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Annual Review of Neuroscience
|
February 1, 2019
Sodium Channels in Human Pain Disorders: Genetics and Pharmacogenomics
Sulayman D Dib-Hajj, Stephen G Waxman
Science Translational Medicine
|
August 15, 2014
Translational pain research: Lessons from genetics and genomics
Sulayman D Dib-Hajj, Stephen G Waxman
The Journal of Clinical Investigation
|
July 1, 2024
Disordered but effective: short linear motifs as gene therapy targets for hyperexcitability disorders
Sulayman D Dib-Hajj, Stephen G Waxman
Neuron
|
September 7, 2023
Na<sub>V</sub>1.7: A central role in pain
Stephen G Waxman, Sulayman D Dib-Hajj
Annals of Neurology
|
June 2, 2005
Erythromelalgia: a hereditary pain syndrome enters the molecular era
Stephen G Waxman, Sulayman D Dib-Hajj
Neuroscience Letters
|
September 7, 2010
Isoform-specific and pan-channel partners regulate trafficking and plasma membrane stability; and alter sodium channel gating properties
Sulayman D Dib-Hajj, Stephen G Waxman
Molecular Brain
|
August 9, 2018
Multiple myosin motors interact with sodium/potassium-ATPase alpha 1 subunits
Bhagirathi Dash, Sulayman D Dib-Hajj, Stephen G Waxman
Molecular Pain
|
June 10, 2010
Effects of ranolazine on wild-type and mutant hNav1.7 channels and on DRG neuron excitability
Mark Estacion, Stephen G Waxman, Sulayman D Dib-Hajj
Molecular Neurobiology
|
November 14, 2002
Structure of the sodium channel gene SCN11A: evidence for intron-to-exon conversion model and implications for gene evolution
Sulayman D Dib-Hajj, Lynda Tyrrell, Stephen G Waxman
Molecular Pharmacology
|
April 19, 2002
Critical molecular determinants of voltage-gated sodium channel sensitivity to mu-conotoxins GIIIA/B
Theodore R Cummins, Fabio Aglieco, Sulayman D Dib-Hajj
Page
of 19
Search research articles
Search
Showing results (1-10 of 184) with videos related to
Sort By:
Page
of 19
Annual Review of Neuroscience
|
February 1, 2019
Sodium Channels in Human Pain Disorders: Genetics and Pharmacogenomics
Sulayman D Dib-Hajj, Stephen G Waxman
Science Translational Medicine
|
August 15, 2014
Translational pain research: Lessons from genetics and genomics
Sulayman D Dib-Hajj, Stephen G Waxman
The Journal of Clinical Investigation
|
July 1, 2024
Disordered but effective: short linear motifs as gene therapy targets for hyperexcitability disorders
Sulayman D Dib-Hajj, Stephen G Waxman
Neuron
|
September 7, 2023
Na<sub>V</sub>1.7: A central role in pain
Stephen G Waxman, Sulayman D Dib-Hajj
Annals of Neurology
|
June 2, 2005
Erythromelalgia: a hereditary pain syndrome enters the molecular era
Stephen G Waxman, Sulayman D Dib-Hajj
Neuroscience Letters
|
September 7, 2010
Isoform-specific and pan-channel partners regulate trafficking and plasma membrane stability; and alter sodium channel gating properties
Sulayman D Dib-Hajj, Stephen G Waxman
Molecular Brain
|
August 9, 2018
Multiple myosin motors interact with sodium/potassium-ATPase alpha 1 subunits
Bhagirathi Dash, Sulayman D Dib-Hajj, Stephen G Waxman
Molecular Pain
|
June 10, 2010
Effects of ranolazine on wild-type and mutant hNav1.7 channels and on DRG neuron excitability
Mark Estacion, Stephen G Waxman, Sulayman D Dib-Hajj
Molecular Neurobiology
|
November 14, 2002
Structure of the sodium channel gene SCN11A: evidence for intron-to-exon conversion model and implications for gene evolution
Sulayman D Dib-Hajj, Lynda Tyrrell, Stephen G Waxman
Molecular Pharmacology
|
April 19, 2002
Critical molecular determinants of voltage-gated sodium channel sensitivity to mu-conotoxins GIIIA/B
Theodore R Cummins, Fabio Aglieco, Sulayman D Dib-Hajj
Page
of 19