Faculty profile

James Eubanks

ResearcherGenetics and DevelopmentUniversity of Toronto

This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of Toronto directory, so their courses and email address may be missing. Find their university profile.

James Eubanks

Researcher

Genetics and Development

Health Sciences

University of Toronto

Toronto, Ontario, Canada

Supervision signals

Has led research grants, which requires an independent research appointment. Ask their department whether they supervise graduate students.
No publications since 2017.
Principal investigator on 7 research grants (7 CIHR), most recently in 2019.

These signals come from public records, including CIHR, NSERC and SSHRC funding decisions. Ask the professor or the graduate program whether they are taking new students.

Academic metrics

Publications

Collaborators

Grants

Publications by year

Counts cover the publications linked to this profile. Citations and the h-index appear when the source records them.

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Signals and details

Research

Mouse Behaviour Epilepsy Rett Syndrome Translational Research Electrophysiology Molecular Genetics Mouse Eeg Analysis Neurodevelopmental Condition

Latest papers

Susceptibility to hippocampal kindling seizures is increased in aging C57 black mice.
IBRO reports · 2017
The double-stranded RNA-binding protein Staufen 2 regulates eye size.
Molecular and cellular neurosciences · 2012
Hippocampal seizures alter the expression of the pannexin and connexin transcriptome.
Journal of neurochemistry · 2010

All 3 publications

Latest funding

Development of TRPM2 Inhibitors for the Treatment of Rett Syndrome
CIHR · 2026 · Co-investigator
$100,000
Delineating the role of the TRPM2 surveillance receptor in Rett syndrome
CIHR · 2019 · Nominated PI
$967,726
Altered Microtubule Regulation: A Novel Mechanism Underlying Rett Syndrome Pathogenesis?
CIHR · 2016 · Nominated PI
$390,150

All 10 grants and awards

Development of TRPM2 Inhibitors for the Treatment of Rett Syndrome

Co-investigatorCIHR2026Project Grant

Principal investigators: Reed, Mark A

Keywords: Alzheimer'S Disease; Commercialization; Drug Discovery; Inhibitors; Neurological Disorders; Rett Syndrome; Small Molecule

$100,000

Delineating the role of the TRPM2 surveillance receptor in Rett syndrome

Nominated PICIHR2019Project Grant

Principal investigators: Eubanks, James H

Keywords: Electrophysiology; Molecular Genetics; Mouse Behaviour; Mouse Eeg Analysis; Neurodevelopmental Condition; Phenotype Rescue; Phenotype Reversal; Transgenic Mice

$967,726

Altered Microtubule Regulation: A Novel Mechanism Underlying Rett Syndrome Pathogenesis?

Nominated PICIHR2016Project Grant

Principal investigators: Eubanks, James H

Keywords: Epilepsy; Histone Deacetylase Type 6; Live Cell Imaging; Microtubule Transport; Mouse Behaviour; Neurodevelopment; Translational Study; Tubulin Regulation

$390,150

Raising Awareness for Rett Syndrome: Connecting Scientists, Clinicians, and Parents

Nominated PICIHR2013Dissemination Events - PA: Musculoskeletal Hlth, Arthritis, Skin & Oral Health

Principal investigators: Eubanks, James H

Keywords: Autism-Spectrum Disorder; Better Treatment Options; Brain And Behavior; Gastrointestinal Impairments; Knowledge Transfer; Orthopedic Interventions; Rett Syndrome; Seizures; Social Welfare And Condition Management; Translational Research

$25,000

The Role Of Histone Deacetylase 6 Complexes In Rett Syndrome Pathophysiology

Nominated PICIHR2012Operating Grant

Principal investigators: Eubanks, James H

Keywords: Behavioral Outcomes; Cell Biology; Developmental Biology; Epigenetics; Epilepsy; Histone Deacetylases; Mouse Models; Protein Acetylation; Rett Syndrome; Translational Research

$390,116

Towards the correction of Rett-like behaviour in MeCP2-deficient mice

Nominated PICIHR2010Operating Grant

Principal investigators: Eubanks, James H

Keywords: Epigenetics; Epilepsy; Mouse Behaviour; Mutant Mice; Neurophysiology; Rett Syndrome

$748,827

Infantile Spasms in Down Syndrome: Correction of the Epileptic Phenotype

Co-investigatorCIHR2010Operating Grant

Principal investigators: Snead, Orlando C

Keywords: Catastrophic Epilepsy; Down Syndrome; Environmental Enrichment; Glur5; Infantile Spasms; Seizures; Ts65dn

$914,579

The Mammalian Sirtuin SIRT3: Mediator of Longevity?

Nominated PICIHR2009Catalyst Grant: Pilot Projects in Aging

Principal investigators: Eubanks, James H

Keywords: Aging; Behaviour; Mitochondria; Molecular Biology; Sirtuin; Transgenic Mouse

$50,000

Delivery improvements for photodynamic therapy

Co-investigatorCIHR2008Operating Grant

Principal investigators: Lilge, Lothar

Keywords: Erythropoetin; Monte Carlo Simulation; Oncology; Optical Sensors; Tissue Response Models

$451,912

From Chromatin to Neurophysiology to Behaviour: Studies to Understand, and Develop Treatment Strategies For, the Autism-Spectrum Disorder Rett Syndrome

Nominated PICIHR2008Emerging Team Grant: From Genes to Proteins, Cells, Tissues and Patients - LOI

Principal investigators: Eubanks, James H

Keywords: Chromatin Biology; Electrophysiology; Induced Pluripotent Stem Cells; Rett Syndrome; Transgenic Mice; Viral-Mediated Gene Transfer

From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.

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James Eubanks

Research

Latest papers

Latest funding

Susceptibility to hippocampal kindling seizures is increased in aging C57 black mice.

The double-stranded RNA-binding protein Staufen 2 regulates eye size.

Hippocampal seizures alter the expression of the pannexin and connexin transcriptome.

Development of TRPM2 Inhibitors for the Treatment of Rett Syndrome

Delineating the role of the TRPM2 surveillance receptor in Rett syndrome

Altered Microtubule Regulation: A Novel Mechanism Underlying Rett Syndrome Pathogenesis?

Raising Awareness for Rett Syndrome: Connecting Scientists, Clinicians, and Parents

The Role Of Histone Deacetylase 6 Complexes In Rett Syndrome Pathophysiology

Towards the correction of Rett-like behaviour in MeCP2-deficient mice

Infantile Spasms in Down Syndrome: Correction of the Epileptic Phenotype

The Mammalian Sirtuin SIRT3: Mediator of Longevity?

Delivery improvements for photodynamic therapy

From Chromatin to Neurophysiology to Behaviour: Studies to Understand, and Develop Treatment Strategies For, the Autism-Spectrum Disorder Rett Syndrome

Frequent collaborators

Rod Bremner