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ROS Generation in Microglia: Understanding Oxidative Stress and Inflammation in Neurodegenerative Disease

Antioxidants, 2020-08, Vol.9 (8), p.743

2020

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Evolution and Functions of Long Noncoding RNAs

Cell, 2009-02, Vol.136 (4), p.629-641

2009

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Oxr1 improves pathogenic cellular features of ALS-associated FUS and TDP-43 mutations

Human molecular genetics, 2015-06, Vol.24 (12), p.3529-3544

2015

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Genomic and transcriptional co-localization of protein-coding and long non-coding RNA pairs in the developing brain

PLoS genetics, 2009-08, Vol.5 (8), p.e1000617-e1000617

2009

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A Transcriptomic Atlas of Mouse Neocortical Layers

Neuron (Cambridge, Mass.), 2011-08, Vol.71 (4), p.605-616

2011

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TLDc proteins: new players in the oxidative stress response and neurological disease

Mammalian genome, 2017-10, Vol.28 (9-10), p.395-406

2017

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Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain

PLoS genetics, 2011-07, Vol.7 (7), p.e1002145-e1002145

2011

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Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxa

PLoS genetics, 2009-12, Vol.5 (12), p.e1000753-e1000753

2009

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Single-copy expression of an amyotrophic lateral sclerosis-linked TDP-43 mutation (M337V) in BAC transgenic mice leads to altered stress granule dynamics and progressive motor dysfunction

Neurobiology of disease, 2019-01, Vol.121, p.148-162

2019

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Oxr1 is essential for protection against oxidative stress-induced neurodegeneration

PLoS genetics, 2011-10, Vol.7 (10), p.e1002338

2011

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The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling

Human molecular genetics, 2007-01, Vol.16 (1), p.92-106

2007

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A Functional Genetic Link between Distinct Developmental Language Disorders

The New England journal of medicine, 2008-11, Vol.359 (22), p.2337-2345

2008

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The antioxidant protein Oxr1 influences aspects of mitochondrial morphology

Free radical biology & medicine, 2016-06, Vol.95, p.255-267

2016

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The Interconnected Mechanisms of Oxidative Stress and Neuroinflammation in Epilepsy

Antioxidants, 2022-01, Vol.11 (1), p.157

2022

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The Evolutionarily Conserved Tre2/Bub2/Cdc16 (TBC), Lysin Motif (LysM), Domain Catalytic (TLDc) Domain Is Neuroprotective against Oxidative Stress

The Journal of biological chemistry, 2016-02, Vol.291 (6), p.2751-2763

2016

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Stereotypic wheel running decreases cortical activity in mice

Nature communications, 2016-10, Vol.7 (1), p.13138-13138, Article 13138

2016

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The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons

Human molecular genetics, 2019-02, Vol.28 (4), p.584-597

2019

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Neuron-specific antioxidant OXR1 extends survival of a mouse model of amyotrophic lateral sclerosis

Brain (London, England : 1878), 2015-05, Vol.138 (Pt 5), p.1167-1181

2015

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The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis

Cell, 2015-07, Vol.162 (3), p.607-621

2015

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Impairment of Macroautophagy in Dopamine Neurons Has Opposing Effects on Parkinsonian Pathology and Behavior

Cell reports (Cambridge), 2019-10, Vol.29 (4), p.920-931.e7

2019

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Laf4/Aff3, a gene involved in intellectual disability, is required for cellular migration in the mouse cerebral cortex

PloS one, 2014-08, Vol.9 (8), p.e105933-e105933

2014

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Temporal transcriptomics suggest that twin-peaking genes reset the clock

eLife, 2015-11, Vol.4

2015

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Deletion of AMPA receptor GluA1 subunit gene (Gria1) causes circadian rhythm disruption and aberrant responses to environmental cues

Translational psychiatry, 2021-11, Vol.11 (1), p.588-17, Article 588

2021

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Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities

Disease models & mechanisms, 2019-02, Vol.12 (2)

2019

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ROS Generation in Microglia: Understanding Oxidative Stress and Inflammation in Neurodegenerative Disease

Evolution and Functions of Long Noncoding RNAs

Oxr1 improves pathogenic cellular features of ALS-associated FUS and TDP-43 mutations

Genomic and transcriptional co-localization of protein-coding and long non-coding RNA pairs in the developing brain

A Transcriptomic Atlas of Mouse Neocortical Layers

TLDc proteins: new players in the oxidative stress response and neurological disease

Mouse genomic variation and its effect on phenotypes and gene regulation

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain

Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxa

Single-copy expression of an amyotrophic lateral sclerosis-linked TDP-43 mutation (M337V) in BAC transgenic mice leads to altered stress granule dynamics and progressive motor dysfunction

Oxr1 is essential for protection against oxidative stress-induced neurodegeneration

The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling

A Functional Genetic Link between Distinct Developmental Language Disorders

The antioxidant protein Oxr1 influences aspects of mitochondrial morphology

The Interconnected Mechanisms of Oxidative Stress and Neuroinflammation in Epilepsy

The Evolutionarily Conserved Tre2/Bub2/Cdc16 (TBC), Lysin Motif (LysM), Domain Catalytic (TLDc) Domain Is Neuroprotective against Oxidative Stress

Stereotypic wheel running decreases cortical activity in mice

The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons

Neuron-specific antioxidant OXR1 extends survival of a mouse model of amyotrophic lateral sclerosis

The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis

Impairment of Macroautophagy in Dopamine Neurons Has Opposing Effects on Parkinsonian Pathology and Behavior

Laf4/Aff3, a gene involved in intellectual disability, is required for cellular migration in the mouse cerebral cortex

Temporal transcriptomics suggest that twin-peaking genes reset the clock

Deletion of AMPA receptor GluA1 subunit gene (Gria1) causes circadian rhythm disruption and aberrant responses to environmental cues

Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities

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