Publications by authors named "Maurice Overzier"

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Learning, memory and blood-brain barrier pathology in Duchenne muscular dystrophy mice lacking Dp427, or Dp427 and Dp140.
Minou Verhaeg, Kevin Adamzek, Davy van de Vijver, Kayleigh Putker, Sarah Engelbeen, Maurice Overzier

Genes Brain Behav· June 2024

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Antisense oligonucleotide-mediated disruption of HTT caspase-6 cleavage site ameliorates the phenotype of YAC128 Huntington disease mice.
Elsa C Kuijper, Maurice Overzier, Ernst Suidgeest, Oleh Dzyubachyk, Cécile Maguin

Neurobiol Dis· January 2024

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Longitudinal Assessment of Creatine Kinase, Creatine/Creatinine, and Myostatin as Monitoring Biomarkers in Becker Muscular Dystrophy.
Nienke M van de Velde, Zaïda Koeks, Mirko Signorelli, Nisha Verwey, Maurice Overzier

Neurology· February 2023

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Huntington Disease Gene Expression Signatures in Blood Compared to Brain of YAC128 Mice as Candidates for Monitoring of Pathology.
Elsa C Kuijper, Lodewijk J A Toonen, Maurice Overzier, Roula Tsonaka, Kristina Hettne

Mol Neurobiol· April 2022

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Broad phenotype of cysteine-altering variants in UK Biobank: CADASIL to nonpenetrance.
Julie W Rutten, Remco J Hack, Marco Duering, Gido Gravesteijn, Johannes G Dauwerse, Maurice Overzier

Neurology· September 2020

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Naturally occurring NOTCH3 exon skipping attenuates NOTCH3 protein aggregation and disease severity in CADASIL patients.
Gido Gravesteijn, Johannes G Dauwerse, Maurice Overzier, Gwendolyn Brouwer, Ingrid Hegeman

Hum Mol Genet· July 2020

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Progression and Classification of Granular Osmiophilic Material (GOM) Deposits in Functionally Characterized Human NOTCH3 Transgenic Mice.
Gido Gravesteijn, Leon P Munting, Maurice Overzier, Aat A Mulder, Ingrid Hegeman

Transl Stroke Res· June 2020

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Implications of increased S100β and Tau5 proteins in dystrophic nerves of two mdx mouse models for Duchenne muscular dystrophy.
Vidya S Krishnan, Annemieke Aartsma-Rus, Maurice Overzier, Cathleen Lutz, Laurent Bogdanik

Mol Cell Neurosci· June 2020

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Natural disease history of the D2 mouse model for Duchenne muscular dystrophy.
Maaike van Putten, Kayleigh Putker, Maurice Overzier, W A Adamzek, Svetlana Pasteuning-Vuhman

FASEB J· July 2019

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Transcriptional profiling and biomarker identification reveal tissue specific effects of expanded ataxin-3 in a spinocerebellar ataxia type 3 mouse model.
Lodewijk J A Toonen, Maurice Overzier, Melvin M Evers, Leticia G Leon, Sander A J van der Zeeuw

Mol Neurodegener· June 2018

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New function of the myostatin/activin type I receptor (ALK4) as a mediator of muscle atrophy and muscle regeneration.
Svitlana Pasteuning-Vuhman, Johanna W Boertje-van der Meulen, Maaike van Putten, Maurice Overzier, Peter Ten Dijke

FASEB J· January 2017

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