Correction: Two ENU-Induced Alleles of Atp2b2 Cause Deafness in Mice

por Carpinelli, Marina R., Manning, Michael G., Kile, Benjamin T., Burt, Rachel A.
Publicado 2013

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

A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination

por Carpinelli, Marina R., Voss, Anne K., Manning, Michael G., Perera, Ashwyn A., Cooray, Anne A., Kile, Benjamin T., Burt, Rachel A.
Publicado 2014

Antibodies against Merozoite Surface Protein (Msp)-1(19) Are a Major Component of the Invasion-Inhibitory Response in Individuals Immune to Malaria

por O'Donnell, Rebecca A., de Koning-Ward, Tania F., Burt, Rachel A., Bockarie, Moses, Reeder, John C., Cowman, Alan F., Crabb, Brendan S.
Publicado 2001

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

A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort

por Downie, Lilian, Halliday, Jane L, Burt, Rachel A, Lunke, Sebastian, Lynch, Elly, Martyn, Melissa, Poulakis, Zeffie, Gaff, Clara, Sung, Valerie, Wake, Melissa, Hunter, Matthew, Saunders, Kerryn, Rose, Elizabeth, Rehm, Heidi L, Amor, David J
Publicado 2017