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Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 gene

Stem cell research, 2019-01, Vol.34, p.101381-101381, Article 101381

2019

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Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene

Stem cell research, 2019-05, Vol.37, p.101438-101438, Article 101438

2019

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Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease

Human molecular genetics, 2001-07, Vol.10 (14), p.1503-1510

2001

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Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice

Journal of medical genetics, 2009-02, Vol.46 (2), p.123-131

2009

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OBINUTUZUMAB PLUS DHAP FOLLOWED BY AUTOLOGOUS STEM CELL TRANSPLANTATION (ASCT) PLUS OBINUTUZUMAB MAINTENANCE PROVIDES A HIGH MRD RESPONSE RATE IN UNTREATED MCL PATIENTS. RESULTS OF LYMA‐101 TRIAL, A LYSA GROUP STUDY

Hematological oncology, 2019-06, Vol.37 (S2), p.44-45

2019

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Retrospective study of allogeneic haematopoietic stem-cell transplantation for myelofibrosis

Bone marrow transplantation (Basingstoke), 2011-04, Vol.46 (4), p.557-561

2011

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BONE MARROW INVOLVEMENT, BUT NO BLOOD INVOLVEMENT, IMPAIRS SURVIVAL IN ANGIOIMMUNOBLASTIC T CELL LYMPHOMA: AN ANCILLARY STUDY OF THE REVAIL TRIAL

Hematological oncology, 2019-06, Vol.37 (S2), p.278-279

2019

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ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia

Leukemia, 1997-09, Vol.11 (9), p.1459-1464

1997

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Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

Nature genetics, 2000-06, Vol.25 (2), p.182-186

2000

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Polydom: a secreted protein with pentraxin, complement control protein, epidermal growth factor and von Willebrand factor A domains

Biochemical journal, 2000-11, Vol.352 Pt 1 (1), p.49-59

2000

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Loss-of-Function Mutations in a Human Gene Related to Chlamydomonas reinhardtii Dynein IC78 Result in Primary Ciliary Dyskinesia

American journal of human genetics, 1999-12, Vol.65 (6), p.1508-1519

1999

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Lymphome méningé primitif : présentation d’un cas et revue de la littérature

La revue de medecine interne, 2012-12, Vol.33, p.A160-A160

2012

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The 12;21 translocation involving TEL and deletion of the other TEL allele : Two frequently associated alterations found in childhood acute lymphoblastic leukemia

Blood, 1996-04, Vol.87 (7), p.2891-2899

1996

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Transcriptional consequences of genomic structural aberrations in breast cancer

Genome research, 2011-05, Vol.21 (5), p.676

2011

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Human Prop-1: cloning, mapping, genomic structure: Mutations in familial combined pituitary hormone deficiency

FEBS letters, 1998-10, Vol.437 (3), p.216-220

1998

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Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization

Prenatal diagnosis, 1994-02, Vol.14 (2), p.79-86

1994

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Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B

American journal of medical genetics, 2003-06, Vol.119A (3), p.257-265

2003

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Diagnostic pré-implantatoire

EMC. Gynécologie-obstétrique, 2004, Vol.1 (2), p.76-87

2004

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The human dynein intermediate chain 2 gene (DNAI2) : cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia

Human genetics, 2000-12, Vol.107 (6), p.642-649

2000

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Allogeneic haematopoietic stem cell transplantation as a curative therapy in primary and secondary myelofibrosis.(Chronic leukaemias)

Bone marrow transplantation (Basingstoke), 2009-03, Vol.43 (S1), p.S261

2009

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Detection of 47,XYY trophoblast fetal cells in maternal blood by fluorescence in situ hybridization after using immunomagnetic lymphocyte depletion and flow cytometry sorting

Fetal diagnosis and therapy, 1992, Vol.7 (3-4), p.190

1992

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Techniques nouvelles en cytogénétique

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 1996, Vol.3, p.S351-S352

1996

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Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 gene

Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene

Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease

Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice

OBINUTUZUMAB PLUS DHAP FOLLOWED BY AUTOLOGOUS STEM CELL TRANSPLANTATION (ASCT) PLUS OBINUTUZUMAB MAINTENANCE PROVIDES A HIGH MRD RESPONSE RATE IN UNTREATED MCL PATIENTS. RESULTS OF LYMA‐101 TRIAL, A LYSA GROUP STUDY

Retrospective study of allogeneic haematopoietic stem-cell transplantation for myelofibrosis

BONE MARROW INVOLVEMENT, BUT NO BLOOD INVOLVEMENT, IMPAIRS SURVIVAL IN ANGIOIMMUNOBLASTIC T CELL LYMPHOMA: AN ANCILLARY STUDY OF THE REVAIL TRIAL

ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

Polydom: a secreted protein with pentraxin, complement control protein, epidermal growth factor and von Willebrand factor A domains

Loss-of-Function Mutations in a Human Gene Related to Chlamydomonas reinhardtii Dynein IC78 Result in Primary Ciliary Dyskinesia

Allogeneic hematopoietic stem cell transplantation allows long-term complete remission and curability in high-risk Waldenström’s macroglobulinemia. Results of a retrospective analysis of the Société Française de Greffe de Moelle et de Thérapie Cellulaire

S103 OBINUTUZUMAB PLUS DHAP FOLLOWED BY AUTOLOGOUS STEM CELL TRANSPLANTATION PLUS OBINUTUZUMAB MAINTENANCE PROVIDES A HIGH MRD RESPONSE RATE IN UNTREATED MCL PATIENTS, LYMA‐101 TRIAL ‐ A LYSA TRIAL

Lymphome méningé primitif : présentation d’un cas et revue de la littérature

The 12;21 translocation involving TEL and deletion of the other TEL allele : Two frequently associated alterations found in childhood acute lymphoblastic leukemia

Transcriptional consequences of genomic structural aberrations in breast cancer

Human Prop-1: cloning, mapping, genomic structure: Mutations in familial combined pituitary hormone deficiency

Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization

Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B

Diagnostic pré-implantatoire

Comprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomes

The human dynein intermediate chain 2 gene (DNAI2) : cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia

Allogeneic haematopoietic stem cell transplantation as a curative therapy in primary and secondary myelofibrosis.(Chronic leukaemias)

Detection of 47,XYY trophoblast fetal cells in maternal blood by fluorescence in situ hybridization after using immunomagnetic lymphocyte depletion and flow cytometry sorting

Techniques nouvelles en cytogénétique

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