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Three‐dimensional genome architecture in health and disease

Clinical genetics, 2019-02, Vol.95 (2), p.189-198

2019

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Dernières nouvelles du chromosome X

Bulletin du cancer, 2021-01, Vol.108 (1), p.129-132

2021

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Digging into X chromosome inactivation

Science (American Association for the Advancement of Science), 2021-11, Vol.374 (6570), p.942-943

2021

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The Spt components of SAGA facilitate TBP binding to a promoter at a post-activator-binding step in vivo

Genes & development, 1999-11, Vol.13 (22), p.2940-2945

1999

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The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain

Nature genetics, 1997-09, Vol.17 (1), p.14-15

1997

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Ftx is a non-coding RNA which affects Xist expression and chromatin structure within the X-inactivation center region

Human molecular genetics, 2011-02, Vol.20 (4), p.705-718

2011

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XACT, a long noncoding transcript coating the active X chromosome in human pluripotent cells

Nature genetics, 2013-03, Vol.45 (3), p.239-241

2013

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A primate-specific retroviral enhancer wires the XACT lncRNA into the core pluripotency network in humans

Nature communications, 2019-12, Vol.10 (1), p.5652-14, Article 5652

2019

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Unraveling hallmark suitability for staging pre- and post-implantation stem cell models

Cell reports (Cambridge), 2024-05, Vol.43 (5), p.114232, Article 114232

2024

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Tsix transcription across the Xist gene alters chromatin conformation without affecting Xist transcription: implications for X-chromosome inactivation

Genes & development, 2005-06, Vol.19 (12), p.1474-1484

2005

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Methylation of Histone H3 at Lys-9 Is an Early Mark on the X Chromosome during X Inactivation

Cell, 2001-12, Vol.107 (6), p.727-738

2001

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Differential Histone H3 Lys-9 and Lys-27 Methylation Profiles on the X Chromosome

Molecular and Cellular Biology, 2004-06, Vol.24 (12), p.5475-5484

2004

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Antisense RNA in imprinting: spreading silence through Air

Trends in genetics, 2002-09, Vol.18 (9), p.434-437

2002

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Cloning and Characterization of a Murine Brain Specific Gene Bpx and Its Human Homologue Lying within the Xic Candidate Region

Human molecular genetics, 1996-01, Vol.5 (1), p.41-49

1996

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An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

Nature genetics, 1998-05, Vol.19 (1), p.15-16

1998

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Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn

Nucleic acids research, 2004, Vol.32 (11), p.3480-3492

2004

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The region 3′ to Xist mediates X chromosome counting and H3 Lys-4 dimethylation within the Xist gene

The EMBO journal, 2004-02, Vol.23 (3), p.594-604

2004

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Promoter-restricted H3 Lys 4 di-methylation is an epigenetic mark for monoallelic expression

Human molecular genetics, 2003-12, Vol.12 (24), p.3343-3348

2003

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The human necdin gene, NDN , is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Nature genetics, 1997-11, Vol.17 (3), p.357-361

1997

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Identification of an S19 pseudogene lying close to the Xist sequence in the mouse

Mammalian genome, 1996-08, Vol.7 (8), p.606-607

1996

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Controlling X-inactivation in mammals: what does the centre hold?

Seminars in cell & developmental biology, 2003-12, Vol.14 (6), p.331-340

2003

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Generation and characterization of an ordered lambda clone array for the 460-kb region surrounding the murine Xist sequence

Mammalian genome, 1994-07, Vol.5 (7), p.416-423

1994

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Improvement of FISH mapping resolution on combed DNA molecules by iterative constrained deconvolution: a quantitative study

Cytogenetic and genome research, 2001-01, Vol.92 (1-2), p.59-62

2001

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Rapid physical mapping of YAC inserts by random integration of I-Sce I sites

Human molecular genetics, 1993-03, Vol.2 (3), p.265-271

1993

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Physical Mapping and YAC Contig Analysis of the Region Surrounding Xist on the Mouse X Chromosome

Genomics (San Diego, Calif.), 1993-03, Vol.15 (3), p.559-569

1993

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Three‐dimensional genome architecture in health and disease

Dernières nouvelles du chromosome X

Digging into X chromosome inactivation

The Spt components of SAGA facilitate TBP binding to a promoter at a post-activator-binding step in vivo

The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain

Ftx is a non-coding RNA which affects Xist expression and chromatin structure within the X-inactivation center region

XACT, a long noncoding transcript coating the active X chromosome in human pluripotent cells

A primate-specific retroviral enhancer wires the XACT lncRNA into the core pluripotency network in humans

Unraveling hallmark suitability for staging pre- and post-implantation stem cell models

Tsix transcription across the Xist gene alters chromatin conformation without affecting Xist transcription: implications for X-chromosome inactivation

Methylation of Histone H3 at Lys-9 Is an Early Mark on the X Chromosome during X Inactivation

Differential Histone H3 Lys-9 and Lys-27 Methylation Profiles on the X Chromosome

Antisense RNA in imprinting: spreading silence through Air

Cloning and Characterization of a Murine Brain Specific Gene Bpx and Its Human Homologue Lying within the Xic Candidate Region

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn

The region 3′ to Xist mediates X chromosome counting and H3 Lys-4 dimethylation within the Xist gene

Promoter-restricted H3 Lys 4 di-methylation is an epigenetic mark for monoallelic expression

The human necdin gene, NDN , is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Identification of an S19 pseudogene lying close to the Xist sequence in the mouse

Controlling X-inactivation in mammals: what does the centre hold?

Generation and characterization of an ordered lambda clone array for the 460-kb region surrounding the murine Xist sequence

Improvement of FISH mapping resolution on combed DNA molecules by iterative constrained deconvolution: a quantitative study

Rapid physical mapping of YAC inserts by random integration of I-Sce I sites

Physical Mapping and YAC Contig Analysis of the Region Surrounding Xist on the Mouse X Chromosome

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