Influence of full-length dystrophin on brain volumes in mouse models of Duchenne muscular dystrophy
Citations Over Time
Abstract
Duchenne muscular dystrophy (DMD) affects besides muscle also the brain, resulting in memory and behavioral problems. The consequences of dystrophinopathy on gross macroscopic alterations are unclear. To elucidate the effect of full-length dystrophin expression on brain morphology, we used high-resolution post-mortem MRI in mouse models that either express 0% (mdx), 100% (BL10) or a low amount of full-length dystrophin (mdx-XistΔhs). While absence or low amounts of full-length dystrophin did not significantly affect whole brain volume and skull morphology, we found differences in volume of individual brain structures. The results are in line with observations in humans, where whole brain volume was found to be reduced only in patients lacking both full-length dystrophin and the shorter isoform Dp140.
Related Papers
- → Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene(1996)478 cited
- → The Frequency of Revertants in mdx Mouse Genetic Models for Duchenne Muscular Dystrophy(1992)140 cited
- → Current Translational Research and Murine Models For Duchenne Muscular Dystrophy(2016)62 cited
- → Marginal Level Dystrophin Expression Improves Clinical Outcome in a Strain of Dystrophin/Utrophin Double Knockout Mice(2010)55 cited
- → Microarray analysis of mdx mice expressing high levels of utrophin: Therapeutic implications for dystrophin deficiency(2008)30 cited