Efficient and versatile CRISPR engineering of human neurons in culture to model neurological disorders von Shah, Ruth R, Cholewa-Waclaw, Justyna, Davies, Faith C J, Paton, Katie M, Chaligne, Ronan, Heard, Edith, Abbott, Catherine M, Bird, Adrian P

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Endogenous epitope tagging of eEF1A2 in mice reveals early embryonic expression of eEF1A2 and subcellular compartmentalisation of neuronal eEF1A1 and eEF1A2 von Davies, Faith C.J., Marshall, Grant F., Pegram, Eleanor, Gadd, Danni, Abbott, Catherine M.

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Face-valid phenotypes in a mouse model of the most common mutation in EEF1A2-related neurodevelopmental disorder von Marshall, Grant F, Fasol, Melissa, Davies, Faith C J, Le Seelleur, Matthew, Fernandez Alvarez, Alejandra, Bennett-Ness, Cavan, Gonzalez-Sulser, Alfredo, Abbott, Catherine M

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Insulin-Like Growth Factor-1 Promotes Wound Healing in Estrogen-Deprived Mice: New Insights into Cutaneous IGF-1R/ERα Cross Talk von Emmerson, Elaine, Campbell, Laura, Davies, Faith C.J., Ross, Nina L., Ashcroft, Gillian S., Krust, Andrée, Chambon, Pierre, Hardman, Matthew J.

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Recapitulation of the EEF1A2 D252H neurodevelopmental disorder-causing missense mutation in mice reveals a toxic gain of function von Davies, Faith C J, Hope, Jilly E, McLachlan, Fiona, Marshall, Grant F, Kaminioti-Dumont, Laura, Qarkaxhija, Vesa, Nunez, Francis, Dando, Owen, Smith, Colin, Wood, Emma, MacDonald, Josephine, Hardt, Oliver, Abbott, Catherine M

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Biallelic mutations in the gene encoding eEF1A2 cause seizures and sudden death in F0 mice von Davies, Faith C. J., Hope, Jilly E., McLachlan, Fiona, Nunez, Francis, Doig, Jennifer, Bengani, Hemant, Smith, Colin, Abbott, Catherine M.

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Haploinsufficiency for translation elongation factor eEF1A2 in aged mouse muscle and neurons is compatible with normal function von Griffiths, Lowri A, Doig, Jennifer, Churchhouse, Antonia M D, Davies, Faith C J, Squires, Charlotte E, Newbery, Helen J, Abbott, Catherine M

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