Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies
Authors
Keywords
-
Journal
FEBS Journal
Volume 280, Issue 17, Pages 4187-4197
Publisher
Wiley
Online
2013-06-29
DOI
10.1111/febs.12412
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Genome editing with RNA-guided Cas9 nuclease in Zebrafish embryos
- (2013) Nannan Chang et al. CELL RESEARCH
- Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker–Warburg syndrome
- (2013) Karen Buysse et al. HUMAN MOLECULAR GENETICS
- Knockdown of desmin in zebrafish larvae affects interfilament spacing and mechanical properties of skeletal muscle
- (2013) Mei Li et al. JOURNAL OF GENERAL PHYSIOLOGY
- Neuromuscular junction abnormalities in DNM2-related centronuclear myopathy
- (2013) Elizabeth M. Gibbs et al. JOURNAL OF MOLECULAR MEDICINE-JMM
- Efficient genome editing in zebrafish using a CRISPR-Cas system
- (2013) Woong Y Hwang et al. NATURE BIOTECHNOLOGY
- RNA-Guided Human Genome Engineering via Cas9
- (2013) P. Mali et al. SCIENCE
- Multiplex Genome Engineering Using CRISPR/Cas Systems
- (2013) L. Cong et al. SCIENCE
- Analysis of Embryonic and Larval Zebrafish Skeletal Myofibers from Dissociated Preparations
- (2013) Eric J. Horstick et al. Jove-Journal of Visualized Experiments
- Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg Syndrome
- (2012) M. Chiara Manzini et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Dominant Mutation of CCDC78 in a Unique Congenital Myopathy with Prominent Internal Nuclei and Atypical Cores
- (2012) Karen Majczenko et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Quantification of birefringence readily measures the level of muscle damage in zebrafish
- (2012) Joachim Berger et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy
- (2012) James J. Dowling et al. BRAIN
- In Vivo Imaging of Molecular Interactions at Damaged Sarcolemma
- (2012) Urmas Roostalu et al. DEVELOPMENTAL CELL
- Zebrafish models flex their muscles to shed light on muscular dystrophies
- (2012) J. Berger et al. Disease Models & Mechanisms
- Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy
- (2012) Hiroaki Mitsuhashi et al. HUMAN MOLECULAR GENETICS
- Hooked! Modeling human disease in zebrafish
- (2012) Cristina Santoriello et al. JOURNAL OF CLINICAL INVESTIGATION
- In vivo genome editing using a high-efficiency TALEN system
- (2012) Victoria M. Bedell et al. NATURE
- Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan
- (2012) Tony Roscioli et al. NATURE GENETICS
- Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy
- (2012) Jaakko Sarparanta et al. NATURE GENETICS
- Muscle diseases in the zebrafish
- (2012) Yung-Yao Lin NEUROMUSCULAR DISORDERS
- A Splice Site Mutation in Laminin-α2 Results in a Severe Muscular Dystrophy and Growth Abnormalities in Zebrafish
- (2012) Vandana A. Gupta et al. PLoS One
- NAD+ Biosynthesis Ameliorates a Zebrafish Model of Muscular Dystrophy
- (2012) Michelle F. Goody et al. PLOS BIOLOGY
- neb: a zebrafish model of nemaline myopathy due to nebulin mutation
- (2011) W. R. Telfer et al. Disease Models & Mechanisms
- The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies
- (2011) Vandana Gupta et al. HUMAN MOLECULAR GENETICS
- Abnormal vascular development in zebrafish models for fukutin and FKRP deficiency
- (2011) Alasdair J. Wood et al. HUMAN MOLECULAR GENETICS
- Zebrafish Fukutin family proteins link the unfolded protein response with dystroglycanopathies
- (2011) Yung-Yao Lin et al. HUMAN MOLECULAR GENETICS
- Connexin 39.9 Protein Is Necessary for Coordinated Activation of Slow-twitch Muscle and Normal Behavior in Zebrafish
- (2011) Hiromi Hirata et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Evaluation of exon-skipping strategies for Duchenne muscular dystrophy utilizing dystrophin-deficient zebrafish
- (2011) Joachim Berger et al. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
- DHODH modulates transcriptional elongation in the neural crest and melanoma
- (2011) Richard Mark White et al. NATURE
- Targeted gene disruption in somatic zebrafish cells using engineered TALENs
- (2011) Jeffry D Sander et al. NATURE BIOTECHNOLOGY
- King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene
- (2011) James J. Dowling et al. NEUROMUSCULAR DISORDERS
- Embryonic Senescence and Laminopathies in a Progeroid Zebrafish Model
- (2011) Eriko Koshimizu et al. PLoS One
- Drug screening in a zebrafish model of Duchenne muscular dystrophy
- (2011) G. Kawahara et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo
- (2010) Lindsay M. Wallace et al. ANNALS OF NEUROLOGY
- RYR1 mutations are a common cause of congenital myopathies with central nuclei
- (2010) J.M. Wilmshurst et al. ANNALS OF NEUROLOGY
- Protein O-mannosylation is necessary for normal embryonic development in zebrafish
- (2010) E. Avsar-Ban et al. GLYCOBIOLOGY
- Zebrafish models of collagen VI-related myopathies
- (2010) W.R. Telfer et al. HUMAN MOLECULAR GENETICS
- Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology
- (2010) Joachim Berger et al. NEUROMUSCULAR DISORDERS
- Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization
- (2010) J. A. Bevilacqua et al. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
- Sildenafil reverses cardiac dysfunction in the mdx mouse model of Duchenne muscular dystrophy
- (2010) C. M. Adamo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- In-vivo characterization of human dilated cardiomyopathy genes in zebrafish
- (2009) Britta Vogel et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Zebrafish models for human FKRP muscular dystrophies
- (2009) Genri Kawahara et al. HUMAN MOLECULAR GENETICS
- Depletion of zebrafish Tcap leads to muscular dystrophy via disrupting sarcomere–membrane interaction, not sarcomere assembly
- (2009) Ruilin Zhang et al. HUMAN MOLECULAR GENETICS
- Loss of Myotubularin Function Results in T-Tubule Disorganization in Zebrafish and Human Myotubular Myopathy
- (2009) James J. Dowling et al. PLoS Genetics
- Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP)
- (2008) Paul Thornhill et al. BRAIN
- Zebrafish integrin-linked kinase is required in skeletal muscles for strengthening the integrin–ECM adhesion complex
- (2008) Ruben Postel et al. DEVELOPMENTAL BIOLOGY
- Genes required for functional glycosylation of dystroglycan are conserved in zebrafish☆☆Sequence data from this article have been deposited with the GenBank Data Library under Accession Nos. DQ826745 (Fukutin), DQ826746 (FKRP), DQ826747 (POMGnT1), DQ826748 (POMT1), and DQ826749 (POMT2).
- (2008) Christopher J. Moore et al. GENOMICS
- Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin
- (2008) Jeffrey R. Guyon et al. HUMAN MOLECULAR GENETICS
- Structure and Function of Skeletal Muscle in Zebrafish Early Larvae
- (2008) Ying Dou et al. JOURNAL OF GENERAL PHYSIOLOGY
- Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle
- (2008) M. J. Jurynec et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Zinc Finger–Based Knockout Punches for Zebrafish Genes
- (2008) Stephen C. Ekker Zebrafish
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started