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Mark I Rees

Showing results (41-50 of 82) with videos related to

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Frontiers in Cellular Neuroscience|April 10, 2023
Complement activation and increased anaphylatoxin receptor expression are associated with cortical grey matter lesions and the compartmentalised inflammatory response of multiple sclerosisRhian Evans, Lewis M Watkins, Kristen Hawkins, et al.
Journal of Cardiovascular Electrophysiology|June 4, 2009
Not all hERG pore domain mutations have a severe phenotype: G584S has an inactivation gating defect with mild phenotype compared to G572S, which has a dominant negative trafficking defect and a severe phenotypeJing Ting Zhao, Adam P Hill, Anthony Varghese, et al.
Heart Rhythm|October 2, 2007
Long QT and Brugada syndrome gene mutations in New ZealandSeo-Kyung Chung, Judith M MacCormick, Caroline H McCulley, et al.
Heart, Lung & Circulation|May 28, 2011
Symptoms and signs associated with syncope in young people with primary cardiac arrhythmiasJudith M MacCormick, Jackie R Crawford, Seo-Kyung Chung, et al.
Neurobiology of Disease|May 5, 2026
A synonymous SLC2A1 variant causes familial epilepsy and paroxysmal exercise-induced dyskinesia by creating aberrant mosaic splicing patternsAdam T Higgins, Fiona Wang, William O Pickrell, et al.
Molecular and Cellular Neurosciences|May 1, 2007
PICK1 interacts with alpha7 neuronal nicotinic acetylcholine receptors and controls their clusteringKristin Baer, Thomas Bürli, Kyung-Hye Huh, et al.
Frontiers in Molecular Neuroscience|April 22, 2010
The glycinergic system in human startle disease: a genetic screening approachJeff S Davies, Seo-Kyung Chung, Rhys H Thomas, et al.
Seizure|December 5, 2021
Epilepsy mortality in Wales during COVID-19Helen Daniels, Arron S Lacey, David Mikadze, et al.
Seizure|October 24, 2017
Validating epilepsy diagnoses in routinely collected dataBeata Fonferko-Shadrach, Arron S Lacey, Catharine P White, et al.
Annals of Neurology|October 27, 2018
Meningeal inflammation and cortical demyelination in acute multiple sclerosisRyan J Bevan, Rhian Evans, Lauren Griffiths, et al.
Pageof 9

Showing results (41-50 of 82) with videos related to

Sort By:
Pageof 9
Frontiers in Cellular Neuroscience|April 10, 2023
Complement activation and increased anaphylatoxin receptor expression are associated with cortical grey matter lesions and the compartmentalised inflammatory response of multiple sclerosisRhian Evans, Lewis M Watkins, Kristen Hawkins, et al.
Journal of Cardiovascular Electrophysiology|June 4, 2009
Not all hERG pore domain mutations have a severe phenotype: G584S has an inactivation gating defect with mild phenotype compared to G572S, which has a dominant negative trafficking defect and a severe phenotypeJing Ting Zhao, Adam P Hill, Anthony Varghese, et al.
Heart Rhythm|October 2, 2007
Long QT and Brugada syndrome gene mutations in New ZealandSeo-Kyung Chung, Judith M MacCormick, Caroline H McCulley, et al.
Heart, Lung & Circulation|May 28, 2011
Symptoms and signs associated with syncope in young people with primary cardiac arrhythmiasJudith M MacCormick, Jackie R Crawford, Seo-Kyung Chung, et al.
Neurobiology of Disease|May 5, 2026
A synonymous SLC2A1 variant causes familial epilepsy and paroxysmal exercise-induced dyskinesia by creating aberrant mosaic splicing patternsAdam T Higgins, Fiona Wang, William O Pickrell, et al.
Molecular and Cellular Neurosciences|May 1, 2007
PICK1 interacts with alpha7 neuronal nicotinic acetylcholine receptors and controls their clusteringKristin Baer, Thomas Bürli, Kyung-Hye Huh, et al.
Frontiers in Molecular Neuroscience|April 22, 2010
The glycinergic system in human startle disease: a genetic screening approachJeff S Davies, Seo-Kyung Chung, Rhys H Thomas, et al.
Seizure|December 5, 2021
Epilepsy mortality in Wales during COVID-19Helen Daniels, Arron S Lacey, David Mikadze, et al.
Seizure|October 24, 2017
Validating epilepsy diagnoses in routinely collected dataBeata Fonferko-Shadrach, Arron S Lacey, Catharine P White, et al.
Annals of Neurology|October 27, 2018
Meningeal inflammation and cortical demyelination in acute multiple sclerosisRyan J Bevan, Rhian Evans, Lauren Griffiths, et al.
Pageof 9