List of works - Xiaoyang Cheng

A Highly Conserved Salt Bridge Stabilizes the Kinked Conformation of β2,3-Sheet Essential for Channel Function of P2X4 Receptors

scientific article published on 10 February 2016

A channelopathy contributes to cerebellar dysfunction in a model of multiple sclerosis.

scientific article published in February 2012

An ankyrinG-binding motif is necessary and sufficient for targeting Nav1.6 sodium channels to axon initial segments and nodes of Ranvier

scientific article

Biphasic modulation of ryanodine binding to sarcoplasmic reticulum vesicles of skeletal muscle by Zn2+ ions.

scientific article published on January 2000

Carbon monoxide dilates cerebral arterioles by enhancing the coupling of Ca2+ sparks to Ca2+-activated K+ channels.

scientific article published in October 2002

De Novo Pathogenic SCN8A Mutation Identified by Whole-Genome Sequencing of a Family Quartet Affected by Infantile Epileptic Encephalopathy and SUDEP ⬇️

scientific article (publication date: 9 March 2012)

Deletion mutation of sodium channel Na(V)1.7 in inherited erythromelalgia: enhanced slow inactivation modulates dorsal root ganglion neuron hyperexcitability.

scientific article published in July 2011

Effect of zinc ions on caffeine-induced contracture in vascular smooth muscle and skeletal muscle of rat.

scientific article

Exploration of the Peptide Recognition of an Amiloride-sensitive FMRFamide Peptide-gated Sodium Channel.

scientific article published on 11 February 2016

FGF13 Selectively Regulates Heat Nociception by Interacting with Nav1.7.

scientific article published on 30 January 2017

Genetic ablation of caveolin-1 modifies Ca2+ spark coupling in murine arterial smooth muscle cells.

scientific article

Intersubunit physical couplings fostered by the left flipper domain facilitate channel opening of P2X4 receptors

scientific article published on 16 March 2017

Mutation I136V alters electrophysiological properties of the Na(v)1.7 channel in a family with onset of erythromelalgia in the second decade

scientific article

Mutations at opposite ends of the DIII/S4-S5 linker of sodium channel Na V 1.7 produce distinct pain disorders

scientific article

N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita.

scientific article published on 20 September 2017

Relative motions between left flipper and dorsal fin domains favour P2X4 receptor activation

scientific article published on 19 June 2014

Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorder.

scientific article published on 22 January 2016

Sodium-calcium exchanger and multiple sodium channel isoforms in intra-epidermal nerve terminals.

scientific article published on 30 November 2010

The nonproton ligand of acid-sensing ion channel 3 activates mollusk-specific FaNaC channels via a mechanism independent of the native FMRFamide peptide.

scientific article published on 9 November 2017

Virus-mediated shRNA knockdown of Na(v)1.3 in rat dorsal root ganglion attenuates nerve injury-induced neuropathic pain

scientific article published on 21 August 2012

[EXPRESS] Nav1.7 is phosphorylated by Fyn tyrosine kinase which modulates channel expression and gating in a cell type-dependent manner.

scientific article

List of works by Xiaoyang Cheng

A Highly Conserved Salt Bridge Stabilizes the Kinked Conformation of β2,3-Sheet Essential for Channel Function of P2X4 Receptors

A channelopathy contributes to cerebellar dysfunction in a model of multiple sclerosis.

An ankyrinG-binding motif is necessary and sufficient for targeting Nav1.6 sodium channels to axon initial segments and nodes of Ranvier

Biphasic modulation of ryanodine binding to sarcoplasmic reticulum vesicles of skeletal muscle by Zn2+ ions.

Carbon monoxide dilates cerebral arterioles by enhancing the coupling of Ca2+ sparks to Ca2+-activated K+ channels.

De Novo Pathogenic SCN8A Mutation Identified by Whole-Genome Sequencing of a Family Quartet Affected by Infantile Epileptic Encephalopathy and SUDEP ⬇️

Deletion mutation of sodium channel Na(V)1.7 in inherited erythromelalgia: enhanced slow inactivation modulates dorsal root ganglion neuron hyperexcitability.

Effect of zinc ions on caffeine-induced contracture in vascular smooth muscle and skeletal muscle of rat.

Exploration of the Peptide Recognition of an Amiloride-sensitive FMRFamide Peptide-gated Sodium Channel.

FGF13 Selectively Regulates Heat Nociception by Interacting with Nav1.7.

Genetic ablation of caveolin-1 modifies Ca2+ spark coupling in murine arterial smooth muscle cells.

Intersubunit physical couplings fostered by the left flipper domain facilitate channel opening of P2X4 receptors

Mutation I136V alters electrophysiological properties of the Na(v)1.7 channel in a family with onset of erythromelalgia in the second decade

Mutations at opposite ends of the DIII/S4-S5 linker of sodium channel Na V 1.7 produce distinct pain disorders

N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita.

Relative motions between left flipper and dorsal fin domains favour P2X4 receptor activation

Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorder.

Sodium-calcium exchanger and multiple sodium channel isoforms in intra-epidermal nerve terminals.

The nonproton ligand of acid-sensing ion channel 3 activates mollusk-specific FaNaC channels via a mechanism independent of the native FMRFamide peptide.

Virus-mediated shRNA knockdown of Na(v)1.3 in rat dorsal root ganglion attenuates nerve injury-induced neuropathic pain

[EXPRESS] Nav1.7 is phosphorylated by Fyn tyrosine kinase which modulates channel expression and gating in a cell type-dependent manner.