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Hierarchical CRMP2 posttranslational modifications control NaV1.7 function

Proceedings of the National Academy of Sciences - PNAS, 2016-12, Vol.113 (52), p.E8443-E8452

2016

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CRMP2 Protein SUMOylation Modulates NaV1.7 Channel Trafficking

The Journal of biological chemistry, 2013-08, Vol.288 (34), p.24316-24331

2013

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Orexin Depolarizes Central Amygdala Neurons via Orexin Receptor 1, Phospholipase C and Sodium-Calcium Exchanger and Modulates Conditioned Fear

Frontiers in neuroscience, 2018-12, Vol.12, p.934-934

2018

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Carbamazepine potentiates the effectiveness of morphine in a rodent model of neuropathic pain

PloS one, 2014-09, Vol.9 (9), p.e107399

2014

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Mining the Na v 1.7 interactome: Opportunities for chronic pain therapeutics

Biochemical pharmacology, 2019-05, Vol.163, p.9

2019

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Sensitization of Ion Channels Contributes to Central and Peripheral Dysfunction in Neurofibromatosis Type 1

Molecular neurobiology, 2017-07, Vol.54 (5), p.3342-3349

2017

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Inhibition of the Ubc9 E2 SUMO-conjugating enzyme-CRMP2 interaction decreases NaV1.7 currents and reverses experimental neuropathic pain

Pain (Amsterdam), 2018-10, Vol.159 (10), p.2115-2127

2018

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Dissecting the role of the CRMP2-neurofibromin complex on pain behaviors

Pain (Amsterdam), 2017-11, Vol.158 (11), p.2203-2221

2017

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The small molecule GAT1508 activates brain-specific GIRK1/2 channel heteromers and facilitates conditioned fear extinction in rodents

The Journal of biological chemistry, 2020-03, Vol.295 (11), p.3614-3634

2020

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Homology‐guided mutational analysis reveals the functional requirements for antinociceptive specificity of collapsin response mediator protein 2‐derived peptides

British journal of pharmacology, 2018-06, Vol.175 (12), p.2244-2260

2018

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Mining the Nav1.7 interactome: Opportunities for chronic pain therapeutics

Biochemical pharmacology, 2019-05, Vol.163, p.9-20

2019

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Chimeric derivatives of functionalized amino acids and α-aminoamides: Compounds with anticonvulsant activity in seizure models and inhibitory actions on central, peripheral, and cardiac isoforms of voltage-gated sodium channels

Bioorganic & medicinal chemistry, 2015-07, Vol.23 (13), p.3655-3666

2015

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Inhibition of Transmitter Release and Attenuation of Anti-retroviral-associated and Tibial Nerve Injury-related Painful Peripheral Neuropathy by Novel Synthetic Ca2+ Channel Peptides

The Journal of biological chemistry, 2012-10, Vol.287 (42), p.35065-35077

2012

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(Biphenyl-4-yl)methylammonium Chlorides: Potent Anticonvulsants That Modulate Na+ Currents

Journal of medicinal chemistry, 2013-07, Vol.56 (14), p.5931-5939

2013

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Substituted N‑(Biphenyl-4′-yl)methyl (R)‑2-Acetamido-3-methoxypropionamides: Potent Anticonvulsants That Affect Frequency (Use) Dependence and Slow Inactivation of Sodium Channels

Journal of medicinal chemistry, 2014-07, Vol.57 (14), p.6165-6182

2014

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Chimeric Agents Derived from the Functionalized Amino Acid, Lacosamide, and the α‑Aminoamide, Safinamide: Evaluation of Their Inhibitory Actions on Voltage-Gated Sodium Channels, and Antiseizure and Antinociception Activities and Comparison with Lacosamide and Safinamide

ACS chemical neuroscience, 2015-02, Vol.6 (2), p.316-330

2015

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Discovery of Lacosamide Affinity Bait Agents That Exhibit Potent Voltage-Gated Sodium Channel Blocking Properties

ACS chemical neuroscience, 2013-03, Vol.4 (3), p.463-474

2013

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Identification of the Benzyloxyphenyl Pharmacophore: A Structural Unit That Promotes Sodium Channel Slow Inactivation

ACS chemical neuroscience, 2012-12, Vol.3 (12), p.1037-1049

2012

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A single structurally conserved SUMOylation site in CRMP2 controls NaV1.7 function

Channels (Austin, Tex.), 2017-07, Vol.11 (4), p.316-328

2017

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S38. Dissecting the Functional Heterogeneity of Serotonergic Systems That Regulate Fear and Panic

