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Journal Articles

High-throughput sequence analysis of the tyrosine kinome in acute myeloid leukemia

Marc M. Loriaux, Ross L. Levine, Jeffrey W. Tyner, Stefan Fröhling, Claudia Scholl, Eric P. Stoffregen, Gerlinde Wernig, Heidi Erickson, Christopher A. Eide, Roland Berger, Olivier A. Bernard, James D. Griffin, Richard M. Stone, Benjamin Lee, Matthew Meyerson, Michael C. Heinrich, Michael W. Deininger, D. Gary Gilliland, Brian J. Druker

Blood (2008) 111 (9): 4788–4796.

https://doi.org/10.1182/blood-2007-07-101394

Published: 2008

Includes: Supplemental data

Journal Articles

Identification of Driver and Passenger Mutations of FLT3 by High-Throughput DNA Sequence Analysis and Functional Assessment of Candidate Alleles.

Blood (2007) 110 (11): 206.

https://doi.org/10.1182/blood.V110.11.206.206

Published: 2007

Journal Articles

High-Throughput Sequence Analysis of the Tyrosine Kinome in Acute Myeloid Leukemia.

Marc Loriaux, Ross Levine, Jeffrey Tyner, Stephan Frohling, Claudia Scholl, Eric Stoffregen, Gerlinde Wernig, Heidi Erickson, Chris Eide, Roland Berger, Olivier Bernard, James Griffin, Richard Stone, Matthew Meyerson, Michael Heinrich, Michael Deininger, Gary Gilliland, Brian Druker

Blood (2007) 110 (11): 886.

https://doi.org/10.1182/blood.V110.11.886.886

Published: 2007

Journal Articles

HOX11L2 / TLX3 is transcriptionally activated through T-cell regulatory elements downstream of BCL11B as a result of the t(5;14)(q35;q32)

Xin-Ying Su, Véronique Della-Valle, Isabelle Andre-Schmutz, Claudie Lemercier, Isabelle Radford-Weiss, Paola Ballerini, Michel Lessard, Marina Lafage-Pochitaloff, Francine Mugneret, Roland Berger, Serge P. Romana, Olivier A. Bernard, Virginie Penard-Lacronique

Blood (2006) 108 (13): 4198–4201.

https://doi.org/10.1182/blood-2006-07-032953

Published: 2006

Includes: Supplemental data

Journal Articles

The t(14;19)(q32;q13) Translocation in B Lymphoproliferative Disorders: A Continuum from Chronic Lymphocytic Leukemia (CLL) to Marginal Zone Lymphoma (MZL)?.

Florence Nguyen-Khac, MD, PhD, Elise Chapiro, MD, Isabelle Radford-Weiss, MD, Christian Bastard, MD,PhD, Leroux Dominique, MD,PhD, Evelyne Callet-Bauchu, MD,PhD, Pascaline Talmant, MD, Isabelle Luquet, MD,PhD, Mozziconacci Marie-Joelle, MD,PhD, Lessard Michel, MD,PhD, Raynaud D. Sophie, MD,PhD, Frederic Davi, MD,PhD, Helene Merle-Beral, MD,PhD, Francoise Berger, MD,PhD, Roland Berger, MD,PhD

Blood (2006) 108 (11): 4944.

https://doi.org/10.1182/blood.V108.11.4944.4944

Published: 2006

Journal Articles

Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia

Elise Chapiro, Lisa Russell, Isabelle Radford-Weiss, Christian Bastard, Michel Lessard, Stephanie Struski, Helene Cave, Sandra Fert-Ferrer, Carole Barin, Odile Maarek, Veronique Della-Valle, Jonathan C. Strefford, Roland Berger, Christine J. Harrison, Olivier A. Bernard, Florence Nguyen-Khac, the Groupe Francophone de Cytogénétique Hématologique

Blood (2006) 108 (10): 3560–3563.

https://doi.org/10.1182/blood-2006-03-010835

Published: 2006

Includes: Supplemental data

Journal Articles

Characterization of 14 NUP214-ABL1 Fusions in T-Cell Acute Lymphoblastic Leukaemia (T-ALL) Exhibits a Genomic Heterogeneity.

Carlos Graux, Marina Lafage, Nicole Dastugue, Francine Mugneret, Roland Berger, Stéphanie Struski, Marie-José Gregoire, Nathalie Nadal, Eric Lippert, Marian Stevens-Kroef, Jan Cools, Anne Hagemeijer, Hélène A. Poirel

Blood (2006) 108 (11): 2075.

https://doi.org/10.1182/blood.V108.11.2075.2075

Published: 2006

Journal Articles

Novel activating JAK2 mutation in a patient with Down syndrome and B-cell precursor acute lymphoblastic leukemia

Sebastien Malinge, Raouf Ben-Abdelali, Catherine Settegrana, Isabelle Radford-Weiss, Marianne Debre, Kheira Beldjord, Elizabeth A. Macintyre, Jean-Luc Villeval, William Vainchenker, Roland Berger, Olivier A. Bernard, Eric Delabesse, Virginie Penard-Lacronique

Blood (2006) 109 (5): 2202–2204.

https://doi.org/10.1182/blood-2006-09-045963

Published: 2006

Includes: Supplemental data

Journal Articles

The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia

Blood (2005) 106 (10): 3377–3379.

https://doi.org/10.1182/blood-2005-05-1898

Published: 2005

Journal Articles

Transcriptional Activation of the Cardiac Homeobox Gene CSX1/NKX2-5 in a B-Cell Chronic Lymphoproliferative Disorder.

