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Publications

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TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43

Godoy-Corchuelo JM. et al, (2023)

Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations.

Ali Z. et al, (2023), Dis Model Mech, 16

FUSDelta14 mutation impairs normal brain development and causes systemic metabolic alterations

Godoy-Corchuelo JM. et al, (2023)

7,8-dihydroxyflavone enhances long-term spatial memory and alters brain volume in wildtype mice.

Rawlings-Mortimer F. et al, (2023), Front Syst Neurosci, 17

Phenotypic and genetic associations of quantitative magnetic susceptibility in UK Biobank brain imaging.

Wang C. et al, (2022), Nat Neurosci, 25, 818 - 831

Non-invasive assessment of skeletal muscle fibrosis in mice using nuclear magnetic resonance imaging and ultrasound shear wave elastography.

Martins-Bach AB. et al, (2021), Sci Rep, 11

Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model.

Fongy A. et al, (2019), Sci Rep, 9

Structural and Functional Alterations of Skeletal Muscle Microvasculature in Dystrophin-Deficient mdx Mice.

Latroche C. et al, (2015), Am J Pathol, 185, 2482 - 2494

A normal life without muscle dystrophin.

Zatz M. et al, (2015), Neuromuscul Disord, 25, 371 - 374

Quantitative T2 combined with texture analysis of nuclear magnetic resonance images identify different degrees of muscle involvement in three mouse models of muscle dystrophy: mdx, Largemyd and mdx/Largemyd.

Martins-Bach AB. et al, (2015), PLoS One, 10

Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies.

Martins PCM. et al, (2013), Dis Model Mech, 6, 1167 - 1174

Metabolic profile of dystrophic mdx mouse muscles analyzed with in vitro magnetic resonance spectroscopy (MRS).

Martins-Bach AB. et al, (2012), Magn Reson Imaging, 30, 1167 - 1176

Include forthcoming?