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Journal of Molecular Medicine (Berlin, Germany)
|
April 24, 2013
Role of dynamin 2 in the disassembly of focal adhesions
Laura Briñas, Stéphane Vassilopoulos, Gisèle Bonne, et al.
Molecular Therapy. Nucleic Acids
|
September 14, 2016
Reprogramming the Dynamin 2 mRNA by Spliceosome-mediated RNA Trans-splicing
Delphine Trochet, Bernard Prudhon, Arnaud Jollet, et al.
Cell Communication and Signaling : CCS
|
October 22, 2025
Lamin A/C protects chromatin accessibility during mechanical loading in human skeletal muscle
Saline Jabre, Emeline Cherchame, Natalia Pinzón, et al.
Scientific Reports
|
February 9, 2019
Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model
Anaïs Fongy, Sestina Falcone, Jeanne Lainé, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
May 7, 2002
The HERV-W/7q family in the human genome. Potential for protein expression and gene regulation
Patrick M Alliel, Jean-Pierre Périn, Danièle Goudou, et al.
American Journal of Human Genetics
|
September 19, 2025
Allele-specific RNAi therapy corrects an extracellular matrix defect in Schuurs-Hoeijmakers syndrome
Lylia Mekzine, Natalia Pinzón, Kamel Mamchaoui, et al.
Neuromuscular Disorders : NMD
|
April 9, 2008
A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findings
Marc Bitoun, Tanya Stojkovic, Bernard Prudhon, et al.
Molecular Therapy. Nucleic Acids
|
September 12, 2022
Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations
Swati Dudhal, Lylia Mekzine, Bernard Prudhon, et al.
Muscle & Nerve
|
December 25, 2003
Neuromuscular expression of the BTB/POZ and zinc finger protein myoneurin
Carmen Cifuentes-Diaz, Marc Bitoun, Daniele Goudou, et al.
Molecular Therapy. Nucleic Acids
|
March 14, 2022
Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy
Delphine Trochet, Bernard Prudhon, Lylia Mekzine, et al.
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of 6
Search research articles
Search
Showing results (11-20 of 54) with videos related to
Sort By:
Page
of 6
Journal of Molecular Medicine (Berlin, Germany)
|
April 24, 2013
Role of dynamin 2 in the disassembly of focal adhesions
Laura Briñas, Stéphane Vassilopoulos, Gisèle Bonne, et al.
Molecular Therapy. Nucleic Acids
|
September 14, 2016
Reprogramming the Dynamin 2 mRNA by Spliceosome-mediated RNA Trans-splicing
Delphine Trochet, Bernard Prudhon, Arnaud Jollet, et al.
Cell Communication and Signaling : CCS
|
October 22, 2025
Lamin A/C protects chromatin accessibility during mechanical loading in human skeletal muscle
Saline Jabre, Emeline Cherchame, Natalia Pinzón, et al.
Scientific Reports
|
February 9, 2019
Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model
Anaïs Fongy, Sestina Falcone, Jeanne Lainé, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
May 7, 2002
The HERV-W/7q family in the human genome. Potential for protein expression and gene regulation
Patrick M Alliel, Jean-Pierre Périn, Danièle Goudou, et al.
American Journal of Human Genetics
|
September 19, 2025
Allele-specific RNAi therapy corrects an extracellular matrix defect in Schuurs-Hoeijmakers syndrome
Lylia Mekzine, Natalia Pinzón, Kamel Mamchaoui, et al.
Neuromuscular Disorders : NMD
|
April 9, 2008
A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findings
Marc Bitoun, Tanya Stojkovic, Bernard Prudhon, et al.
Molecular Therapy. Nucleic Acids
|
September 12, 2022
Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations
Swati Dudhal, Lylia Mekzine, Bernard Prudhon, et al.
Muscle & Nerve
|
December 25, 2003
Neuromuscular expression of the BTB/POZ and zinc finger protein myoneurin
Carmen Cifuentes-Diaz, Marc Bitoun, Daniele Goudou, et al.
Molecular Therapy. Nucleic Acids
|
March 14, 2022
Benefits of therapy by dynamin-2-mutant-specific silencing are maintained with time in a mouse model of dominant centronuclear myopathy
Delphine Trochet, Bernard Prudhon, Lylia Mekzine, et al.
Page
of 6