Emmanuelle Bitoun, Ph.D.

Affiliations: 
Physiology, Anatomy and Genetics University of Oxford, Oxford, United Kingdom 
Area:
Ataxia
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"Emmanuelle Bitoun"
Mean distance: 19.03 (cluster 28)
 
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Publications

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Li R, Bitoun E, Altemose N, et al. (2019) A high-resolution map of non-crossover events reveals impacts of genetic diversity on mammalian meiotic recombination. Nature Communications. 10: 3900
Davies B, Hatton E, Altemose N, et al. (2016) Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice. Nature
Paton L, Bitoun E, Kenyon J, et al. (2014) A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathology. The Journal of Biological Chemistry. 289: 26709-21
Oliver PL, Finelli MJ, Edwards B, et al. (2011) Oxr1 is essential for protection against oxidative stress-induced neurodegeneration. Plos Genetics. 7: e1002338
Bitoun E, Finelli MJ, Oliver PL, et al. (2009) AF4 is a critical regulator of the IGF-1 signaling pathway during Purkinje cell development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 15366-74
Schmitt I, Bitoun E, Manto M. (2009) PTPRR, cerebellum, and motor coordination. Cerebellum (London, England). 8: 71-3
Bitoun E, Davies KE. (2009) The robotic mouse: understanding the role of AF4, a cofactor of transcriptional elongation and chromatin remodelling, in purkinje cell function. Cerebellum (London, England). 8: 175-83
Vereshchagina N, Ramel MC, Bitoun E, et al. (2008) The protein phosphatase PP2A-B' subunit Widerborst is a negative regulator of cytoplasmic activated Akt and lipid metabolism in Drosophila. Journal of Cell Science. 121: 3383-92
Oliver PL, Bitoun E, Davies KE. (2007) Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 412-24
Mazereeuw-Hautier J, Bitoun E, Chevrant-Breton J, et al. (2007) Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients. The British Journal of Dermatology. 156: 1015-9
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