MicroRNAs in mouse development and disease

por Lewis, Morag A., Steel, Karen P.
Publicado 2010

Reversal of an existing hearing loss by gene activation in Spns2 mutant mice

por Martelletti, Elisa, Ingham, Neil J., Steel, Karen P.
Publicado 2023

The deaf mouse mutant whirler suggests a role for whirlin in actin filament dynamics and stereocilia development

por Mogensen, Mette M, Rzadzinska, Agnieszka, Steel, Karen P
Publicado 2007

Specific expression of Kcna10, Pxn and Odf2 in the organ of Corti

por Carlisle, Francesca A., Steel, Karen P., Lewis, Morag A.
Publicado 2012

Investigating the characteristics of genes and variants associated with self-reported hearing difficulty in older adults in the UK Biobank

por Lewis, Morag A., Schulte, Bradley A., Dubno, Judy R., Steel, Karen P.
Publicado 2022

Catweasel mice: A novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome

por Bosman, Erika A., Quint, Elizabeth, Fuchs, Helmut, Hrabé de Angelis, Martin, Steel, Karen P.
Publicado 2009

MyosinVIIa Interacts with Twinfilin-2 at the Tips of Mechanosensory Stereocilia in the Inner Ear

por Rzadzinska, Agnieszka K., Nevalainen, Elisa M., Prosser, Haydn M., Lappalainen, Pekka, Steel, Karen P.
Publicado 2009

Emx2 and early hair cell development in the mouse inner ear

por Holley, Matthew, Rhodes, Charlotte, Kneebone, Adam, Herde, Michel K., Fleming, Michelle, Steel, Karen P.
Publicado 2010

Study of smell and reproductive organs in a mouse model for CHARGE syndrome

por Bergman, Jorieke EH, Bosman, Erika A, van Ravenswaaij-Arts, Conny MA, Steel, Karen P
Publicado 2010

Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1

por Bosman, Erika A., Estabel, Jeanne, Ismail, Ozama, Podrini, Christine, White, Jacqueline K., Steel, Karen P.
Publicado 2012

Hearing impairment due to Mir183/96/182 mutations suggests both loss-of-function and gain-of-function effects

por Lewis, Morag A., Di Domenico, Francesca, Ingham, Neil J., Prosser, Haydn M., Steel, Karen P.
Publicado 2021

A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice

por Calvert, Jennifer A., Dedos, Skarlatos G., Hawker, Kelvin, Fleming, Michelle, Lewis, Morag A., Steel, Karen P.
Publicado 2011

Auditory Function in the Tc1 Mouse Model of Down Syndrome Suggests a Limited Region of Human Chromosome 21 Involved in Otitis Media

por Kuhn, Stephanie, Ingham, Neil, Pearson, Selina, Gribble, Susan M., Clayton, Stephen, Steel, Karen P., Marcotti, Walter
Publicado 2012

Expression and Replication Studies to Identify New Candidate Genes Involved in Normal Hearing Function

por Girotto, Giorgia, Vuckovic, Dragana, Buniello, Annalisa, Lorente-Cánovas, Beatriz, Lewis, Morag, Gasparini, Paolo, Steel, Karen P.
Publicado 2014

Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells

por Lorente-Cánovas, Beatriz, Eckrich, Stephanie, Lewis, Morag A., Johnson, Stuart L., Marcotti, Walter, Steel, Karen P.
Publicado 2022

Headbobber: A Combined Morphogenetic and Cochleosaccular Mouse Model to Study 10qter Deletions in Human Deafness

por Buniello, Annalisa, Hardisty-Hughes, Rachel E., Pass, Johanna C., Bober, Eva, Smith, Richard J., Steel, Karen P.
Publicado 2013

Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice

por Martelletti, Elisa, Ingham, Neil J., Houston, Oliver, Pass, Johanna C., Chen, Jing, Marcotti, Walter, Steel, Karen P.
Publicado 2020

Mice deficient in H(+)-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear

por Lorente-Cánovas, Beatriz, Ingham, Neil, Norgett, Elizabeth E., Golder, Zoe J., Karet Frankl, Fiona E., Steel, Karen P.
Publicado 2013

A reduction in Ptprq associated with specific features of the deafness phenotype of the miR-96 mutant mouse diminuendo

por Chen, Jing, Johnson, Stuart L, Lewis, Morag A, Hilton, Jennifer M, Huma, Andreea, Marcotti, Walter, Steel, Karen P
Publicado 2014

Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss

por Ingham, Neil J., Banafshe, Navid, Panganiban, Clarisse, Crunden, Julia L., Chen, Jing, Lewis, Morag A., Steel, Karen P.
Publicado 2021