Xinying Su, MD, Maryvonne Busson, Eric Delabesse, MD, PhD, Zahia Azgui, MD, Roland Berger, MD, PhD, Hélène Merle-Beral, MD, PhD, Olivier A. Bernard, PhD, Florence Nguyen-Khac, MD, PhD

Blood (2004) 104 (11): 4269.

https://doi.org/10.1182/blood.V104.11.4269.4269

Published: 2004

Journal Articles

M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: a report of 59 cases by the Groupe Français d'Hématologie Cellulaire (GFHC) and the Groupe Français de Cytogénétique Hématologique (GFCH)

Blood (2003) 101 (4): 1277–1283.

https://doi.org/10.1182/blood-2002-05-1474

Published: 2003

Journal Articles

HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis

Paola Ballerini, Annick Blaise, Maryvonne Busson-Le Coniat, Xin Ying Su, Jessica Zucman-Rossi, Mircea Adam, Jacqueline van den Akker, Christine Perot, Beatrice Pellegrino, Judith Landman-Parker, Luc Douay, Roland Berger, Olivier A. Bernard

Blood (2002) 100 (3): 991–997.

https://doi.org/10.1182/blood-2001-11-0093

Published: 2002

Journal Articles

Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Français de Cytogénétique Hématologique (GFCH)

Nicole Dastugue, Marina Lafage-Pochitaloff, Marie-Pierre Pagès, Isabelle Radford, Christian Bastard, Pascaline Talmant, Marie Joelle Mozziconacci, Claude Léonard, Christelle Bilhou-Nabéra, Christine Cabrol, Anne-Marie Capodano, Pascale Cornillet-Lefebvre, Michel Lessard, Francine Mugneret, Christine Pérot, Sylvie Taviaux, Odile Fenneteaux, Eliane Duchayne, Roland Berger

Blood (2002) 100 (2): 618–626.

https://doi.org/10.1182/blood-2001-12-0241

Published: 2002

Journal Articles

Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party

Blood (2000) 96 (4): 1297–1308.

https://doi.org/10.1182/blood.V96.4.1297

Published: 2000

Journal Articles

Transforming properties of chimeric TEL-JAK proteins in Ba/F3 cells

Virginie Lacronique, Anthony Boureux, Richard Monni, Stephanie Dumon, Martine Mauchauffé, Patrick Mayeux, Fabrice Gouilleux, Roland Berger, Sylvie Gisselbrecht, Jacques Ghysdael, Olivier A. Bernard

Blood (2000) 95 (6): 2076–2083.

https://doi.org/10.1182/blood.V95.6.2076

Published: 2000

Journal Articles

Fusion of Huntingtin Interacting Protein 1 to Platelet-Derived Growth Factor β Receptor (PDGFβR) in Chronic Myelomonocytic Leukemia With t(5;7)(q33;q11.2)

Theodora S. Ross, Olivier A. Bernard, Roland Berger, D. Gary Gilliland

Blood (1998) 91 (12): 4419–4426.

https://doi.org/10.1182/blood.V91.12.4419

Published: 1998

Journal Articles

AF6q21, a Novel Partner of the MLL Gene in t(6; 11)(q21; q23), Defines a Forkhead Transcriptional Factor Subfamily

Josette Hillion, Maryvonne Le Coniat, Philippe Jonveaux, Roland Berger, O.A. Bernard

Blood (1997) 90 (9): 3714–3719.

https://doi.org/10.1182/blood.V90.9.3714

Published: 1997

NARROW

High-throughput sequence analysis of the tyrosine kinome in acute myeloid leukemia

Identification of Driver and Passenger Mutations of FLT3 by High-Throughput DNA Sequence Analysis and Functional Assessment of Candidate Alleles.

High-Throughput Sequence Analysis of the Tyrosine Kinome in Acute Myeloid Leukemia.

HOX11L2 / TLX3 is transcriptionally activated through T-cell regulatory elements downstream of BCL11B as a result of the t(5;14)(q35;q32)

The t(14;19)(q32;q13) Translocation in B Lymphoproliferative Disorders: A Continuum from Chronic Lymphocytic Leukemia (CLL) to Marginal Zone Lymphoma (MZL)?.

Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia

Characterization of 14 NUP214-ABL1 Fusions in T-Cell Acute Lymphoblastic Leukaemia (T-ALL) Exhibits a Genomic Heterogeneity.

Novel activating JAK2 mutation in a patient with Down syndrome and B-cell precursor acute lymphoblastic leukemia

The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia

Transcriptional Activation of the Cardiac Homeobox Gene CSX1/NKX2-5 in a B-Cell Chronic Lymphoproliferative Disorder.

M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: a report of 59 cases by the Groupe Français d'Hématologie Cellulaire (GFHC) and the Groupe Français de Cytogénétique Hématologique (GFCH)

HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis

Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Français de Cytogénétique Hématologique (GFCH)

Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party

Transforming properties of chimeric TEL-JAK proteins in Ba/F3 cells

Fusion of Huntingtin Interacting Protein 1 to Platelet-Derived Growth Factor β Receptor (PDGFβR) in Chronic Myelomonocytic Leukemia With t(5;7)(q33;q11.2)

AF6q21, a Novel Partner of the MLL Gene in t(6; 11)(q21; q23), Defines a Forkhead Transcriptional Factor Subfamily

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American Society of Hematology

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American Society of Hematology

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