Zobrazeno 1 - 10
of 11
pro vyhledávání: '"David Avran"'
Autor:
Jean Soulier, François Sigaux, Hugues de Thé, Claude Gazin, Jean-Jacques Diaz, Emmanuelle Clappier, Hervé Dombret, André Baruchel, Jules P. Meijerink, Pieter Van Vlierberghe, Tom Taghon, Isabelle André-Schmutz, Gerben Menschaert, Wouter Van Loocke, Jessica G. Buijs-Gladdines, Willem K. Smits, Marika Pla, Lucie Hernandez, Godelieve Meunier, Delphine Briot, Gabriel Thérizols, Marc Delord, Samuel Quentin, Frédéric Catez, Eulalia Genesca, David Avran, Tiama El-Chaar, Stéphanie Gachet
Differentially Expressed Proteins Deleted versus non-deleted clones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::271857d373d87f7754090d9a8c66e7c1
https://doi.org/10.1158/2159-8290.22533191.v1
https://doi.org/10.1158/2159-8290.22533191.v1
Autor:
Jean Soulier, François Sigaux, Hugues de Thé, Claude Gazin, Jean-Jacques Diaz, Emmanuelle Clappier, Hervé Dombret, André Baruchel, Jules P. Meijerink, Pieter Van Vlierberghe, Tom Taghon, Isabelle André-Schmutz, Gerben Menschaert, Wouter Van Loocke, Jessica G. Buijs-Gladdines, Willem K. Smits, Marika Pla, Lucie Hernandez, Godelieve Meunier, Delphine Briot, Gabriel Thérizols, Marc Delord, Samuel Quentin, Frédéric Catez, Eulalia Genesca, David Avran, Tiama El-Chaar, Stéphanie Gachet
Differentially expressed genes in Xenograted T-ALL shSYNCRIP-SNHG5 versus ShCtrl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49f0baf6c4edbe82832f8d3e87bb143e
https://doi.org/10.1158/2159-8290.22533185.v1
https://doi.org/10.1158/2159-8290.22533185.v1
Autor:
Jean Soulier, François Sigaux, Hugues de Thé, Claude Gazin, Jean-Jacques Diaz, Emmanuelle Clappier, Hervé Dombret, André Baruchel, Jules P. Meijerink, Pieter Van Vlierberghe, Tom Taghon, Isabelle André-Schmutz, Gerben Menschaert, Wouter Van Loocke, Jessica G. Buijs-Gladdines, Willem K. Smits, Marika Pla, Lucie Hernandez, Godelieve Meunier, Delphine Briot, Gabriel Thérizols, Marc Delord, Samuel Quentin, Frédéric Catez, Eulalia Genesca, David Avran, Tiama El-Chaar, Stéphanie Gachet
Differentially translated transcripts - translatome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::374114b4001261d1ee7665b17215fae0
https://doi.org/10.1158/2159-8290.22533188.v1
https://doi.org/10.1158/2159-8290.22533188.v1
Autor:
Jean Soulier, François Sigaux, Hugues de Thé, Claude Gazin, Jean-Jacques Diaz, Emmanuelle Clappier, Hervé Dombret, André Baruchel, Jules P. Meijerink, Pieter Van Vlierberghe, Tom Taghon, Isabelle André-Schmutz, Gerben Menschaert, Wouter Van Loocke, Jessica G. Buijs-Gladdines, Willem K. Smits, Marika Pla, Lucie Hernandez, Godelieve Meunier, Delphine Briot, Gabriel Thérizols, Marc Delord, Samuel Quentin, Frédéric Catez, Eulalia Genesca, David Avran, Tiama El-Chaar, Stéphanie Gachet
Supp Fig. S1-6, Supp Tables S1-S3, Supp Methods and References
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c126e285664795ed7837b709d7613fde
https://doi.org/10.1158/2159-8290.22533194
https://doi.org/10.1158/2159-8290.22533194
Autor:
Jean Soulier, François Sigaux, Hugues de Thé, Claude Gazin, Jean-Jacques Diaz, Emmanuelle Clappier, Hervé Dombret, André Baruchel, Jules P. Meijerink, Pieter Van Vlierberghe, Tom Taghon, Isabelle André-Schmutz, Gerben Menschaert, Wouter Van Loocke, Jessica G. Buijs-Gladdines, Willem K. Smits, Marika Pla, Lucie Hernandez, Godelieve Meunier, Delphine Briot, Gabriel Thérizols, Marc Delord, Samuel Quentin, Frédéric Catez, Eulalia Genesca, David Avran, Tiama El-Chaar, Stéphanie Gachet
Deletion of chromosome 6q is a well-recognized abnormality found in poor-prognosis T-cell acute lymphoblastic leukemia (T-ALL). Using integrated genomic approaches, we identified two candidate haploinsufficient genes contiguous at 6q14, SYNCRIP (enco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e40b504a7e1e61dc754363e5c823e52
