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Nathalie Pironon

Showing results (1-10 of 8) with videos related to

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BMC Genomics|March 25, 2010
Molecular and evolutionary characteristics of the fraction of human alpha satellite DNA associated with CENP-A at the centromeres of chromosomes 1, 5, 19, and 21Nathalie Pironon, Jacques Puechberty, Gérard Roizès
Methods in Molecular Biology (Clifton, N.J.)|November 30, 2018
Correction to: Antisense-Mediated Splice Modulation to Reframe TranscriptsMatthias Titeux, Sandrina Turczynski, Nathalie Pironon, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 2, 2018
Antisense-Mediated Splice Modulation to Reframe TranscriptsMatthias Titeux, Sandrina Turczynski, Nathalie Pironon, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 29, 2012
Antisense-mediated exon skipping to reframe transcriptsSandrina Turczynski, Matthias Titeux, Nathalie Pironon, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 2024
Splice modulation strategy applied to deep intronic variants in <i>COL7A1</i> causing recessive dystrophic epidermolysis bullosaNathalie Pironon, Emmanuelle Bourrat, Catherine Prost, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 21, 2010
SIN retroviral vectors expressing COL7A1 under human promoters for ex vivo gene therapy of recessive dystrophic epidermolysis bullosaMatthias Titeux, Valérie Pendaries, Maria A Zanta-Boussif, et al.
European Journal of Human Genetics : EJHG|December 5, 2024
Novel variants impairing Sp1 transcription factor binding in the COL7A1 promoter cause mild cases of recessive dystrophic epidermolysis bullosaNathalie Pironon, Artyom Gasparyan, María Joao Yubero, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2025
A recurrent de novo damaging variant in <i>EMP2</i> causes progressive symmetric erythrokeratodermaXingyuan Jiang, Ryland D Mortlock, Nathalie Pironon, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
BMC Genomics|March 25, 2010
Molecular and evolutionary characteristics of the fraction of human alpha satellite DNA associated with CENP-A at the centromeres of chromosomes 1, 5, 19, and 21Nathalie Pironon, Jacques Puechberty, Gérard Roizès
Methods in Molecular Biology (Clifton, N.J.)|November 30, 2018
Correction to: Antisense-Mediated Splice Modulation to Reframe TranscriptsMatthias Titeux, Sandrina Turczynski, Nathalie Pironon, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 2, 2018
Antisense-Mediated Splice Modulation to Reframe TranscriptsMatthias Titeux, Sandrina Turczynski, Nathalie Pironon, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 29, 2012
Antisense-mediated exon skipping to reframe transcriptsSandrina Turczynski, Matthias Titeux, Nathalie Pironon, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 2024
Splice modulation strategy applied to deep intronic variants in <i>COL7A1</i> causing recessive dystrophic epidermolysis bullosaNathalie Pironon, Emmanuelle Bourrat, Catherine Prost, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 21, 2010
SIN retroviral vectors expressing COL7A1 under human promoters for ex vivo gene therapy of recessive dystrophic epidermolysis bullosaMatthias Titeux, Valérie Pendaries, Maria A Zanta-Boussif, et al.
European Journal of Human Genetics : EJHG|December 5, 2024
Novel variants impairing Sp1 transcription factor binding in the COL7A1 promoter cause mild cases of recessive dystrophic epidermolysis bullosaNathalie Pironon, Artyom Gasparyan, María Joao Yubero, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 4, 2025
A recurrent de novo damaging variant in <i>EMP2</i> causes progressive symmetric erythrokeratodermaXingyuan Jiang, Ryland D Mortlock, Nathalie Pironon, et al.
Pageof 1