Functional insights from genetic channelopathies [electronic resource] / Stephanie Schorge.

By: Schorge, Stephanie [spk]Material type: FilmFilmSeries: Henry Stewart talksBiomedical & life sciences collection. Genetic basis of neurological disorders: Publisher: London : Henry Stewart Talks, 2014Description: 1 online resource (1 streaming video file (50 min.) : color, sound)Subject(s): Epilepsy -- Genetic aspects | Ion channels | Nervous system -- Diseases -- Genetic aspects | Ataxia -- genetics | Ataxia -- physiopathology | Channelopathies | Epilepsy -- genetics | Epilepsy -- physiopathology | Ion Channels -- genetics | Ion Channels -- physiology | Myotonia CongenitaOnline resources: Click here to access online | Series
Contents:
Contents: Channelopathies in the Genomic Era -- Introduction to ion channels -- The example of Hyperekplexia -- Transcriptional regulation defects of ion channels are associated with cases of schizophrenia and epilepsy -- Ion channels mRNA processing in myotonia congenita and epilepsy -- Ion channel misfolding and episodic ataxia type 1 -- Ion channel mistrafficking and epilepsy -- Ion channel degradation and Spinocerebellar ataxia type 6 -- concluding remarks.
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Animated audio-visual presentation with synchronized narration.

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Contents: Channelopathies in the Genomic Era -- Introduction to ion channels -- The example of Hyperekplexia -- Transcriptional regulation defects of ion channels are associated with cases of schizophrenia and epilepsy -- Ion channels mRNA processing in myotonia congenita and epilepsy -- Ion channel misfolding and episodic ataxia type 1 -- Ion channel mistrafficking and epilepsy -- Ion channel degradation and Spinocerebellar ataxia type 6 -- concluding remarks.

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