Biological psychiatry (1969), 2019-05, Vol.85 (10), p.S311-S311

2019

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Role of PSD95 and nNOS Interaction in Gene Regulation following Fear Conditioning and Implications for Molecular Mechanisms Underlying Post-Traumatic Stress Disorder

Biological psychiatry (1969), 2020-05, Vol.87 (9), p.S334

2020

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F10. Cue-Induced Conditioned Fear Learning Requires Orexin Receptor 1 Signaling in the Central Amygdala

Biological psychiatry (1969), 2019-05, Vol.85 (10), p.S216-S217

2019

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74. Mechanisms of Agoraphobia: Contribution of Orexin and mGluR2 Signaling in the Amygdala

Biological psychiatry (1969), 2019-05, Vol.85 (10), p.S30-S31

2019

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77822 PSD95-nNOS interaction alters the basolateral amygdala transcriptome following fear conditioning: implications for molecular mechanisms underlying PTSD

Journal of clinical and translational science, 2021-03, Vol.5 (s1), p.23-23

2021

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4335 Role of PSD95 and nNOS interaction in gene regulation following fear conditioning and implications for molecular mechanisms underlying PTSD

Journal of clinical and translational science, 2020-06, Vol.4 (s1), p.15-16

2020

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Hierarchical CRMP2 posttranslational modifications control NaV1.7 function

CRMP2 Protein SUMOylation Modulates NaV1.7 Channel Trafficking

Orexin Depolarizes Central Amygdala Neurons via Orexin Receptor 1, Phospholipase C and Sodium-Calcium Exchanger and Modulates Conditioned Fear

Carbamazepine potentiates the effectiveness of morphine in a rodent model of neuropathic pain

Mining the Na v 1.7 interactome: Opportunities for chronic pain therapeutics

Sensitization of Ion Channels Contributes to Central and Peripheral Dysfunction in Neurofibromatosis Type 1

Inhibition of the Ubc9 E2 SUMO-conjugating enzyme-CRMP2 interaction decreases NaV1.7 currents and reverses experimental neuropathic pain

Dissecting the role of the CRMP2-neurofibromin complex on pain behaviors

The small molecule GAT1508 activates brain-specific GIRK1/2 channel heteromers and facilitates conditioned fear extinction in rodents

Homology‐guided mutational analysis reveals the functional requirements for antinociceptive specificity of collapsin response mediator protein 2‐derived peptides

Mining the Nav1.7 interactome: Opportunities for chronic pain therapeutics

Chimeric derivatives of functionalized amino acids and α-aminoamides: Compounds with anticonvulsant activity in seizure models and inhibitory actions on central, peripheral, and cardiac isoforms of voltage-gated sodium channels

Inhibition of Transmitter Release and Attenuation of Anti-retroviral-associated and Tibial Nerve Injury-related Painful Peripheral Neuropathy by Novel Synthetic Ca2+ Channel Peptides

(Biphenyl-4-yl)methylammonium Chlorides: Potent Anticonvulsants That Modulate Na+ Currents

Substituted N‑(Biphenyl-4′-yl)methyl (R)‑2-Acetamido-3-methoxypropionamides: Potent Anticonvulsants That Affect Frequency (Use) Dependence and Slow Inactivation of Sodium Channels

Chimeric Agents Derived from the Functionalized Amino Acid, Lacosamide, and the α‑Aminoamide, Safinamide: Evaluation of Their Inhibitory Actions on Voltage-Gated Sodium Channels, and Antiseizure and Antinociception Activities and Comparison with Lacosamide and Safinamide

Discovery of Lacosamide Affinity Bait Agents That Exhibit Potent Voltage-Gated Sodium Channel Blocking Properties

Identification of the Benzyloxyphenyl Pharmacophore: A Structural Unit That Promotes Sodium Channel Slow Inactivation

A single structurally conserved SUMOylation site in CRMP2 controls NaV1.7 function

S38. Dissecting the Functional Heterogeneity of Serotonergic Systems That Regulate Fear and Panic

Role of PSD95 and nNOS Interaction in Gene Regulation following Fear Conditioning and Implications for Molecular Mechanisms Underlying Post-Traumatic Stress Disorder

F10. Cue-Induced Conditioned Fear Learning Requires Orexin Receptor 1 Signaling in the Central Amygdala

74. Mechanisms of Agoraphobia: Contribution of Orexin and mGluR2 Signaling in the Amygdala

77822 PSD95-nNOS interaction alters the basolateral amygdala transcriptome following fear conditioning: implications for molecular mechanisms underlying PTSD

4335 Role of PSD95 and nNOS interaction in gene regulation following fear conditioning and implications for molecular mechanisms underlying PTSD

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