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Progressive impairment of muscle regeneration in muscleblind-like 3 isoform knockout mice.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 17, p. 3547, doi. 10.1093/hmg/ddt209
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- Publication type:
- Article
Partners in crime: bidirectional transcription in unstable microsatellite disease.
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- Human Molecular Genetics, 2010, v. 19, n. R1, p. R77, doi. 10.1093/hmg/ddq132
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- Publication type:
- Article
Transcriptional and post-transcriptional impact of toxic RNA in myotonic dystrophy.
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- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1471, doi. 10.1093/hmg/ddp058
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- Publication type:
- Article
Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2087, doi. 10.1093/hmg/ddl132
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- Publication type:
- Article
Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons.
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- Human Molecular Genetics, 2004, v. 13, n. 24, p. 3079, doi. 10.1093/hmg/ddh327
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- Publication type:
- Article
MBNL1-mediated regulation of differentiation RNAs promotes myofibroblast transformation and the fibrotic response.
- Published in:
- Nature Communications, 2015, v. 6, n. 12, p. 10084, doi. 10.1038/ncomms10084
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- Publication type:
- Article
Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy.
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- Nature Communications, 2015, v. 6, n. 5, p. 7205, doi. 10.1038/ncomms8205
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- Publication type:
- Article
Choroid plexus mis-splicing and altered cerebrospinal fluid composition in myotonic dystrophy type 1.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4217, doi. 10.1093/brain/awad148
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- Publication type:
- Article
Splicing biomarkers of disease severity in myotonic dystrophy.
- Published in:
- Annals of Neurology, 2013, v. 74, n. 6, p. 862, doi. 10.1002/ana.23992
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- Publication type:
- Article
Control of cleavage site selection during mRNA 3' end formation by a yeast hnRNP.
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- EMBO Journal, 1998, v. 17, n. 24, p. 7454, doi. 10.1093/emboj/17.24.7454
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- Publication type:
- Article
Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 13, p. 3365, doi. 10.3390/ijms20133365
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- Publication type:
- Article
Identification of a (CUG)n Triplet Repeat RNA-Binding Protein and Its Expression in Myotonic Dystrophy.
- Published in:
- Nucleic Acids Research, 1996, v. 24, n. 22, p. 4407, doi. 10.1093/nar/24.22.4407
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- Publication type:
- Article
SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets.
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- Database: The Journal of Biological Databases & Curation, 2017, v. 2017, n. 1, p. 1, doi. 10.1093/database/bax071
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- Publication type:
- Article
RNA Gain-of-Function in Spinocerebellar Ataxia Type 8.
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- PLoS Genetics, 2009, v. 5, n. 8, p. 1, doi. 10.1371/journal.pgen.1000600
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- Article
Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy.
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- Nature Structural & Molecular Biology, 2010, v. 17, n. 2, p. 187, doi. 10.1038/nsmb.1720
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- Publication type:
- Article
Precise temporal regulation of alternative splicing during neural development.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04559-0
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- Publication type:
- Article
Muscleblind-like 1 is required for normal heart valve development in vivo.
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- BMC Developmental Biology, 2015, v. 15, p. 1, doi. 10.1186/s12861-015-0087-4
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- Publication type:
- Article
Methylphenidate Attenuates the Cognitive and Mood Alterations Observed in Mbnl2 Knockout Mice and Reduces Microglia Overexpression.
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- Cerebral Cortex, 2019, v. 29, n. 7, p. 2978, doi. 10.1093/cercor/bhy164
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- Publication type:
- Article
Compound loss of muscleblind-like function in myotonic dystrophy.
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- EMBO Molecular Medicine, 2013, v. 5, n. 12, p. 1887, doi. 10.1002/emmm.201303275
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- Publication type:
- Article
Muscleblind-Like 1 Knockout Mice Reveal Novel Splicing Defects in the Myotonic Dystrophy Brain.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0033218
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- Publication type:
- Article
Genome Modification Leads to Phenotype Reversal in Human Myotonic Dystrophy Type 1 Induced Pluripotent Stem Cell-Derived Neural Stem Cells.
