Publications by authors named "Alexandra Erven"

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Cognitive Rehabilitation for Attention and Memory in people with Multiple Sclerosis: study protocol for a randomised controlled trial (CRAMMS).
Nadina B Lincoln, Roshan das Nair, Lucy Bradshaw, Cris S Constantinescu, Avril E R Drummond, Alexandra Erven

Trials· December 2015

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Tmc1 is necessary for normal functional maturation and survival of inner and outer hair cells in the mouse cochlea.
Walter Marcotti, Alexandra Erven, Stuart L Johnson, Karen P Steel, Corné J Kros

J Physiol· August 2006

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Two quantitative trait loci affecting progressive hearing loss in 101/H mice.
Tomoji Mashimo, Alexandra E Erven, Sarah L Spiden, Jean-Louis Guénet, Karen P Steel

Mamm Genome· August 2006

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Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders.
Sohaila Rastan, Tertius Hough, Amy Kierman, Rachel Hardisty, Alexandra Erven

Genetica· September 2004

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An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice.
Nadav Ahituv, Alexandra Erven, Helmut Fuchs, Keren Guy, Ruth Ashery-Padan

Mamm Genome· June 2004

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The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media.
Rachel E Hardisty, Alexandra Erven, Karen Logan, Susan Morse, Sylvia Guionaud

J Assoc Res Otolaryngol· June 2003

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A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil.
Alexandra Erven, Michael J Skynner, Katsuzumi Okumura, Shin-ichiro Takebayashi, Steve D M Brown

Eur J Neurosci· October 2002

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Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
Sarah Vreugde, Alexandra Erven, Corné J Kros, Walter Marcotti, Helmut Fuchs

Nat Genet· March 2002

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ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis.
Amy E Kiernan, Alexandra Erven, Stéphanie Voegeling, Jo Peters, Pat Nolan

Mamm Genome· March 2002

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