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Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease

PloS one, 2020-03, Vol.15 (3), p.e0230566-e0230566

2020

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Cryptic Amyloidogenic Elements in the 3′ UTRs of Neurofilament Genes Trigger Axonal Neuropathy

American journal of human genetics, 2016-04, Vol.98 (4), p.597-614

2016

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A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure

PloS one, 2017-12, Vol.12 (12), p.e0189324-e0189324

2017

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Gastrointestinal Dysfunction in Genetically Defined Neurodevelopmental Disorders

Seminars in neurology, 2023-08, Vol.43 (4), p.645

2023

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Drugs prescribed for Phelan-McDermid syndrome differentially impact sensory behaviors in shank3 zebrafish models. [version 1; peer review: 2 approved with reservations]

F1000 research, 2023, Vol.12, p.84

2023

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Intestinal dysmotility in a zebrafish ( Danio rerio ) shank3a;shank3b mutant model of autism

Molecular autism, 2019-01, Vol.10 (1), p.3-3, Article 3

2019

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Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish

Frontiers in molecular neuroscience, 2016-07, Vol.9, p.55-55

2016

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Context-dependent hyperactivity in syngap1a and syngap1b zebrafish models of SYNGAP1-related disorder

Frontiers in molecular neuroscience, 2024-07, Vol.17, p.1401746

2024

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Drugs prescribed for Phelan-McDermid syndrome differentially impact sensory behaviors in shank3 zebrafish models. [version 2; peer review: 2 approved]

F1000 research, 2023, Vol.12, p.84-84

2023

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Spatial patterning of excitatory and inhibitory neuropil territories during spinal circuit development

Journal of comparative neurology (1911), 2017-05, Vol.525 (7), p.1649-1667

2017

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Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis

Human molecular genetics, 2015-07, Vol.24 (14), p.4006-4023

2015

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Elevated preoptic brain activity in zebrafish glial glycine transporter mutants is linked to lethargy-like behaviors and delayed emergence from anesthesia

Scientific reports, 2021-02, Vol.11 (1), p.3148-3148, Article 3148

2021

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Distinct phenotypes in zebrafish models of human startle disease

Neurobiology of disease, 2013-12, Vol.60, p.139-151

2013

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The Gut-Brain-Microbiome Axis and Its Link to Autism: Emerging Insights and the Potential of Zebrafish Models

Frontiers in cell and developmental biology, 2021-04, Vol.9, p.662916-662916

2021

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Zebrafish: A Pharmacogenetic Model for Anesthesia

Methods in enzymology, 2018, Vol.602, p.189-209

2018

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Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficits

Communications biology, 2021-12, Vol.4 (1), p.1411-1411, Article 1411

2021

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CoREST: A Functional Corepressor Required for Regulation of Neural-Specific Gene Expression

Proceedings of the National Academy of Sciences - PNAS, 1999-08, Vol.96 (17), p.9873-9878

1999

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Synaptic Homeostasis in a Zebrafish Glial Glycine Transporter Mutant

Journal of neurophysiology, 2008-10, Vol.100 (4), p.1716-1723

2008

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Knock-down DHDDS expression induces photoreceptor degeneration in zebrafish

Advances in experimental medicine and biology, 2014, Vol.801, p.543

2014

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A Conserved Role But Different Partners for the Transcriptional Corepressor CoREST in Fly and Mammalian Nervous System Formation

The Journal of neuroscience, 2004-08, Vol.24 (32), p.7186-7193

2004

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Glycinergic synapse development, plasticity, and homeostasis in zebrafish

Frontiers in molecular neuroscience, 2009-01, Vol.2, p.30-30

2009

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Translocation of CaM kinase II to synaptic sites in vivo

Nature neuroscience, 2003-03, Vol.6 (3), p.217-218

2003

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Crossing the blood–brain–barrier with transferrin conjugated carbon dots: A zebrafish model study

Colloids and surfaces, B, Biointerfaces, 2016-09, Vol.145, p.251-256

2016

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Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Nature genetics, 2020-05, Vol.52 (5), p.473-481

2020

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Tryptophan carbon dots and their ability to cross the blood-brain barrier

Colloids and surfaces, B, Biointerfaces, 2019-04, Vol.176, p.488-493

2019

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Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease

Cryptic Amyloidogenic Elements in the 3′ UTRs of Neurofilament Genes Trigger Axonal Neuropathy

A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure

Gastrointestinal Dysfunction in Genetically Defined Neurodevelopmental Disorders

Drugs prescribed for Phelan-McDermid syndrome differentially impact sensory behaviors in shank3 zebrafish models. [version 1; peer review: 2 approved with reservations]

Intestinal dysmotility in a zebrafish ( Danio rerio ) shank3a;shank3b mutant model of autism

Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish

Context-dependent hyperactivity in syngap1a and syngap1b zebrafish models of SYNGAP1-related disorder

Drugs prescribed for Phelan-McDermid syndrome differentially impact sensory behaviors in shank3 zebrafish models. [version 2; peer review: 2 approved]

Spatial patterning of excitatory and inhibitory neuropil territories during spinal circuit development

Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis

Elevated preoptic brain activity in zebrafish glial glycine transporter mutants is linked to lethargy-like behaviors and delayed emergence from anesthesia

Distinct phenotypes in zebrafish models of human startle disease

The Gut-Brain-Microbiome Axis and Its Link to Autism: Emerging Insights and the Potential of Zebrafish Models

Zebrafish: A Pharmacogenetic Model for Anesthesia

Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficits

CoREST: A Functional Corepressor Required for Regulation of Neural-Specific Gene Expression

Synaptic Homeostasis in a Zebrafish Glial Glycine Transporter Mutant

Knock-down DHDDS expression induces photoreceptor degeneration in zebrafish

A Conserved Role But Different Partners for the Transcriptional Corepressor CoREST in Fly and Mammalian Nervous System Formation

Glycinergic synapse development, plasticity, and homeostasis in zebrafish

Translocation of CaM kinase II to synaptic sites in vivo

Crossing the blood–brain–barrier with transferrin conjugated carbon dots: A zebrafish model study

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Tryptophan carbon dots and their ability to cross the blood-brain barrier

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