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Orientation-dependent Dxz4 contacts shape the 3D structure of the inactive X chromosome

Nature communications, 2018-04, Vol.9 (1), p.1445-17, Article 1445

2018

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The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned

Nature genetics, 1996-11, Vol.14 (3), p.292-299

1996

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DNA deletion associated with hereditary neuropathy with liability to pressure palsies

Cell, 1993-01, Vol.72 (1), p.143-151

1993

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CD40 Ligand Gene Defects Responsible for X-Linked Hyper-IgM Syndrome

Science (American Association for the Advancement of Science), 1993-02, Vol.259 (5097), p.990-993

1993

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The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome

Nature genetics, 1999-07, Vol.22 (3), p.223-224

1999

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Escape from X inactivation in human and mouse

Trends in Genetics, 1995, Vol.11 (1), p.17-22

Disteche, Christine M.

1995

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Escape from X inactivation

Cytogenetic and Genome Research, 2002-01, Vol.99 (1-4), p.36-43

2002

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The Human Acid Ceramidase Gene (ASAH): Structure, Chromosomal Location, Mutation Analysis, and Expression

Genomics (San Diego, Calif.), 1999-12, Vol.62 (2), p.223-231

1999

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Boundaries between Chromosomal Domains of X Inactivation and Escape Bind CTCF and Lack CpG Methylation during Early Development

Developmental cell, 2005, Vol.8 (1), p.31-42

2005

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Cloning and Primary Structure of a Human Islet Isoform of Glutamic Acid Decarboxylase from Chromosome 10

Proceedings of the National Academy of Sciences - PNAS, 1991-10, Vol.88 (19), p.8337-8341

1991

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The amphiregulin gene encodes a novel epidermal growth factor-related protein with tumor-inhibitory activity

Molecular and Cellular Biology, 1990-05, Vol.10 (5), p.1969-1981

1990

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Molecular cloning of human Syk. A B cell protein-tyrosine kinase associated with the surface immunoglobulin M-B cell receptor complex

The Journal of biological chemistry, 1994-04, Vol.269 (16), p.12310-12319

1994

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Down syndrome : molecular mapping of the congenital heart disease and duodenal stenosis

American journal of human genetics, 1992-02, Vol.50 (2), p.294-302

1992

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Structural characterization and chromosomal location of the gene encoding human platelet glycoprotein Ib beta

The Journal of biological chemistry, 1994-07, Vol.269 (26), p.17424-17427

1994

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Ring X and Other Structural X Chromosome Abnormalities: X Inactivation and Phenotype

Seminars in reproductive medicine, 2001, Vol.19 (2), p.147-158

2001

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RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS

Prenatal diagnosis, 1997-03, Vol.17 (3), p.201-242

1997

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Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangements

Ultrasound in obstetrics & gynecology, 2003-06, Vol.21 (6), p.609-615

2003

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Escapees on the X Chromosome

Proceedings of the National Academy of Sciences - PNAS, 1999-12, Vol.96 (25), p.14180-14182

Disteche, Christine M.

1999

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Isolation and chromosomal localization of cDNAs encoding a novel human lymphocyte cell surface molecule, LAM-1. Homology with the mouse lymphocyte homing receptor and other human adhesion proteins

The Journal of experimental medicine, 1989-07, Vol.170 (1), p.123-133

1989

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Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty

Genomics (San Diego, Calif.), 1996-07, Vol.35 (2), p.346-352

1996

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Recurrent Duplication and Deletion Polymorphisms on the Long Arm of the Y Chromosome in Normal Males

Human molecular genetics, 1996-11, Vol.5 (11), p.1767-1775

1996

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cDNA Cloning and Chromosome Mapping of the Human Fe65 Gene: Interaction of the Conserved Cytoplasmic Domains of the Human β-amyloid Precursor Protein and Its Homologues with the Mouse Fe65 Protein

Human molecular genetics, 1996-10, Vol.5 (10), p.1589-1598

1996

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Gene dosage in the evolution and function of mammalian sex chromosomes

Cytogenetic and genome research, 1998-01, Vol.80 (1-4), p.94-103

1998

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Human and rabbit paraoxonases: Purification, cloning, sequencing, mapping and role of polymorphism in organophosphate detoxification

Chemico-biological interactions, 1993-06, Vol.87 (1), p.35-48

1993

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Human Huntingtin Derived from YAC Transgenes Compensates for Loss of Murine Huntingtin by Rescue of the Embryonic Lethal Phenotype

Human molecular genetics, 1996-12, Vol.5 (12), p.1875-1885

1996

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Orientation-dependent Dxz4 contacts shape the 3D structure of the inactive X chromosome

The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

CD40 Ligand Gene Defects Responsible for X-Linked Hyper-IgM Syndrome

The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome

Escape from X inactivation in human and mouse

Escape from X inactivation

The Human Acid Ceramidase Gene (ASAH): Structure, Chromosomal Location, Mutation Analysis, and Expression

Boundaries between Chromosomal Domains of X Inactivation and Escape Bind CTCF and Lack CpG Methylation during Early Development

Cloning and Primary Structure of a Human Islet Isoform of Glutamic Acid Decarboxylase from Chromosome 10

The amphiregulin gene encodes a novel epidermal growth factor-related protein with tumor-inhibitory activity

Molecular cloning of human Syk. A B cell protein-tyrosine kinase associated with the surface immunoglobulin M-B cell receptor complex

Down syndrome : molecular mapping of the congenital heart disease and duodenal stenosis

Structural characterization and chromosomal location of the gene encoding human platelet glycoprotein Ib beta

Ring X and Other Structural X Chromosome Abnormalities: X Inactivation and Phenotype

RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS

Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangements

Escapees on the X Chromosome

Isolation and chromosomal localization of cDNAs encoding a novel human lymphocyte cell surface molecule, LAM-1. Homology with the mouse lymphocyte homing receptor and other human adhesion proteins

Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty

Recurrent Duplication and Deletion Polymorphisms on the Long Arm of the Y Chromosome in Normal Males

cDNA Cloning and Chromosome Mapping of the Human Fe65 Gene: Interaction of the Conserved Cytoplasmic Domains of the Human β-amyloid Precursor Protein and Its Homologues with the Mouse Fe65 Protein

Gene dosage in the evolution and function of mammalian sex chromosomes

Human and rabbit paraoxonases: Purification, cloning, sequencing, mapping and role of polymorphism in organophosphate detoxification

Human Huntingtin Derived from YAC Transgenes Compensates for Loss of Murine Huntingtin by Rescue of the Embryonic Lethal Phenotype

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