Soenen V - Search Results

1

Mechanisms of genesis of variant translocation in chronic myeloid leukemia are not correlated with ABL1 or BCR deletion status or response to imatinib therapy.

Richebourg S, Eclache V, Perot C, Portnoi MF, Van den Akker J, Terré C, Maareck O, Soenen V, Viguié F, Laï JL, Andrieux J, Corm S, Roche-Lestienne C; Fi-LMC Group. Richebourg S, et al. Among authors: soenen v. Cancer Genet Cytogenet. 2008 Apr 15;182(2):95-102. doi: 10.1016/j.cancergencyto.2008.01.005. Cancer Genet Cytogenet. 2008. PMID: 18406870

2

Chromosomal insertion involving MLL in childhood acute myeloblastic leukemia (M4).

Lafay-Cousin L, Soenen V, Mazingue F, Preudhomme C, Laï JL, Andrieux J. Lafay-Cousin L, et al. Among authors: soenen v. Cancer Genet Cytogenet. 2004 Apr 15;150(2):153-5. doi: 10.1016/j.cancergencyto.2003.08.006. Cancer Genet Cytogenet. 2004. PMID: 15066323

3

17p Deletion in acute myeloid leukemia and myelodysplastic syndrome. Analysis of breakpoints and deleted segments by fluorescence in situ.

Soenen V, Preudhomme C, Roumier C, Daudignon A, Laï JL, Fenaux P. Soenen V, et al. Blood. 1998 Feb 1;91(3):1008-15. Blood. 1998. PMID: 9446663 Free article.

4

p190 bcr-abl rearrangement: a secondary cytogenetic event in some chronic myeloid disorders?

Roumier C, Daudignon A, Soenen V, Dupriez B, Wetterwald M, Lai JL, Cosson A, Fenaux P, Preudhomme C. Roumier C, et al. Among authors: soenen v. Haematologica. 1999 Dec;84(12):1075-80. Haematologica. 1999. PMID: 10586207

5

Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3).

Nicodème F, Geffroy S, Conti M, Delobel B, Soenen V, Grardel N, Porte H, Copin MC, Laï JL, Andrieux J. Nicodème F, et al. Among authors: soenen v. Genes Chromosomes Cancer. 2005 Oct;44(2):154-60. doi: 10.1002/gcc.20225. Genes Chromosomes Cancer. 2005. PMID: 15942943

6

Identification of a YAC spanning the translocation breakpoint t(8;22) associated with acute monocytic leukemia.

Soenen V, Chaffanet M, Preudhomme C, Dib A, Lai JL, Fletcher JA, Birnbaurn D, Pébusque MJ. Soenen V, et al. Genes Chromosomes Cancer. 1996 Mar;15(3):191-4. doi: 10.1002/(SICI)1098-2264(199603)15:3<191::AID-GCC9>3.0.CO;2-Y. Genes Chromosomes Cancer. 1996. PMID: 8721686

7

Prognostic significance of p16INK4a immunocytochemistry in adult ALL with standard risk karyotype.

Soenen V, Lepelley P, Gyan E, Preudhomme C, Lai JL, Bauters F, Fenaux P, Quesnel B. Soenen V, et al. Leukemia. 2001 Jul;15(7):1054-9. doi: 10.1038/sj.leu.2402153. Leukemia. 2001. PMID: 11455973

8

FISH analysis with a YAC probe improves detection of LAZ3/BCL6 rearrangement in non-Hodgkin's lymphoma.

Roumier C, Galiègue-Zouitina S, Bastard C, Soenen V, Laï JL, Denis C, Buchonnet G, Kerckaert JP, Cosson A, Fenaux P, Preudhomme C. Roumier C, et al. Among authors: soenen v. Hematol J. 2000;1(2):117-25. doi: 10.1038/sj.thj.6200002. Hematol J. 2000. PMID: 11920179

9

Combined immunophenotyping and in situ hybridization (FICTION): a rapid method to study cell lineage involvement in myelodysplastic syndromes.

Soenen V, Fenaux P, Flactif M, Lepelley P, Lai JL, Cosson A, Preudhomme C. Soenen V, et al. Br J Haematol. 1995 Jul;90(3):701-6. doi: 10.1111/j.1365-2141.1995.tb05604.x. Br J Haematol. 1995. PMID: 7647013

10

Myelodysplasia during the course of myeloma. Restriction of 17p deletion and p53 overexpression to myeloid cells.

Soenen V, Preudhomme C, Roumier C, Laï JL, Lepelley P, Facon T, Pagniez D, Fenaux P. Soenen V, et al. Leukemia. 1998 Feb;12(2):238-41. doi: 10.1038/sj.leu.2400909. Leukemia. 1998. PMID: 9519788

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