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An open source microcontroller based flume for evaluating swimming performance of larval, juvenile, and adult zebrafish.
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- PLoS ONE, 2018, v. 13, n. 6, p. 1, doi. 10.1371/journal.pone.0199712
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- Article
Fam65b is important for formation of the HDAC6-dysferlin protein complex during myogenic cell differentiation.
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- FASEB Journal, 2014, v. 28, n. 7, p. 2955, doi. 10.1096/fj.13-246470
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- Article
α-Actinin-2 deficiency results in sarcomeric defects in zebrafish that cannot be rescued by α-actinin-3 revealing functional differences between sarcomeric isoforms.
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- FASEB Journal, 2012, v. 26, n. 5, p. 1892, doi. 10.1096/fj.11-194548
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- Article
α-Actinin-2 deficiency results in sarcomeric defects in zebrafish that cannot be rescued by α-actinin-3 revealing functional differences between sarcomeric isoforms.
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- FASEB Journal, 2012, v. 26, n. 5, p. 1892, doi. 10.1096/fj.11-194548
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- Publication type:
- Article
Diagnosis and cell-based therapy for Duchenne muscular dystrophy in humans, mice, and zebrafish.
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- Journal of Human Genetics, 2006, v. 51, n. 5, p. 397, doi. 10.1007/s10038-006-0374-9
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- Article
A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).
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- Human Molecular Genetics, 2014, v. 23, n. 15, p. 4103, doi. 10.1093/hmg/ddu127
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- Publication type:
- Article
Human skeletal muscle xenograft as a new preclinical model for muscle disorders.
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- Human Molecular Genetics, 2014, v. 23, n. 12, p. 3180, doi. 10.1093/hmg/ddu028
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- Article
Dystrophic muscle improvement in zebrafish via increased heme oxygenase signaling.
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- Human Molecular Genetics, 2014, v. 23, n. 7, p. 1869, doi. 10.1093/hmg/ddt579
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- Article
Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 568, doi. 10.1093/hmg/dds467
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- Article
Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis.
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- Human Molecular Genetics, 2012, v. 21, n. 20, p. 4419, doi. 10.1093/hmg/dds284
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- Article
The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies.
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- Human Molecular Genetics, 2011, v. 20, n. 9, p. 1712, doi. 10.1093/hmg/ddr047
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- Article
Zebrafish models for human FKRP muscular dystrophies.
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- Human Molecular Genetics, 2010, v. 19, n. 4, p. 623, doi. 10.1093/hmg/ddp528
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- Article
Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.
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- Human Molecular Genetics, 2009, v. 18, n. 1, p. 202, doi. 10.1093/hmg/ddn337
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- Publication type:
- Article
Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy.
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- Science Translational Medicine, 2020, v. 12, n. 536, p. 1, doi. 10.1126/scitranslmed.aay0271
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- Article
Zebrafish orthologs of human muscular dystrophy genes.
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- BMC Genomics, 2007, v. 8, p. 79, doi. 10.1186/1471-2164-8-79
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- Article
A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function.
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- European Journal of Human Genetics, 2012, v. 20, n. 4, p. 404, doi. 10.1038/ejhg.2011.213
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- Article
Dystrophin distribution in heterozygote mdx mice.
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- Muscle & Nerve, 1989, v. 12, n. 10, p. 861, doi. 10.1002/mus.880121013
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- Article
Dystrophin is a tumor suppressor in human cancers with myogenic programs.
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- Nature Genetics, 2014, v. 46, n. 6, p. 601, doi. 10.1038/ng.2974
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- Article
Stem and Progenitor Cells in Skeletal Muscle Development, Maintenance, and Therapy.
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- Molecular Therapy, 2007, v. 15, n. 5, p. 867, doi. 10.1038/mt.sj.6300145
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- Article
Microarray analysis of normal and dystrophic skeletal muscle
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- International Journal of Developmental Neuroscience, 2002, v. 20, n. 3-5, p. 359, doi. 10.1016/S0736-5748(02)00041-2
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- Article
Reproducibility of gene expression across generations of Affymetrix microarrays.
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- BMC Bioinformatics, 2003, v. 4, p. 27, doi. 10.1186/1471-2105-4-27
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- Article
The influence of muscle type and dystrophin deficiency on murine expression profiles.
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- Mammalian Genome, 2005, v. 16, n. 10, p. 739, doi. 10.1007/s00335-005-0053-8
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- Publication type:
- Article
The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs.
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- Nature, 1988, v. 334, n. 6178, p. 154, doi. 10.1038/334154a0
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- Article
Immunoelectron microscopic localization of dystrophin in myofibres.
