List of works - Lucie Tosca

An atypical human induced pluripotent stem cell line with a complex, stable, and balanced genomic rearrangement including a large de novo 1q uniparental disomy.

scientific article

Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23

scientific article

Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility.

scientific article published on 10 September 2011

Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts

scientific article published on 16 September 2015

Confined blood chimerism in a monochorionic dizygotic sex discordant twin pregnancy conceived after induced ovulation

article by Anne Mayeur Le Bras et al published 2 March 2016 in Birth Defects Research Part A: Clinical and Molecular Teratology

Different routes lead to apoptosis in unfertilized sea urchin eggs.

scientific article published in March 2014

Disrupted filamin A/αβ interaction induces macrothrombocytopenia by increasing RhoA activity

scientific article published on 02 January 2019

Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease

scientific article

Genomic instability of human embryonic stem cell lines using different passaging culture methods.

scientific article published on 23 April 2015

Human embryonic stem cell-derived cardiac progenitors for severe heart failure treatment: first clinical case report: Figure 1

scientific article published on 19 May 2015

In Vitro Gamete Differentiation from Pluripotent Stem Cells as a Promising Therapy for Infertility.

scientific article published on 12 February 2016

Induced pluripotent stem cell generation from a man carrying a complex chromosomal rearrangement as a genetic model for infertility studies

scientific article published on 03 January 2017

Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: a two-hit case with more severe clinical manifestations

scientific article published on 7 July 2015

Level of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia.

scientific article

Messenger RNA- versus retrovirus-based induced pluripotent stem cell reprogramming strategies: analysis of genomic integrity.

scientific article published on 15 April 2014

Modeling the influence of stromal microenvironment in the selection of ENU-induced BCR-ABL1 mutants by tyrosine kinase inhibitors.

scientific article published on 30 January 2014

PLCγ, G-protein of the Gαq type and cADPr pathway are associated to trigger the fertilization Ca2+ signal in the sea urchin egg ⬇️

scientific article published on July 10, 2012

Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly

scientific article

Risk of tumorigenicity in mesenchymal stromal cell-based therapies--bridging scientific observations and regulatory viewpoints

scientific article published on 18 April 2013

SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplication

scientific article published on 29 January 2014

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

scientific article

Small Supernumerary Marker Chromosomes in Human Infertility

scientific article

Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions.

scientific article published on 24 September 2012

Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations

scientific article published on 14 March 2012

Towards a clinical use of human embryonic stem cell-derived cardiac progenitors: a translational experience

scientific article

Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice

scientific article published on 18 June 2015

List of works by Lucie Tosca

An atypical human induced pluripotent stem cell line with a complex, stable, and balanced genomic rearrangement including a large de novo 1q uniparental disomy.

Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23

Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility.

Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts

Confined blood chimerism in a monochorionic dizygotic sex discordant twin pregnancy conceived after induced ovulation

Different routes lead to apoptosis in unfertilized sea urchin eggs.

Disrupted filamin A/αβ interaction induces macrothrombocytopenia by increasing RhoA activity

Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease

Genomic instability of human embryonic stem cell lines using different passaging culture methods.

Human embryonic stem cell-derived cardiac progenitors for severe heart failure treatment: first clinical case report: Figure 1

In Vitro Gamete Differentiation from Pluripotent Stem Cells as a Promising Therapy for Infertility.

Induced pluripotent stem cell generation from a man carrying a complex chromosomal rearrangement as a genetic model for infertility studies

Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: a two-hit case with more severe clinical manifestations

Level of RUNX1 activity is critical for leukemic predisposition but not for thrombocytopenia.

Messenger RNA- versus retrovirus-based induced pluripotent stem cell reprogramming strategies: analysis of genomic integrity.

Modeling the influence of stromal microenvironment in the selection of ENU-induced BCR-ABL1 mutants by tyrosine kinase inhibitors.

PLCγ, G-protein of the Gαq type and cADPr pathway are associated to trigger the fertilization Ca2+ signal in the sea urchin egg ⬇️

Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly

Risk of tumorigenicity in mesenchymal stromal cell-based therapies--bridging scientific observations and regulatory viewpoints

SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplication

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

Small Supernumerary Marker Chromosomes in Human Infertility

Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions.

Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations

Towards a clinical use of human embryonic stem cell-derived cardiac progenitors: a translational experience

Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice