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Elife|October 27, 2017
A map of human PRDM9 binding provides evidence for novel behaviors of PRDM9 and other zinc-finger proteins in meiosisNicolas Altemose, Nudrat Noor, Emmanuelle Bitoun, et al.The Journal of Biological Chemistry|August 10, 2014
A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathologyLeigh Paton, Emmanuelle Bitoun, Janet Kenyon, et al.Plos Genetics|October 27, 2011
Oxr1 is essential for protection against oxidative stress-induced neurodegenerationPeter L Oliver, Mattéa J Finelli, Benjamin Edwards, et al.The Journal of Investigative Dermatology|February 14, 2002
Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 familiesEmmanuelle Bitoun, Stéphane Chavanas, Alan D Irvine, et al.Human Molecular Genetics|August 14, 2003
LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndromeEmmanuelle Bitoun, Alessia Micheloni, Laurence Lamant, et al.The Journal of Investigative Dermatology|January 29, 2005
LEKTI is localized in lamellar granules, separated from KLK5 and KLK7, and is secreted in the extracellular spaces of the superficial stratum granulosumAkemi Ishida-Yamamoto, Céline Deraison, Chrystelle Bonnart, et al.Nature|February 4, 2016
Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in miceBenjamin Davies, Edouard Hatton, Nicolas Altemose, et al.Pageof 2