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    Results: 1 to 20 of 45

    1.

    An activating mutation in the CSF3R gene induces a hereditary chronic neutrophilia.

    Plo I, Zhang Y, Le Couédic JP, Nakatake M, Boulet JM, Itaya M, Smith SO, Debili N, Constantinescu SN, Vainchenker W, Louache F, de Botton S.

    J Exp Med. 2009 Aug 3;206(8):1701-7. Epub 2009 Jul 20.PMID: 19620628 [PubMed - indexed for MEDLINE]Related articles

    2.

    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.

    N Engl J Med. 2009 May 28;360(22):2289-301.PMID: 19474426 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Evidence for MPL W515L/K mutations in hematopoietic stem cells in primitive myelofibrosis.

    Chaligné R, James C, Tonetti C, Besancenot R, Le Couédic JP, Fava F, Mazurier F, Godin I, Maloum K, Larbret F, Lécluse Y, Vainchenker W, Giraudier S.

    Blood. 2007 Nov 15;110(10):3735-43. Epub 2007 Aug 20.PMID: 17709604 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Mutations in JAK2V617F homologous domain of JAK genes are uncommon in solid tumors.

    Motté N, Saulnier P, Le Couedic JP, Soria JC, Delaloge S, Boige V, Pautier P, Vainchenker W, Bidart JM, Villeval JL.

    Int J Cancer. 2007 Nov 1;121(9):2113-5. No abstract available. PMID: 17631640 [PubMed - indexed for MEDLINE]Related articles

    5.

    The JAK2 617V>F mutation triggers erythropoietin hypersensitivity and terminal erythroid amplification in primary cells from patients with polycythemia vera.

    Dupont S, Massé A, James C, Teyssandier I, Lécluse Y, Larbret F, Ugo V, Saulnier P, Koscielny S, Le Couédic JP, Casadevall N, Vainchenker W, Delhommeau F.

    Blood. 2007 Aug 1;110(3):1013-21. Epub 2007 Mar 27.PMID: 17389763 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Proplatelet formation is regulated by the Rho/ROCK pathway.

    Chang Y, Auradé F, Larbret F, Zhang Y, Le Couedic JP, Momeux L, Larghero J, Bertoglio J, Louache F, Cramer E, Vainchenker W, Debili N.

    Blood. 2007 May 15;109(10):4229-36. Epub 2007 Jan 23.PMID: 17244674 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Evidence that the JAK2 G1849T (V617F) mutation occurs in a lymphomyeloid progenitor in polycythemia vera and idiopathic myelofibrosis.

    Delhommeau F, Dupont S, Tonetti C, Massé A, Godin I, Le Couedic JP, Debili N, Saulnier P, Casadevall N, Vainchenker W, Giraudier S.

    Blood. 2007 Jan 1;109(1):71-7. Epub 2006 Sep 5.PMID: 16954506 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera.

    James C, Ugo V, Le Couédic JP, Staerk J, Delhommeau F, Lacout C, Garçon L, Raslova H, Berger R, Bennaceur-Griscelli A, Villeval JL, Constantinescu SN, Casadevall N, Vainchenker W.

    Nature. 2005 Apr 28;434(7037):1144-8.PMID: 15793561 [PubMed - indexed for MEDLINE]Related articles

    9.

    Gfi-1B plays a critical role in terminal differentiation of normal and transformed erythroid progenitor cells.

    Garçon L, Lacout C, Svinartchouk F, Le Couédic JP, Villeval JL, Vainchenker W, Duménil D.

    Blood. 2005 Feb 15;105(4):1448-55. Epub 2004 Oct 26.PMID: 15507521 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia.

    Raslova H, Komura E, Le Couédic JP, Larbret F, Debili N, Feunteun J, Danos O, Albagli O, Vainchenker W, Favier R.

    J Clin Invest. 2004 Jul;114(1):77-84.PMID: 15232614 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Megakaryocyte polyploidization is associated with a functional gene amplification.

    Raslova H, Roy L, Vourc'h C, Le Couedic JP, Brison O, Metivier D, Feunteun J, Kroemer G, Debili N, Vainchenker W.

    Blood. 2003 Jan 15;101(2):541-4. Epub 2002 Sep 5.PMID: 12393414 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Role of p21(Cip1/Waf1) in cell-cycle exit of endomitotic megakaryocytes.

    Baccini V, Roy L, Vitrat N, Chagraoui H, Sabri S, Le Couedic JP, Debili N, Wendling F, Vainchenker W.

    Blood. 2001 Dec 1;98(12):3274-82.PMID: 11719364 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Expression and function of the collagen receptor GPVI during megakaryocyte maturation.

    Lagrue-Lak-Hal AH, Debili N, Kingbury G, Lecut C, Le Couedic JP, Villeval JL, Jandrot-Perrus M, Vainchenker W.

    J Biol Chem. 2001 May 4;276(18):15316-25. Epub 2001 Jan 16.PMID: 11278467 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Myelofibrosis: experimental models and human studies.

    Taskin AL, Cohen-Solal K, Le Couedic JP, Abina MA, Villeval JL, Debili N, Casadevall N, Vainchenker W, Wendling F.

    Stem Cells. 1998;16 Suppl 2:155-64. Review.PMID: 11012187 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Cloning, characterization, and functional studies of human and mouse glycoprotein VI: a platelet-specific collagen receptor from the immunoglobulin superfamily.

    Jandrot-Perrus M, Busfield S, Lagrue AH, Xiong X, Debili N, Chickering T, Le Couedic JP, Goodearl A, Dussault B, Fraser C, Vainchenker W, Villeval JL.

    Blood. 2000 Sep 1;96(5):1798-807.PMID: 10961879 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Existence of a differentiation blockage at the stage of a megakaryocyte precursor in the thrombocytopenia and absent radii (TAR) syndrome.

    Letestu R, Vitrat N, Massé A, Le Couedic JP, Lazar V, Rameau P, Wendling F, Vuillier J, Boutard P, Plouvier E, Plasse M, Favier R, Vainchenker W, Debili N.

    Blood. 2000 Mar 1;95(5):1633-41.PMID: 10688818 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Endomitosis of human megakaryocytes are due to abortive mitosis.

    Vitrat N, Cohen-Solal K, Pique C, Le Couedic JP, Norol F, Larsen AK, Katz A, Vainchenker W, Debili N.

    Blood. 1998 May 15;91(10):3711-23.PMID: 9573008 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Missense mutation of the erythropoietin receptor is a rare event in human erythroid malignancies.

    Le Couedic JP, Mitjavila MT, Villeval JL, Feger F, Gobert S, Mayeux P, Casadevall N, Vainchenker W.

    Blood. 1996 Feb 15;87(4):1502-11.PMID: 8608241 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Gene analysis in 18 cases of cutaneous lymphoid infiltrates of uncertain significance.

    Wechsler J, Bagot M, Henni T, Le Couedic JP, Gaulard P, Zafrani ES.

    Arch Pathol Lab Med. 1995 Feb;119(2):157-62.PMID: 7848063 [PubMed - indexed for MEDLINE]Related articles

    20.

    Role of granulocyte-macrophage colony-stimulating factor, interleukin-3 and interleukin-5 in the eosinophilia associated with T cell lymphoma.

    Fermand JP, Mitjavila MT, Le Couedic JP, Tsapis A, Berger R, Modigliani R, Seligmann M, Brouet JC, Vainchenker W.

    Br J Haematol. 1993 Mar;83(3):359-64.PMID: 8485042 [PubMed - indexed for MEDLINE]Related articles

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