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Page 1
BACH2 promotes indolent clinical presentation in Waldenström macroglobulinemia.
Herbaux C, Bertrand E, Marot G, Roumier C, Poret N, Soenen V, Nibourel O, Roche-Lestienne C, Broucqsault N, Galiègue-Zouitina S, Boyle EM, Fouquet G, Renneville A, Tricot S, Morschhauser F, Preudhomme C, Quesnel B, Poulain S, Leleu X. Herbaux C, et al. Among authors: bertrand e. Oncotarget. 2016 Jun 7;8(34):57451-57459. doi: 10.18632/oncotarget.9917. eCollection 2017 Aug 22. Oncotarget. 2016. PMID: 28924457 Free PMC article.
MYD88 L265P mutation in Waldenstrom macroglobulinemia.
Poulain S, Roumier C, Decambron A, Renneville A, Herbaux C, Bertrand E, Tricot S, Daudignon A, Galiègue-Zouitina S, Soenen V, Theisen O, Grardel N, Nibourel O, Roche-Lestienne C, Quesnel B, Duthilleul P, Preudhomme C, Leleu X. Poulain S, et al. Among authors: bertrand e. Blood. 2013 May 30;121(22):4504-11. doi: 10.1182/blood-2012-06-436329. Epub 2013 Mar 26. Blood. 2013. PMID: 23532735 Free article.
Genome wide SNP array identified multiple mechanisms of genetic changes in Waldenstrom macroglobulinemia.
Poulain S, Roumier C, Galiègue-Zouitina S, Daudignon A, Herbaux C, Aiijou R, Lainelle A, Broucqsault N, Bertrand E, Manier S, Renneville A, Soenen V, Tricot S, Roche-Lestienne C, Duthilleul P, Preudhomme C, Quesnel B, Morel P, Leleu X. Poulain S, et al. Among authors: bertrand e. Am J Hematol. 2013 Nov;88(11):948-54. doi: 10.1002/ajh.23545. Epub 2013 Aug 30. Am J Hematol. 2013. PMID: 23861223 Free article.
Genomic Landscape of CXCR4 Mutations in Waldenström Macroglobulinemia.
Poulain S, Roumier C, Venet-Caillault A, Figeac M, Herbaux C, Marot G, Doye E, Bertrand E, Geffroy S, Lepretre F, Nibourel O, Decambron A, Boyle EM, Renneville A, Tricot S, Daudignon A, Quesnel B, Duthilleul P, Preudhomme C, Leleu X. Poulain S, et al. Among authors: bertrand e. Clin Cancer Res. 2016 Mar 15;22(6):1480-8. doi: 10.1158/1078-0432.CCR-15-0646. Epub 2015 Oct 21. Clin Cancer Res. 2016. PMID: 26490317
TP53 Mutation and Its Prognostic Significance in Waldenstrom's Macroglobulinemia.
Poulain S, Roumier C, Bertrand E, Renneville A, Caillault-Venet A, Doye E, Geffroy S, Sebda S, Nibourel O, Nudel M, Herbaux C, Renaud L, Tomowiak C, Guidez S, Tricot S, Roche-Lestienne C, Quesnel B, Preudhomme C, Leleu X. Poulain S, et al. Among authors: bertrand e. Clin Cancer Res. 2017 Oct 15;23(20):6325-6335. doi: 10.1158/1078-0432.CCR-17-0007. Epub 2017 Jul 28. Clin Cancer Res. 2017. PMID: 28754818
MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome.
Poulain S, Boyle EM, Roumier C, Demarquette H, Wemeau M, Geffroy S, Herbaux C, Bertrand E, Hivert B, Terriou L, Verrier A, Pollet JP, Maurage CA, Onraed B, Morschhauser F, Quesnel B, Duthilleul P, Preudhomme C, Leleu X. Poulain S, et al. Among authors: bertrand e. Br J Haematol. 2014 Nov;167(4):506-13. doi: 10.1111/bjh.13078. Epub 2014 Aug 27. Br J Haematol. 2014. PMID: 25160558 Free article. Clinical Trial.
Preclinical evaluation of invariant natural killer T cells in the 5T33 multiple myeloma model.
Nur H, Fostier K, Aspeslagh S, Renmans W, Bertrand E, Leleu X, Favreau M, Breckpot K, Schots R, De Waele M, Van Valckenborgh E, De Bruyne E, Facon T, Elewaut D, Vanderkerken K, Menu E. Nur H, et al. Among authors: bertrand e. PLoS One. 2013 May 31;8(5):e65075. doi: 10.1371/journal.pone.0065075. Print 2013. PLoS One. 2013. PMID: 23741460 Free PMC article.
[Stem cell transplantation unit: Guidelines from the francophone Society of bone marrow transplantation and cellular therapy (SFGM-TC)].
Faucher C, Adam C, Bancillon N, Bertrand E, Colledani F, de Berranger E, Denis V, Girard I, Hamzy F, Loukili N, Mannone L, Mercier L, Perrin A, Vasseur A, Asma Q, Bompoint C, Yafour N, Yakoub-Agha I, Jost E. Faucher C, et al. Among authors: bertrand e. Bull Cancer. 2019 Jan;106(1S):S1-S9. doi: 10.1016/j.bulcan.2018.11.005. Epub 2018 Dec 21. Bull Cancer. 2019. PMID: 30580913 Free article. French.
591 results