« Stat5a and Stat5b: fraternal twins of signal transduction and transcriptional activation », Cytokine Growth Factor Rev., vol. 10, no 2, , p. 131–57 (PMID10743504, DOI10.1016/S1359-6101(99)00011-8)
« Signal transducer and activator of transcription 5A/B in prostate and breast cancers », Endocr. Relat. Cancer, vol. 15, no 2, , p. 367–90 (PMID18508994, DOI10.1677/ERC-08-0013, lire en ligne)
« Inhibitors of Stat5 protein signalling », MedChemComm, vol. 3, no 1, , p. 22 (DOI10.1039/C1MD00175B)
« Epigenetic repression of the Igk locus by STAT5-mediated recruitment of the histone methyltransferase Ezh2 », Nat. Immunol., vol. 12, no 12, , p. 1212–20 (PMID22037603, PMCID3233979, DOI10.1038/ni.2136)
« Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells », Nat. Med., vol. 2, no 5, , p. 561–6 (PMID8616716, DOI10.1038/nm0596-561)
« A FLT3-targeted tyrosine kinase inhibitor is cytotoxic to leukemia cells in vitro and in vivo », Blood, vol. 99, no 11, , p. 3885–91 (PMID12010785, DOI10.1182/blood.V99.11.3885)
« CYT387, a selective JAK1/JAK2 inhibitor: in vitro assessment of kinase selectivity and preclinical studies using cell lines and primary cells from polycythemia vera patients », Leukemia, vol. 23, no 8, , p. 1441–5 (PMID19295546, DOI10.1038/leu.2009.50)
« Specific inhibition of Stat5a/b promotes apoptosis of IL-2-responsive primary and tumor-derived lymphoid cells », J. Immunol., vol. 171, no 8, , p. 3919–27 (PMID14530308, DOI10.4049/jimmunol.171.8.3919, lire en ligne)
« Stat3 as a molecular target in RNA interference-based treatment of oral squamous cell carcinoma », Oncol. Rep., vol. 20, no 4, , p. 873–8 (PMID18813829, DOI10.3892/or_00000085)
« Small molecule STAT5-SH2 domain inhibitors exhibit potent antileukemia activity », J. Med. Chem., vol. 55, no 3, , p. 1047–55 (PMID22148584, DOI10.1021/jm200720n)
« Signal transducer and activator of transcription 5A/B in prostate and breast cancers », Endocr. Relat. Cancer, vol. 15, no 2, , p. 367–90 (PMID18508994, DOI10.1677/ERC-08-0013, lire en ligne)
« Specific inhibition of Stat5a/b promotes apoptosis of IL-2-responsive primary and tumor-derived lymphoid cells », J. Immunol., vol. 171, no 8, , p. 3919–27 (PMID14530308, DOI10.4049/jimmunol.171.8.3919, lire en ligne)
« Stat5a and Stat5b: fraternal twins of signal transduction and transcriptional activation », Cytokine Growth Factor Rev., vol. 10, no 2, , p. 131–57 (PMID10743504, DOI10.1016/S1359-6101(99)00011-8)
« Signal transducer and activator of transcription 5A/B in prostate and breast cancers », Endocr. Relat. Cancer, vol. 15, no 2, , p. 367–90 (PMID18508994, DOI10.1677/ERC-08-0013, lire en ligne)
« Epigenetic repression of the Igk locus by STAT5-mediated recruitment of the histone methyltransferase Ezh2 », Nat. Immunol., vol. 12, no 12, , p. 1212–20 (PMID22037603, PMCID3233979, DOI10.1038/ni.2136)
« Constitutive activation of STAT5 by the BCR-ABL oncogene in chronic myelogenous leukemia », Oncogene, vol. 13, no 2, , p. 247–54 (PMID8710363)
« Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells », Nat. Med., vol. 2, no 5, , p. 561–6 (PMID8616716, DOI10.1038/nm0596-561)
« A FLT3-targeted tyrosine kinase inhibitor is cytotoxic to leukemia cells in vitro and in vivo », Blood, vol. 99, no 11, , p. 3885–91 (PMID12010785, DOI10.1182/blood.V99.11.3885)
« CYT387, a selective JAK1/JAK2 inhibitor: in vitro assessment of kinase selectivity and preclinical studies using cell lines and primary cells from polycythemia vera patients », Leukemia, vol. 23, no 8, , p. 1441–5 (PMID19295546, DOI10.1038/leu.2009.50)
« Specific inhibition of Stat5a/b promotes apoptosis of IL-2-responsive primary and tumor-derived lymphoid cells », J. Immunol., vol. 171, no 8, , p. 3919–27 (PMID14530308, DOI10.4049/jimmunol.171.8.3919, lire en ligne)
« Stat3 as a molecular target in RNA interference-based treatment of oral squamous cell carcinoma », Oncol. Rep., vol. 20, no 4, , p. 873–8 (PMID18813829, DOI10.3892/or_00000085)
« Small molecule STAT5-SH2 domain inhibitors exhibit potent antileukemia activity », J. Med. Chem., vol. 55, no 3, , p. 1047–55 (PMID22148584, DOI10.1021/jm200720n)