Lista de obras - Gérard Tachdjian - Dominio Público Uruguay

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

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

artículo científico publicado en 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

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

artículo científico publicado en 2019

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

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

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

artículo científico publicado en 2013

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

artículo científico publicado en 2014

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

artículo científico publicado en 2012

Shortening gametes co-incubation time improves live birth rate for couples with a history of fragmented embryos.

artículo científico publicado en 2017

Small Supernumerary Marker Chromosomes in Human Infertility

artículo científico publicado en 2015

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

artículo científico publicado en 2012

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

artículo científico publicado en 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 2015

WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion.

artículo científico publicado en 2017

Lista de obras de Gérard Tachdjian

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

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

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.

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

Shortening gametes co-incubation time improves live birth rate for couples with a history of fragmented embryos.

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

WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion.