Maaike A. Van Putten
Leiden, ZH, Netherlands
Last Updated: 09/26/2026
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Found 72 publications
Four new mouse models of Duchenne muscular dystrophy with clinically relevant exon deletions in the human DMD gene.
Journal: Disease models & mechanisms
Published: February 12, 2026
Unraveling the spatial landscape of dystrophinopathies: a transcriptomic approach to Becker and Duchenne muscular dystrophies.
Journal: The Journal of pathology
Published: November 10, 2025
Myonuclear Domain-Associated and Central Nucleation-Dependent Spatial Restriction of Dystrophin Protein Expression.
Journal: Journal of cachexia, sarcopenia and muscle
Published: October 02, 2025
Antisense-mediated exon skipping therapy improves neuromuscular junction deficits in a Duchenne muscular dystrophy mouse model.
Journal: Neuromuscular disorders : NMD
Published: August 27, 2025
Regional Expression of Dystrophin Gene Transcripts and Proteins in the Mouse Brain.
Journal: Cells
Published: August 06, 2025
Understanding Duchenne muscular dystrophy-associated brain pathology.
Journal: Disease models & mechanisms
Published: August 01, 2025
A two-site collaborative study of electrical impedance myography for evaluation of disease progression in murine Duchenne muscular dystrophy models.
Journal: Scientific reports
Published: April 22, 2025
Antisense oligonucleotide-mediated redirection of Igf1 alternative polyadenylation.
Journal: Neuromuscular disorders : NMD
Published: December 19, 2024
Identification of suitable qPCR reference genes for the normalization of gene expression in the BL10-mdx and D2-mdx mouse models of Duchenne muscular dystrophy.
Journal: PloS one
Published: November 12, 2024
The behavioural consequences of dystrophinopathy.
Journal: Disease models & mechanisms
Published: August 02, 2024
Antisense Oligonucleotide-Mediated Downregulation of IGFBPs Enhances IGF-1 Signaling.
Journal: Journal of neuromuscular diseases
Published: January 08, 2024
Last Updated: 09/26/2026