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Maaike van Putten

Showing results (41-50 of 61) with videos related to

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Neuromuscular Disorders : NMD|November 9, 2025
Antisense-mediated exon skipping therapy improves neuromuscular junction deficits in a Duchenne muscular dystrophy mouse modelElizabeth M van der Pijl, Svetlana Pasteuning-Vuhman, Johanna Boertje-van der Meulen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 6, 2013
Low dystrophin levels increase survival and improve muscle pathology and function in dystrophin/utrophin double-knockout miceMaaike van Putten, Margriet Hulsker, Courtney Young, et al.
Cells|September 26, 2025
Regional Expression of Dystrophin Gene Transcripts and Proteins in the Mouse BrainKonstantina Tetorou, Artadokht Aghaeipour, Shunyi Ma, et al.
Plos One|February 22, 2018
A dystrophic Duchenne mouse model for testing human antisense oligonucleotidesMarcel Veltrop, Laura van Vliet, Margriet Hulsker, et al.
Plos One|December 28, 2020
Detailed genetic and functional analysis of the hDMDdel52/mdx mouse modelAlper Yavas, Rudie Weij, Maaike van Putten, et al.
Journal of Cachexia, Sarcopenia and Muscle|April 7, 2026
Myonuclear Domain-Associated and Central Nucleation-Dependent Spatial Restriction of Dystrophin Protein ExpressionKatarzyna Chwalenia, Vivi-Yun Feng, Nicole Hemmer, et al.
Plos One|February 24, 2012
The effects of low levels of dystrophin on mouse muscle function and pathologyMaaike van Putten, Margriet Hulsker, Vishna Devi Nadarajah, et al.
Neuromuscular Disorders : NMD|January 31, 2012
Comparison of skeletal muscle pathology and motor function of dystrophin and utrophin deficient mouse strainsMaaike van Putten, Darshan Kumar, Margriet Hulsker, et al.
Biomedicines|December 23, 2023
Networking to Optimize <i>Dmd</i> exon 53 Skipping in the Brain of <i>mdx52</i> Mouse ModelMathilde Doisy, Ophélie Vacca, Claire Fergus, et al.
Scientific Reports|September 26, 2025
A two-site collaborative study of electrical impedance myography for evaluation of disease progression in murine Duchenne muscular dystrophy modelsPaola Mantuano, Maaike van Putten, Buket Sonbas Cobb, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Neuromuscular Disorders : NMD|November 9, 2025
Antisense-mediated exon skipping therapy improves neuromuscular junction deficits in a Duchenne muscular dystrophy mouse modelElizabeth M van der Pijl, Svetlana Pasteuning-Vuhman, Johanna Boertje-van der Meulen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 6, 2013
Low dystrophin levels increase survival and improve muscle pathology and function in dystrophin/utrophin double-knockout miceMaaike van Putten, Margriet Hulsker, Courtney Young, et al.
Cells|September 26, 2025
Regional Expression of Dystrophin Gene Transcripts and Proteins in the Mouse BrainKonstantina Tetorou, Artadokht Aghaeipour, Shunyi Ma, et al.
Plos One|February 22, 2018
A dystrophic Duchenne mouse model for testing human antisense oligonucleotidesMarcel Veltrop, Laura van Vliet, Margriet Hulsker, et al.
Plos One|December 28, 2020
Detailed genetic and functional analysis of the hDMDdel52/mdx mouse modelAlper Yavas, Rudie Weij, Maaike van Putten, et al.
Journal of Cachexia, Sarcopenia and Muscle|April 7, 2026
Myonuclear Domain-Associated and Central Nucleation-Dependent Spatial Restriction of Dystrophin Protein ExpressionKatarzyna Chwalenia, Vivi-Yun Feng, Nicole Hemmer, et al.
Plos One|February 24, 2012
The effects of low levels of dystrophin on mouse muscle function and pathologyMaaike van Putten, Margriet Hulsker, Vishna Devi Nadarajah, et al.
Neuromuscular Disorders : NMD|January 31, 2012
Comparison of skeletal muscle pathology and motor function of dystrophin and utrophin deficient mouse strainsMaaike van Putten, Darshan Kumar, Margriet Hulsker, et al.
Biomedicines|December 23, 2023
Networking to Optimize <i>Dmd</i> exon 53 Skipping in the Brain of <i>mdx52</i> Mouse ModelMathilde Doisy, Ophélie Vacca, Claire Fergus, et al.
Scientific Reports|September 26, 2025
A two-site collaborative study of electrical impedance myography for evaluation of disease progression in murine Duchenne muscular dystrophy modelsPaola Mantuano, Maaike van Putten, Buket Sonbas Cobb, et al.
Pageof 7