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The emerging use of zebrafish to model metabolic disease

Disease models & mechanisms, 2013-09, Vol.6 (5), p.1080-1088

2013

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A systematic genome-wide analysis of zebrafish protein-coding gene function

Nature (London), 2013-04, Vol.496 (7446), p.494-497

2013

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Genetic Screen for Postembryonic Development in the Zebrafish ( Danio rerio ): Dominant Mutations Affecting Adult Form

Genetics (Austin), 2017-10, Vol.207 (2), p.609-623

2017

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Mutations in C10orf11, a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism

American journal of human genetics, 2013-03, Vol.92 (3), p.415-421

2013

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The gene regulatory basis of genetic compensation during neural crest induction

PLoS genetics, 2019-06, Vol.15 (6), p.e1008213-e1008213

2019

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The Ribosome Biogenesis Protein Nol9 Is Essential for Definitive Hematopoiesis and Pancreas Morphogenesis in Zebrafish

PLoS genetics, 2015-12, Vol.11 (12), p.e1005677-e1005677

2015

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Common and distinct transcriptional signatures of mammalian embryonic lethality

Nature communications, 2019-06, Vol.10 (1), p.2792-16, Article 2792

2019

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Identification of slit3 as a locus affecting nicotine preference in zebrafish and human smoking behaviour

eLife, 2020-03, Vol.9

2020

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Loss of the chromatin modifier Kdm2aa causes BrafV600E-independent spontaneous melanoma in zebrafish

PLoS genetics, 2017-08, Vol.13 (8), p.e1006959

2017

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Zebrafish mutants identify an essential role for laminins in notochord formation

Development (Cambridge), 2002-07, Vol.129 (13), p.3137-3146

2002

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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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Identification of a plant isoflavonoid that causes biliary atresia

Science translational medicine, 2015-05, Vol.7 (286), p.286ra67

2015

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Genetic screens for mutations affecting development of Xenopus tropicalis

PLoS genetics, 2006-06, Vol.2 (6), p.e91

2006

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A new patient‐derived iPSC model for dystroglycanopathies validates a compound that increases glycosylation of α‐dystroglycan

EMBO reports, 2019-11, Vol.20 (11), p.e47967-n/a

2019

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gridlock , a localized heritable vascular patterning defect in the zebrafish

Nature medicine, 1995-11, Vol.1 (11), p.1143-1147

1995

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Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

Human molecular genetics, 2005-11, Vol.14 (22), p.3463-3476

2005

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Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function

Acta neuropathologica, 2015-09, Vol.130 (3), p.389-406

2015

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Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation

Nature (London), 2000-05, Vol.405 (6782), p.76-81

2000

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Multi-allelic phenotyping – A systematic approach for the simultaneous analysis of multiple induced mutations

Methods (San Diego, Calif.), 2013-08, Vol.62 (3), p.197-206

2013

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Organ-specific requirements for Hdac1 in liver and pancreas formation

Developmental biology, 2008-10, Vol.322 (2), p.237-250

2008

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Visualisation and quantification of morphogen gradient formation in the zebrafish

PLoS biology, 2009-05, Vol.7 (5), p.e1000101-e1000101

2009

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High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping

BMC genomics, 2015-08, Vol.16 (1), p.578-578, Article 578

2015

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Midline signals regulate retinal neurogenesis in zebrafish

Neuron (Cambridge, Mass.), 2000-08, Vol.27 (2), p.251-263

2000

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A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon

Genes & development, 2001-06, Vol.15 (11), p.1427-1434

2001

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The emerging use of zebrafish to model metabolic disease

A systematic genome-wide analysis of zebrafish protein-coding gene function

Genetic Screen for Postembryonic Development in the Zebrafish ( Danio rerio ): Dominant Mutations Affecting Adult Form

Mutations in C10orf11, a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism

The gene regulatory basis of genetic compensation during neural crest induction

The Ribosome Biogenesis Protein Nol9 Is Essential for Definitive Hematopoiesis and Pancreas Morphogenesis in Zebrafish

Common and distinct transcriptional signatures of mammalian embryonic lethality

Identification of slit3 as a locus affecting nicotine preference in zebrafish and human smoking behaviour

Loss of the chromatin modifier Kdm2aa causes BrafV600E-independent spontaneous melanoma in zebrafish

Zebrafish mutants identify an essential role for laminins in notochord formation

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

Identification of a plant isoflavonoid that causes biliary atresia

Genetic screens for mutations affecting development of Xenopus tropicalis

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome

A new patient‐derived iPSC model for dystroglycanopathies validates a compound that increases glycosylation of α‐dystroglycan

gridlock , a localized heritable vascular patterning defect in the zebrafish

Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function

Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation

Multi-allelic phenotyping – A systematic approach for the simultaneous analysis of multiple induced mutations

Organ-specific requirements for Hdac1 in liver and pancreas formation

Visualisation and quantification of morphogen gradient formation in the zebrafish

High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping

Midline signals regulate retinal neurogenesis in zebrafish

A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon

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