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.
Duchenne muscular dystrophy (DMD) is an X-linked disorder that is caused by mutations in the DMD gene, leading to progressive muscle wasting and weakness. There is currently no cure for DMD. The BL10-mdx mouse is the most commonly used model in preclinical DMD studies, but it exhibits a mild disease...
Saved in:
| Main Authors: | Kayleigh Putker, Anne-Fleur Schneider, Davy Van De Vijver, John Hildyard, Annemieke Aartsma-Rus, Maaike van Putten |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2025-01-01
|
| Series: | PLoS ONE |
| Online Access: | https://doi.org/10.1371/journal.pone.0318944 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Transcriptomic profiling of skeletal muscle in the DMD mdx rat model of Duchenne muscular dystrophy
by: Abdolvahab Ebrahimpour Gorji, et al.
Published: (2025-08-01) -
Importância do camundongo mdx na fisiopatologia da distrofia muscular de Duchenne The importance of mdx mouse in the pathophysiology of Duchenne's muscular distrophy
by: Sandra Lopes Seixas, et al.
Published: (1997-09-01) -
Respiratory pathology in the mdx/utrn -/- mouse: A murine model for Duchenne Muscular Dystrophy (DMD).
by: Marán Y Hernández Rodríguez, et al.
Published: (2025-01-01) -
Dystropathology increases energy expenditure and protein turnover in the mdx mouse model of duchenne muscular dystrophy.
by: Hannah G Radley-Crabb, et al.
Published: (2014-01-01) -
Brain glucose metabolism as a neuronal substrate of the abnormal behavioral response to stress in the mdx mouse, a model of Duchenne muscular dystrophy
by: Sébastien Goutal, et al.
Published: (2025-01-01)