A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia
Arnaud, Lionel, Saison, Carole, Helias, Virginie, Lucien, Nicole, Steschenko, Dominique, Giarratana, Marie-Catherine, Prehu, Claude, Foliguet, Bernard, Montout, Lory, de Brevern, Alexandre G., Francina, Alain, Ripoche, Pierre, Fenneteau, Odile, Da Costa, Lydie, Peyrard, Thierry, Coghlan, Gail, Illum, Niels, Birgens, Henrik, Tamary, Hannah, Iolascon, Achille, Delaunay, Jean, Tchernia, Gil, Cartron, Jean-Pierre
Published in American journal of human genetics (12.11.2010)
Published in American journal of human genetics (12.11.2010)
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Impaired ribosome biogenesis in Diamond-Blackfan anemia
Choesmel, Valérie, Bacqueville, Daniel, Rouquette, Jacques, Noaillac-Depeyre, Jacqueline, Fribourg, Sébastien, Crétien, Aurore, Leblanc, Thierry, Tchernia, Gil, Da Costa, Lydie, Gleizes, Pierre-Emmanuel
Published in Blood (01.02.2007)
Published in Blood (01.02.2007)
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Role of the interaction between Lu/BCAM and the spectrin‐based membrane skeleton in the increased adhesion of hereditary spherocytosis red cells to laminin
Gauthier, Emilie, El Nemer, Wassim, Wautier, Marie P., Renaud, Olivier, Tchernia, Gil, Delaunay, Jean, Le Van Kim, Caroline, Colin, Yves
Published in British journal of haematology (01.02.2010)
Published in British journal of haematology (01.02.2010)
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Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis
Bader-Meunier, Brigitte, Gauthier, Frédéric, Archambaud, Frédérique, Cynober, Thérèse, Miélot, Francoise, Dommergues, Jean-Paul, Warszawski, Josiane, Mohandas, Narla, Tchernia, Gil
Published in Blood (15.01.2001)
Published in Blood (15.01.2001)
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Frequency of Immune Thrombocytopenia in Newborns: A Prospective Study
Dreyfus, Marie, Kaplan, Cécile, Verdy, Elizabeth, Schlegel, Nicole, Durand-Zaleski, Isabelle, Tchernia, Gil
Published in Blood (15.06.1997)
Published in Blood (15.06.1997)
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Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia
Cretien, Aurore, Hurtaud, Corinne, Moniz, Helene, Proust, Alexis, Marie, Isabelle, Wagner-Ballon, Orianne, Choesmel, Valerie, Gleizes, Pierre-Emmanuel, Leblanc, Thierry, Delaunay, Jean, Tchernia, Gil, Mohandas, Narla, Da Costa, Lydie
Published in Haematologica (Roma) (01.11.2008)
Published in Haematologica (Roma) (01.11.2008)
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Ribosomal protein S19 expression during erythroid differentiation
Da Costa, Lydie, Narla, Goutham, Willig, Thiébaut-Noel, Peters, Luanne L., Parra, Marilyn, Fixler, Jason, Tchernia, Gil, Mohandas, Narla
Published in Blood (01.01.2003)
Published in Blood (01.01.2003)
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Association between myeloid malignancies and acquired deficit in protein 4.1R: A retrospective analysis of six patients
Alanio‐Bréchot, Cécile, Schischmanoff, Pierre‐Olivier, Fénéant‐Thibault, Madeleine, Cynober, Thérèse, Tchernia, Gil, Delaunay, Jean, Garçon, Loïc
Published in American journal of hematology (01.04.2008)
Published in American journal of hematology (01.04.2008)
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Pregnancy-Associated Thrombocytopenia Revisited: Assessment and Follow-Up of 50 Cases
Ajzenberg, Nadine, Dreyfus, Marie, Kaplan, Cécile, Yvart, Jeannine, Weill, Bernard, Tchernia, Gil
Published in Blood (15.12.1998)
Published in Blood (15.12.1998)
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Identification of Microdeletions Spanning the Diamond-Blackfan Anemia Locus on 19q13 and Evidence for Genetic Heterogeneity
Gustavsson, Peter, Garelli, Emanuela, Draptchinskaia, Natalia, Ball, Sarah, Willig, Thiébaut-Noël, Tentler, Dimitri, Dianzani, Irma, Punnett, Hope H., Shafer, Frank E., Cario, Holger, Ramenghi, Ugo, Glomstein, Anders, Pfeiffer, Rudolf A., Goringe, Andy, Olivieri, Nancy F., Smibert, Elizabeth, Tchernia, Gil, Elinder, Göran, Dahl, Niklas
