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192 results
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Cytosine arabinoside induces costimulatory molecule expression in acute myeloid leukemia cells.
Vereecque R, Saudemont A, Quesnel B. Vereecque R, et al. Among authors: quesnel b. Leukemia. 2004 Jul;18(7):1223-30. doi: 10.1038/sj.leu.2403391. Leukemia. 2004. PMID: 15152266
Haemostatic and proteolytic markers in acute non lymphoid leukemia: a source of multiple informations.
Goudemand J, Caron C, Quesnel B. Goudemand J, et al. Among authors: quesnel b. Nouv Rev Fr Hematol. 1991;33(2):207-8. Nouv Rev Fr Hematol. 1991. PMID: 1766856 No abstract available.
Inactivation of the retinoblastoma gene appears to be very uncommon in myelodysplastic syndromes.
Preudhomme C, Vachee A, Lepelley P, Vanrumbeke M, Zandecki M, Quesnel B, Cosson A, Fenaux P. Preudhomme C, et al. Among authors: quesnel b. Br J Haematol. 1994 May;87(1):61-7. doi: 10.1111/j.1365-2141.1994.tb04871.x. Br J Haematol. 1994. PMID: 7524620
c-mpl expression in hematologic disorders.
Bouscary D, Prudhomme C, Quesnel B, Melle J, Picard F, Dreyfus F. Bouscary D, et al. Among authors: quesnel b. Leuk Lymphoma. 1995 Mar;17(1-2):19-26. doi: 10.3109/10428199509051699. Leuk Lymphoma. 1995. PMID: 7773160 Review.
p16 gene homozygous deletions in acute lymphoblastic leukemia.
Quesnel B, Preudhomme C, Philippe N, Vanrumbeke M, Dervite I, Lai JL, Bauters F, Wattel E, Fenaux P. Quesnel B, et al. Blood. 1995 Feb 1;85(3):657-63. Blood. 1995. PMID: 7833469
Relationship between p53 gene mutations and multidrug resistance (mdr1) gene expression in myelodysplastic syndromes.
Preudhomme C, Lepelley P, Vachee A, Soenen V, Quesnel B, Cosson A, Fenaux P. Preudhomme C, et al. Among authors: quesnel b. Leukemia. 1993 Nov;7(11):1888-90. Leukemia. 1993. PMID: 7901457
Detection of p53 mutations in hematological malignancies: comparison between immunocytochemistry and DNA analysis.
Lepelley P, Preudhomme C, Vanrumbeke M, Quesnel B, Cosson A, Fenaux P. Lepelley P, et al. Among authors: quesnel b. Leukemia. 1994 Aug;8(8):1342-9. Leukemia. 1994. PMID: 8057671
Absence of rearrangement of the neurofibromatosis 1 (NF1) gene in myelodysplastic syndromes and acute myeloid leukemia.
Quesnel B, Preudhomme C, Vanrumbeke M, Vachee A, Lai JL, Fenaux P. Quesnel B, et al. Leukemia. 1994 May;8(5):878-80. Leukemia. 1994. PMID: 8182944
Therapy-related acute myeloid leukemia with t(8;21), inv(16), and t(8;16): a report on 25 cases and review of the literature.
Quesnel B, Kantarjian H, Bjergaard JP, Brault P, Estey E, Lai JL, Tilly H, Stoppa AM, Archimbaud E, Harousseau JL, et al. Quesnel B, et al. J Clin Oncol. 1993 Dec;11(12):2370-9. doi: 10.1200/JCO.1993.11.12.2370. J Clin Oncol. 1993. PMID: 8246025 Review.
Rare occurrence of mutations of the FLR exon of the neurofibromatosis 1 (NF1) gene in myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML).
Preudhomme C, Vachee A, Quesnel B, Wattel E, Cosson A, Fenaux P. Preudhomme C, et al. Among authors: quesnel b. Leukemia. 1993 Jul;7(7):1071. Leukemia. 1993. PMID: 8321023 No abstract available.
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