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Items: 17

1.

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

Altemose N, Noor N, Bitoun E, Tumian A, Imbeault M, Chapman JR, Aricescu AR, Myers SR.

Elife. 2017 Oct 26;6. pii: e28383. doi: 10.7554/eLife.28383.

2.

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

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, Camerini-Otero RD, Myers SR, Donnelly P.

Nature. 2016 Feb 11;530(7589):171-176. doi: 10.1038/nature16931. Epub 2016 Feb 3.

3.

A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathology.

Paton L, Bitoun E, Kenyon J, Priestman DA, Oliver PL, Edwards B, Platt FM, Davies KE.

J Biol Chem. 2014 Sep 26;289(39):26709-21. doi: 10.1074/jbc.M114.586156. Epub 2014 Aug 8.

4.

Oxr1 is essential for protection against oxidative stress-induced neurodegeneration.

Oliver PL, Finelli MJ, Edwards B, Bitoun E, Butts DL, Becker EB, Cheeseman MT, Davies B, Davies KE.

PLoS Genet. 2011 Oct;7(10):e1002338. doi: 10.1371/journal.pgen.1002338. Epub 2011 Oct 20.

5.

AF4 is a critical regulator of the IGF-1 signaling pathway during Purkinje cell development.

Bitoun E, Finelli MJ, Oliver PL, Lee S, Davies KE.

J Neurosci. 2009 Dec 9;29(49):15366-74. doi: 10.1523/JNEUROSCI.5188-09.2009.

6.

PTPRR, cerebellum, and motor coordination.

Schmitt I, Bitoun E, Manto M.

Cerebellum. 2009 Jun;8(2):71-3. doi: 10.1007/s12311-009-0118-4. Review.

PMID:
19488825
7.

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

Bitoun E, Davies KE.

Cerebellum. 2009 Sep;8(3):175-83. doi: 10.1007/s12311-009-0101-0. Epub 2009 Apr 2. Review.

PMID:
19340490
8.

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

Vereshchagina N, Ramel MC, Bitoun E, Wilson C.

J Cell Sci. 2008 Oct 15;121(Pt 20):3383-92. doi: 10.1242/jcs.035220. Epub 2008 Sep 30.

9.

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

Oliver PL, Bitoun E, Davies KE.

Mamm Genome. 2007 Jul;18(6-7):412-24. Epub 2007 May 21. Review.

10.

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

Mazereeuw-Hautier J, Bitoun E, Chevrant-Breton J, Man SY, Bodemer C, Prins C, Antille C, Saurat JH, Atherton D, Harper JI, Kelsell DP, Hovnanian A.

Br J Dermatol. 2007 May;156(5):1015-9. Epub 2007 Mar 23. Review.

PMID:
17381453
11.
12.

The robotic mouse: unravelling the function of AF4 in the cerebellum.

Bitoun E, Davies KE.

Cerebellum. 2005;4(4):250-60. Review.

PMID:
16321881
13.

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

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.

J Invest Dermatol. 2005 Feb;124(2):360-6.

14.

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

Oliver PL, Bitoun E, Clark J, Jones EL, Davies KE.

Proc Natl Acad Sci U S A. 2004 Oct 12;101(41):14901-6. Epub 2004 Sep 30.

15.

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

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.

Hum Mol Genet. 2003 Oct 1;12(19):2417-30. Epub 2003 Jul 29.

PMID:
12915442
16.

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

Bitoun E, Bodemer C, Amiel J, de Prost Y, Stoll C, Calvas P, Hovnanian A.

Prenat Diagn. 2002 Feb;22(2):121-6.

PMID:
11857617
17.

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

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.

J Invest Dermatol. 2002 Feb;118(2):352-61.

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