Dorota Gibbins
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Dissecting the contribution of human chromosome 21 syntenic regions to recognition memory processes in adult and aged mouse models of Down syndrome.
Journal: Frontiers in behavioral neuroscience
Published: May 05, 2024
Investigating brain alterations in the Dp1Tyb mouse model of Down syndrome.
Journal: Neurobiology of disease
Published: February 06, 2024
Increased dosage of DYRK1A leads to congenital heart defects in a mouse model of Down syndrome.
Journal: Science translational medicine
Published: January 24, 2024
Craniofacial dysmorphology in Down syndrome is caused by increased dosage of Dyrk1a and at least three other genes.
Journal: Development (Cambridge, England)
Published: June 27, 2022
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes.
Journal: Disease models & mechanisms
Published: June 09, 2021
In vivo and ex vivo analyses of amyloid toxicity in the Tc1 mouse model of Down syndrome.
Journal: Journal of psychopharmacology (Oxford, England)
Published: December 08, 2017
Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration.
Journal: PLoS genetics
Published: June 27, 2017
Aging rather than aneuploidy affects monoamine neurotransmitters in brain regions of Down syndrome mouse models.
Journal: Neurobiology of disease
Published: April 11, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026