Michael E. Hildebrand

发表

Contributions of T-Type Voltage-Gated Calcium Channels to Postsynaptic Calcium Signaling within Purkinje Neurons

Philippe Isope, P. Isope, T. Snutch, 2010, The Cerebellum.

A novel slow-inactivation-specific ion channel modulator attenuates neuropathic pain

Gerald W. Zamponi, David Parker, Hassan Pajouhesh, 2011, PAIN®.

Functional Coupling between mGluR1 and Cav3.1 T-Type Calcium Channels Contributes to Parallel Fiber-Induced Fast Calcium Signaling within Purkinje Cell Dendritic Spines

Masahiko Watanabe, Masanobu Kano, Toni Schneider, 2009, The Journal of Neuroscience.

Selective Inhibition of Cav3.3 T-type Calcium Channels by Gαq/11-coupled Muscarinic Acetylcholine Receptors*

T. Snutch, Esperanza García, G. Zamponi, 2007, Journal of Biological Chemistry.

Conserved contributions of NMDA receptor subtypes to synaptic responses in lamina II spinal neurons across early postnatal development

Michael E. Hildebrand, Hadir Mahmoud, Newton Martin, 2020, Molecular Brain.

The Human Motoneuron Expression Signature is Defined by ALS-Related Genes

Ariel J. Levine, M. Nalls, V. Menon, 2022 .

A cellular taxonomy of the adult human spinal cord

Ariel J. Levine, M. Nalls, V. Menon, 2022, Neuron.

Potentiation of Synaptic GluN2B NMDAR Currents by Fyn Kinase Is Gated through BDNF-Mediated Disinhibition in Spinal Pain Processing.

P. Lombroso, Jian Xu, S. Beggs, 2016, Cell reports.

The T‐type calcium channel antagonist, Z944, reduces spinal excitability and pain hypersensitivity

Erika K. Harding, R. Bonin, M. Salter, 2021, British journal of pharmacology.

Sexual dimorphism in a neuronal mechanism of spinal hyperexcitability across rodent and human models of pathological pain

Y. de Koninck, P. Lombroso, Jian Xu, 2021, bioRxiv.

Potentiation of Synaptic G luN 2 BNMDARCurrents by Fyn Kinase Is Gated through BDNF-Mediated Disinhibition in Spinal Pain Processing Graphical

P. Lombroso, Jian Xu, S. Beggs, 2016 .

Contributions of T-Type Voltage-Gated Calcium Channels to Postsynaptic Calcium Signaling within Purkinje Neurons

P. Isope, T. Snutch, Michael E. Hildebrand, 2010, The Cerebellum.

Ion Channels and Electrophysiological Properties of Astrocytes: Implications for Emergent Stimulation Technologies

Chris Rudyk, Michael E. Hildebrand, N. Salmaso, 2021, Frontiers in Cellular Neuroscience.

GluN2B and GluN2D NMDARs dominate synaptic responses in the adult spinal cord

Erika K. Harding, S. Beggs, M. Salter, 2014, Scientific Reports.

Calcium-permeable ion channels in pain signaling.

C. Altier, M. Salter, T. Trang, 2014, Physiological reviews.

Activation of Corticotropin-Releasing Factor Receptor 1 Selectively Inhibits CaV3.2 T-Type Calcium Channels

T. Soong, T. Snutch, M. C. Liang, 2008, Molecular Pharmacology.

T-type calcium channels

M. C. Liang, Ping Liao, Michael E. Hildebrand, 2008 .

Mammalian Voltage-Gated Calcium Channels Are Potently Blocked by the Pyrethroid Insecticide Allethrin

T. Snutch, J. McRory, Michael E. Hildebrand, 2004, Journal of Pharmacology and Experimental Therapeutics.

The CACNA1F Gene Encodes an L-Type Calcium Channel with Unique Biophysical Properties and Tissue Distribution

Aaron M. Beedle, Terrance P Snutch, Lina Chen, 2004, The Journal of Neuroscience.

Functional implications of a novel EA2 mutation in the P/Q‐type calcium channel

T. Bird, T. Snutch, S. Spacey, 2004, Annals of neurology.

Loss of STEP61 couples disinhibition to N-methyl-d-aspartate receptor potentiation in rodent and human spinal pain processing

Y. de Koninck, P. Lombroso, Jian Xu, 2019, Brain : a journal of neurology.

Contributions of T-type calcium channels to the pathophysiology of pain signaling

T. Snutch, Michael E. Hildebrand, 2006 .

RESEARCH PAPER The transient receptor potential channel antagonist SKF96365 is a potent blocker of low-voltage-activated T-type calcium channels

T. Snutch, Esperanza García, Michael E. Hildebrand, 2010 .

Inhibition of High Voltage-Activated Calcium Channels by Spider Toxin PnTx3-6

C. Kushmerick, T. Snutch, Esperanza García, 2005, Journal of Pharmacology and Experimental Therapeutics.

Advances and Barriers in Understanding Presynaptic N-Methyl-D-Aspartate Receptors in Spinal Pain Processing

Michael E. Hildebrand, Annemarie Dedek, 2022, Frontiers in Molecular Neuroscience.

Differential expression of GluN2 NMDA receptor subunits in the dorsal horn of male and female rats

Chris Rudyk, Michael E. Hildebrand, N. Salmaso, 2021, Channels.

Identification of sodium channel isoforms that mediate action potential firing in lamina I/II spinal cord neurons

M. Salter, T. Snutch, Paula L. Smith, 2011, Molecular pain.

T-Type Calcium Channels and Epilepsy

T. Snutch, S. Cain, Michael E. Hildebrand, 2014 .

Cord Pain Processing Circuits Moving From an Averaged to Specific View of Spinal

Masahiko Watanabe, A. Todd, R. Callister, 2015 .

Conserved contributions of NMDA receptor subtypes to synaptic responses in lamina II spinal neurons across early postnatal development

Michael E. Hildebrand, Hadir Mahmoud, Newton Martin, 2020, Molecular Brain.

The transient receptor potential channel antagonist SKF96365 is a potent blocker of low‐voltage‐activated T‐type calcium channels

T. Snutch, T. Snutch, Esperanza García, 2010, British journal of pharmacology.

Heterogeneity of synaptic NMDA receptor responses within individual lamina I pain processing neurons across sex in rats and humans

Michael E. Hildebrand, J. Krajewski, Eve C. Tsai, 2023, bioRxiv.

A novel slow-inactivation-specific ion channel modulator attenuates neuropathic pain

S. Arneric, C. Bladen, F. Belardetti, 2011, PAIN®.