C. Broccardo

发表

The scl +18/19 Stem Cell Enhancer Is Not Required for Hematopoiesis: Identification of a 5′ Bifunctional Hematopoietic-Endothelial Enhancer Bound by Fli-1 and Elf-1

B. Göttgens, A. Green, C. Begley, 2004, Molecular and Cellular Biology.

B-cell regulator of immunoglobulin heavy-chain transcription (Bright)/ARID3a is a direct target of the oncomir microRNA-125b in progenitor B-cells

P. Brousset, É. Coyaud, B. Mari, 2012, Leukemia.

Wide diversity of PAX5 alterations in B-ALL: a Groupe Francophone de Cytogenetique Hematologique study.

P. Brousset, É. Coyaud, B. Poppe, 2010, Blood.

Deletion of the Scl +19 enhancer increases the blood stem cell compartment without affecting the formation of mature blood lineages

B. Göttgens, A. Green, L. Scott, 2012, Experimental hematology.

Identification of GSX2 and AF10 as NUP98 partner genes in myeloid malignancies

O. Bernard, V. Penard-Lacronique, E. Delabesse, 2013, Blood Cancer Journal.

ATP‐binding cassette transporter 1 (ABCA1) deficiency decreases platelet reactivity and reduces thromboxane A2 production independently of hematopoietic ABCA1

B. Payrastre, P. Le Faouder, J. Bertrand-Michel, 2016, Journal of thrombosis and haemostasis : JTH.

Retroviral transduction of lineage antigen-negative ((Lin−) cells: a valuable alternative for the generation of T cell receptor (TCR) retrogenic mice.

C. Viret, S. Guerder, C. Broccardo, 2012, Journal of immunological methods.

Identification of a transforming MYB-GATA1 fusion gene in acute basophilic leukemia: a new entity in male infants.

P. Brousset, E. Lippert, C. Demur, 2011, Blood.

Wide diversity of PAX 5 alterations in BALL : a GFCH ( Groupe Francophone de Cytogénétique Hématologique ) study

P. Brousset, É. Coyaud, B. Poppe, 2010 .

Germline PAX5 mutation predisposes to familial B acute lymphoblastic leukemia.

C. Preudhomme, Aurélie Caillault, C. Berthon, 2020, Blood.

PAX5-AUTS2 fusion resulting from t(7;9)(q11.2;p13.2) can now be classified as recurrent in B cell acute lymphoblastic leukemia.

P. Brousset, É. Coyaud, N. Dastugue, 2010, Leukemia research.

High density lipoprotein deficiency and foam cell accumulation in mice with targeted disruption of ATP-binding cassette transporter-1.

C. Gabel, J. Mcneish, G. Chimini, 2000, Proceedings of the National Academy of Sciences of the United States of America.

by Fli-1 and Elf-1 Bound Hematopoietic-Endothelial Enhancer Bifunctional ' of a 5 Required for Hematopoiesis: Identification +18/19 Stem Cell Enhancer Is Not scl The

B. Göttgens, A. Green, S. Kinston, 2014 .

NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis

G. Leverger, I. Radford‐Weiss, I. Luquet, 2017, Leukemia.

PAX5A and PAX5B isoforms are both efficient to drive B cell differentiation

M. Cogné, E. Delabesse, C. Broccardo, 2018, Oncotarget.

A novel PAX5-ELN fusion protein identified in B-cell acute lymphoblastic leukemia acts as a dominant negative on wild-type PAX5.

P. Brousset, G. Delsol, N. Dastugue, 2007, Blood.

A novel PAX 5-ELN fusion protein identified in B-cell acute lymphoblastic leukemia acts as a dominant negative on wild-type PAX 5

P. Brousset, G. Delsol, N. Dastugue, 2007 .

A novel PAX 5-ELN fusion protein identified in B-cell acute lymphoblastic leukemia acts as a dominant negative on the wild type PAX 5 Running title : PAX 5-ELN fusion gene in BALL

P. Brousset, G. Delsol, N. Dastugue, 2006 .

PAX5-ELN oncoprotein promotes multistep B-cell acute lymphoblastic leukemia in mice

P. Brousset, A. Khamlichi, M. Bousquet, 2018, Proceedings of the National Academy of Sciences.

PAX5 mutations occur frequently in adult B-cell progenitor acute lymphoblastic leukemia and PAX5 haploinsufficiency is associated with BCR-ABL1 and TCF3-PBX1 fusion genes: a GRAALL study

J. D. Vos, P. Brousset, J. Soulier, 2009, Leukemia.

The ABCA subclass of mammalian transporters.

M. Luciani, G. Chimini, C. Broccardo, 1999, Biochimica et biophysica acta.

ABC1 promotes engulfment of apoptotic cells and transbilayer redistribution of phosphatidylserine.

Yannick Hamon, Didier Marguet, D. Marguet, 2000, Nature Cell Biology.

The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11

O. Dovey, G. Vassiliou, L. Michaux, 2021, Blood advances.

Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA7 gene encoding a novel ABCA transporter

P. Denéfle, L. Schriml, M. Mattei, 2001, Cytogenetic and Genome Research.

Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA 7 gene encoding a novel ABCA transporter

P. Denéfle, L. Schriml, M. Mattei, 2001 .

Homeobox NKX2-3 promotes marginal-zone lymphomagenesis by activating B-cell receptor signalling and shaping lymphocyte dynamics

R. Siebert, A. Salar, P. Brousset, 2016, Nature Communications.

Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred.

P. Denéfle, H. Brewer, M. Dinger, 1999, Proceedings of the National Academy of Sciences of the United States of America.

RET fusion genes are associated with chronic myelomonocytic leukemia and enhance monocytic differentiation

C. Deswarte, E. Lippert, C. Demur, 2012, Leukemia.

Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice

T. Langmann, K. Lackner, G. Schmitz, 2000, Nature Genetics.

ATP‐binding cassette transporter hallmarks tissue macrophages and modulates cytokine‐triggered polarization programs

G. Chimini, P. Naquet, L. Pradel, 2009, European journal of immunology.

ABCA2 is a marker of neural progenitors and neuronal subsets in the adult rodent brain

A. Nieoullon, G. Rougon, G. Chazal, 2006, Journal of neurochemistry.

Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)

J. Mandel, G. Chimini, C. Broccardo, 1998, European Journal of Human Genetics.

Animal Cytogenetics and Comparative Mapping

P. Denéfle, L. Schriml, M. Luciani, 2001 .

Loss of HSC stemness identity is associated with exhaustion and hyporesponsiveness in GATA2 deficiency syndrome

E. Delabesse, C. Broccardo, N. Prade, 2023, bioRxiv.

Identification of novel, clonally stable, somatic mutations targeting transcription factors PAX5 and NKX2-3, the epigenetic regulator LRIF1, and BRAF in a case of atypical B-cell chronic lymphocytic leukemia harboring a t(14;18)(q32;q21)

O. Casasnovas, M. Callanan, Y. Duffourd, 2021, Cold Spring Harbor molecular case studies.

Stem cell–like reprogramming is required for leukemia-initiating activity in B-ALL

A. Khamlichi, I. Luquet, C. Broccardo, 2023, The Journal of experimental medicine.