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Arnaud F Klein

Showing results (1-10 of 15) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|October 6, 2019
FISH Protocol for Myotonic Dystrophy Type 1 CellsArnaud F Klein, Ludovic Arandel, Joelle Marie, et al.
Frontiers in Neurology|June 8, 2018
Cells of Matter-<i>In Vitro</i> Models for Myotonic DystrophyMagdalena Matloka, Arnaud F Klein, Frédérique Rau, et al.
Nature Structural & Molecular Biology|December 28, 2010
Selective silencing of mutated mRNAs in DM1 by using modified hU7-snRNAsVirginie François, Arnaud F Klein, Cyriaque Beley, et al.
Nucleic Acids Research|December 14, 2011
New function for the RNA helicase p68/DDX5 as a modifier of MBNL1 activity on expanded CUG repeatsFrançois-Xavier Laurent, Alain Sureau, Arnaud F Klein, et al.
The American Journal of Pathology|February 28, 2009
Large CTG repeats trigger p16-dependent premature senescence in myotonic dystrophy type 1 muscle precursor cellsAnne Bigot, Arnaud F Klein, Erwan Gasnier, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 9, 2021
Comprehensive transcriptome-wide analysis of spliceopathy correction of myotonic dystrophy using CRISPR-Cas9 in iPSCs-derived cardiomyocytesSumitava Dastidar, Debanjana Majumdar, Jaitip Tipanee, et al.
Experimental Cell Research|March 28, 2008
PABPN1 polyalanine tract deletion and long expansions modify its aggregation pattern and expressionArnaud F Klein, Mitsuru Ebihara, Christine Alexander, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 30, 2019
Genome Editing of Expanded CTG Repeats within the Human DMPK Gene Reduces Nuclear RNA Foci in the Muscle of DM1 MiceMirella Lo Scrudato, Karine Poulard, Célia Sourd, et al.
Neurobiology of Disease|July 25, 2006
The dynamism of PABPN1 nuclear inclusions during the cell cycleA Marie-Josée Sasseville, Antoine W Caron, Lucie Bourget, et al.
The Journal of Clinical Investigation|September 4, 2019
Peptide-conjugated oligonucleotides evoke long-lasting myotonic dystrophy correction in patient-derived cells and miceArnaud F Klein, Miguel A Varela, Ludovic Arandel, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|October 6, 2019
FISH Protocol for Myotonic Dystrophy Type 1 CellsArnaud F Klein, Ludovic Arandel, Joelle Marie, et al.
Frontiers in Neurology|June 8, 2018
Cells of Matter-<i>In Vitro</i> Models for Myotonic DystrophyMagdalena Matloka, Arnaud F Klein, Frédérique Rau, et al.
Nature Structural & Molecular Biology|December 28, 2010
Selective silencing of mutated mRNAs in DM1 by using modified hU7-snRNAsVirginie François, Arnaud F Klein, Cyriaque Beley, et al.
Nucleic Acids Research|December 14, 2011
New function for the RNA helicase p68/DDX5 as a modifier of MBNL1 activity on expanded CUG repeatsFrançois-Xavier Laurent, Alain Sureau, Arnaud F Klein, et al.
The American Journal of Pathology|February 28, 2009
Large CTG repeats trigger p16-dependent premature senescence in myotonic dystrophy type 1 muscle precursor cellsAnne Bigot, Arnaud F Klein, Erwan Gasnier, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 9, 2021
Comprehensive transcriptome-wide analysis of spliceopathy correction of myotonic dystrophy using CRISPR-Cas9 in iPSCs-derived cardiomyocytesSumitava Dastidar, Debanjana Majumdar, Jaitip Tipanee, et al.
Experimental Cell Research|March 28, 2008
PABPN1 polyalanine tract deletion and long expansions modify its aggregation pattern and expressionArnaud F Klein, Mitsuru Ebihara, Christine Alexander, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 30, 2019
Genome Editing of Expanded CTG Repeats within the Human DMPK Gene Reduces Nuclear RNA Foci in the Muscle of DM1 MiceMirella Lo Scrudato, Karine Poulard, Célia Sourd, et al.
Neurobiology of Disease|July 25, 2006
The dynamism of PABPN1 nuclear inclusions during the cell cycleA Marie-Josée Sasseville, Antoine W Caron, Lucie Bourget, et al.
The Journal of Clinical Investigation|September 4, 2019
Peptide-conjugated oligonucleotides evoke long-lasting myotonic dystrophy correction in patient-derived cells and miceArnaud F Klein, Miguel A Varela, Ludovic Arandel, et al.
Pageof 2