Rodent models in Down syndrome research: impact and future opportunities

Y Herault, JM Delabar, EMC Fisher… - Disease models & …, 2017 - journals.biologists.com
Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse
models with Down-syndrome-related features has been developed to understand this …

Transchromosomic technology for genomically humanized animals

T Moriwaki, S Abe, M Oshimura, Y Kazuki - Experimental Cell Research, 2020 - Elsevier
Abstract “Genomically” humanized animals are invaluable tools for generating human
disease models and for biomedical research. Humanized animal models have generally …

Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A

TL Nguyen, A Duchon… - Disease models & …, 2018 - journals.biologists.com
Growing evidence supports the implication of DYRK1A in the development of cognitive
deficits seen in Down syndrome (DS) and Alzheimer's disease (AD). We here demonstrate …

[HTML][HTML] A transchromosomic rat model with human chromosome 21 shows robust Down syndrome features

Y Kazuki, FJ Gao, M Yamakawa, M Hirabayashi… - The American Journal of …, 2022 - cell.com
Progress in earlier detection and clinical management has increased life expectancy and
quality of life in people with Down syndrome (DS). However, no drug has been approved to …

[HTML][HTML] Tissue magnetic susceptibility mapping as a marker of tau pathology in Alzheimer's disease

J O'callaghan, H Holmes, N Powell, JA Wells, O Ismail… - Neuroimage, 2017 - Elsevier
Alzheimer's disease is connected to a number of other neurodegenerative conditions,
known collectively as 'tauopathies', by the presence of aggregated tau protein in the brain …

AAV5-miHTT-mediated huntingtin lowering improves brain health in a Huntington's disease mouse model

SB Thomson, A Stam, C Brouwers, V Fodale… - Brain, 2023 - academic.oup.com
Huntingtin (HTT)-lowering therapies show great promise in treating Huntington's disease.
We have developed a microRNA targeting human HTT that is delivered in an adeno …

Comparison of In Vivo and Ex Vivo MRI for the Detection of Structural Abnormalities in a Mouse Model of Tauopathy

HE Holmes, NM Powell, D Ma, O Ismail… - Frontiers in …, 2017 - frontiersin.org
With increasingly large numbers of mouse models of human disease dedicated to MRI
studies, compromises between in vivo and ex vivo MRI must be fully understood in order to …

Study the Longitudinal in vivo and Cross-Sectional ex vivo Brain Volume Difference for Disease Progression and Treatment Effect on Mouse Model of Tauopathy …

D Ma, HE Holmes, MJ Cardoso, M Modat… - Frontiers in …, 2019 - frontiersin.org
Brain volume measurements extracted from structural MRI data sets are a widely accepted
neuroimaging biomarker to study mouse models of neurodegeneration. Whether to acquire …

[HTML][HTML] Investigating brain alterations in the Dp1Tyb mouse model of Down syndrome

ME Serrano, E Kim, B Siow, D Ma, L Rojo… - Neurobiology of …, 2023 - Elsevier
Down syndrome (DS) is one of the most common birth defects and the most prevalent
genetic form of intellectual disability. DS arises from trisomy of chromosome 21, but its …

Sammba-MRI: a library for processing SmAll-MaMmal BrAin MRI data in python

M Celestine, NA Nadkarni, CM Garin… - Frontiers in …, 2020 - frontiersin.org
Small-mammal neuroimaging offers incredible opportunities to investigate structural and
functional aspects of the brain. Many tools have been developed in the last decade to …