[HTML][HTML] A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

…, A Ayadi, L Becker, A Blake, D Brooker, H Cater… - Genome biology, 2013 - Springer
Background The mouse inbred line C57BL/6J is widely used in mouse genetics and its
genome has been incorporated into many genetic reference populations. More recently large …

A tissue level tolerance criterion for living brain developed with an in vitro model of traumatic mechanical loading

B Morrison, HL Cater, CCB Wang, FC Thomas… - 2003 - sae.org
Traumatic brain injury (TBI) is caused by brain deformations resulting in the pathophysiological
activation of cellular cascades which produce delayed cell damage and death. …

An in vitro model of traumatic brain injury utilising two-dimensional stretch of organotypic hippocampal slice cultures

B Morrison III, HL Cater, CD Benham… - Journal of neuroscience …, 2006 - Elsevier
Traumatic brain injury (TBI) is caused by rapid deformation of the brain, resulting in a
cascade of pathological events and ultimately neurodegeneration. Understanding how the …

[HTML][HTML] Assessing mouse behaviour throughout the light/dark cycle using automated in-cage analysis tools

…, S Wells, RR Sillito, JD Armstrong, HL Cater… - Journal of neuroscience …, 2018 - Elsevier
An important factor in reducing variability in mouse test outcomes has been to develop assays
that can be used for continuous automated home cage assessment. Our experience has …

Temporal development of hippocampal cell death is dependent on tissue strain but not strain rate

HL Cater, LE Sundstrom, B Morrison III - Journal of biomechanics, 2006 - Elsevier
Deformation of brain tissue in response to mechanical loading of the head is the root-cause
of traumatic brain injury (TBI). Even below ultimate failure limits, deformation activates …

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

…, DH Busch, JN Bussell, J Calzada-Wack, H Cater… - Nature …, 2015 - nature.com
The function of the majority of genes in the mouse and human genomes remains unknown.
The mouse embryonic stem cell knockout resource provides a basis for the characterization …

[HTML][HTML] A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction

…, NJ Ingham, S Greenaway, L Santos, H Cater… - Nature …, 2017 - nature.com
The developmental and physiological complexity of the auditory system is likely reflected in
the underlying set of genes involved in auditory function. In humans, over 150 non-…

[HTML][HTML] Analysis of individual mouse activity in group housed animals of different inbred strains using a novel automated home cage analysis system

RS Bains, HL Cater, RR Sillito, A Chartsias… - Frontiers in behavioral …, 2016 - frontiersin.org
Central nervous system disorders such as autism as well as the range of neurodegenerative
diseases such as Huntington's disease are commonly investigated using genetically altered …

[HTML][HTML] Human and mouse essentiality screens as a resource for disease gene discovery

…, H Wardle-Jones, S Wells, L Teboul, H Cater… - Nature …, 2020 - nature.com
The identification of causal variants in sequencing studies remains a considerable challenge
that can be partially addressed by new gene-specific knowledge. Here, we integrate …

[HTML][HTML] Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

…, L Teboul, RKA Bunton-Stasyshyn, H Cater… - Nature Cardiovascular …, 2022 - nature.com
Clinical presentation of congenital heart disease is heterogeneous, making identification of
the disease-causing genes and their genetic pathways and mechanisms of action …