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TRPV1 Receptors in the CNS Play a Key Role in Broad-Spectrum Analgesia of TRPV1 Antagonists

The Journal of neuroscience, 2006-09, Vol.26 (37), p.9385-9393

2006

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Distribution and functional characterization of human Nav1.3 splice variants

The European journal of neuroscience, 2005-07, Vol.22 (1), p.1-9

2005

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Elevated temperatures alter TRPV1 agonist-evoked excitability of dorsal root ganglion neurons

Inflammation research, 2008-09, Vol.57 (9), p.404-409

2008

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Spontaneous and gamma-aminobutyric acid (GABA)-activated GABA(A) receptor channels formed by epsilon subunit-containing isoforms

Molecular pharmacology, 1999-01, Vol.55 (1), p.168-178

1999

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Incorporation of the pi subunit into functional gamma-aminobutyric Acid(A) receptors

Molecular pharmacology, 1999-09, Vol.56 (3), p.598-610

1999

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Functional Expression of L-, N-, P/Q-, and R-Type Calcium Channels in the Human NT2-N Cell Line

Journal of neurophysiology, 2000-12, Vol.84 (6), p.2933-2944

2000

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Small-conductance calcium-activated potassium currents in mouse hyperexcitable denervated skeletal muscle

The Journal of physiology, 2001-10, Vol.536 (2), p.397-407

2001

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Involvement of the TTX-resistant sodium channel Nav 1.8 in inflammatory and neuropathic, but not post-operative, pain states

Pain (Amsterdam), 2006-07, Vol.123 (1), p.75-82

2006

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GABA(A) receptors expressed in undifferentiated human teratocarcinoma NT2 cells differ from those expressed by differentiated NT2-N cells

The Journal of neuroscience, 1999-08, Vol.19 (16), p.7057-7065

1999

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534 Defining a mechanistic link between TRPV3 activity and psoriasis through IL-1α and EGFR signaling pathways

Journal of investigative dermatology, 2016-05, Vol.136 (5), p.S94-S94

2016

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Drama and Theatre in Urban Contexts

1, 2013

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Cohort Profile: The Applied Research Group for Kids (TARGet Kids!)

International journal of epidemiology, 2015-06, Vol.44 (3), p.776-788

2015

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A-1048400 is a novel, orally active, state-dependent neuronal calcium channel blocker that produces dose-dependent antinociception without altering hemodynamic function in rats

Biochemical pharmacology, 2012-02, Vol.83 (3), p.406-418

2012

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Contrasting actions of lanthanum on different recombinant gamma-aminobutyric acid receptor isoforms expressed in L929 fibroblasts

Molecular pharmacology, 1997-02, Vol.51 (2), p.328-335

1997

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Domains Responsible for Constitutive and Ca2+-Dependent Interactions between Calmodulin and Small Conductance Ca2+-Activated Potassium Channels

The Journal of neuroscience, 1999-10, Vol.19 (20), p.8830-8838

1999

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Domains responsible for constitutive and Ca(2+)-dependent interactions between calmodulin and small conductance Ca(2+)-activated potassium channels

The Journal of neuroscience, 1999-10, Vol.19 (20), p.8830

1999

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Association between total duration of breastfeeding and iron deficiency

Pediatrics (Evanston), 2013-05, Vol.131 (5), p.e1530-e1537

2013

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Expression of Functional GABA A Receptors in Transfected L929 Cells Isolated by Immunomagnetic Bead Separation

Neuropharmacology, 1997-01, Vol.36 (1), p.63-73

1997

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Pharmacology of modality-specific transient receptor potential vanilloid-1 antagonists that do not alter body temperature

The Journal of pharmacology and experimental therapeutics, 2012-08, Vol.342 (2), p.416-428

2012

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Respiration and Parturition Affected by Conditional Overexpression of the Ca2+-Activated K+Channel Subunit, SK3

