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Direct measurement of TRPV4 and PIEZO1 activity reveals multiple mechanotransduction pathways in chondrocytes

eLife, 2017-01, Vol.6

2017

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Regulation of body weight and energy homeostasis by neuronal cell adhesion molecule 1

Nature neuroscience, 2017-08, Vol.20 (8), p.1096-1103

2017

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Small-molecule inhibition of STOML3 oligomerization reverses pathological mechanical hypersensitivity

Nature neuroscience, 2017-02, Vol.20 (2), p.209-218

2017

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Hypofunctional TrkA Accounts for the Absence of Pain Sensitization in the African Naked Mole-Rat

Cell reports (Cambridge), 2016-10, Vol.17 (3), p.748-758

2016

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Human α3β4 neuronal nicotinic receptors show different stoichiometry if they are expressed in Xenopus oocytes or mammalian HEK293 cells

PloS one, 2010-10, Vol.5 (10), p.e13611-e13611

2010

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Stoichiometry and Pharmacology of Two Human α4β2 Nicotinic Receptor Types

Journal of molecular neuroscience, 2006, Vol.30 (1-2), p.95-96

2006

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Sensory mechanotransduction at membrane-matrix interfaces

Pflügers Archiv, 2015-01, Vol.467 (1), p.121-132

2015

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alpha 4 beta 2 Nicotinic Receptors with High and Low Acetylcholine Sensitivity: Pharmacology, Stoichiometry, and Sensitivity to Long-Term Exposure to Nicotine

Molecular pharmacology, 2006-08, Vol.70 (2), p.755-768

2006

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α4β2 Nicotinic Receptors with High and Low Acetylcholine Sensitivity: Pharmacology, Stoichiometry, and Sensitivity to Long-Term Exposure to Nicotine

Molecular pharmacology, 2006-08, Vol.70 (2), p.755-768

2006

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GABA Blocks Pathological but Not Acute TRPV1 Pain Signals

Cell, 2015-02, Vol.160 (4), p.759-770

2015

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SUMOylation of Enzymes and Ion Channels in Sensory Neurons Protects against Metabolic Dysfunction, Neuropathy, and Sensory Loss in Diabetes

Neuron (Cambridge, Mass.), 2020-09, Vol.107 (6), p.1141-1159.e7

2020

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Human alpha 3 beta 4 Neuronal Nicotinic Receptors Show Different Stoichiometry if They Are Expressed in Xenopus Oocytes or Mammalian HEK293 Cells

PloS one, 2010-10, Vol.5

2010

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The α1K276E startle disease mutation reveals multiple intermediate states in the gating of glycine receptors

The Journal of neuroscience, 2012-01, Vol.32 (4), p.1336-1352

2012

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The kinetic properties of the [alpha]3 rat glycine receptor make it suitable for mediating fast synaptic inhibition

The Journal of physiology, 2013-07, Vol.591 (13), p.3289

2013

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The kinetic properties of the α3 rat glycine receptor make it suitable for mediating fast synaptic inhibition

The Journal of physiology, 2013-07, Vol.591 (13), p.3289-3308

2013

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The kinetic properties of the alpha 3 rat glycine receptor make it suitable for mediating fast synaptic inhibition

The Journal of physiology, 2013-07, Vol.591 (13), p.3289-3308

2013

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The Activation Mechanism of Rat α3 Homomeric Glycine Receptors

Biophysical journal, 2013-01, Vol.104 (2), p.638a-638a

2013

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Chloride ions in the pore of glycine and GABA channels shape the time course and voltage dependence of agonist currents

The Journal of neuroscience, 2011-10, Vol.31 (40), p.14095-14106

2011

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Phosphorylation and Function of α4β2 Receptor

Journal of molecular neuroscience, 2006-09, Vol.30 (1-2), p.97-98

2006

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Sazetidine-A Is a Potent and Selective Agonist at Native and Recombinant α4β2 Nicotinic Acetylcholine Receptors

Molecular pharmacology, 2008-06, Vol.73 (6), p.1838-1843

2008

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Sazetidine-A is a potent and selective agonist at native and recombinant alpha 4 beta 2 nicotinic acetylcholine receptors

Molecular pharmacology, 2008-06, Vol.73 (6), p.1838-1843

2008

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Molecular Determinants in Glycine and GABA-A Receptors that Sense Intracellular Chloride Concentration

Biophysical journal, 2010-01, Vol.98 (3), p.704a-704a

2010

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The K276E Startle Disease Mutation in the Glycine Receptor: Effects on Channel Gating

Biophysical journal, 2011-02, Vol.100 (3), p.433a-433a

2011

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Experimentally induced aggressiveness in heroin-dependent patients treated with buprenorphine: Comparison of patients receiving methadone and healthy subjects

Psychiatry research, 2007-01, Vol.149 (1), p.201-213

2007

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Direct measurement of TRPV4 and PIEZO1 activity reveals multiple mechanotransduction pathways in chondrocytes

TMEM87a/Elkin1, a component of a novel mechanoelectrical transduction pathway, modulates melanoma adhesion and migration

Regulation of body weight and energy homeostasis by neuronal cell adhesion molecule 1

Small-molecule inhibition of STOML3 oligomerization reverses pathological mechanical hypersensitivity

Hypofunctional TrkA Accounts for the Absence of Pain Sensitization in the African Naked Mole-Rat

Human α3β4 neuronal nicotinic receptors show different stoichiometry if they are expressed in Xenopus oocytes or mammalian HEK293 cells

Stoichiometry and Pharmacology of Two Human α4β2 Nicotinic Receptor Types

Sensory mechanotransduction at membrane-matrix interfaces

alpha 4 beta 2 Nicotinic Receptors with High and Low Acetylcholine Sensitivity: Pharmacology, Stoichiometry, and Sensitivity to Long-Term Exposure to Nicotine

α4β2 Nicotinic Receptors with High and Low Acetylcholine Sensitivity: Pharmacology, Stoichiometry, and Sensitivity to Long-Term Exposure to Nicotine

GABA Blocks Pathological but Not Acute TRPV1 Pain Signals

SUMOylation of Enzymes and Ion Channels in Sensory Neurons Protects against Metabolic Dysfunction, Neuropathy, and Sensory Loss in Diabetes

Human alpha 3 beta 4 Neuronal Nicotinic Receptors Show Different Stoichiometry if They Are Expressed in Xenopus Oocytes or Mammalian HEK293 Cells

The α1K276E startle disease mutation reveals multiple intermediate states in the gating of glycine receptors

The kinetic properties of the [alpha]3 rat glycine receptor make it suitable for mediating fast synaptic inhibition

The kinetic properties of the α3 rat glycine receptor make it suitable for mediating fast synaptic inhibition

The kinetic properties of the alpha 3 rat glycine receptor make it suitable for mediating fast synaptic inhibition

The Activation Mechanism of Rat α3 Homomeric Glycine Receptors

Chloride ions in the pore of glycine and GABA channels shape the time course and voltage dependence of agonist currents

Phosphorylation and Function of α4β2 Receptor

Sazetidine-A Is a Potent and Selective Agonist at Native and Recombinant α4β2 Nicotinic Acetylcholine Receptors

Sazetidine-A is a potent and selective agonist at native and recombinant alpha 4 beta 2 nicotinic acetylcholine receptors

Molecular Determinants in Glycine and GABA-A Receptors that Sense Intracellular Chloride Concentration

The K276E Startle Disease Mutation in the Glycine Receptor: Effects on Channel Gating

Experimentally induced aggressiveness in heroin-dependent patients treated with buprenorphine: Comparison of patients receiving methadone and healthy subjects

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