https://doi.org/10.1158/2159-8290.c.6546977
https://doi.org/10.1158/2159-8290.c.6546977
Autor:
Sarah Spyridakis Coquery, Alexandre Georges, Anne Cortey, Corinne Floch, David Avran, Edith Gatbois, Claire Mehler-Jacob, Matthieu de Stampa
Publikováno v:
European Journal of Pediatrics. 181:3075-3084
Neonatal jaundice is common and associated with delay in hospital discharge and risk of neurological sequelae if not treated. The objectives of the study were to report on our experience of the monitoring and treatment of neonatal jaundice in a home
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbc964fb53fa62f20e94a59cede71496
https://doi.org/10.1007/s00431-022-04461-4
https://doi.org/10.1007/s00431-022-04461-4
Autor:
Wouter Van Loocke, Hervé Dombret, Samuel Quentin, Claude Gazin, David Avran, Pieter Van Vlierberghe, François Sigaux, André Baruchel, Delphine Briot, Jean-Jacques Diaz, Stéphanie Gachet, Tom Taghon, Emmanuelle Clappier, Gerben Menschaert, Tiama El-Chaar, Jules P.P. Meijerink, Marika Pla, Eulàlia Genescà, Jessica G.C.A.M. Buijs-Gladdines, Isabelle André-Schmutz, Jean Soulier, Marc Delord, Frédéric Catez, Lucie Hernandez, Willem K. Smits, Godelieve Meunier, Gabriel Therizols
Publikováno v:
Cancer Discovery
Cancer Discovery, 2018, ⟨10.1158/2159-8290.CD-17-0831⟩
Cancer Discovery, American Association for Cancer Research, 2018, ⟨10.1158/2159-8290.CD-17-0831⟩
Cancer Discovery, 2018, ⟨10.1158/2159-8290.CD-17-0831⟩
Cancer Discovery, American Association for Cancer Research, 2018, ⟨10.1158/2159-8290.CD-17-0831⟩
Deletion of chromosome 6q is a well-recognized abnormality found in poor-prognosis T-cell acute lymphoblastic leukemia (T-ALL). Using integrated genomic approaches, we identified two candidate haploinsufficient genes contiguous at 6q14, SYNCRIP (enco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf028ce74fad78e6b8390e626d815e0a
https://hal.univ-lorraine.fr/hal-01908797
https://hal.univ-lorraine.fr/hal-01908797
Autor:
L. Hauser, Marie Belloy, Philippe Bierling, Nourredine AitOubelli, David Avran, Béatrice Pangon, Stéphane Bonacorsi, M. Simonet, Laurence Raoult, Senbetta Menasie, A. Beyloune, Typhaine Billard-Pomares
Publikováno v:
Transfusion. 56:1311-1313
BACKGROUND Transfusion-transmitted bacterial infection (TTBI) is still one of the most feared complications of blood transfusion. CASE REPORT We report a fatal case involving an 8-year-old child with congenital dyskeratosis complicated by severe apla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f084872b5fdf538b2eaeccd04aadf4a
https://doi.org/10.1111/trf.13589
https://doi.org/10.1111/trf.13589
Publikováno v:
European Journal of Pediatrics. 173:1659-1661
Although the incidence of sudden unexpected death in infancy (SUDI) decreased markedly after campaigns to promote supine positioning during sleeping, it has remained unchanged over the last decade. Epidemiological data suggest a role for new causes s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7462d051237bd8d15c09aeac7841e0c
https://doi.org/10.1007/s00431-013-2238-6
https://doi.org/10.1007/s00431-013-2238-6
Publikováno v:
Case Reports. 2014:bcr2014204706-bcr2014204706
A 5-year-old boy from the Congo, was admitted for hyperleucocytic acute lymphoblastic leukaemia, with a high risk of tumour lysis syndrome (TLS). He had splenomegaly and mediastinal lymphadenopathy on chest X-ray. We started steroids and hyperhydrati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b500e6df8933ac2e544d3a0b4152368b
https://doi.org/10.1136/bcr-2014-204706
https://doi.org/10.1136/bcr-2014-204706