F. Parmentier

发表

Standardized nested polymerase chain reaction-based assay for detection of human immunodeficiency virus type 1 DNA in whole blood lysates

V. Barlet, J. Chermann, C. Bastard, 1993, Journal of clinical microbiology.

Increased trisomy 12 frequency and a biased IgVH 3-21 gene usage characterize small lymphocytic lymphoma.

C. Bastard, P. Morel, P. Duthilleul, 2010, Leukemia research.

Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1/S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease

F. Jardin, J. Picquenot, H. Tilly, 2009, Leukemia.

Transformation of an Unclassified Myeloproliferative Neoplasm with a Rare BCR-JAK2 Fusion Transcript Resulting from the Translocation (9;22)(p24;q11)

F. Jardin, H. Tilly, C. Bastard, 2015, Case reports in hematology.

Characterisation of BCL2-JH rearrangements in follicular lymphoma: PCR detection of 3′ BCL2 breakpoints and evidence of a new cluster

F. Jardin, A. Stamatoullas, S. Leprêtre, 2000, Leukemia.

Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients

S. Leprêtre, H. Tilly, T. Frebourg, 2007, Leukemia.

Detection of gene copy number aberrations in mantle cell lymphoma by a single quantitative multiplex PCR assay: clinicopathological relevance and prognosis value

F. Jardin, J. Picquenot, H. Lanic, 2009, British journal of haematology.

Intronic BCL-6 mutations are preferentially targeted to the translocated allele in t(3;14)(q27;q32) non-Hodgkin B-cell lymphoma.

F. Jardin, J. Picquenot, H. Tilly, 2003, Blood.

The isotype of the BCR as a surrogate for the GCB and ABC molecular subtypes in diffuse large B-cell lymphoma

F. Jardin, J. Picquenot, S. Mareschal, 2011, Leukemia.

Promoter Shuffling by Sequential Genomic Rearrangements in Follicular Lymphoma Reveals an Ongoing Genomic Instability at the BCL6 Locus.

F. Jardin, J. Picquenot, H. Tilly, 2006 .

Expression profile of serotonin4 (5-HT4) receptors in adrenocortical aldosterone-producing adenomas.

H. Vaudry, C. Bastard, P. Plouin, 2005, European journal of endocrinology.

Fetuin-B, a second member of the fetuin family in mammals.

M. Daveau, A. Husson, P. Ruminy, 2000, The Biochemical journal.

Familial adrenocorticotropin-independent macronodular adrenal hyperplasia with aberrant serotonin and vasopressin adrenal receptors.

P. Caron, M. Plantavid, A. Lacroix, 2007, European journal of endocrinology.

Overexpression of serotonin4 receptors in cisapride-responsive adrenocorticotropin-independent bilateral macronodular adrenal hyperplasia causing Cushing's syndrome.

A. Tabarin, H. Vaudry, Jacques Young, 2003, The Journal of clinical endocrinology and metabolism.

Follicular lymphoma without t(14;18) and with BCL-6 rearrangement: a lymphoma subtype with distinct pathological, molecular and clinical characteristics

F. Jardin, P. Gaulard, A. Stamatoullas, 2002, Leukemia.

Several mechanisms lead to the inactivation of the CDKN2A (P16), P14ARF, or CDKN2B (P15) genes in the GCB and ABC molecular DLBCL subtypes

F. Jardin, J. Picquenot, S. Mareschal, 2012, Genes, chromosomes & cancer.

Diffuse large B-cell lymphomas with CDKN2A deletion have a distinct gene expression signature and a poor prognosis under R-CHOP treatment: a GELA study.

T. Molina, F. Jardin, G. Salles, 2010, Blood.

Clinical and biological relevance of single-nucleotide polymorphisms and acquired somatic mutations of the BCL6 first intron in follicular lymphoma

F. Jardin, J. Picquenot, H. Tilly, 2005, Leukemia.

From bloodjournal.hematologylibrary.org at PENN STATE UNIVERSITY on February 28, 2013. For personal use only.

F. Jardin, J. Picquenot, H. Tilly, 2006 .

Recurrent disruption of the Iμ splice donor site in t(14;18) positive lymphomas : A potential molecular basis for aberrant downstream class switch recombination

F. Jardin, J. Picquenot, H. Tilly, 2007 .

Distribution of BCL2 breakpoints in follicular lymphoma and correlation with clinical features: specific subtypes or same disease?

F. Jardin, S. Leprêtre, H. Tilly, 2002, Leukemia.

Gene Expression Profile Analysis According to Recurrent Gene Copy Number Abnormalities Defines a Diffuse Large B-Cell Lymphoma Subgroup Characterized by 9p21 Locus Deletion, Ribosome Machinery Deregulation and Poor Prognosis. A GELA Study

T. Molina, F. Jardin, G. Salles, 2008 .

Detection of somatic quantitative genetic alterations by multiplex polymerase chain reaction for the prediction of outcome in diffuse large B-cell lymphomas

F. Jardin, J. Picquenot, H. Tilly, 2008, Haematologica.

Two patterns of chromosomal breakpoint locations on the immunoglobulin heavy-chain locus in B-cell lymphomas with t(3;14)(q27;q32): relevance to histology

F. Jardin, P. Gaulard, J. Picquenot, 2006, Oncogene.

Novel Ig V gene features of t(14;18) and t(3;14) de novo diffuse large B-cell lymphoma displaying germinal center-B cell like and non-germinal center-B cell like markers

F. Jardin, S. Leprêtre, H. Tilly, 2006, Leukemia.

Recurrent disruption of the Imu splice donor site in t(14;18) positive lymphomas: a potential molecular basis for aberrant downstream class switch recombination.

F. Jardin, J. Picquenot, H. Tilly, 2007, Genes, chromosomes & cancer.

Abnormal sensitivity of cortisol-producing adrenocortical adenomas to serotonin: in vivo and in vitro studies.

H. Vaudry, A. Laquérriere, Y. Reznik, 2005, The Journal of clinical endocrinology and metabolism.

Follicle center lymphoma is associated with significantly elevated levels of BCL-6 expression among lymphoma subtypes, independent of chromosome 3q27 rearrangements

F. Jardin, A. Stamatoullas, S. Leprêtre, 2002, Leukemia.

F. Jardin, J. Picquenot, H. Tilly, 2009, Leukemia.

TET2 and TP53 mutations are frequently observed in blastic plasmacytoid dendritic cell neoplasm

F. Jardin, A. Stamatoullas, J. Picquenot, 2011, British journal of haematology.

Follicular Lymphoma: Early Direct or Late from Fl Progenitor Cells Mutation Patterns Suggest Different Progression Pathways in Μ S

F. Jardin, J. Picquenot, H. Tilly, 2022 .