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Molecular Therapy. Nucleic Acids
|
March 31, 2022
mRNA-mediated delivery of gene editing tools to human primary muscle stem cells
Christian Stadelmann, Silvia Di Francescantonio, Andreas Marg, et al.
Molecular Therapy. Nucleic Acids
|
March 3, 2023
Cas9-induced single cut enables highly efficient and template-free repair of a muscular dystrophy causing founder mutation
Stefanie Müthel, Andreas Marg, Busem Ignak, et al.
Traffic (Copenhagen, Denmark)
|
June 12, 2012
Sarcolemmal repair is a slow process and includes EHD2
Andreas Marg, Verena Schoewel, Tobias Timmel, et al.
Plos One
|
November 28, 2012
Dysferlin-peptides reallocate mutated dysferlin thereby restoring function
Verena Schoewel, Andreas Marg, Severine Kunz, et al.
The Journal of Clinical Investigation
|
August 27, 2014
Human satellite cells have regenerative capacity and are genetically manipulable
Andreas Marg, Helena Escobar, Sina Gloy, et al.
Clinical and Vaccine Immunology : CVI
|
October 6, 2006
Development of novel immunoglobulin G (IgG), IgA, and IgM enzyme immunoassays based on recombinant Puumala and Dobrava hantavirus nucleocapsid proteins
Helga Meisel, Anne Wolbert, Ausra Razanskiene, et al.
Animal Models and Experimental Medicine
|
October 8, 2022
Human primary muscle stem cells regenerate injured urethral sphincter in athymic rats
Biniam M Bekele, Verena Schöwel-Wolf, Janine Kieshauer, et al.
Molecular Therapy. Nucleic Acids
|
October 7, 2018
Exon Skipping in a Dysf-Missense Mutant Mouse Model
Jakub Malcher, Leonie Heidt, Aurélie Goyenvalle, et al.
Journal of Autoimmunity
|
August 15, 2016
The immunoproteasomes are key to regulate myokines and MHC class I expression in idiopathic inflammatory myopathies
Salyan Bhattarai, Khetam Ghannam, Sabine Krause, et al.
Nature Communications
|
January 3, 2025
Gene-editing in patient and humanized-mice primary muscle stem cells rescues dysferlin expression in dysferlin-deficient muscular dystrophy
Helena Escobar, Silvia Di Francescantonio, Julia Smirnova, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Molecular Therapy. Nucleic Acids
|
March 31, 2022
mRNA-mediated delivery of gene editing tools to human primary muscle stem cells
Christian Stadelmann, Silvia Di Francescantonio, Andreas Marg, et al.
Molecular Therapy. Nucleic Acids
|
March 3, 2023
Cas9-induced single cut enables highly efficient and template-free repair of a muscular dystrophy causing founder mutation
Stefanie Müthel, Andreas Marg, Busem Ignak, et al.
Traffic (Copenhagen, Denmark)
|
June 12, 2012
Sarcolemmal repair is a slow process and includes EHD2
Andreas Marg, Verena Schoewel, Tobias Timmel, et al.
Plos One
|
November 28, 2012
Dysferlin-peptides reallocate mutated dysferlin thereby restoring function
Verena Schoewel, Andreas Marg, Severine Kunz, et al.
The Journal of Clinical Investigation
|
August 27, 2014
Human satellite cells have regenerative capacity and are genetically manipulable
Andreas Marg, Helena Escobar, Sina Gloy, et al.
Clinical and Vaccine Immunology : CVI
|
October 6, 2006
Development of novel immunoglobulin G (IgG), IgA, and IgM enzyme immunoassays based on recombinant Puumala and Dobrava hantavirus nucleocapsid proteins
Helga Meisel, Anne Wolbert, Ausra Razanskiene, et al.
Animal Models and Experimental Medicine
|
October 8, 2022
Human primary muscle stem cells regenerate injured urethral sphincter in athymic rats
Biniam M Bekele, Verena Schöwel-Wolf, Janine Kieshauer, et al.
Molecular Therapy. Nucleic Acids
|
October 7, 2018
Exon Skipping in a Dysf-Missense Mutant Mouse Model
Jakub Malcher, Leonie Heidt, Aurélie Goyenvalle, et al.
Journal of Autoimmunity
|
August 15, 2016
The immunoproteasomes are key to regulate myokines and MHC class I expression in idiopathic inflammatory myopathies
Salyan Bhattarai, Khetam Ghannam, Sabine Krause, et al.
Nature Communications
|
January 3, 2025
Gene-editing in patient and humanized-mice primary muscle stem cells rescues dysferlin expression in dysferlin-deficient muscular dystrophy
Helena Escobar, Silvia Di Francescantonio, Julia Smirnova, et al.
Page
of 3