Worldwide-Sodium-Channel-Seminars

Past Events

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Dravet syndrome is severe childhood-onset epilepsy, caused by loss of function mutations in the SCN1A gene. Novel therapies aim to restore SCN1A expression in order to address all disease manifestations.

Lille, France

Past Events

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This meeting will be dedicated to exploring ion channel regulation from molecular biophysics to physiology and clinical applications in cancer biology. Meeting will also include one ECS session: "Calcium signaling in cancer".

Worldwide-Sodium-Channel-Seminars

Past Events

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Repurposing VGSC-inhibiting medications to cancer may hold promise for reducing metastasis.

AnnaGrekaWebinar-2022 - Life Sciences Switzerland

Past Events

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Anna Greka leads a program focused on dissecting fundamental mechanisms of disrupted cellular homeostasis in genetically-defined kidney, metabolic and degenerative diseases...

Worldwide-Sodium-Channel-Seminars

Past Events

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The pharmacological activity of pain-causing toxins can provide critical insights into the molecular mechanisms underpinning sensory neuron function and pain...

Metrion Biosciences

Past Events

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Many de novo missense mutations of SCN8A, the gene that encodes for Nav1.6, have been identified and patients have seizure onset between birth and 12 months of age...