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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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Correction of Heritable Epigenetic Defects Using Editing Tools

International journal of molecular sciences, 2021-04, Vol.22 (8), p.3966

2021

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Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome

Frontiers in molecular neuroscience, 2018-02, Vol.11, p.31-31

2018

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Pluripotency-independent induction of human trophoblast stem cells from fibroblasts

Nature communications, 2023-06, Vol.14 (1), p.3359-3359, Article 3359

2023

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Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus

Nature communications, 2024-04, Vol.15 (1), p.3270-3270, Article 3270

2024

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Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells

Genes, 2016-09, Vol.7 (10), p.77

2016

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The Contribution of Pluripotent Stem Cell (PSC)-Based Models to the Study of Fragile X Syndrome (FXS)

Brain sciences, 2019-02, Vol.9 (2), p.42

2019

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FMR1 Epigenetic Silencing Commonly Occurs in Undifferentiated Fragile X-Affected Embryonic Stem Cells

Stem cell reports, 2014-11, Vol.3 (5), p.699-706

2014

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Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells

Stem cell reports, 2015-08, Vol.5 (2), p.221-231

2015

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Genetic Manipulation of Human Embryonic Stem Cells

Methods in molecular biology (Clifton, N.J.), 2016-01, Vol.1307, p.149

Eiges, Rachel

2016

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Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis

PloS one, 2015-10, Vol.10 (10), p.e0138893-e0138893

2015

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Marked Differences in C9orf72 Methylation Status and Isoform Expression between C9/ALS Human Embryonic and Induced Pluripotent Stem Cells

Stem cell reports, 2016-11, Vol.7 (5), p.927-940

2016

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GNE is involved in the early development of skeletal and cardiac muscle

PloS one, 2011-06, Vol.6 (6), p.e21389-e21389

2011

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DMPK hypermethylation in sperm cells of myotonic dystrophy type 1 patients

European journal of human genetics : EJHG, 2022-08, Vol.30 (8), p.980-983

2022

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The G-rich Repeats in FMR1 and C9orf72 Loci Are Hotspots for Local Unpairing of DNA

Genetics (Austin), 2018-12, Vol.210 (4), p.1239-1252

2018

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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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A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay

Neurobiology of aging, 2021-10, Vol.106, p.1-6

2021

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Genetic manipulation of human embryonic stem cells by transfection

Methods in molecular biology (Clifton, N.J.), 2006, Vol.331, p.221

Eiges, Rachel

2006

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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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Induced neuronal differentiation of human embryonic stem cells

Brain research, 2001-09, Vol.913 (2), p.201-205

2001

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Human embryonic stem cells as a powerful tool for studying human embryogenesis

Pediatric research, 2006-08, Vol.60 (2), p.111-117

2006

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DNMT3B splicing dysregulation mediated by SMCHD1 loss contributes to DUX4 overexpression and FSHD pathogenesis

Science advances, 2024-05, Vol.10 (22), p.eadn7732-eadn7732

2024

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Prevention of Lysosomal Storage Diseases and Derivation of Mutant Stem Cell Lines by Preimplantation Genetic Diagnosis

Molecular Biology International, 2012-01, Vol.2012 (2012), p.304-312

2012

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Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation

Cells (Basel, Switzerland), 2023-09, Vol.12 (18), p.2330

2023

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Temporal gene expression during differentiation of human embryonic stem cells and embryoid bodies

Human reproduction (Oxford), 2004-12, Vol.19 (12), p.2875-2883

2004

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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

Correction of Heritable Epigenetic Defects Using Editing Tools

Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome

Pluripotency-independent induction of human trophoblast stem cells from fibroblasts

Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus

Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells

The Contribution of Pluripotent Stem Cell (PSC)-Based Models to the Study of Fragile X Syndrome (FXS)

FMR1 Epigenetic Silencing Commonly Occurs in Undifferentiated Fragile X-Affected Embryonic Stem Cells

Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells

Genetic Manipulation of Human Embryonic Stem Cells

Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis

Marked Differences in C9orf72 Methylation Status and Isoform Expression between C9/ALS Human Embryonic and Induced Pluripotent Stem Cells

GNE is involved in the early development of skeletal and cardiac muscle

DMPK hypermethylation in sperm cells of myotonic dystrophy type 1 patients

The G-rich Repeats in FMR1 and C9orf72 Loci Are Hotspots for Local Unpairing of DNA

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

A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay

Genetic manipulation of human embryonic stem cells by transfection

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

Induced neuronal differentiation of human embryonic stem cells

Human embryonic stem cells as a powerful tool for studying human embryogenesis

DNMT3B splicing dysregulation mediated by SMCHD1 loss contributes to DUX4 overexpression and FSHD pathogenesis

Prevention of Lysosomal Storage Diseases and Derivation of Mutant Stem Cell Lines by Preimplantation Genetic Diagnosis

Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation

Temporal gene expression during differentiation of human embryonic stem cells and embryoid bodies

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