Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Leite, Betty"'
Autor:
Fagnan, Alexandre 1, 2, Bagger, Frederik Otzen 3, 4, 5, 6, *, Piqué-Borràs, Maria-Riera 3, 4, *, Ignacimouttou, Cathy 1, 2, *, Caulier, Alexis 7, 8, Lopez, Cécile K. 1, 2, Robert, Elie 1, 2, Uzan, Benjamin 9, Gelsi-Boyer, Véronique 10, 11, Aid, Zakia 1, 2, Thirant, Cécile 1, 2, Moll, Ute 12, 13, Tauchmann, Samantha 3, 4, Kurtovic-Kozaric, Amina 14, Maciejewski, Jaroslaw 15, Dierks, Christine 16, Spinelli, Orietta 17, Salmoiraghi, Silvia 17, 18, Pabst, Thomas 19, Shimoda, Kazuya 20, Deleuze, Virginie 21, 22, Lapillonne, Hélène 23, Sweeney, Connor 24, De Mas, Véronique 25, Leite, Betty 26, Kadri, Zahra 27, Malinge, Sébastien 1, 28, de Botton, Stéphane 1, 2, Micol, Jean-Baptiste 1, Kile, Benjamin 29, Carmichael, Catherine L. 29, Iacobucci, Ilaria 30, Mullighan, Charles G. 30, 31, Carroll, Martin 32, Valent, Peter 33, 34, Bernard, Olivier A. 1, 2, Delabesse, Eric 25, Vyas, Paresh 24, Birnbaum, Daniel 10, 11, Anguita, Eduardo 35, 36, 37, 38, Garçon, Loïc 7, 8, Soler, Eric 21, 22, Schwaller, Juerg 2, 3, 4, †, Mercher, Thomas 1, 1, 2, †
Publikováno v:
In Blood 6 August 2020 136(6):698-714
Autor:
Manchev, Vladimir T., Bouzid, Hind, Antony-Debré, Iléana, Leite, Betty, Meurice, Guillaume, Droin, Nathalie, Prebet, Thomas, Costello, Régis T., Vainchenker, William, Plo, Isabelle, Diop, M'boyba, Macintyre, Elizabeth, Asnafi, Vahid, Favier, Rémi, Baccini, Véronique, Raslova, Hana
Publikováno v:
Journal of Cellular and Molecular Medicine
Journal of Cellular and Molecular Medicine, 2017, 21 (6), pp.1237-1242. ⟨10.1111/jcmm.13051⟩
Journal of Cellular and Molecular Medicine, Wiley Open Access, 2017, 21 (6), pp.1237-1242. ⟨10.1111/jcmm.13051⟩
Journal of Cellular and Molecular Medicine, 2017, 21 (6), pp.1237-1242. ⟨10.1111/jcmm.13051⟩
Journal of Cellular and Molecular Medicine, Wiley Open Access, 2017, 21 (6), pp.1237-1242. ⟨10.1111/jcmm.13051⟩
International audience; Familial platelet disorder with predisposition to acute myeloid leukaemia (FPD/AML) is characterized by germline RUNX1 mutations, thrombocy-topaenia, platelet dysfunction and a risk of developing acute myeloid and in rare case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e7bbf85c193f1de64606e85d40ebada0
https://hal.sorbonne-universite.fr/hal-01537098/file/Manchev_et_al-2017-Journal_of_Cellular_and_Molecular_Medicine.pdf
https://hal.sorbonne-universite.fr/hal-01537098/file/Manchev_et_al-2017-Journal_of_Cellular_and_Molecular_Medicine.pdf
Autor:
Fagnan, Alexandre, Bagger, Frederik Otzen, Piqué-Borràs, Maria-Riera, Ignacimouttou, Cathy, Caulier, Alexis, Lopez, Cécile K, Robert, Elie, Uzan, Benjamin, Gelsi-Boyer, Véronique, Aid, Zakia, Thirant, Cécile, Moll, Ute, Tauchmann, Samantha, Kurtovic-Kozaric, Amina, Maciejewski, Jaroslaw, Dierks, Christine, Spinelli, Orietta, Salmoiraghi, Silvia, Pabst, Thomas, Shimoda, Kazuya, Deleuze, Virginie, Lapillonne, Hélène, Sweeney, Connor, De Mas, Véronique, Leite, Betty, Kadri, Zahra, Malinge, Sébastien, De Botton, Stéphane, Micol, Jean-Baptiste, Kile, Benjamin, Carmichael, Catherine L, Iacobucci, Ilaria, Mullighan, Charles G, Carroll, Martin, Valent, Peter, Bernard, Olivier A, Delabesse, Eric, Vyas, Paresh, Birnbaum, Daniel, Anguita, Eduardo, Garçon, Loïc, Soler, Eric, Schwaller, Juerg, Mercher, Thomas
Acute erythroleukemia (AEL or acute myeloid leukemia [AML]-M6) is a rare but aggressive hematologic malignancy. Previous studies showed that AEL leukemic cells often carry complex karyotypes and mutations in known AML-associated oncogenes. To better
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a34b77752bab3522659e30baac7e9c3e