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- Stem Cells, 2015, v. 33, n. 6, p. 1829, doi. 10.1002/stem.1970
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- Publication type:
- Article
Muscleblind proteins regulate alternative splicing.
- Published in:
- EMBO Journal, 2004, v. 23, n. 15, p. 3103, doi. 10.1038/sj.emboj.7600300
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- Publication type:
- Article
Dual requirement for yeast hnRNP Nab2p in mRNA poly(A) tail length control and nuclear export.
- Published in:
- EMBO Journal, 2002, v. 21, n. 7, p. 1800, doi. 10.1093/emboj/21.7.1800
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- Publication type:
- Article
Recruitment of human muscleblind proteins to (CUG)<sub>n</sub> expansions associated with myotonic dystrophy.
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- EMBO Journal, 2000, v. 19, n. 17, p. 4439, doi. 10.1093/emboj/19.17.4439
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- Publication type:
- Article
Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy.
- Published in:
- 2007
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- Publication type:
- journal article
Spaceflight effects on human vascular smooth muscle cell phenotype and function.
- Published in:
- NPJ Microgravity, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41526-024-00380-w
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- Article
Retraction Note: Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype.
- Published in:
- 2017
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- Correction Notice
Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype.
- Published in:
- Acta Neuropathologica Communications, 2016, v. 4, p. 1, doi. 10.1186/s40478-016-0393-5
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- Publication type:
- Article
MBNL splicing activity depends on RNA binding site structural context.
- Published in:
- Nucleic Acids Research, 2018, v. 46, n. 17, p. 9119, doi. 10.1093/nar/gky565
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- Publication type:
- Article
Prediction of clustered RNA-binding protein motif sites in the mammalian genome.
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- Nucleic Acids Research, 2013, v. 41, n. 14, p. 6793, doi. 10.1093/nar/gkt421
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- Publication type:
- Article
The X-linked splicing regulator MBNL3 has been co-opted to restrict placental growth in eutherians.
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- PLoS Biology, 2022, v. 20, n. 4, p. 1, doi. 10.1371/journal.pbio.3001615
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- Article
Muscleblind-like 1 interacts with RNA hairpins in splicing target and pathogenic RNAs.
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- Nucleic Acids Research, 2007, v. 35, n. 16, p. 5474, doi. 10.1093/nar/gkm601
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- Publication type:
- Article
Identification of NH...N hydrogen bonds by magic angle spinning solid state NMR in a double‐stranded RNA associated with myotonic dystrophy.
- Published in:
- Nucleic Acids Research, 2004, v. 32, n. 3, p. 1177, doi. 10.1093/nar/gkh288
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- Publication type:
- Article
Visualization of double-stranded RNAs from the myotonic dystrophy protein kinase gene and interactions with CUG-binding protein.
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- Nucleic Acids Research, 1999, v. 27, n. 17, p. 3534, doi. 10.1093/nar/27.17.3534
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- Publication type:
- Article
Loss of MBNL1 induces RNA misprocessing in the thymus and peripheral blood.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15962-x
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- Publication type:
- Article
Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour.
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- 2013
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- Publication type:
- journal article
Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour.
- Published in:
- Brain: A Journal of Neurology, 2013, v. 136, n. 3, p. 957
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- Publication type:
- Article
Dynamic balance between activation and repression regulates pre-mRNA alternative splicing during heart development.
- Published in:
- Developmental Dynamics, 2005, v. 233, n. 3, p. 783
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- Publication type:
- Article
Constraints on the Structure of (CUG)<sub>97</sub> RNA from Magic-Angle-Spinning Solid-State NMR Spectroscopy.
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 34, p. 5620, doi. 10.1002/anie.200600769
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- Publication type:
- Article
Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 19, p. 2165, doi. 10.1093/hmg/10.19.2165
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- Publication type:
- Article