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Denis Furling

Showing results (71-80 of 80) with videos related to

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Disease Models & Mechanisms|February 12, 2017
Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compoundsLudovic Arandel, Micaela Polay Espinoza, Magdalena Matloka, et al.
Nature Biomedical Engineering|February 11, 2022
Reversal of RNA toxicity in myotonic dystrophy via a decoy RNA-binding protein with high affinity for expanded CUG repeatsLudovic Arandel, Magdalena Matloka, Arnaud F Klein, et al.
Nature Communications|May 29, 2015
Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophyFrédérique Rau, Jeanne Lainé, Laetitita Ramanoudjame, et al.
Cell Reports|June 29, 2017
Downregulation of the Glial GLT1 Glutamate Transporter and Purkinje Cell Dysfunction in a Mouse Model of Myotonic DystrophyGéraldine Sicot, Laurent Servais, Diana M Dinca, et al.
Nature Communications|May 24, 2018
rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differencesChantal Sellier, Estefanía Cerro-Herreros, Markus Blatter, et al.
Neurology. Genetics|March 4, 2021
New recessive mutations in <i>SYT2</i> causing severe presynaptic congenital myasthenic syndromesStéphanie Bauché, Alain Sureau, Damien Sternberg, et al.
Nucleic Acids Research|June 28, 2018
Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cellsSumitava Dastidar, Simon Ardui, Kshitiz Singh, et al.
The Journal of Biological Chemistry|April 2, 2011
Analysis of exonic regions involved in nuclear localization, splicing activity, and dimerization of Muscleblind-like-1 isoformsHélène Tran, Nathalie Gourrier, Camille Lemercier-Neuillet, et al.
Nature Medicine|May 31, 2011
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophyCharlotte Fugier, Arnaud F Klein, Caroline Hammer, et al.
Nature Communications|April 12, 2016
Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophyFernande Freyermuth, Frédérique Rau, Yosuke Kokunai, et al.
Pageof 8

Showing results (71-80 of 80) with videos related to

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Pageof 8
You have reached the last page of results.This site can display upto 80 results.
Disease Models & Mechanisms|February 12, 2017
Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compoundsLudovic Arandel, Micaela Polay Espinoza, Magdalena Matloka, et al.
Nature Biomedical Engineering|February 11, 2022
Reversal of RNA toxicity in myotonic dystrophy via a decoy RNA-binding protein with high affinity for expanded CUG repeatsLudovic Arandel, Magdalena Matloka, Arnaud F Klein, et al.
Nature Communications|May 29, 2015
Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophyFrédérique Rau, Jeanne Lainé, Laetitita Ramanoudjame, et al.
Cell Reports|June 29, 2017
Downregulation of the Glial GLT1 Glutamate Transporter and Purkinje Cell Dysfunction in a Mouse Model of Myotonic DystrophyGéraldine Sicot, Laurent Servais, Diana M Dinca, et al.
Nature Communications|May 24, 2018
rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differencesChantal Sellier, Estefanía Cerro-Herreros, Markus Blatter, et al.
Neurology. Genetics|March 4, 2021
New recessive mutations in <i>SYT2</i> causing severe presynaptic congenital myasthenic syndromesStéphanie Bauché, Alain Sureau, Damien Sternberg, et al.
Nucleic Acids Research|June 28, 2018
Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cellsSumitava Dastidar, Simon Ardui, Kshitiz Singh, et al.
The Journal of Biological Chemistry|April 2, 2011
Analysis of exonic regions involved in nuclear localization, splicing activity, and dimerization of Muscleblind-like-1 isoformsHélène Tran, Nathalie Gourrier, Camille Lemercier-Neuillet, et al.
Nature Medicine|May 31, 2011
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophyCharlotte Fugier, Arnaud F Klein, Caroline Hammer, et al.
Nature Communications|April 12, 2016
Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophyFernande Freyermuth, Frédérique Rau, Yosuke Kokunai, et al.
Pageof 8