Hearing Function, Degeneration, and Disease: Spotlight on the Stria Vascularis

por Thulasiram, Matsya R, Ogier, Jacqueline M, Dabdoub, Alain
Publicado 2022

ASK1 inhibition: a therapeutic strategy with multi-system benefits

por Ogier, Jacqueline M., Nayagam, Bryony A., Lockhart, Paul J.
Publicado 2020

Organotypic Culture of Neonatal Murine Inner Ear Explants

por Ogier, Jacqueline M., Burt, Rachel A., Drury, Hannah R., Lim, Rebecca, Nayagam, Bryony A.
Publicado 2019

CHD7 Deficiency in “Looper”, a New Mouse Model of CHARGE Syndrome, Results in Ossicle Malformation, Otosclerosis and Hearing Impairment

por Ogier, Jacqueline M., Carpinelli, Marina R., Arhatari, Benedicta D., Symons, R. C. Andrew, Kile, Benjamin T., Burt, Rachel A.
Publicado 2014

An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome

por Ogier, Jacqueline M., Arhatari, Benedicta D., Carpinelli, Marina R., McColl, Bradley K., Wilson, Michael A., Burt, Rachel A.
Publicado 2018

ASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death

por Ogier, Jacqueline M., Gao, Yujing, Dunne, Eileen M., Wilson, Michael A., Ranganathan, Sarath C., Tesch, Gregory H., Nikolic Paterson, David J., Dabdoub, Alain, Burt, Rachel A., Nayagam, Bryony A., Lockhart, Paul J.
Publicado 2022

Correction to: ASK1 is a novel molecular target for preventing aminoglycoside‑induced hair cell death

por Ogier, Jacqueline M., Gao, Yujing, Dunne, Eileen M., Wilson, Michael A., Ranganathan, Sarath C., Tesch, Gregory H., Nikolic Paterson, David J., Dabdoub, Alain, Burt, Rachel A., Nayagam, Bryony A., Lockhart, Paul J.
Publicado 2022