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Analysis of CpG Suppression in Methylated and Nonmethylated Species

Proceedings of the National Academy of Sciences - PNAS, 1992-02, Vol.89 (3), p.957-961

1992

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Polymerase Chain Reaction-Aided Genomic Sequencing of an X Chromosome- Linked CpG Island: Methylation Patterns Suggest Clonal Inheritance, CpG Site Autonomy, and an Explanation of Activity State Stability

Proceedings of the National Academy of Sciences - PNAS, 1990-11, Vol.87 (21), p.8252-8256

1990

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Association of fragile X syndrome with delayed replication of the FMR1 gene

Cell, 1993-07, Vol.73 (7), p.1403-1409

1993

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The DNMT3B DNA Methyltransferase Gene Is Mutated in the ICF Immunodeficiency Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1999-12, Vol.96 (25), p.14412-14417

1999

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Methylation analysis of CGG sites in the CpG island of the human FMR1 gene

Human molecular genetics, 1992-11, Vol.1 (8), p.571-578

1992

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Role of Late Replication Timing in the Silencing of X-Linked Genes

Human molecular genetics, 1996-09, Vol.5 (9), p.1345-1353

1996

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Mammalian X-Chromosome Inactivation

Annual review of genetics, 1983-01, Vol.17 (1), p.155-190

1983

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Allele-specific replication timing in imprinted domains: absence of asynchrony at several loci

Human molecular genetics, 1995-12, Vol.4 (12), p.2287-2293

1995

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Demethylation of specific sites in the 5' region of the inactive X-linked human phosphoglycerate kinase gene correlates with the appearance of nuclease sensitivity and gene expression

Molecular and Cellular Biology, 1988-11, Vol.8 (11), p.4692-4699

1988

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5-Azacytidine-induced reactivation of the human X chromosome-linked PGK1 gene is associated with a large region of cytosine demethylation in the 5' CpG island

Proceedings of the National Academy of Sciences - PNAS, 1990-06, Vol.87 (11), p.4174-4178

1990

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Analysis of a paracentric inversion in human oocytes: nonhomologous pairing in pachytene

Human genetics, 1999-09, Vol.105 (3), p.191-196

1999

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ICF syndrome cells as a model system for studying X chromosome inactivation

Cytogenetic and Genome Research, 2002-01, Vol.99 (1-4), p.25-29

2002

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Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant

Human molecular genetics, 2000-11, Vol.9 (18), p.2575-2587

2000

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An analysis of meiotic pairing in trisomy 21 oocytes using fluorescent in situ hybridization

Cytogenetic and genome research, 1998-01, Vol.80 (1-4), p.48-53

1998

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High Rate of Recombination and Double Crossovers in the Mouse Pseudoautosomal Region during Male Meiosis

Proceedings of the National Academy of Sciences - PNAS, 1987-10, Vol.84 (20), p.7218-7220

1987

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Reverse replication timing for the XIST gene in human fibroblasts

Human molecular genetics, 1995-05, Vol.4 (5), p.813-820

1995

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A Potentially Critical Hpa II Site of the X Chromosome-Linked PGK1 Gene is Unmethylated Prior to the Onset of Meiosis of Human Oogenic Cells

Proceedings of the National Academy of Sciences - PNAS, 1992-02, Vol.89 (4), p.1413-1417

1992

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Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication

Human genetics, 2001-10, Vol.109 (4), p.452-462

2001

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Constitutive phosphorylation of ATM in lymphoblastoid cell lines from patients with ICF syndrome without downstream kinase activity

DNA repair, 2006-04, Vol.5 (4), p.432-443

2006

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Hemimethylation and hypersensitivity are early events in transcriptional reactivation of human inactive X-linked genes in a hamster x human somatic cell hybrid

Molecular and Cellular Biology, 1992-09, Vol.12 (9), p.3819-3826

1992

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Chromosome painting analysis of early oogenesis in human trisomy 18

Cytogenetic and genome research, 1995-01, Vol.70 (3-4), p.205-210

1995

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A fluorescent in situ hybridization analysis of X chromosome pairing in early human female meiosis

Human genetics, 1994-10, Vol.94 (4), p.389-394

1994

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Transformation with DNA from 5-azacytidine-Reactivated X Chromosomes

Proceedings of the National Academy of Sciences - PNAS, 1982-04, Vol.79 (7), p.2352-2354

1982

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A Variable Domain of Delayed Replication in FRAXA Fragile X Chromosomes: X Inactivation-Like Spread of Late Replication

Proceedings of the National Academy of Sciences - PNAS, 1997-04, Vol.94 (9), p.4587-4592

1997

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Linkage of the Steroid Sulfatase Gene to the Sex-Reversed Mutation in the Mouse

Genetics (Austin), 1987-07, Vol.116 (3), p.465-468

1987

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Analysis of CpG Suppression in Methylated and Nonmethylated Species

Polymerase Chain Reaction-Aided Genomic Sequencing of an X Chromosome- Linked CpG Island: Methylation Patterns Suggest Clonal Inheritance, CpG Site Autonomy, and an Explanation of Activity State Stability

Association of fragile X syndrome with delayed replication of the FMR1 gene

The DNMT3B DNA Methyltransferase Gene Is Mutated in the ICF Immunodeficiency Syndrome

Methylation analysis of CGG sites in the CpG island of the human FMR1 gene

Role of Late Replication Timing in the Silencing of X-Linked Genes

Mammalian X-Chromosome Inactivation

Allele-specific replication timing in imprinted domains: absence of asynchrony at several loci

Demethylation of specific sites in the 5' region of the inactive X-linked human phosphoglycerate kinase gene correlates with the appearance of nuclease sensitivity and gene expression

5-Azacytidine-induced reactivation of the human X chromosome-linked PGK1 gene is associated with a large region of cytosine demethylation in the 5' CpG island

Analysis of a paracentric inversion in human oocytes: nonhomologous pairing in pachytene

ICF syndrome cells as a model system for studying X chromosome inactivation

Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant

An analysis of meiotic pairing in trisomy 21 oocytes using fluorescent in situ hybridization

High Rate of Recombination and Double Crossovers in the Mouse Pseudoautosomal Region during Male Meiosis

Reverse replication timing for the XIST gene in human fibroblasts

A Potentially Critical Hpa II Site of the X Chromosome-Linked PGK1 Gene is Unmethylated Prior to the Onset of Meiosis of Human Oogenic Cells

Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication

Constitutive phosphorylation of ATM in lymphoblastoid cell lines from patients with ICF syndrome without downstream kinase activity

Hemimethylation and hypersensitivity are early events in transcriptional reactivation of human inactive X-linked genes in a hamster x human somatic cell hybrid

Chromosome painting analysis of early oogenesis in human trisomy 18

A fluorescent in situ hybridization analysis of X chromosome pairing in early human female meiosis

Transformation with DNA from 5-azacytidine-Reactivated X Chromosomes

A Variable Domain of Delayed Replication in FRAXA Fragile X Chromosomes: X Inactivation-Like Spread of Late Replication

Linkage of the Steroid Sulfatase Gene to the Sex-Reversed Mutation in the Mouse

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