Aurea B. Bach-Martins

Oxford, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications

Corrigendum to "TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43" [Neurobiology of disease Volume 193, April 2024, 106437].

Corrigendum to "TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43" [Neurobiology of disease Volume 193, April 2024, 106437].

Journal: Neurobiology of disease
Published: October 27, 2024

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

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

Journal: Neurobiology of disease
Published: December 15, 2023

Lasting dynamic effects of the psychedelic 2,5-dimethoxy-4-iodoamphetamine ((±)-DOI) on cognitive flexibility.

Lasting dynamic effects of the psychedelic 2,5-dimethoxy-4-iodoamphetamine ((±)-DOI) on cognitive flexibility.

Journal: Molecular psychiatry
Published: July 05, 2023

Protocol for tissue processing and paraffin embedding of mouse brains following ex vivo MRI.

Protocol for tissue processing and paraffin embedding of mouse brains following ex vivo MRI.

Journal: STAR protocols
Published: June 01, 2023

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

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

Journal: Disease models & mechanisms
Published: March 21, 2023

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

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

Journal: Frontiers in systems neuroscience
Published: December 30, 2022

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

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

Journal: Nature neuroscience
Published: August 11, 2021

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

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

Journal: Scientific reports
Published: March 03, 2020

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

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

Journal: Scientific reports
Published: November 14, 2018

A normal life without muscle dystrophin.

A normal life without muscle dystrophin.

Journal: Neuromuscular disorders : NMD
Published: November 27, 2014

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

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

Journal: The American journal of pathology
Published: November 18, 2014

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.

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.

Journal: PloS one
Published: August 19, 2014
Showing 1-12 of 13

Last Updated: 09/26/2026