Emma J Kenyon

Emma J Kenyon
Swansea University | SWAN · Institute of Life Science "ILS"

PhD

About

22
Publications
6,615
Reads
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4,731
Citations
Introduction
Emma J Kenyon is a lecturer in neuroscience in the Medical School at Swansea University. the the Department of Neuroscience, University of Sussex. Emma does research in Physiology and Genetics. Their current project is 'Mechanisms of aminoglycoside ototoxicity: towards the design of otoprotective agents.'
Additional affiliations
August 2013 - March 2019
University of Sussex
Position
  • PostDoc Position
November 2011 - July 2013
University of Birmingham
Position
  • PostDoc Position
June 2009 - November 2011
Wellcome Sanger Institute
Position
  • Annotator
Education
September 2002 - September 2006
University College London
Field of study
  • Developmental Biology
September 2001 - August 2002
King's College London
Field of study
  • Biomedical Science
September 1998 - July 2001
King's College London
Field of study
  • Pharmacology

Publications

Publications (22)
Article
Full-text available
The styryl dye FM1-43 is widely used to study endocytosis but behaves as a permeant blocker of the mechano-electrical transducer (MET) channel in sensory hair cells, loading rapidly and specifically into the cytoplasm of hair cells in a MET channel-dependent manner. Patch clamp recordings of mouse outer hair cells (OHCs) were used to determine how...
Article
Full-text available
Coastal vegetative ecosystems are among the most threatened in the world, facing multiple anthropogenic stressors. A good example of this is seagrass, which supports carbon capture, coastal stabilization, and biodiversity, but is declining globally at an alarming rate. To understand the causes and consequences of changes to these ecosystems, we nee...
Article
Full-text available
To identify small molecules that shield mammalian sensory hair cells from the ototoxic side effects of aminoglycoside antibiotics we screened 10,240 compounds, selecting those that protected against neomycin and gentamicin in zebrafish lateral-line hair cells and, when retested in mouse cochlear cultures, prevented gentamicin-induced death of outer...
Article
Full-text available
In isolated or declining populations, viability may be compromised further by loss of genetic diversity. Therefore, it is important to understand the relationship between long-term ecological trajectories and population genetic structure. However, opportunities to combine these types of data are rare, especially in natural systems. Using an existin...
Article
Full-text available
Aminoglycosides (AGs) are broad-spectrum antibiotics used for the treatment of serious bacterial infections but have use-limiting side effects including irreversible hearing loss. Here, we assessed the otoprotective profile of carvedilol in mouse cochlear culture and in vivo zebrafish assays and investigated its mechanism of protection which we fou...
Poster
Drug discovery for novel compounds with antimicrobial activity and efflux pump inhibition against Mycobacterium tuberculosis.
Article
Full-text available
Aminoglycoside antibiotics are used to treat life-threatening bacterial infections but can cause deafness due to hair cell death in the inner ear. Compounds have been described that protect zebrafish lateral line hair cells from aminoglycosides, but few are effective in the cochlea. As the aminoglycosides interact with several ion channels, includi...
Article
Full-text available
Aminoglycoside antibiotics are widely used for the treatment of life-threatening bacterial infections, but cause permanent hearing loss in a substantial proportion of treated patients. The sensory hair cells of the inner ear are damaged following entry of these antibiotics via the mechano-electrical transducer (MET) channels located at the tips of...
Article
Full-text available
Background: Birt-Hogg-Dubé syndrome (BHD) is a dominantly inherited familial cancer syndrome characterised by the development of benign skin fibrofolliculomas, multiple lung and kidney cysts, spontaneous pneumothorax and susceptibility to renal cell carcinoma. BHD is caused by mutations in the gene encoding Folliculin (FLCN). Little is known about...
Article
Full-text available
Measurement of population persistence is a long-standing problem in ecology; in particular, whether it is possible to gain insights into persistence without long time-series. Fractal measurements of spatial patterns, such as the Korcak exponent or boundary dimension, have been proposed as indicators of the persistence of underlying dynamics. Here w...
Article
Full-text available
The RAB5 gene family is the best characterised of all human RAB families and is essential for in vitro homotypic fusion of early endosomes. In recent years, the disruption or activation of Rab5 family proteins has been used as a tool to understand growth factor signal transduction in whole animal systems such as Drosophila melanogaster and zebrafis...
Article
Full-text available
Zebrafish have become a popular organism for the study of vertebrate gene function. The virtually transparent embryos of this species, and the ability to accelerate genetic studies by gene knockdown or overexpression, have led to the widespread use of zebrafish in the detailed investigation of vertebrate gene function and increasingly, the study of...
Article
Full-text available
It is well known that ecological processes such as population regulation and natural enemy interactions potentially occur over a range of spatial scales, and there is a substantial body of literature developing theoretical understanding of the interplay between these processes. However, there are comparatively few studies quantifying the long-term...
Article
Full-text available
The role of disease in the long-term dynamics of threatened species is poorly quantified, as well as being under-represented in ecology and conservation management. To understand persistent host-pathogen interaction operating in a vulnerable habitat, we quantified dynamics driving patterns of seagrass density using a longitudinal study in a relativ...
Article
Full-text available
Mutations in the SHOX gene are responsible for Leri-Weill Dyschondrosteosis, a disorder characterised by mesomelic limb shortening. Recent investigations into regulatory elements surrounding SHOX have shown that deletions of conserved non-coding elements (CNEs) downstream of the SHOX gene produce a phenotype indistinguishable from Leri-Weill Dyscho...
Article
Full-text available
Worldwide, seagrasses face threats including climate change, disease and anthropogenic disturbance, with populations at the extremes of species' distributions likely presaging future problems elsewhere in their geographical ranges. At the geographic limits of two marine macrophytes (Zostera marina and Posidonia oceanica) and under intense urbanizat...
Article
Estrogen replacement therapy (ERT) improves blood flow through various mechanisms including an augmented release of nitric oxide (NO). We report on the long-term effects of estrogen loss on vascular function and endothelial regulation. Male, female, ovariectomized and ovariectomized+ERT treated rats were used. Female rats were ovariectomized at 12...

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