | FLAVOPROTEIN AUTOFLUORESCENCE | BRAIN
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 02/2019, Volume 509, Issue 2, pp. 384 - 389
Alternative splicing (AS) is dysregulated in Type 1 diabetic (T1D) hearts but mechanisms responsible are unclear. Here, we provide evidence that the RNA... 
PTBP1 | Alternative splicing | Diabetic heart | RNA binding proteins | CELF | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRACT BINDING-PROTEIN | PRE-MESSENGER-RNA | EXON 6B | ANTAGONISTIC REGULATION | PATHOGENESIS | BIOPHYSICS | REPRESSION | CARDIAC-HYPERTROPHY | MBNL | EXPRESSION
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 04/2018, Volume 46, Issue 6, pp. 3152 - 3168
Abstract The muscleblind-like (MBNL) family of proteins are key developmental regulators of alternative splicing. Sequestration of MBNL proteins by expanded... 
MYOTONIC-DYSTROPHY TYPE-1 | ZINC FINGERS | MUSCLEBLIND PROTEINS | CARDIAC TROPONIN-T | MBNL PROTEINS | BIOCHEMISTRY & MOLECULAR BIOLOGY | IN-VIVO | DISEASE | NUCLEAR FOCI | PRE-MESSENGER-RNA | EXPANDED-REPEAT TRANSCRIPTS | RNA and RNA-protein complexes
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 04/2019, Volume 20, Issue 8, p. 1938
Circular RNAs (circRNAs) constitute a recently re-discovered class of non-coding RNAs functioning as sponges for miRNAs and proteins, affecting RNA splicing... 
Alternative splicing | Circular RNA | Muscular dystrophies | TRIPLET REPEAT | ABUNDANT | alternative splicing | BIOCHEMISTRY & MOLECULAR BIOLOGY | RECEPTOR | BINDING PROTEIN | FAILURE | CHEMISTRY, MULTIDISCIPLINARY | BIOMARKERS | DISRUPTION | circular RNA | MBNL PROTEINS | PLASMA MICRORNAS | GENE-EXPRESSION | muscular dystrophies | Life Sciences
Journal Article
Cell reports, 8/2015, Volume 12, Issue 7, pp. 1159 - 1168
For some neurological disorders, disease is primarily RNA-mediated due to expression of non-coding microsatellite expansion RNAs (RNA exp ). Toxicity is... 
myotonic dystrophy | microsatellite | non-coding RNA | RNA processing | RNA-mediated disease | MBNL
Journal Article
Journal Article
Molecular Cell, ISSN 1097-2765, 02/2017, Volume 65, Issue 3, pp. 539 - 553.e7
Journal Article
Genes and Development, ISSN 0890-9369, 2017, Volume 31, Issue 11, pp. 1067 - 1068
Journal Article
Drug Metabolism and Disposition, ISSN 0090-9556, 03/2019, Volume 47, Issue 3, pp. 314 - 319
Sulfotransferase 4A1 (SULT4A1) is a sulfotransferase-like protein that is highly conserved between species. In human tissues, there are two transcripts, one... 
PHARMACOLOGY & PHARMACY | MECHANISMS | MBNL PROTEINS | BRAIN | Phenotypes | Animal models | Transcription | Splicing | Exons | Embryo cells | Differentiation (biology) | Stem cell transplantation | Cell differentiation | Gene expression | Tissues | Human tissues | Proteins | Time dependence | Ribonucleic acids | Sulfotransferase | Stem cells | Protein expression | CelF protein | RNA processing | Splicing factors | Pluripotency
Journal Article
Molecular Cell, ISSN 1097-2765, 10/2016, Volume 64, Issue 2, pp. 294 - 306
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 06/2015, Volume 58, Issue 15, pp. 5770 - 5780
Myotonic dystrophy type 1 (DM1) is a disease characterized by errors in alternative splicing, or "mis-splicing". The causative agent of mis-splicing in DM1 is... 
PENTAMIDINE | SKELETAL-MUSCLE | CHEMISTRY, MEDICINAL | DNA MINOR-GROOVE | ANALOGS | IN-VIVO | MBNL | DM1 | BINDING | PRE-MESSENGER-RNA | CUG REPEATS | Animals | Cells, Cultured | Myotonic Dystrophy - drug therapy | Amidines - therapeutic use | Male | Amidines - pharmacology | Structure-Activity Relationship | Amidines - chemistry | Disease Models, Animal | Index Medicus
Journal Article