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Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissues

Proceedings of the National Academy of Sciences - PNAS, 2010-05, Vol.107 (20), p.9281-9286

2010

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Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions

Human molecular genetics, 2008-09, Vol.17 (18), p.2776-2789

2008

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Regulation of DNA methylation activity through Dnmt3L promoter methylation by Dnmt3 enzymes in embryonic development

Human molecular genetics, 2008-09, Vol.17 (17), p.2654-2664

2008

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Altered heterochromatin organization after perinatal exposure to zidovudine

Antiviral therapy, 2007-01, Vol.12 (2), p.179-187

2007

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Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

Nature genetics, 1995-10, Vol.11 (2), p.144-149

1995

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Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

Nature (London), 1999-11, Vol.402 (6758), p.187-191

1999

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Defective B-cell-negative selection and terminal differentiation in the ICF syndrome

Blood, 2004-04, Vol.103 (7), p.2683-2690

2004

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Chromosome methylation patterns during mammalian preimplantation development

Genes & development, 1998-07, Vol.12 (14), p.2108-2113

1998

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Whole-genome methylation scan in ICF syndrome : hypomethylation of non-satellite DNA repeats D4Z4 and NBL2

Human molecular genetics, 2000-03, Vol.9 (4), p.597-604

2000

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Altered Heterochromatin Organization after Perinatal Exposure to Zidovudine

Antiviral therapy, 2007-04, Vol.12 (3), p.429-430

2007

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Early prenatal diagnosis of ICF syndrome by mutation detection

Prenatal diagnosis, 2007-11, Vol.27 (11), p.1075-1078

2007

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Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients

Human molecular genetics, 1994-12, Vol.3 (12), p.2093-2102

1994

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α-Satellite DNA methylation in normal individuals and in ICF patients : heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

Human genetics, 1997-06, Vol.99 (6), p.738-745

1997

Volltextzugriff (PDF)

EMR1, an unusual member in the family of hormone receptors with seven transmembrane segments

Genomics (San Diego, Calif.), 1995-03, Vol.26 (2), p.334-344

1995

Volltextzugriff (PDF)

cDNA, Gene Structure, and Chromosomal Localization of Human GAR1 (CNCG3L), a Homolog of the Third Subunit of Bovine Photoreceptor cGMP-Gated Channel

Genomics (San Diego, Calif.), 1995-07, Vol.28 (1), p.32-38

1995

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Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization

Human genetics, 1989-08, Vol.83 (1), p.33-36

1989

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A 37-kb Fragment Common to the Pericentromeric Region of Human Chromosomes 13 and 21 and to the Ancestral Inactive Centromere of Chromosome 2

Genomics (San Diego, Calif.), 1993-03, Vol.15 (3), p.576-581

1993

Volltextzugriff (PDF)

LAG-3, a novel lymphocyte activation gene closely related to CD4

The Journal of experimental medicine, 1990-05, Vol.171 (5), p.1393-1405

1990

Volltextzugriff (PDF)

Abnormal methylation does not prevent X inactivation in ICF patients

Cytogenetics and cell genetics, 1999, Vol.84 (3-4), p.245

1999

Volltextzugriff (PDF)

Localization of a 900-bp-long fragment of the human choline acetyltransferase gene to 10q11.2 by nonradioactive in situ hybridization

Genomics (San Diego, Calif.), 1991, Vol.9 (1), p.210-212

1991

Volltextzugriff (PDF)

The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease

American journal of human genetics, 1997, Vol.60 (1), p.72-79

1997

Volltextzugriff (PDF)

High recurrence of rearrangements involving chromosome 14 in an ataxia telangiectasia lymphoblastoid cell line and in its mutagen-treated derivatives

Human genetics, 1991-03, Vol.86 (5), p.475-480

1991

Volltextzugriff (PDF)

Mapping of Single-Copy DNA Sequences on Human Chromosomes by in situ Hybridization with Biotinylated Probes: Enhancement of Detection Sensitivity by Intensified-Fluorescence Digital-Imaging Microscopy

Proceedings of the National Academy of Sciences - PNAS, 1989, Vol.86 (2), p.582-586

1989

Volltextzugriff (PDF)

Aneuploidy in human lymphocytes: an extensive study of eight individuals of various ages

Mutation research. DNAging : genetic instability and aging, 1993, Vol.295 (2), p.71-80

1993

Volltextzugriff (PDF)

Detection of G-C rich heterochromatin by 5-azacytidine in mammals

Human genetics, 1981-01, Vol.57 (2), p.134-137

1981

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Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissues

Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions

Regulation of DNA methylation activity through Dnmt3L promoter methylation by Dnmt3 enzymes in embryonic development

Altered heterochromatin organization after perinatal exposure to zidovudine

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

Defective B-cell-negative selection and terminal differentiation in the ICF syndrome

Chromosome methylation patterns during mammalian preimplantation development

Whole-genome methylation scan in ICF syndrome : hypomethylation of non-satellite DNA repeats D4Z4 and NBL2

Altered Heterochromatin Organization after Perinatal Exposure to Zidovudine

Early prenatal diagnosis of ICF syndrome by mutation detection

Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients

α-Satellite DNA methylation in normal individuals and in ICF patients : heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

EMR1, an unusual member in the family of hormone receptors with seven transmembrane segments

cDNA, Gene Structure, and Chromosomal Localization of Human GAR1 (CNCG3L), a Homolog of the Third Subunit of Bovine Photoreceptor cGMP-Gated Channel

Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization

A 37-kb Fragment Common to the Pericentromeric Region of Human Chromosomes 13 and 21 and to the Ancestral Inactive Centromere of Chromosome 2

LAG-3, a novel lymphocyte activation gene closely related to CD4

Abnormal methylation does not prevent X inactivation in ICF patients

Localization of a 900-bp-long fragment of the human choline acetyltransferase gene to 10q11.2 by nonradioactive in situ hybridization

The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease

High recurrence of rearrangements involving chromosome 14 in an ataxia telangiectasia lymphoblastoid cell line and in its mutagen-treated derivatives

Mapping of Single-Copy DNA Sequences on Human Chromosomes by in situ Hybridization with Biotinylated Probes: Enhancement of Detection Sensitivity by Intensified-Fluorescence Digital-Imaging Microscopy

Aneuploidy in human lymphocytes: an extensive study of eight individuals of various ages

Detection of G-C rich heterochromatin by 5-azacytidine in mammals

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