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Alfred L George

Showing results (131-140 of 296) with videos related to

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Neuromuscular Disorders : NMD|September 11, 2007
Reduced expression of Kir6.2/SUR2A subunits explains KATP deficiency in K+-depleted ratsDomenico Tricarico, Antonietta Mele, Birgit Liss, et al.
Heart Rhythm|February 4, 2009
A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndromeLia Crotti, Marzena A Lewandowska, Peter J Schwartz, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 populationVlasta Bari, Andrea Marchi, Giulia Girardengo, et al.
The Journal of Physiology|January 13, 2010
The KATP channel is a molecular sensor of atrophy in skeletal muscleDomenico Tricarico, Antonietta Mele, Giulia Maria Camerino, et al.
Pharmacogenetics|September 30, 2003
Genotype-phenotype associations for common CYP3A4 and CYP3A5 variants in the basal and induced metabolism of midazolam in European- and African-American men and womenMichael D Floyd, Guillermo Gervasini, Andrew L Masica, et al.
Plos One|February 6, 2013
A data similarity-based strategy for meta-analysis of transcriptional profiles in cancerQingchao Qiu, Pengcheng Lu, Yuzhu Xiang, et al.
Circulation|April 2, 2008
Cardiac sodium channel (SCN5A) variants associated with atrial fibrillationDawood Darbar, Prince J Kannankeril, Brian S Donahue, et al.
Kidney International|June 18, 2004
Mutant prenyltransferase-like mitochondrial protein (PLMP) and mitochondrial abnormalities in kd/kd miceMin Peng, Leonard Jarett, Ray Meade, et al.
The Journal of Biological Chemistry|February 18, 2021
Disease-linked supertrafficking of a potassium channelHui Huang, Laura M Chamness, Carlos G Vanoye, et al.
Biorxiv : the Preprint Server for Biology|August 6, 2025
Machine Learning Resolves Functional Phenotypes and Therapeutic Responses in KCNQ2 Developmental Epileptic Encephalopathy iPSC ModelsDina Simkin, Syed M A Wafa, Mennat Gharib, et al.
Pageof 30

Showing results (131-140 of 296) with videos related to

Sort By:
Pageof 30
Neuromuscular Disorders : NMD|September 11, 2007
Reduced expression of Kir6.2/SUR2A subunits explains KATP deficiency in K+-depleted ratsDomenico Tricarico, Antonietta Mele, Birgit Liss, et al.
Heart Rhythm|February 4, 2009
A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndromeLia Crotti, Marzena A Lewandowska, Peter J Schwartz, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 populationVlasta Bari, Andrea Marchi, Giulia Girardengo, et al.
The Journal of Physiology|January 13, 2010
The KATP channel is a molecular sensor of atrophy in skeletal muscleDomenico Tricarico, Antonietta Mele, Giulia Maria Camerino, et al.
Pharmacogenetics|September 30, 2003
Genotype-phenotype associations for common CYP3A4 and CYP3A5 variants in the basal and induced metabolism of midazolam in European- and African-American men and womenMichael D Floyd, Guillermo Gervasini, Andrew L Masica, et al.
Plos One|February 6, 2013
A data similarity-based strategy for meta-analysis of transcriptional profiles in cancerQingchao Qiu, Pengcheng Lu, Yuzhu Xiang, et al.
Circulation|April 2, 2008
Cardiac sodium channel (SCN5A) variants associated with atrial fibrillationDawood Darbar, Prince J Kannankeril, Brian S Donahue, et al.
Kidney International|June 18, 2004
Mutant prenyltransferase-like mitochondrial protein (PLMP) and mitochondrial abnormalities in kd/kd miceMin Peng, Leonard Jarett, Ray Meade, et al.
The Journal of Biological Chemistry|February 18, 2021
Disease-linked supertrafficking of a potassium channelHui Huang, Laura M Chamness, Carlos G Vanoye, et al.
Biorxiv : the Preprint Server for Biology|August 6, 2025
Machine Learning Resolves Functional Phenotypes and Therapeutic Responses in KCNQ2 Developmental Epileptic Encephalopathy iPSC ModelsDina Simkin, Syed M A Wafa, Mennat Gharib, et al.
Pageof 30