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Benjamin Currall

Showing results (1-10 of 21) with videos related to

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Journal of Neurophysiology|August 5, 2011
The roles of conserved and nonconserved cysteinyl residues in the oligomerization and function of mammalian prestinBenjamin Currall, Danielle Rossino, Heather Jensen-Smith, et al.
Brain Research|April 22, 2006
Studying inner ear protein-protein interactions using FRET and FLIMRichard Hallworth, Benjamin Currall, Michael G Nichols, et al.
Hearing Research|October 30, 2007
Streptomycin and gentamicin have no immediate effect on outer hair cell electromotilityXiang Wang, Shuping Jia, Benjamin Currall, et al.
Developmental Neurobiology|April 20, 2007
Prestin-prestin and prestin-GLUT5 interactions in HEK293T cellsXudong Wu, Benjamin Currall, Tetsuji Yamashita, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 8, 2008
Fluorescence microscopy methods in the study of protein structure and functionHeather Jensen-Smith, Benjamin Currall, Danielle Rossino, et al.
Biorxiv : the Preprint Server for Biology|October 9, 2023
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous systemRicardo Harripaul, Elisabetta Morini, Monica Salani, et al.
Scientific Reports|January 4, 2024
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous systemRicardo Harripaul, Elisabetta Morini, Monica Salani, et al.
Cell Reports Methods|December 13, 2023
Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR librariesXander Nuttle, Nicholas D Burt, Benjamin Currall, et al.
American Journal of Human Genetics|October 21, 2021
Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelinAloysius Domingo, Rachita Yadav, Shivangi Shah, et al.
Human Molecular Genetics|December 28, 2018
Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactionsThomas Arbogast, Parisa Razaz, Jacob Ellegood, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Journal of Neurophysiology|August 5, 2011
The roles of conserved and nonconserved cysteinyl residues in the oligomerization and function of mammalian prestinBenjamin Currall, Danielle Rossino, Heather Jensen-Smith, et al.
Brain Research|April 22, 2006
Studying inner ear protein-protein interactions using FRET and FLIMRichard Hallworth, Benjamin Currall, Michael G Nichols, et al.
Hearing Research|October 30, 2007
Streptomycin and gentamicin have no immediate effect on outer hair cell electromotilityXiang Wang, Shuping Jia, Benjamin Currall, et al.
Developmental Neurobiology|April 20, 2007
Prestin-prestin and prestin-GLUT5 interactions in HEK293T cellsXudong Wu, Benjamin Currall, Tetsuji Yamashita, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 8, 2008
Fluorescence microscopy methods in the study of protein structure and functionHeather Jensen-Smith, Benjamin Currall, Danielle Rossino, et al.
Biorxiv : the Preprint Server for Biology|October 9, 2023
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous systemRicardo Harripaul, Elisabetta Morini, Monica Salani, et al.
Scientific Reports|January 4, 2024
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous systemRicardo Harripaul, Elisabetta Morini, Monica Salani, et al.
Cell Reports Methods|December 13, 2023
Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR librariesXander Nuttle, Nicholas D Burt, Benjamin Currall, et al.
American Journal of Human Genetics|October 21, 2021
Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelinAloysius Domingo, Rachita Yadav, Shivangi Shah, et al.
Human Molecular Genetics|December 28, 2018
Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactionsThomas Arbogast, Parisa Razaz, Jacob Ellegood, et al.
Pageof 3