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Vertebrate features revealed in the rudimentary eye of the Pacific hagfish ( Eptatretus stoutii )

Proceedings of the Royal Society. B, Biological sciences, 2021-01, Vol.288 (1942), p.20202187-20202187

2021

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Seizures are a druggable mechanistic link between TBI and subsequent tauopathy

eLife, 2021-02, Vol.10

2021

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Sleep is bi-directionally modified by amyloid beta oligomers

eLife, 2020-07, Vol.9

2020

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Regeneration of cone photoreceptors when cell ablation is primarily restricted to a particular cone subtype

PloS one, 2013-01, Vol.8 (1), p.e55410

2013

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CB1 and CB2 receptors play differential roles in early zebrafish locomotor development

Journal of experimental biology, 2019, Vol.222

2019

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Protein Misfolding in Prion and Prion-Like Diseases: Reconsidering a Required Role for Protein Loss-of-Function

Journal of Alzheimer's disease, 2016-08, Vol.54 (1), p.3-29

2016

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Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ9-tetrahydrocannabinol

Scientific reports, 2021-06, Vol.11 (1), p.11515-11515, Article 11515

2021

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Tryptophan 32 mediates SOD1 toxicity in a in vivo motor neuron model of ALS and is a promising target for small molecule therapeutics

Neurobiology of disease, 2019-04, Vol.124, p.297-310

2019

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Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary Glaucoma

International journal of molecular sciences, 2023-10, Vol.24 (19), p.14423

2023

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Prion-Like Propagation Mechanisms in Tauopathies and Traumatic Brain Injury: Challenges and Prospects

Biomolecules (Basel, Switzerland), 2020-10, Vol.10 (11), p.1487

2020

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Ontogeny of cone photoreceptor mosaics in zebrafish

Journal of comparative neurology (1911), 2010-10, Vol.518 (20), p.4182-4195

2010

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Functional Domains and Evolutionary History of the PMEL and GPNMB Family Proteins

Molecules (Basel, Switzerland), 2021-06, Vol.26 (12), p.3529

2021

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Amyloid beta precursor protein and prion protein have a conserved interaction affecting cell adhesion and CNS development

PloS one, 2012-12, Vol.7 (12), p.e51305

2012

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Rapid Recovery of Visual Function Associated with Blue Cone Ablation in Zebrafish

PloS one, 2016-11, Vol.11 (11), p.e0166932-e0166932

2016

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Zebrafish Models of Photoreceptor Dysfunction and Degeneration

Biomolecules (Basel, Switzerland), 2021-01, Vol.11 (1), p.78

2021

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Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

Human molecular genetics, 2010-01, Vol.19 (2), p.287-298

2010

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Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina

Frontiers in cell and developmental biology, 2022-01, Vol.10, p.822358

2022

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A complex regulatory network of transcription factors critical for ocular development and disease

Human molecular genetics, 2011-04, Vol.20 (8), p.1610-1624

2011

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gdf6a is required for cone photoreceptor subtype differentiation and for the actions of tbx2b in determining rod versus cone photoreceptor fate

PloS one, 2014-03, Vol.9 (3), p.e92991-e92991

2014

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Reduced Abundance and Subverted Functions of Proteins in Prion-Like Diseases: Gained Functions Fascinate but Lost Functions Affect Aetiology

International journal of molecular sciences, 2017-10, Vol.18 (10), p.2223

2017

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Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies

Human molecular genetics, 2013-04, Vol.22 (7), p.1432-1442

2013

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Transmission from the dominant input shapes the stereotypic ratio of photoreceptor inputs onto horizontal cells

Nature communications, 2014-05, Vol.5 (1), p.3699-3699, Article 3699

2014

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Bright and High-Performance Genetically Encoded Ca2+ Indicator Based on mNeonGreen Fluorescent Protein

ACS sensors, 2020-07, Vol.5 (7), p.1959-1968

2020

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Targeted mutation of the gene encoding prion protein in zebrafish reveals a conserved role in neuron excitability

Neurobiology of disease, 2013-07, Vol.55, p.11-25

2013

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The intrigue is infectious: Impacts of prion protein during neural development

Developmental biology, 2018-09, Vol.441 (1), p.1-3

Allison, W. Ted

2018

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Vertebrate features revealed in the rudimentary eye of the Pacific hagfish ( Eptatretus stoutii )

Seizures are a druggable mechanistic link between TBI and subsequent tauopathy

Sleep is bi-directionally modified by amyloid beta oligomers

Regeneration of cone photoreceptors when cell ablation is primarily restricted to a particular cone subtype

CB1 and CB2 receptors play differential roles in early zebrafish locomotor development

Protein Misfolding in Prion and Prion-Like Diseases: Reconsidering a Required Role for Protein Loss-of-Function

Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ9-tetrahydrocannabinol

Tryptophan 32 mediates SOD1 toxicity in a in vivo motor neuron model of ALS and is a promising target for small molecule therapeutics

Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary Glaucoma

Prion-Like Propagation Mechanisms in Tauopathies and Traumatic Brain Injury: Challenges and Prospects

Ontogeny of cone photoreceptor mosaics in zebrafish

Functional Domains and Evolutionary History of the PMEL and GPNMB Family Proteins

Amyloid beta precursor protein and prion protein have a conserved interaction affecting cell adhesion and CNS development

Rapid Recovery of Visual Function Associated with Blue Cone Ablation in Zebrafish

Zebrafish Models of Photoreceptor Dysfunction and Degeneration

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

Hagfish to Illuminate the Developmental and Evolutionary Origins of the Vertebrate Retina

A complex regulatory network of transcription factors critical for ocular development and disease

gdf6a is required for cone photoreceptor subtype differentiation and for the actions of tbx2b in determining rod versus cone photoreceptor fate

Reduced Abundance and Subverted Functions of Proteins in Prion-Like Diseases: Gained Functions Fascinate but Lost Functions Affect Aetiology

Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies

Transmission from the dominant input shapes the stereotypic ratio of photoreceptor inputs onto horizontal cells

Bright and High-Performance Genetically Encoded Ca2+ Indicator Based on mNeonGreen Fluorescent Protein

Targeted mutation of the gene encoding prion protein in zebrafish reveals a conserved role in neuron excitability

The intrigue is infectious: Impacts of prion protein during neural development

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