| Year |
Citation |
Score |
| 2020 |
Wells D, Bitoun E, Moralli D, Zhang G, Hinch A, Jankowska J, Donnelly P, Green C, Myers SR. ZCWPW1 is recruited to recombination hotspots by PRDM9, and is essential for meiotic double strand break repair. Elife. 9. PMID 32744506 DOI: 10.7554/Elife.53392 |
0.338 |
|
| 2017 |
Altemose N, Noor N, Bitoun E, Tumian A, Imbeault M, Chapman JR, Aricescu AR, Myers SR. A map of human PRDM9 binding provides evidence for novel behaviors of PRDM9 and other zinc-finger proteins in meiosis. Elife. 6. PMID 29072575 DOI: 10.7554/Elife.28383 |
0.344 |
|
| 2017 |
Altemose N, Noor N, Bitoun E, Tumian A, Imbeault M, Chapman JR, Aricescu AR, Myers SR. Author response: A map of human PRDM9 binding provides evidence for novel behaviors of PRDM9 and other zinc-finger proteins in meiosis Elife. DOI: 10.7554/Elife.28383.038 |
0.309 |
|
| 2016 |
Davies B, Hatton E, Altemose N, Hussin JG, Pratto F, Zhang G, Hinch AG, Moralli D, Biggs D, Diaz R, Preece C, Li R, Bitoun E, Brick K, Green CM, et al. Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice. Nature. PMID 26840484 DOI: 10.1038/Nature16931 |
0.349 |
|
| 2014 |
Paton L, Bitoun E, Kenyon J, Priestman DA, Oliver PL, Edwards B, Platt FM, Davies KE. A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathology. The Journal of Biological Chemistry. 289: 26709-21. PMID 25107912 DOI: 10.1074/Jbc.M114.586156 |
0.686 |
|
| 2011 |
Oliver PL, Finelli MJ, Edwards B, Bitoun E, Butts DL, Becker EB, Cheeseman MT, Davies B, Davies KE. Oxr1 is essential for protection against oxidative stress-induced neurodegeneration. Plos Genetics. 7: e1002338. PMID 22028674 DOI: 10.1371/Journal.Pgen.1002338 |
0.608 |
|
| 2009 |
Bitoun E, Finelli MJ, Oliver PL, Lee S, Davies KE. 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. PMID 20007461 DOI: 10.1523/Jneurosci.5188-09.2009 |
0.684 |
|
| 2009 |
Schmitt I, Bitoun E, Manto M. PTPRR, cerebellum, and motor coordination. Cerebellum (London, England). 8: 71-3. PMID 19488825 DOI: 10.1007/S12311-009-0118-4 |
0.392 |
|
| 2009 |
Bitoun E, Davies KE. 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. PMID 19340490 DOI: 10.1007/S12311-009-0101-0 |
0.653 |
|
| 2007 |
Oliver PL, Bitoun E, Davies KE. 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. PMID 17514509 DOI: 10.1007/S00335-007-9014-8 |
0.664 |
|
| 2007 |
Bitoun E, Oliver PL, Davies KE. The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling. Human Molecular Genetics. 16: 92-106. PMID 17135274 DOI: 10.1093/Hmg/Ddl444 |
0.679 |
|
| 2005 |
Bitoun E, Davies KE. The robotic mouse: unravelling the function of AF4 in the cerebellum. Cerebellum (London, England). 4: 250-60. PMID 16321881 DOI: 10.1080/14734220500325897 |
0.645 |
|
| 2005 |
Ishida-Yamamoto A, Deraison C, Bonnart C, Bitoun E, Robinson R, O'Brien TJ, Wakamatsu K, Ohtsubo S, Takahashi H, Hashimoto Y, Dopping-Hepenstal PJ, McGrath JA, Iizuka H, Richard G, Hovnanian A. LEKTI is localized in lamellar granules, separated from KLK5 and KLK7, and is secreted in the extracellular spaces of the superficial stratum granulosum. The Journal of Investigative Dermatology. 124: 360-6. PMID 15675955 DOI: 10.1111/J.0022-202X.2004.23583.X |
0.316 |
|
| 2004 |
Oliver PL, Bitoun E, Clark J, Jones EL, Davies KE. Mediation of Af4 protein function in the cerebellum by Siah proteins. Proceedings of the National Academy of Sciences of the United States of America. 101: 14901-6. PMID 15459319 DOI: 10.1073/Pnas.0406196101 |
0.693 |
|
| 2003 |
Bitoun E, Micheloni A, Lamant L, Bonnart C, Tartaglia-Polcini A, Cobbold C, Al Saati T, Mariotti F, Mazereeuw-Hautier J, Boralevi F, Hohl D, Harper J, Bodemer C, D'Alessio M, Hovnanian A. LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome. Human Molecular Genetics. 12: 2417-30. PMID 12915442 DOI: 10.1093/Hmg/Ddg247 |
0.355 |
|
| 2002 |
Bitoun E, Chavanas S, Irvine AD, Lonie L, Bodemer C, Paradisi M, Hamel-Teillac D, Ansai S, Mitsuhashi Y, Taïeb A, de Prost Y, Zambruno G, Harper JI, Hovnanian A. Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families. The Journal of Investigative Dermatology. 118: 352-61. PMID 11841556 DOI: 10.1046/J.1523-1747.2002.01603.X |
0.384 |
|
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