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Jarid2 Is Implicated in the Initial Xist-Induced Targeting of PRC2 to the Inactive X Chromosome

Molecular cell, 2014-01, Vol.53 (2), p.301-316

2014

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Imprinting fidelity in mouse iPSCs depends on sex of donor cell and medium formulation

Nature communications, 2022-09, Vol.13 (1), p.5432-20, Article 5432

2022

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The Implication of Early Chromatin Changes in X Chromosome Inactivation

Cell, 2019-01, Vol.176 (1-2), p.182-197.e23

2019

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Generation and characterization of induced pluripotent stem cell line (IBBISTi004-A) from an Angelman syndrome patient carrying a class II deletion of the maternal chromosome 15q11.2-q13

Stem cell research, 2022-05, Vol.61, p.102757-102757, Article 102757

2022

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The role of Xist‐mediated Polycomb recruitment in the initiation of X‐chromosome inactivation

EMBO reports, 2019-10, Vol.20 (10), p.e48019-n/a

2019

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Systematic Discovery of Xist RNA Binding Proteins

Cell, 2015-04, Vol.161 (2), p.404-416

2015

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Genomic imprinting at the mammalian Dlk1-Dio3 domain

Trends in genetics, 2008-06, Vol.24 (6), p.306-316

2008

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The tandem repeat modules of Xist lncRNA: a swiss army knife for the control of X-chromosome inactivation

Biochemical Society transactions, 2021-12, Vol.49 (6), p.2549-2560

2021

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Evolutionary diversity and developmental regulation of X-chromosome inactivation

Human genetics, 2011-08, Vol.130 (2), p.307-327

2011

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H4K20me1 and H3K27me3 are concurrently loaded onto the inactive X chromosome but dispensable for inducing gene silencing

EMBO reports, 2021-03, Vol.22 (3), p.e51989-n/a

2021

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The influence of DNA methylation on monoallelic expression

Essays in biochemistry, 2019-12, Vol.63 (6), p.663-676

2019

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Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying MYBPC3 nonsense mutations

Stem cell research, 2024-04, Vol.76, p.103362-103362, Article 103362

2024

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Gene dosage effects of the imprinted delta-like homologue 1 (dlk1/pref1) in development: implications for the evolution of imprinting

PLoS genetics, 2009-02, Vol.5 (2), p.e1000392-e1000392

2009

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Generation of induced pluripotent stem cells from an individual with early onset and severe hypertrophic cardiomyopathy linked to MYBPC3: c.772G > A mutation

Human cell : official journal of Human Cell Research Society, 2024, Vol.37 (4), p.1205-1214

2024

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IMPLICON: an ultra-deep sequencing method to uncover DNA methylation at imprinted regions

Nucleic acids research, 2020-09, Vol.48 (16), p.e92-e92

2020

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Stem cell models of Angelman syndrome

Frontiers in cell and developmental biology, 2023-10, Vol.11, p.1274040-1274040

2023

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Generation and characterization of induced pluripotent stem cells heterozygous for the Portuguese BRCA2 founder mutation

Stem cell research, 2021-05, Vol.53, p.102364-102364, Article 102364

2021

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Angelman syndrome: a journey through the brain

The FEBS journal, 2020-06, Vol.287 (11), p.2154-2175

2020

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LncRNAs regulating stemness in aging

Aging cell, 2019-02, Vol.18 (1), p.e12870-n/a

2019

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DLK1/PREF1 regulates nutrient metabolism and protects from steatosis

Proceedings of the National Academy of Sciences - PNAS, 2014-11, Vol.111 (45), p.16088-16093

2014

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Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying the MYBPC3 missense c.1484G>A mutation

Stem cell research, 2024-02, Vol.74, p.103282-103282, Article 103282

2024

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Editorial: Legacies of epigenetic perturbations

Frontiers in cell and developmental biology, 2023-06, Vol.11, p.1228115-1228115

2023

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Differential regulation of imprinting in the murine embryo and placenta by the Dlk1-Dio3 imprinting control region

Development (Cambridge), 2007-01, Vol.134 (2), p.417-426

2007

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Patient-derived induced pluripotent stem cells to study non-canonical splicing variants associated with Hypertrophic Cardiomyopathy

Stem cell research, 2024-12, Vol.81, p.103582, Article 103582

2024

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Genomic imprinting

Current biology, 2004-08, Vol.14 (16), p.R646-R649

2004

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Jarid2 Is Implicated in the Initial Xist-Induced Targeting of PRC2 to the Inactive X Chromosome

Imprinting fidelity in mouse iPSCs depends on sex of donor cell and medium formulation

The Implication of Early Chromatin Changes in X Chromosome Inactivation

Generation and characterization of induced pluripotent stem cell line (IBBISTi004-A) from an Angelman syndrome patient carrying a class II deletion of the maternal chromosome 15q11.2-q13

The role of Xist‐mediated Polycomb recruitment in the initiation of X‐chromosome inactivation

Systematic Discovery of Xist RNA Binding Proteins

Genomic imprinting at the mammalian Dlk1-Dio3 domain

The tandem repeat modules of Xist lncRNA: a swiss army knife for the control of X-chromosome inactivation

Evolutionary diversity and developmental regulation of X-chromosome inactivation

H4K20me1 and H3K27me3 are concurrently loaded onto the inactive X chromosome but dispensable for inducing gene silencing

The influence of DNA methylation on monoallelic expression

Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying MYBPC3 nonsense mutations

Gene dosage effects of the imprinted delta-like homologue 1 (dlk1/pref1) in development: implications for the evolution of imprinting

Generation of induced pluripotent stem cells from an individual with early onset and severe hypertrophic cardiomyopathy linked to MYBPC3: c.772G > A mutation

IMPLICON: an ultra-deep sequencing method to uncover DNA methylation at imprinted regions

Stem cell models of Angelman syndrome

Generation and characterization of induced pluripotent stem cells heterozygous for the Portuguese BRCA2 founder mutation

Angelman syndrome: a journey through the brain

LncRNAs regulating stemness in aging

DLK1/PREF1 regulates nutrient metabolism and protects from steatosis

Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying the MYBPC3 missense c.1484G>A mutation

Editorial: Legacies of epigenetic perturbations

Differential regulation of imprinting in the murine embryo and placenta by the Dlk1-Dio3 imprinting control region

Patient-derived induced pluripotent stem cells to study non-canonical splicing variants associated with Hypertrophic Cardiomyopathy

Genomic imprinting

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