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- Nature, 1988, v. 333, n. 6176, p. 863, doi. 10.1038/333863a0
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- Publication type:
- Article
Subcellular fractionation of dystrophin to the triads of skeletal muscle.
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- Nature, 1987, v. 330, n. 6150, p. 754, doi. 10.1038/330754a0
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- Publication type:
- Article
Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.
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- Nature, 1985, v. 316, n. 6031, p. 842, doi. 10.1038/316842a0
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- Article
Characteristics and Predictive Value of Blood Transcriptome Signature in Males with Autism Spectrum Disorders.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0049475
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- Publication type:
- Article
A Splice Site Mutation in Laminin-α2 Results in a Severe Muscular Dystrophy and Growth Abnormalities in Zebrafish.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043794
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- Publication type:
- Article
High-Density Genomewide Linkage Analysis of Exceptional Human Longevity Identifies Multiple Novel Loci.
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- PLoS ONE, 2010, v. 5, n. 8, p. 1, doi. 10.1371/journal.pone.0012432
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- Article
Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics.
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- Nature Genetics, 1998, v. 20, n. 1, p. 83, doi. 10.1038/1753
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- Article
MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms.
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- 2014
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- Publication type:
- journal article
MicroRNA-486--dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy--associated symptoms.
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- Journal of Clinical Investigation, 2014, v. 124, n. 6, p. 2651, doi. 10.1172/JCI73579
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- Article
Comment on "Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients".
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- 2009
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- Publication type:
- commentary
Dystrophin expression in the mdx mouse restored by stem cell transplantation.
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- Nature, 1999, v. 401, n. 6751, p. 390, doi. 10.1038/43922
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- Article
Dystrophin and Its Isoforms.
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- Brain Pathology, 1996, v. 6, n. 1, p. 25, doi. 10.1111/j.1750-3639.1996.tb00780.x
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- Article
LGMD2I in a North American population.
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- BMC Musculoskeletal Disorders, 2007, v. 8, p. 115, doi. 10.1186/1471-2474-8-115
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- Article
Beta-synemin expression in cardiotoxin-injected rat skeletal muscle.
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- BMC Musculoskeletal Disorders, 2007, v. 8, p. 40, doi. 10.1186/1471-2474-8-40
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- Publication type:
- Article
Transcriptome-scale similarities between mouse and human skeletal muscles with normal and myopathic phenotypes.
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- BMC Musculoskeletal Disorders, 2006, v. 7, p. 23, doi. 10.1186/1471-2474-7-23
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- Publication type:
- Article
Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE.
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- BMC Medical Genetics, 2011, v. 12, n. 1, p. 87, doi. 10.1186/1471-2350-12-87
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- Publication type:
- Article
Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis.
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- Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-16
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- Publication type:
- Article
Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel disease.
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- PLoS ONE, 2019, v. 14, n. 10, p. 1, doi. 10.1371/journal.pone.0222952
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- Publication type:
- Article
miRNAs in normal and diseased skeletal muscle.
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- Journal of Cellular & Molecular Medicine, 2009, v. 13, n. 1, p. 2, doi. 10.1111/j.1582-4934.2008.00524.x
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- Publication type:
- Article
Expression profiling and identification of novel genes involved in myogenic differentiation.
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- FASEB Journal, 2004, v. 18, n. 2, p. 403, doi. 10.1096/fj.03-0568fje
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- Publication type:
- Article
hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologies.
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- 2021
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- Publication type:
- journal article
Homozygous nonsense mutation in SGCA is a common cause of limb-girdle muscular dystrophy in Assiut, Egypt.
- Published in:
- 2016
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- Publication type:
- journal article
Isolation and transcriptome analysis of adult zebrafish cells enriched for skeletal muscle progenitors.
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- Muscle & Nerve, 2011, v. 43, n. 5, p. 741, doi. 10.1002/mus.21972
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- Publication type:
- Article
Inefficient dystrophin expression after cord blood transplantation in Duchenne muscular dystrophy.
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- Muscle & Nerve, 2010, v. 41, n. 6, p. 746, doi. 10.1002/mus.21702
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- Publication type:
- Article
CXCR4 enhances engraftment of muscle progenitor cells.
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- Muscle & Nerve, 2009, v. 40, n. 4, p. 562, doi. 10.1002/mus.21317
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- Publication type:
- Article
Expression of synemin in the mouse spinal cord.
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- Muscle & Nerve, 2009, v. 39, n. 5, p. 634, doi. 10.1002/mus.21221
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- Article
Synemin expression in brain.
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- Muscle & Nerve, 2007, v. 36, n. 4, p. 497, doi. 10.1002/mus.20847
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- Publication type:
- Article