E. Bitoun

发表

ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair

P. Donnelly, S. Myers, C. Green, 2020, eLife.

A map of human PRDM9 binding provides evidence for novel behaviors of PRDM9 and other zinc-finger proteins in meiosis

S. Myers, Nudrat Noor, A. R. Aricescu, 2017, eLife.

LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome.

C. Bodemer, D. Hohl, A. Hovnanian, 2003, Human molecular genetics.

Keratitis–ichthyosis–deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients

C. Bodemer, C. Prins, J. Saurat, 2007, The British journal of dermatology.

ZCWPW1 is recruited to recombination hotspots by PRDM9, and is essential for meiotic double strand break repair

P. Donnelly, S. Myers, C. Green, 2019, bioRxiv.

The robotic mouse: Unravelling the function of AF4 in the cerebellum

K. Davies, E. Bitoun, 2005, The Cerebellum.

P. Oliver, E. Bitoun, Kay E. Davies, 2021, Handbook of the Cerebellum and Cerebellar Disorders.

Mediation of Af4 protein function in the cerebellum by Siah proteins.

K. Davies, P. Oliver, E. Bitoun, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Prenatal diagnosis of a lethal form of Netherton syndrome by SPINK5 mutation analysis

C. Bodemer, C. Stoll, P. Calvas, 2002, Prenatal diagnosis.

Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families.

C. Bodemer, A. Hovnanian, A. Irvine, 2002, The Journal of investigative dermatology.

LEKTI is localized in lamellar granules, separated from KLK5 and KLK7, and is secreted in the extracellular spaces of the superficial stratum granulosum.

A. Ishida-Yamamoto, J. McGrath, G. Richard, 2005, The Journal of investigative dermatology.

AF4 Is a Critical Regulator of the IGF-1 Signaling Pathway during Purkinje Cell Development

K. Davies, P. Oliver, E. Bitoun, 2009, The Journal of Neuroscience.

The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling.

K. Davies, P. Oliver, E. Bitoun, 2007, Human molecular genetics.

A high-resolution map of non-crossover events reveals impacts of genetic diversity on mammalian meiotic recombination

S. Myers, R. Davies, B. Davies, 2018, Nature Communications.

Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice

P. Donnelly, S. Myers, D. Biggs, 2016, Nature.

Oxr1 Is Essential for Protection against Oxidative Stress-Induced Neurodegeneration

K. Davies, P. Oliver, Esther B. E. Becker, 2011, PLoS genetics.

The protein phosphatase PP2A-B′ subunit Widerborst is a negative regulator of cytoplasmic activated Akt and lipid metabolism in Drosophila

Clive Wilson, E. Bitoun, N. Vereshchagina, 2008, Journal of Cell Science.

Human PRDM9 can bind and activate promoters, and other zinc-finger proteins associate with reduced recombination in cis

S. Myers, Nudrat Noor, J. R. Chapman, 2017, bioRxiv.

Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease

K. Davies, P. Oliver, E. Bitoun, 2007, Mammalian Genome.

The Robotic Mouse: Understanding the Role of AF4, a Cofactor of Transcriptional Elongation and Chromatin Remodelling, in Purkinje Cell Function

K. Davies, E. Bitoun, 2009, The Cerebellum.

PTPRR, Cerebellum, and Motor Coordination

M. Manto, I. Schmitt, E. Bitoun, 2009, The Cerebellum.

A Novel Mouse Model of a Patient Mucolipidosis II Mutation Recapitulates Disease Pathology

K. Davies, P. Oliver, J. Kenyon, 2014, The Journal of Biological Chemistry.

Title: A high-resolution map of non-crossover events in mice reveals impacts of genetic diversity on meiotic recombination Authors:

S. Myers, R. Davies, B. Davies, 2018 .