about
Development and evolution of the muscles of the pelvic finThe zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.The caveolin-cavin system plays a conserved and critical role in mechanoprotection of skeletal muscle.A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafishMorphogenesis and cell fate determination within the adaxial cell equivalence group of the zebrafish myotomeThe zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachmentZebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle functionIn vivo characterization of microglial engulfment of dying neurons in the zebrafish spinal cord.FishNet: an online database of zebrafish anatomy.Mutant human FUS Is ubiquitously mislocalized and generates persistent stress granules in primary cultured transgenic zebrafish cellsFgf-dependent glial cell bridges facilitate spinal cord regeneration in zebrafish.Mechanoprotection by skeletal muscle caveolaeLoss of Tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy.Modular Detection of GFP-Labeled Proteins for Rapid Screening by Electron Microscopy in Cells and Organisms.A plasmid library of full-length zebrafish rab proteins for in vivo cell biology.Genetic basis of hindlimb loss in a naturally occurring vertebrate model.Temperature and the expression of seven muscle-specific protein genes during embryogenesis in the Atlantic cod Gadus morhua L.Temperature and the expression of myogenic regulatory factors (MRFs) and myosin heavy chain isoforms during embryogenesis in the common carp Cyprinus carpio L.Stages of embryonic development in the Atlantic cod Gadus morhua.The in vivo performance of an enzyme-assisted self-assembled peptide/protein hydrogel.Morphology of pelvic fin loss in a zebrafish strain (Danio rerio).Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology.Haematopoietic stem cell induction by somite-derived endothelial cells controlled by meox1.Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle.Scube activity is necessary for Hedgehog signal transduction in vivo.Muscle Stem Cells Undergo Extensive Clonal Drift during Tissue Growth via Meox1-Mediated Induction of G2 Cell-Cycle Arrest.Asymmetric division of clonal muscle stem cells coordinates muscle regeneration in vivo.Caveolae Protect Notochord Cells against Catastrophic Mechanical Failure during Development.Whole-somite rotation generates muscle progenitor cell compartments in the developing zebrafish embryo.Correlative light and electron microscopic detection of GFP-labeled proteins using modular APEX.A Tol2 Gateway-Compatible Toolbox for the Study of the Nervous System and Neurodegenerative Disease.New Transgenic Lines for Localization of GFP-Tagged Proteins by Electron Microscopy.Characterization of the laminin gene family and evolution in zebrafish.Ultrastructural localisation of protein interactions using conditionally stable nanobodies.Novel Transgenic Lines to Label Sarcolemma and Myofibrils of the MusculatureA somitic contribution to the apical ectodermal ridge is essential for fin formationMyosin Vb is required for correct trafficking of N‐cadherin and cardiac chamber ballooningA variable undecad repeat domain in cavin1 regulates caveola formation and stabilityKBTBD13 is an actin-binding protein that modulates muscle kineticsCellular rescue in a zebrafish model of congenital muscular dystrophy type 1A
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Thomas E Hall
@nl
Thomas E Hall
@sl
Thomas E. Hall
@en
Thomas E. Hall
@es
Thomas Hall
@fr
type
label
Thomas E Hall
@nl
Thomas E Hall
@sl
Thomas E. Hall
@en
Thomas E. Hall
@es
Thomas Hall
@fr
prefLabel
Thomas E Hall
@nl
Thomas E Hall
@sl
Thomas E. Hall
@en
Thomas E. Hall
@es
Thomas Hall
@fr
P1053
J-2125-2014
P106
P1153
8758255300
P21
P31
P3829
P496
0000-0002-7718-7614