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The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome

Nature genetics, 2014-06, Vol.46 (6), p.551-557

2014

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Identifying regulators of parental imprinting by CRISPR/Cas9 screening in haploid human embryonic stem cells

Nature communications, 2021-11, Vol.12 (1), p.6718-6718, Article 6718

2021

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Selective Elimination of Human Pluripotent Stem Cells by an Oleate Synthesis Inhibitor Discovered in a High-Throughput Screen

Cell stem cell, 2013-02, Vol.12 (2), p.167-179

2013

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Reversion of FMR1 Methylation and Silencing by Editing the Triplet Repeats in Fragile X iPSC-Derived Neurons

Cell reports (Cambridge), 2015-10, Vol.13 (2), p.234-241

2015

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Distinct Imprinting Signatures and Biased Differentiation of Human Androgenetic and Parthenogenetic Embryonic Stem Cells

Cell stem cell, 2019-09, Vol.25 (3), p.419-432.e9

2019

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Differentiation and isolation of hepatic-like cells from human embryonic stem cells

Differentiation (London), 2004-06, Vol.72 (5), p.230-238

2004

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Effects of Eight Growth Factors on the Differentiation of Cells Derived from Human Embryonic Stem Cells

Proceedings of the National Academy of Sciences - PNAS, 2000-10, Vol.97 (21), p.11307-11312

2000

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Teratogen screening using transcriptome profiling of differentiating human embryonic stem cells

Journal of cellular and molecular medicine, 2011-06, Vol.15 (6), p.1393-1401

2011

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Human Pluripotent Stem Cells with Distinct X Inactivation Status Show Molecular and Cellular Differences Controlled by the X-Linked ELK-1 Gene

Cell reports (Cambridge), 2013-07, Vol.4 (2), p.262-270

2013

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Molecular Characterization of Down Syndrome Embryonic Stem Cells Reveals a Role for RUNX1 in Neural Differentiation

Stem cell reports, 2016-10, Vol.7 (4), p.777-786

2016

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Human Embryonic Stem Cells as Models for Aneuploid Chromosomal Syndromes

Stem cells (Dayton, Ohio), 2010-09, Vol.28 (9), p.1530-1540

2010

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Establishment of human embryonic stem cell-transfected clones carrying a marker for undifferentiated cells

Current biology, 2001-04, Vol.11 (7), p.514-518

2001

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Aberrant DNA methylation in ES cells

PloS one, 2014-05, Vol.9 (5), p.e96090-e96090

2014

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Molecular Analysis of LEFTY‐Expressing Cells in Early Human Embryoid Bodies

Stem cells (Dayton, Ohio), 2007-02, Vol.25 (2), p.465-472

2007

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Genome-wide Screen for Culture Adaptation and Tumorigenicity-Related Genes in Human Pluripotent Stem Cells

iScience, 2019-01, Vol.11, p.398-408

2019

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Derivation and differentiation of haploid human embryonic stem cells

Nature (London), 2016-04, Vol.532 (7597), p.107-111

2016

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Global analysis of parental imprinting in human parthenogenetic induced pluripotent stem cells

Nature structural & molecular biology, 2011-06, Vol.18 (6), p.735-741

2011

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The Effect of Overexpression of Pdx1 and Foxa2 on the Differentiation of Human Embryonic Stem Cells into Pancreatic Cells

Stem cells (Dayton, Ohio), 2006-08, Vol.24 (8), p.1923-1930

2006

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Genome-wide screening for genes involved in the epigenetic basis of fragile X syndrome

Stem cell reports, 2022-05, Vol.17 (5), p.1048-1058

2022

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Differentiation of uniparental human embryonic stem cells into granulosa cells reveals a paternal contribution to gonadal development

Stem cell reports, 2023-04, Vol.18 (4), p.817-828

2023

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Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos

Cell stem cell, 2007-11, Vol.1 (5), p.568

2007

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Reprogramming of the MHC-I and Its Regulation by NFκB in Human-Induced Pluripotent Stem Cells

Stem cells (Dayton, Ohio), 2012-12, Vol.30 (12), p.2700-2708

2012

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Developmental Study of Fragile X Syndrome Using Human Embryonic Stem Cells Derived from Preimplantation Genetically Diagnosed Embryos

Cell stem cell, 2007-11, Vol.1 (5), p.568-577

2007

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The Tmp Gene, Encoding a Membrane Protein, Is a c-Myc Target with a Tumorigenic Activity

Molecular and Cellular Biology, 1999-05, Vol.19 (5), p.3529-3539

1999

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Epigenetic mechanism of FMR1 inactivation in Fragile X syndrome

The International journal of developmental biology, 2017, Vol.61 (3-4-5), p.285-292

2017

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The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome

Identifying regulators of parental imprinting by CRISPR/Cas9 screening in haploid human embryonic stem cells

Selective Elimination of Human Pluripotent Stem Cells by an Oleate Synthesis Inhibitor Discovered in a High-Throughput Screen

Reversion of FMR1 Methylation and Silencing by Editing the Triplet Repeats in Fragile X iPSC-Derived Neurons

Distinct Imprinting Signatures and Biased Differentiation of Human Androgenetic and Parthenogenetic Embryonic Stem Cells

Differentiation and isolation of hepatic-like cells from human embryonic stem cells

Effects of Eight Growth Factors on the Differentiation of Cells Derived from Human Embryonic Stem Cells

Teratogen screening using transcriptome profiling of differentiating human embryonic stem cells

Human Pluripotent Stem Cells with Distinct X Inactivation Status Show Molecular and Cellular Differences Controlled by the X-Linked ELK-1 Gene

Molecular Characterization of Down Syndrome Embryonic Stem Cells Reveals a Role for RUNX1 in Neural Differentiation

Human Embryonic Stem Cells as Models for Aneuploid Chromosomal Syndromes

Establishment of human embryonic stem cell-transfected clones carrying a marker for undifferentiated cells

Aberrant DNA methylation in ES cells

Molecular Analysis of LEFTY‐Expressing Cells in Early Human Embryoid Bodies

Genome-wide Screen for Culture Adaptation and Tumorigenicity-Related Genes in Human Pluripotent Stem Cells

Derivation and differentiation of haploid human embryonic stem cells

Global analysis of parental imprinting in human parthenogenetic induced pluripotent stem cells

The Effect of Overexpression of Pdx1 and Foxa2 on the Differentiation of Human Embryonic Stem Cells into Pancreatic Cells

Genome-wide screening for genes involved in the epigenetic basis of fragile X syndrome

Differentiation of uniparental human embryonic stem cells into granulosa cells reveals a paternal contribution to gonadal development

Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos

Reprogramming of the MHC-I and Its Regulation by NFκB in Human-Induced Pluripotent Stem Cells

Developmental Study of Fragile X Syndrome Using Human Embryonic Stem Cells Derived from Preimplantation Genetically Diagnosed Embryos

The Tmp Gene, Encoding a Membrane Protein, Is a c-Myc Target with a Tumorigenic Activity

Epigenetic mechanism of FMR1 inactivation in Fragile X syndrome

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