Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Marie Céline Deau"'
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Helios represses megakaryocyte priming in hematopoietic stem and progenitor cells
Autor: Marie-Céline Deau, Angela M. Thornton, Stephanie Gras, Leif Carlsson, Vincent Mittelheisser, Susan Chan, Giovanni Cova, Peggy Kirstetter, Chiara Taroni, Bernard Jost, Ethan M. Shevach, Marie Cerciat, Matthieu Jung, Christelle Thibault-Carpentier, Qi Cai, Philippe Kastner, Muriel Philipps
Publikováno v: Journal of Experimental Medicine
Journal of Experimental Medicine, 2021, 218 (10), pp.e20202317. ⟨10.1084/jem.20202317⟩
Journal of Experimental Medicine, Rockefeller University Press, 2021, 218 (10), ⟨10.1084/jem.20202317⟩
International audience; Our understanding of cell fate decisions in hematopoietic stem cells is incomplete. Here, we show that the transcription factor Helios is highly expressed in murine hematopoietic stem and progenitor cells (HSPCs), where it is
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa67fa174402716bd69ba0708bdaf889
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-189179
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3
MYB-GATA1fusion promotes basophilic leukaemia: involvement of interleukin-33 and nerve growth factor receptors
Autor: Valérie Prouzet-Mauléon, Jean-Max Pasquet, Marie-Céline Deau, Hayssam Soueidan, Philippe Brunet de la Grange, François Moreau-Gaudry, S. Ducassou, Bruno Cardinaud, Pierre Brousset, Francois-Xavier Mahon, Michel Arock, Cathy Quelen, Eric Lippert
Publikováno v: The Journal of Pathology. 242:347-357
Acute basophilic leukaemia (ABL) is a rare subtype of acute myeloblastic leukaemia. We previously described a recurrent t(X;6)(p11;q23) translocation generating an MYB-GATA1 fusion gene in male infants with ABL. To better understand its role, the chi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bf8b74d77ed030b120d09f7077055e9c
https://doi.org/10.1002/path.4908
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5
Loss of ARHGEF1 causes a human primary antibody deficiency
Autor: Anne Durandy, Sébastien Lofek, Hicham Lamrini, Eric Oksenhendler, Loic Chentout, Isabelle André-Schmutz, Elizabeth Macintyre, Sven Kracker, Marie-Céline Deau, Marc Bras, Lucie Heurtier, Amélie Trinquand, Marina Cavazzana, Amine Bouafia, Véronique Meignin, Olivier Alibeu, Alain Fischer, Julie Bruneau, Thierry Jo Molina, Capucine Picard
Publikováno v: Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2019, 129 (3), pp.1047-1060. ⟨10.1172/jci120572⟩
ARHGEF1 is a RhoA-specific guanine nucleotide exchange factor expressed in hematopoietic cells. We used whole-exome sequencing to identify compound heterozygous mutations in ARHGEF1, resulting in the loss of ARHGEF1 protein expression in 2 primary an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78c605f59403518da995ceb2250c379c
https://hal.archives-ouvertes.fr/hal-02323397
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6
A human immunodeficiency caused by mutations in the PIK3R1 gene
Autor: Lucie Heurtier, Patrick Nitschke, Christine Bole-Feysot, Anne Durandy, Pierre Frange, Alain Fischer, Sven Kracker, Felipe Suarez, Marie-Céline Deau, Capucine Picard, Marina Cavazzana
Publikováno v: Journal of Clinical Investigation
Recently, patient mutations that activate PI3K signaling have been linked to a primary antibody deficiency. Here, we used whole-exome sequencing and characterized the molecular defects in 4 patients from 3 unrelated families diagnosed with hypogammag
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27cb32a36877c7833c552ad821087b96
https://europepmc.org/articles/PMC4396486/
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7
An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complex
Autor: Jacek Majewski, Nada Jabado, Marina Cavazzana, Alain Fischer, Jeremy Schwartzentruber, Anne Durandy, Monique Forveille, Michel C. Nussenzweig, Sven Kracker, Necil Kutukculer, Cyrille Cuenin, Anna Gazumyan, Kevin M. McBride, Suranjith L. Seneviratne, Michela Di Virgilio, Zdenko Herceg, Bodo Grimbacher, Marie Céline Deau
Publikováno v: Journal of Allergy and Clinical Immunology
The Journal of Allergy and Clinical Immunology
WOS: 000352238600023
PubMed ID: 25312759
Background: Immunoglobulin class-switch recombination defects (CSR-D) are rare primary immunodeficiencies characterized by impaired production of switched immunoglobulin isotypes and normal or elevat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1257dab9395b3f780555e3870ffa61c0
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8
Hyper-activated PI3K-δ in immunodeficiency
Autor: Lucie Heurtier, Marie-Céline Deau, Sven Kracker
Publikováno v: Oncotarget
The class I phosphoinositide 3-kinases (PI3Ks) are especially involved in the cell response to extracellular signals and convert phosphatidylinositol-(4,5)-bisphosphate (PIP2) into phosphatidylinositol-(3,4,5)-triphosphate (PIP3), an important intrac
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8749587af3ef872f083e0fa7203bffe4
http://europepmc.org/articles/PMC4621884
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