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Linking life‐history theory and metabolic theory explains the offspring size‐temperature relationship

Ecology letters, 2019-03, Vol.22 (3), p.518-526

2019

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Genetic compensation triggered by actin mutation prevents the muscle damage caused by loss of actin protein

PLoS genetics, 2018-02, Vol.14 (2), p.e1007212-e1007212

2018

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In vivo wall shear measurements within the developing zebrafish heart

PloS one, 2013-10, Vol.8 (10), p.e75722-e75722

2013

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The role of ADHD associated genes in neurodevelopment

Developmental biology, 2018-06, Vol.438 (2), p.69-83

2018

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Sample drift correction following 4D confocal time-lapse imaging

Journal of visualized experiments, 2014-04 (86)

2014

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FLNC myofibrillar myopathy results from impaired autophagy and protein insufficiency

Human molecular genetics, 2016-06, Vol.25 (11), p.2131-2142

2016

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Expression of the Z Variant of α1-Antitrypsin Suppresses Hepatic Cholesterol Biosynthesis in Transgenic Zebrafish

International journal of molecular sciences, 2023-01, Vol.24 (3), p.2475

2023

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Zebrafish models of BAG3 myofibrillar myopathy suggest a toxic gain of function leading to BAG3 insufficiency

Acta neuropathologica, 2014-12, Vol.128 (6), p.821-833

2014

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Does the cost of development scale allometrically with offspring size?

Functional ecology, 2018-03, Vol.32 (3), p.762-772

2018

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Using Touch-evoked Response and Locomotion Assays to Assess Muscle Performance and Function in Zebrafish

Journal of visualized experiments, 2016-10 (116)

2016

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Novel preclinical model for CDKL5 deficiency disorder

Disease models & mechanisms, 2022-03, Vol.15 (3)

2022

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Production of zebrafish cardiospheres and cardiac progenitor cells in vitro and three‐dimensional culture of adult zebrafish cardiac tissue in scaffolds

Biotechnology and bioengineering, 2017-09, Vol.114 (9), p.2142-2148

2017

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zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin α2-deficient congenital muscular dystrophy

Proceedings of the National Academy of Sciences - PNAS, 2007-04, Vol.104 (17), p.7092-7097

2007

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Whole-Somite Rotation Generates Muscle Progenitor Cell Compartments in the Developing Zebrafish Embryo

Developmental cell, 2007-02, Vol.12 (2), p.207-219

2007

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Characterization and investigation of zebrafish models of filamin-related myofibrillar myopathy

Human molecular genetics, 2012-09, Vol.21 (18), p.4073-4083

2012

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Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo

Development (Cambridge), 2003-12, Vol.130 (23), p.5851-5860

2003

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Genome-wide identification of conserved intronic non-coding sequences using a Bayesian segmentation approach

BMC genomics, 2017-03, Vol.18 (1), p.259-259, Article 259

2017

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The genetics of vertebrate myogenesis

Nature reviews. Drug discovery, 2008-08, Vol.9 (8), p.632-646

2008

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Zebrafish prox1b mutants develop a lymphatic vasculature, and prox1b does not specifically mark lymphatic endothelial cells

PloS one, 2011-12, Vol.6 (12), p.e28934-e28934

2011

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Muscle Pathology in Dystrophic Rats and Zebrafish Is Unresponsive to Taurine Treatment, Compared to the mdx Mouse Model for Duchenne Muscular Dystrophy

Metabolites, 2023-02, Vol.13 (2), p.232

2023

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Testing of therapies in a novel nebulin nemaline myopathy model demonstrate a lack of efficacy

Acta neuropathologica communications, 2018-05, Vol.6 (1), p.40-10, Article 40

2018

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Manipulation of Proteostasis Networks in Transgenic ZAAT Zebrafish via CRISPR-Cas9 Gene Editing

Methods in molecular biology (Clifton, N.J.), 2024, Vol.2750, p.19

2024

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The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment

Development (Cambridge), 2009-10, Vol.136 (19), p.3367-3376

2009

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Immuno Correlative Light and Electron Microscopy on Tokuyasu Cryosections

Methods in Cell Biology, 2014, Vol.124, p.241-258

2014

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The structure and evolution of the melanocortin and MCH receptors in fish and mammals

Genomics (San Diego, Calif.), 2003-02, Vol.81 (2), p.184-191

2003

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Linking life‐history theory and metabolic theory explains the offspring size‐temperature relationship

Genetic compensation triggered by actin mutation prevents the muscle damage caused by loss of actin protein

In vivo wall shear measurements within the developing zebrafish heart

The role of ADHD associated genes in neurodevelopment

Sample drift correction following 4D confocal time-lapse imaging

FLNC myofibrillar myopathy results from impaired autophagy and protein insufficiency

Expression of the Z Variant of α1-Antitrypsin Suppresses Hepatic Cholesterol Biosynthesis in Transgenic Zebrafish

Zebrafish models of BAG3 myofibrillar myopathy suggest a toxic gain of function leading to BAG3 insufficiency

Does the cost of development scale allometrically with offspring size?

Using Touch-evoked Response and Locomotion Assays to Assess Muscle Performance and Function in Zebrafish

Novel preclinical model for CDKL5 deficiency disorder

Production of zebrafish cardiospheres and cardiac progenitor cells in vitro and three‐dimensional culture of adult zebrafish cardiac tissue in scaffolds

zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin α2-deficient congenital muscular dystrophy

Whole-Somite Rotation Generates Muscle Progenitor Cell Compartments in the Developing Zebrafish Embryo

Characterization and investigation of zebrafish models of filamin-related myofibrillar myopathy

Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo

Genome-wide identification of conserved intronic non-coding sequences using a Bayesian segmentation approach

The genetics of vertebrate myogenesis

Zebrafish prox1b mutants develop a lymphatic vasculature, and prox1b does not specifically mark lymphatic endothelial cells

Muscle Pathology in Dystrophic Rats and Zebrafish Is Unresponsive to Taurine Treatment, Compared to the mdx Mouse Model for Duchenne Muscular Dystrophy

Testing of therapies in a novel nebulin nemaline myopathy model demonstrate a lack of efficacy

Manipulation of Proteostasis Networks in Transgenic ZAAT Zebrafish via CRISPR-Cas9 Gene Editing

The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment

Immuno Correlative Light and Electron Microscopy on Tokuyasu Cryosections

The structure and evolution of the melanocortin and MCH receptors in fish and mammals

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