Control of muscle fibre-type diversity during embryonic development: the zebrafish paradigm
about
"Slow" skeletal muscles across vertebrate speciesZebrafish: A Model for the Study of Toxicants Affecting Muscle Development and FunctionRecent advances using zebrafish animal models for muscle disease drug discoveryA defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome.Zebrafish ambra1a and ambra1b knockdown impairs skeletal muscle development.Swimming-induced exercise promotes hypertrophy and vascularization of fast skeletal muscle fibres and activation of myogenic and angiogenic transcriptional programs in adult zebrafish.Zebrafish foxc1a plays a crucial role in early somitogenesis by restricting the expression of aldh1a2 directly.Isolation of Novel CreERT2-Driver Lines in Zebrafish Using an Unbiased Gene Trap ApproachMotoneuron axon pathfinding errors in zebrafish: differential effects related to concentration and timing of nicotine exposureSix1 homeoprotein drives myofiber type IIA specialization in soleus muscle.Skeletal muscle fiber type: using insights from muscle developmental biology to dissect targets for susceptibility and resistance to muscle disease.Comparative myogenesis in teleosts and mammals.Canonical and non-canonical Hedgehog signalling and the control of metabolism.Tmem2 regulates cell-matrix interactions that are essential for muscle fiber attachmentThe role of Sox6 in zebrafish muscle fiber type specificationRequirement of the fusogenic micropeptide myomixer for muscle formation in zebrafish.Transient cardiomyocyte fusion regulates cardiac development in zebrafish.Promoter architecture and transcriptional regulation of musculoskeletal embryonic nuclear protein 1b (mustn1b) gene in zebrafish.Copper pyrithione, a booster biocide, induces abnormal muscle and notochord architecture in zebrafish embryogenesis.Regulation of posterior body and epidermal morphogenesis in zebrafish by localized Yap1 and Wwtr1.WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome.Proteomic profiling of muscle fibre type shifting in neuromuscular diseases.Differential Cellular Responses to Hedgehog Signalling in Vertebrates-What is the Role of Competence?[Potential of the zebrafish model to study congenital muscular dystrophies].Emerging Roles of DYRK Kinases in Embryogenesis and Hedgehog Pathway Control.Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy.Principles Governing Locomotion in Vertebrates: Lessons From ZebrafishGenes Show Spatiotemporal Expression during Murine Tongue and Eyelid Development
P2860
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P2860
Control of muscle fibre-type diversity during embryonic development: the zebrafish paradigm
description
2013 nî lūn-bûn
@nan
2013 թուականին հրատարակուած գիտական յօդուած
@hyw
2013 թվականին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@ast
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@en
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@nl
type
label
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@ast
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@en
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@nl
prefLabel
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@ast
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@en
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@nl
P3181
P1476
Control of muscle fibre-type d ...... opment: the zebrafish paradigm
@en
P2093
Harriet E. Jackson
P304
P3181
P356
10.1016/J.MOD.2013.06.001
P407
P577
2013-01-01T00:00:00Z