Published in American journal of human genetics (01.11.1998)
Published in American journal of human genetics (01.11.1998)
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Recurrent V75M mutation within the Wiskott-Aldrich syndrome protein: description of a homozygous female patient
Proust, Alexis, Guillet, Benoît, Pellier, Isabelle, Rachieru, Petronela, Hoarau, Cyrille, Claeyssens, Ségolène, Léonard, Claude, Charrier, Sabine, Vainchenker, William, Tchernia, Gil, Delaunay, Jean
Published in European journal of haematology (01.07.2005)
Published in European journal of haematology (01.07.2005)
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Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French children
Bader-Meunier, Brigitte, Leverger, Guy, Tchernia, Gil, Schischmanoff, Olivier, Cynober, Thérèse, Bernaudin, Françoise, Leblanc, Thierry, Munzer, Martine, Roda, Laurent, Soler, Christine, Thuret, Isabelle, Delaunay, Jean
Published in Journal of pediatric hematology/oncology (01.08.2005)
Published in Journal of pediatric hematology/oncology (01.08.2005)
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Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects
Dhermy, Didier, Galand, Colette, Bournier, Odile, Boulanger, Laurent, Cynober, Thérèse, Schismanoff, Pierre Olivier, Bursaux, Elisabeth, Tchernia Boivin, Gil, Pierre, Garbarz, Michel
Published in British journal of haematology (01.07.1997)
Published in British journal of haematology (01.07.1997)
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Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study
Pincez, Thomas, Guitton, Corinne, Gauthier, Frédéric, de Lambert, Guénolée, Picard, Véronique, Fénéant-Thibault, Madeleine, Turhan, Ali, Mohandas, Narla, Tchernia, Gil, Garçon, Loïc
Published in Blood (24.03.2016)
Published in Blood (24.03.2016)
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Human blood IgM “memory” B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire
Weller, Sandra, Braun, Moritz C., Tan, Bruce K., Rosenwald, Andreas, Cordier, Corinne, Conley, Mary Ellen, Plebani, Alessandro, Kumararatne, Dinakhanta S., Bonnet, Damien, Tournilhac, Olivier, Tchernia, Gil, Steiniger, Birte, Staudt, Louis M., Casanova, Jean-Laurent, Reynaud, Claude-Agnès, Weill, Jean-Claude
Published in Blood (01.12.2004)
Published in Blood (01.12.2004)
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Long-Term Follow up of the Beneficial Effects and of Issues in Subtotal Splenectomy for Hereditary Spherocytosis
Pincez, Thomas, Guitton, Corinne, Gauthier, Frederic, Lambert, Guenolee, Picard, Veronique, feneant Thibault, Madeleine, Mohandas, Narla, Tchernia, Gil, Garcon, Loic
Published in Blood (03.12.2015)
Published in Blood (03.12.2015)
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Ribosomal Protein S24 Gene Is Mutated in Diamond-Blackfan Anemia
Gazda, Hanna T., Grabowska, Agnieszka, Merida-Long, Lilia B., Latawiec, Elzbieta, Schneider, Hal E., Lipton, Jeffrey M., Vlachos, Adrianna, Atsidaftos, Eva, Ball, Sarah E., Orfali, Karen A., Niewiadomska, Edyta, Da Costa, Lydie, Tchernia, Gil, Niemeyer, Charlotte, Meerpohl, Joerg J., Stahl, Joachim, Schratt, Gerhard, Glader, Bertil, Backer, Karen, Wong, Carolyn, Nathan, David G., Beggs, Alan H., Sieff, Colin A.
Published in American journal of human genetics (01.12.2006)
Published in American journal of human genetics (01.12.2006)
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Subtotal and total splenectomy for hereditary pyropoikilocytosis: Benefits and outcomes
Pincez, Thomas, Guitton, Corinne, Landman‐Parker, Judith, Brousse, Valentine, Gauthier, Frédéric, Da Costa, Lydie, Ghazal, Kaldoun, Dufillot, Denis, Tchernia, Gil, Picard, Véronique, Garçon, Loïc
Published in American journal of hematology (01.10.2018)
Published in American journal of hematology (01.10.2018)
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