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X-chromosome inactivation: molecular mechanisms and genetic consequences

Trends in genetics, 1994-07, Vol.10 (7), p.230-235

Migeon, Barbara R.

1994

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Differential X Reactivation in Human Placental Cells: Implications for Reversal of X Inactivation

American journal of human genetics, 2005-09, Vol.77 (3), p.355-364

2005

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Non-random X chromosome inactivation in mammalian cells

Cytogenetic and genome research, 1998-01, Vol.80 (1-4), p.142-148

Migeon, B R

1998

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X chromosome inactivation: theme and variations

Cytogenetic and Genome Research, 2002-01, Vol.99 (1-4), p.8-16

Migeon, B.R.

2002

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The severe phenotype of females with Tiny Ring X chromosomes is associated with inability of these chromosomes to undergo X inactivation

American journal of human genetics, 1994-09, Vol.55 (3), p.497-504

1994

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The human NTT gene : Identification of a novel 17-kb noncoding nuclear RNA expressed in activated CD4+ T cells

Genomics (San Diego, Calif.), 1997-01, Vol.39 (2), p.171-184

1997

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DNA Methylation Stabilizes X Chromosome Inactivation in Eutherians but not in Marsupials: Evidence for Multistep Maintenance of Mammalian X Dosage Compensation

Proceedings of the National Academy of Sciences - PNAS, 1987-09, Vol.84 (17), p.6210-6214

1987

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The Human Female Paradox: Biological Disadvantage Preimplantation, Biological Advantage, Thereafter

Current Opinion in Gynecology and Obstetrics, 2021-02, Vol.4 (1), p.397-404

BR, Migeon

2021

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Human X Inactivation Center Induces Random X Chromosome Inactivation in Male Transgenic Mice

Genomics (San Diego, Calif.), 1999-07, Vol.59 (2), p.113-121

1999

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Deficient Transcription of XIST from Tiny Ring X Chromosomes in Females with Severe Phenotypes

Proceedings of the National Academy of Sciences - PNAS, 1993-12, Vol.90 (24), p.12025-12029

1993

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Identification of TSIX, Encoding an RNA Antisense to Human XIST, Reveals Differences from its Murine Counterpart: Implications for X Inactivation

American journal of human genetics, 2001-11, Vol.69 (5), p.951-960

2001

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Asynchronous Replication of Homologous Loci on Human Active and Inactive X Chromosomes

Proceedings of the National Academy of Sciences - PNAS, 1990-05, Vol.87 (10), p.3685-3689

1990

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Lack of X inactivation associated with maternal X isodisomy : Evidence for a counting mechanism prior to X inactivation during human embryogenesis

American journal of human genetics, 1996, Vol.58 (1), p.161-170

1996

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Studies of X inactivation and isodisomy in twins provide further evidence that X chromosome is not involved in Rett syndrome

American journal of human genetics, 1995-03, Vol.56 (3), p.647-653

1995

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Methylation of the Hypoxanthine Phosphoribosyltransferase Locus on the Human X Chromosome: Implications for X-Chromosome Inactivation

Proceedings of the National Academy of Sciences - PNAS, 1984-05, Vol.81 (9), p.2806-2810

1984

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The role of X inactivation and cellular mosaicism in women's health and sex-specific diseases

JAMA : the journal of the American Medical Association, 2006-03, Vol.295 (12), p.1428

Migeon, Barbara R

2006

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Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA

The EMBO journal, 1988-02, Vol.7 (2), p.401-406

1988

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Adrenoleukodystrophy: Evidence for X Linkage, Inactivation, and Selection Favoring the Mutant Allele in Heterozygous Cells

Proceedings of the National Academy of Sciences - PNAS, 1981-08, Vol.78 (8), p.5066-5070

1981

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Incomplete X Chromosome Dosage Compensation in Chorionic Villi of Human Placenta

Proceedings of the National Academy of Sciences - PNAS, 1985-05, Vol.82 (10), p.3390-3394

1985

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The Barr Body is a Looped X Chromosome Formed by Telomere Association

Proceedings of the National Academy of Sciences - PNAS, 1991-07, Vol.88 (14), p.6191-6195

1991

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Studies of the Locus for Androgen Receptor: Localization on the Human X Chromosome and Evidence for Homology with the Tfm Locus in the Mouse

Proceedings of the National Academy of Sciences - PNAS, 1981-10, Vol.78 (10), p.6339-6343

1981

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Characterization of a Cloned DNA Sequence That is Present at Centromeres of All Human Autosomes and the X Chromosome and Shows Polymorphic Variation

Proceedings of the National Academy of Sciences - PNAS, 1984-08, Vol.81 (15), p.4884-4888

1984

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Clusters of CpG dinucleotides implicated by nuclease hypersensitivity as control elements of housekeeping genes

Nature (London), 1985-04, Vol.314 (6010), p.467-469

1985

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Selection against lethal alleles in females heterozygous for incontinentia pigmenti

American journal of human genetics, 1989, Vol.44 (1), p.100-106

1989

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Effect of ageing on reactivation of the human X-linked HPRT locus

Nature (London), 1988-09, Vol.335 (6185), p.93-96

1988

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X-chromosome inactivation: molecular mechanisms and genetic consequences

Differential X Reactivation in Human Placental Cells: Implications for Reversal of X Inactivation

Non-random X chromosome inactivation in mammalian cells

X chromosome inactivation: theme and variations

The severe phenotype of females with Tiny Ring X chromosomes is associated with inability of these chromosomes to undergo X inactivation

The human NTT gene : Identification of a novel 17-kb noncoding nuclear RNA expressed in activated CD4+ T cells

DNA Methylation Stabilizes X Chromosome Inactivation in Eutherians but not in Marsupials: Evidence for Multistep Maintenance of Mammalian X Dosage Compensation

The Human Female Paradox: Biological Disadvantage Preimplantation, Biological Advantage, Thereafter

Human X Inactivation Center Induces Random X Chromosome Inactivation in Male Transgenic Mice

Deficient Transcription of XIST from Tiny Ring X Chromosomes in Females with Severe Phenotypes

Identification of TSIX, Encoding an RNA Antisense to Human XIST, Reveals Differences from its Murine Counterpart: Implications for X Inactivation

Asynchronous Replication of Homologous Loci on Human Active and Inactive X Chromosomes

Lack of X inactivation associated with maternal X isodisomy : Evidence for a counting mechanism prior to X inactivation during human embryogenesis

Studies of X inactivation and isodisomy in twins provide further evidence that X chromosome is not involved in Rett syndrome

Methylation of the Hypoxanthine Phosphoribosyltransferase Locus on the Human X Chromosome: Implications for X-Chromosome Inactivation

The role of X inactivation and cellular mosaicism in women's health and sex-specific diseases

Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA

Adrenoleukodystrophy: Evidence for X Linkage, Inactivation, and Selection Favoring the Mutant Allele in Heterozygous Cells

Incomplete X Chromosome Dosage Compensation in Chorionic Villi of Human Placenta

The Barr Body is a Looped X Chromosome Formed by Telomere Association

Studies of the Locus for Androgen Receptor: Localization on the Human X Chromosome and Evidence for Homology with the Tfm Locus in the Mouse

Characterization of a Cloned DNA Sequence That is Present at Centromeres of All Human Autosomes and the X Chromosome and Shows Polymorphic Variation

Clusters of CpG dinucleotides implicated by nuclease hypersensitivity as control elements of housekeeping genes

Selection against lethal alleles in females heterozygous for incontinentia pigmenti

Effect of ageing on reactivation of the human X-linked HPRT locus

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