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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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Molecular Mechanisms of Skewed X-Chromosome Inactivation in Female Hemophilia Patients—Lessons from Wide Genome Analyses

International journal of molecular sciences, 2021-08, Vol.22 (16), p.9074

2021

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Human Naive Pluripotent Stem Cells Model X Chromosome Dampening and X Inactivation

Cell stem cell, 2017-01, Vol.20 (1), p.87-101

2017

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The role of the Xist 5' m6A region and RBM15 in X chromosome inactivation

Wellcome open research, 2020, Vol.5, p.31

2020

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evolution of X chromosome inactivation in mammals: the demise of Ohno’s hypothesis?

Cellular and molecular life sciences : CMLS, 2014-04, Vol.71 (8), p.1383-1394

2014

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Analysis of X chromosome inactivation and prenatal diagnosis for a Chinese pedigree with loss of heterozygosity at Xq22.1q22.3

Zhonghua yi xue yi chuan xue za zhi, 2024-03, Vol.41 (3), p.326

2024

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PCGF3/5–PRC1 initiates Polycomb recruitment in X chromosome inactivation

Science (American Association for the Advancement of Science), 2017-06, Vol.356 (6342), p.1081-1084

2017

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X-chromosome inactivation in female patients with Fabry disease

Clinical genetics, 2016-01, Vol.89 (1), p.44-54

2016

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Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X‐chromosome inactivation

Journal of thrombosis and haemostasis, 2015-04, Vol.13 (4), p.530-539

2015

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Corrigendum to “Genome-Wide RNAi Screen Identify Melanoma-Associated Antigen Mageb3 Involved in X Chromosome Inactivation” [J. Mol. Biol. 430 (2018) 2734–2746]

Journal of molecular biology, 2019-09, Vol.431 (19), p.3943-3943

2019

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X-chromosome inactivation in development and cancer

FEBS letters, 2014-08, Vol.588 (15), p.2514-2522

2014

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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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Spread of X‐chromosome inactivation into autosomal regions in patients with unbalanced X‐autosome translocations and its phenotypic effects

American journal of medical genetics. Part A, 2021-08, Vol.185 (8), p.2295-2305

2021

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Eutherian mammals use diverse strategies to initiate X―chromosome inactivation during development

Nature (London), 2011-04, Vol.472 (7343), p.370-374

2011

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The Long Noncoding RNA, Jpx, Is a Molecular Switch for X Chromosome Inactivation

Cell, 2010-10, Vol.143 (3), p.390-403

2010

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Complexities of X chromosome inactivation status in female human induced pluripotent stem cells-a brief review and scientific update for autism research

Journal of neurodevelopmental disorders, 2016-06, Vol.8 (1), p.22-22, Article 22

2016

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Cellular resolution maps of X chromosome inactivation: implications for neural development, function, and disease

Neuron (Cambridge, Mass.), 2014-01, Vol.81 (1), p.103-119

2014

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Female predisposition to TLR7-driven autoimmunity: gene dosage and the escape from X chromosome inactivation

Seminars in immunopathology, 2019-03, Vol.41 (2), p.153-164

2019

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X chromosome inactivation: new players in the initiation of gene silencing [version 1; peer review: 2 approved]

F1000 research, 2017, Vol.6, p.344

2017

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Age‐dependent skewing of X chromosome inactivation appears delayed in centenarians’ offspring. Is there a role for allelic imbalance in Healthy Aging and Longevity?

Aging cell, 2012-04, Vol.11 (2), p.277-283

2012

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Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation

Human genetics, 2012, Vol.131 (1), p.121-130

2012

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A novel 1‐bp deletion mutation and extremely skewed X‐chromosome inactivation causing severe X‐linked hypohidrotic ectodermal dysplasia in a Chinese girl

Clinical and experimental dermatology, 2018-01, Vol.43 (1), p.60-62

2018

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X-Chromosome Genetic Association Test Accounting for X-Inactivation, Skewed X-Inactivation, and Escape from X-Inactivation: X-Chromosome Genetic Association Test

Genetic epidemiology, 2014-09, Vol.38 (6), p.483-493

2014

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Regulation of X-chromosome inactivation by the X-inactivation centre

Nature reviews. Genetics, 2011-06, Vol.12 (6), p.429

2011

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cross-species comparison of escape from X inactivation in Eutheria: implications for evolution of X chromosome inactivation

Chromosoma, 2012-02, Vol.121 (1), p.71-78

2012

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

Molecular Mechanisms of Skewed X-Chromosome Inactivation in Female Hemophilia Patients—Lessons from Wide Genome Analyses

Human Naive Pluripotent Stem Cells Model X Chromosome Dampening and X Inactivation

The role of the Xist 5' m6A region and RBM15 in X chromosome inactivation

evolution of X chromosome inactivation in mammals: the demise of Ohno’s hypothesis?

Analysis of X chromosome inactivation and prenatal diagnosis for a Chinese pedigree with loss of heterozygosity at Xq22.1q22.3

PCGF3/5–PRC1 initiates Polycomb recruitment in X chromosome inactivation

X-chromosome inactivation in female patients with Fabry disease

Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X‐chromosome inactivation

Corrigendum to “Genome-Wide RNAi Screen Identify Melanoma-Associated Antigen Mageb3 Involved in X Chromosome Inactivation” [J. Mol. Biol. 430 (2018) 2734–2746]

X-chromosome inactivation in development and cancer

The Implication of Early Chromatin Changes in X Chromosome Inactivation

Spread of X‐chromosome inactivation into autosomal regions in patients with unbalanced X‐autosome translocations and its phenotypic effects

Eutherian mammals use diverse strategies to initiate X―chromosome inactivation during development

The Long Noncoding RNA, Jpx, Is a Molecular Switch for X Chromosome Inactivation

Complexities of X chromosome inactivation status in female human induced pluripotent stem cells-a brief review and scientific update for autism research

Cellular resolution maps of X chromosome inactivation: implications for neural development, function, and disease

Female predisposition to TLR7-driven autoimmunity: gene dosage and the escape from X chromosome inactivation

X chromosome inactivation: new players in the initiation of gene silencing [version 1; peer review: 2 approved]

Age‐dependent skewing of X chromosome inactivation appears delayed in centenarians’ offspring. Is there a role for allelic imbalance in Healthy Aging and Longevity?

Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation

A novel 1‐bp deletion mutation and extremely skewed X‐chromosome inactivation causing severe X‐linked hypohidrotic ectodermal dysplasia in a Chinese girl

X-Chromosome Genetic Association Test Accounting for X-Inactivation, Skewed X-Inactivation, and Escape from X-Inactivation: X-Chromosome Genetic Association Test

Regulation of X-chromosome inactivation by the X-inactivation centre

cross-species comparison of escape from X inactivation in Eutheria: implications for evolution of X chromosome inactivation

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