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109 results

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Page 1
Mutation in TET2 in myeloid cancers.
Delhommeau F, Dupont S, Della Valle V, James C, Trannoy S, Massé A, Kosmider O, Le Couedic JP, Robert F, Alberdi A, Lécluse Y, Plo I, Dreyfus FJ, Marzac C, Casadevall N, Lacombe C, Romana SP, Dessen P, Soulier J, Viguié F, Fontenay M, Vainchenker W, Bernard OA. Delhommeau F, et al. Among authors: romana sp. N Engl J Med. 2009 May 28;360(22):2289-301. doi: 10.1056/NEJMoa0810069. N Engl J Med. 2009. PMID: 19474426 Free article.
NUP98-MLL fusion in human acute myeloblastic leukemia.
Kaltenbach S, Soler G, Barin C, Gervais C, Bernard OA, Penard-Lacronique V, Romana SP. Kaltenbach S, et al. Among authors: romana sp. Blood. 2010 Sep 30;116(13):2332-5. doi: 10.1182/blood-2010-04-277806. Epub 2010 Jun 17. Blood. 2010. PMID: 20558618 Free article.
Functional analysis of the NUP98-CCDC28A fusion protein.
Petit A, Ragu C, Soler G, Ottolenghi C, Schluth C, Radford-Weiss I, Schneider-Maunoury S, Callebaut I, Dastugue N, Drabkin HA, Bernard OA, Romana S, Penard-Lacronique V. Petit A, et al. Haematologica. 2012 Mar;97(3):379-87. doi: 10.3324/haematol.2011.047969. Epub 2011 Nov 4. Haematologica. 2012. PMID: 22058212 Free PMC article.
HOX11L2/TLX3 is transcriptionally activated through T-cell regulatory elements downstream of BCL11B as a result of the t(5;14)(q35;q32).
Su XY, Della-Valle V, Andre-Schmutz I, Lemercier C, Radford-Weiss I, Ballerini P, Lessard M, Lafage-Pochitaloff M, Mugneret F, Berger R, Romana SP, Bernard OA, Penard-Lacronique V. Su XY, et al. Among authors: romana sp. Blood. 2006 Dec 15;108(13):4198-201. doi: 10.1182/blood-2006-07-032953. Epub 2006 Aug 22. Blood. 2006. PMID: 16926283 Free article. Clinical Trial.
Acute megakaryoblastic leukemia and loss of the RUNX1 gene.
Berger R, Busson M, Dastugue N, Radford-Weiss I, Michaux L, Hagemeijer A, Quilichini B, Benattar L, Bernard O, Romana SP. Berger R, et al. Among authors: romana sp. Cancer Genet Cytogenet. 2006 Jan 1;164(1):71-3. doi: 10.1016/j.cancergencyto.2005.05.002. Cancer Genet Cytogenet. 2006. PMID: 16364766
Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth.
Malan V, Chevallier S, Soler G, Coubes C, Lacombe D, Pasquier L, Soulier J, Morichon-Delvallez N, Turleau C, Munnich A, Romana S, Vekemans M, Cormier-Daire V, Colleaux L. Malan V, et al. Eur J Hum Genet. 2010 Feb;18(2):227-32. doi: 10.1038/ejhg.2009.162. Epub 2009 Oct 21. Eur J Hum Genet. 2010. PMID: 19844265 Free PMC article.
109 results