Science (American Association for the Advancement of Science), 2000-09, Vol.289 (5486), p.1942-1946

2000

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BL-1249 [(5,6,7,8-tetrahydro-naphthalen-1-yl)-[2-(1H-tetrazol-5-yl)-phenyl]-amine]: a putative potassium channel opener with bladder-relaxant properties

The Journal of pharmacology and experimental therapeutics, 2005-04, Vol.313 (1), p.250-259

2005

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Development and validation of a medium-throughput electrophysiological assay for KCNQ2/3 channel openers using QPatch HT

Assay and drug development technologies, 2013-02, Vol.11 (1), p.17-24

2013

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Respiration and parturition affected by conditional overexpression of the Ca(2+)-activated K(+) channel subunit, SK3

Science (American Association for the Advancement of Science), 2000-09, Vol.289 (5486), p.1942-1946

2000

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TRPV1 Receptors in the CNS Play a Key Role in Broad-Spectrum Analgesia of TRPV1 Antagonists

Distribution and functional characterization of human Nav1.3 splice variants

Elevated temperatures alter TRPV1 agonist-evoked excitability of dorsal root ganglion neurons

Spontaneous and gamma-aminobutyric acid (GABA)-activated GABA(A) receptor channels formed by epsilon subunit-containing isoforms

Incorporation of the pi subunit into functional gamma-aminobutyric Acid(A) receptors

Functional Expression of L-, N-, P/Q-, and R-Type Calcium Channels in the Human NT2-N Cell Line

Small-conductance calcium-activated potassium currents in mouse hyperexcitable denervated skeletal muscle

Involvement of the TTX-resistant sodium channel Nav 1.8 in inflammatory and neuropathic, but not post-operative, pain states

GABA(A) receptors expressed in undifferentiated human teratocarcinoma NT2 cells differ from those expressed by differentiated NT2-N cells

534 Defining a mechanistic link between TRPV3 activity and psoriasis through IL-1α and EGFR signaling pathways

Drama and Theatre in Urban Contexts

Cohort Profile: The Applied Research Group for Kids (TARGet Kids!)

A-1048400 is a novel, orally active, state-dependent neuronal calcium channel blocker that produces dose-dependent antinociception without altering hemodynamic function in rats

Contrasting actions of lanthanum on different recombinant gamma-aminobutyric acid receptor isoforms expressed in L929 fibroblasts

Domains Responsible for Constitutive and Ca2+-Dependent Interactions between Calmodulin and Small Conductance Ca2+-Activated Potassium Channels

Domains responsible for constitutive and Ca(2+)-dependent interactions between calmodulin and small conductance Ca(2+)-activated potassium channels

Association between total duration of breastfeeding and iron deficiency

Expression of Functional GABA A Receptors in Transfected L929 Cells Isolated by Immunomagnetic Bead Separation

Pharmacology of modality-specific transient receptor potential vanilloid-1 antagonists that do not alter body temperature

Respiration and Parturition Affected by Conditional Overexpression of the Ca2+-Activated K+Channel Subunit, SK3

BL-1249 [(5,6,7,8-tetrahydro-naphthalen-1-yl)-[2-(1H-tetrazol-5-yl)-phenyl]-amine]: a putative potassium channel opener with bladder-relaxant properties

Development and validation of a medium-throughput electrophysiological assay for KCNQ2/3 channel openers using QPatch HT

Respiration and parturition affected by conditional overexpression of the Ca(2+)-activated K(+) channel subunit, SK3

Synthesis and Pharmacology of (Pyridin-2-yl)methanol Derivatives as Novel and Selective Transient Receptor Potential Vanilloid 3 Antagonists

A-995662 [(R)-8-(4-methyl-5-(4-(trifluoromethyl)phenyl)oxazol-2-ylamino)-1,2,3,4-tetrahydronaphthalen-2-ol], a novel, selective TRPV1 receptor antagonist, reduces spinal release of glutamate and CGRP in a rat knee joint pain model

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