Publications by authors named "Emmanuelle Bitoun"

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ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair.
Daniel Wells, Emmanuelle Bitoun, Daniela Moralli, Gang Zhang, Anjali Hinch

Elife· August 2020

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A high-resolution map of non-crossover events reveals impacts of genetic diversity on mammalian meiotic recombination.
Ran Li, Emmanuelle Bitoun, Nicolas Altemose, Robert W Davies, Benjamin Davies

Nat Commun· August 2019

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A map of human PRDM9 binding provides evidence for novel behaviors of PRDM9 and other zinc-finger proteins in meiosis.
Nicolas Altemose, Nudrat Noor, Emmanuelle Bitoun, Afidalina Tumian, Michael Imbeault

Elife· October 2017

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Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice.
Benjamin Davies, Edouard Hatton, Nicolas Altemose, Julie G Hussin, Florencia Pratto, Emmanuelle Bitoun

Nature· February 2016

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A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathology.
Leigh Paton, Emmanuelle Bitoun, Janet Kenyon, David A Priestman, Peter L Oliver

J Biol Chem· September 2014

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Oxr1 is essential for protection against oxidative stress-induced neurodegeneration.
Peter L Oliver, Mattéa J Finelli, Benjamin Edwards, Emmanuelle Bitoun, Darcy L Butts

PLoS Genet· October 2011

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AF4 is a critical regulator of the IGF-1 signaling pathway during Purkinje cell development.
Emmanuelle Bitoun, Mattéa J Finelli, Peter L Oliver, Sheena Lee, Kay E Davies

J Neurosci· December 2009

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The robotic mouse: understanding the role of AF4, a cofactor of transcriptional elongation and chromatin remodelling, in purkinje cell function.
Emmanuelle Bitoun, Kay E Davies

Cerebellum· September 2009

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PTPRR, cerebellum, and motor coordination.
Ina Schmitt, Emmanuelle Bitoun, Mario Manto

Cerebellum· June 2009

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The protein phosphatase PP2A-B' subunit Widerborst is a negative regulator of cytoplasmic activated Akt and lipid metabolism in Drosophila.
Natalia Vereshchagina, Marie-Christine Ramel, Emmanuelle Bitoun, Clive Wilson

J Cell Sci· October 2008

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Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease.
Peter L Oliver, Emmanuelle Bitoun, Kay E Davies

Mamm Genome· July 2007

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The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling.
Emmanuelle Bitoun, Peter L Oliver, Kay E Davies

Hum Mol Genet· January 2007

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The robotic mouse: unravelling the function of AF4 in the cerebellum.
Emmanuelle Bitoun, Kay Elizabeth Davies

Cerebellum· January 2006

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LEKTI is localized in lamellar granules, separated from KLK5 and KLK7, and is secreted in the extracellular spaces of the superficial stratum granulosum.
Akemi Ishida-Yamamoto, Céline Deraison, Chrystelle Bonnart, Emmanuelle Bitoun, Ross Robinson

J Invest Dermatol· February 2005

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Mediation of Af4 protein function in the cerebellum by Siah proteins.
Peter L Oliver, Emmanuelle Bitoun, Joanne Clark, Emma L Jones, Kay E Davies

Proc Natl Acad Sci U S A· October 2004

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LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome.
Emmanuelle Bitoun, Alessia Micheloni, Laurence Lamant, Chrystelle Bonnart, Alessandro Tartaglia-Polcini

Hum Mol Genet· October 2003

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Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families.
Emmanuelle Bitoun, Stéphane Chavanas, Alan D Irvine, Lorne Lonie, Christine Bodemer

J Invest Dermatol· February 2002

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