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Grant F Marshall

Showing results (1-10 of 6) with videos related to

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Disease Models & Mechanisms|February 23, 2021
Modelling epilepsy in the mouse: challenges and solutionsGrant F Marshall, Alfredo Gonzalez-Sulser, Catherine M Abbott
Molecular and Cellular Neurosciences|July 10, 2023
Endogenous epitope tagging of eEF1A2 in mice reveals early embryonic expression of eEF1A2 and subcellular compartmentalisation of neuronal eEF1A1 and eEF1A2Faith C J Davies, Grant F Marshall, Eleanor Pegram, et al.
Disease Models & Mechanisms|January 5, 2024
Face-valid phenotypes in a mouse model of the most common mutation in EEF1A2-related neurodevelopmental disorderGrant F Marshall, Melissa Fasol, Faith C J Davies, et al.
Brain Communications|April 14, 2025
Absence of GluN2A in hippocampal CA1 neurons leads to altered dendritic structure and reduced frequency of miniature excitatory synaptic eventsFarhana Yasmin, Katie F M Marwick, Daniel W Hunter, et al.
Human Molecular Genetics|March 12, 2020
Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of functionFaith C J Davies, Jilly E Hope, Fiona McLachlan, et al.
Nature Genetics|June 12, 2026
A progeria syndrome links DNA hypermethylation to age-related pathologyDan Sarni, Gráinne Neary, Paula L Carroll, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Disease Models & Mechanisms|February 23, 2021
Modelling epilepsy in the mouse: challenges and solutionsGrant F Marshall, Alfredo Gonzalez-Sulser, Catherine M Abbott
Molecular and Cellular Neurosciences|July 10, 2023
Endogenous epitope tagging of eEF1A2 in mice reveals early embryonic expression of eEF1A2 and subcellular compartmentalisation of neuronal eEF1A1 and eEF1A2Faith C J Davies, Grant F Marshall, Eleanor Pegram, et al.
Disease Models & Mechanisms|January 5, 2024
Face-valid phenotypes in a mouse model of the most common mutation in EEF1A2-related neurodevelopmental disorderGrant F Marshall, Melissa Fasol, Faith C J Davies, et al.
Brain Communications|April 14, 2025
Absence of GluN2A in hippocampal CA1 neurons leads to altered dendritic structure and reduced frequency of miniature excitatory synaptic eventsFarhana Yasmin, Katie F M Marwick, Daniel W Hunter, et al.
Human Molecular Genetics|March 12, 2020
Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of functionFaith C J Davies, Jilly E Hope, Fiona McLachlan, et al.
Nature Genetics|June 12, 2026
A progeria syndrome links DNA hypermethylation to age-related pathologyDan Sarni, Gráinne Neary, Paula L Carroll, et al.
Pageof 1