Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Jean Briere"'
Autor:
Jean Briere
Publikováno v:
Bulletin de l'Académie Nationale de Médecine. 191:535-548
An increased platelet number in blood depends on a limited spectrum of causes, which aren't always simple to identify. Secondary thrombocytosis is a reactive process in relation with acute or chronic inflammatory diseases, or asplenia. The infrequent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a18b22c1429ea8d4c3cd95f4f98701d4
https://doi.org/10.1016/s0001-4079(19)33043-2
https://doi.org/10.1016/s0001-4079(19)33043-2
Autor:
Devinder Gill, E. Van Den Neste, B. Glass, Dc Linch, Christian Gisselbrecht, Noel-Jean Milpied, Catherine Thieblemont, John Radford, Craig H. Moskowitz, Marek Trneny, David D.F. Ma, Ofer Shpilberg, Gilles Salles, Jean Briere, Nicolas Ketterer, Nicolas Mounier, Norbert Schmitz, Ulrich Dührsen
Publikováno v:
Bone marrow transplantation. 51(1)
Salvage chemotherapy followed by autologous stem cell transplantation (ASCT) is the standard second-line treatment for relapsed and refractory diffuse large B-cell lymphoma (DLBCL). However, the strategy is less clear in patients who require third-li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81a76c0e46900df4023283c89f9c23d6
https://pubmed.ncbi.nlm.nih.gov/26437065
https://pubmed.ncbi.nlm.nih.gov/26437065
Autor:
Jean-François Bernard, Jean-Didier Rain, Jean-Jacques Kiladjian, Christine Chomienne, Jean Briere, Pierre Fenaux
Publikováno v:
Seminars in Thrombosis and Hemostasis. 32:417-421
Despite recent discoveries made in myeloproliferative disorders other than chronic myelogenous leukemia, which it is hoped will result in earlier diagnosis, and better evaluation and management of patients, hematological evolution to myelofibrosis, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77e47245d7103c9a0a188ad1c2ed2694
https://doi.org/10.1055/s-2006-942762
https://doi.org/10.1055/s-2006-942762
Autor:
Nicola Vahsen, Pier G. Mastroberardino, Frank Madeo, Nicholas Joza, Noelia Casares, Guido Kroemer, Silvia Engelhardt, Najet Debili, Silke Wissing, Hermann Schägger, Paule Bénit, Pierre Rustin, Olivier Feraud, Vladimir Lazar, Josef M. Penninger, Marie O. Pequignot, Jean Briere, Nathanael Larochette, Céline Candé, Mauro Piacentini
Publikováno v:
The EMBO Journal. 23:4679-4689
Apoptosis-inducing factor (AIF) is a mitochondrial flavoprotein that, after apoptosis induction, translocates to the nucleus where it participates in apoptotic chromatinolysis. Here, we show that human or mouse cells lacking AIF as a result of homolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e578f4247502c38ba134e3694c9559f4
https://doi.org/10.1038/sj.emboj.7600461
https://doi.org/10.1038/sj.emboj.7600461
Publikováno v:
Pathologie Biologie. 52:289-293
Despite a prolonged survival of around 15 years linked to a prolonged complete remission induced by myelosuppression, myeloproliferative syndromes such as polycythemia vera (PV) and essential thrombosis (ET) remain at risk of lethal adverse affects s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::832d927813191a81ba3716ba72c4b594
https://doi.org/10.1016/j.patbio.2004.03.017
https://doi.org/10.1016/j.patbio.2004.03.017
Autor:
Yasmine Chait, Annie Bezeaud, Marie-Hélène Denninger, Dominique Valla, Marie-Claude Guillin, Jean Briere, Serge Erlinger, Sophie Hillaire, Nicole Casadevall
Publikováno v:
Hepatology. 31:587-591
According to a recent hypothesis, venous thrombosis results from the concurrence of several factors. This hypothesis was assessed in patients with portal or hepatic venous thrombosis by simultaneously investigating most of the currently identified pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::747afddd86f5d8d6d7ebeddab3c2e811
https://doi.org/10.1002/hep.510310307
https://doi.org/10.1002/hep.510310307
Autor:
Jean Briere, N. Elkassar
Publikováno v:
Baillière's Clinical Haematology. 11:787-801
Our current understanding of the pathogenesis of the myeloproliferative disorders is based on the assumption that they represent a clonal disorder resulting from transformation of a haematopoietic stem cell. Clonality assays exploit the fact that fem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c44b54741579a32c461c568eced657a
https://doi.org/10.1016/s0950-3536(98)80039-5
https://doi.org/10.1016/s0950-3536(98)80039-5
Autor:
C. Gardin, Gilles Hetet, Jean Briere, Bernard Grandchamp, N. Elkassar, Jean-Jacques Kiladjian
Publikováno v:
Leukemia. 11:1821-1826
Essential thrombocythemia (ET) is a myeloproliferative disorder associated with megakaryocytic hyperplasia and thrombocytosis. In this disease, in vitro autonomous growth of megakaryocytic colonies has been demonstrated by various investigators. This
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3893bd300d5b87a7d6e8bc9ccba58b52
https://doi.org/10.1038/sj.leu.2400845
https://doi.org/10.1038/sj.leu.2400845
Publikováno v:
Baillière's Clinical Haematology. 10:65-88
Increased megakaryocyte (MK) proliferation in bone marrow is a feature common to the three Ph-negative myeloproliferative disorders (MPDs), i.e. essential thrombocythaemia (ET), polycythaemia vera (PV), and myelofibrosis with splenic myeloid metaplas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::735bcce17d87de2f66438b7272825a4c
https://doi.org/10.1016/s0950-3536(97)80051-0
https://doi.org/10.1016/s0950-3536(97)80051-0
Publikováno v:
Journal of Laboratory and Clinical Medicine. 127:382-390
We have previously reported that platelet factor 4 (PF4) inhibits human erythroleukemic (HEL) cell growth in a dose-dependent fashion in vitro and that PF4 binds to HEL cells in a specific, saturable, and concentration-dependent manner. In this artic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c0ff4c036c4974776d8ab1839b2883d
https://doi.org/10.1016/s0022-2143(96)90186-9
https://doi.org/10.1016/s0022-2143(96)90186-9