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Transposable elements in the mammalian germline: a comfortable niche or a deadly trap?

Heredity, 2010-07, Vol.105 (1), p.92-104

2010

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Dnmt3L and the Establishment of Maternal Genomic Imprints

Science (American Association for the Advancement of Science), 2001-12, Vol.294 (5551), p.2536-2539

2001

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Do assisted reproductive technologies and in vitro embryo culture influence the epigenetic control of imprinted genes and transposable elements in children?

Human reproduction (Oxford), 2021-02, Vol.36 (2), p.479-492

2021

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Identification and resolution of artifacts in the interpretation of imprinted gene expression

Briefings in functional genomics, 2010-12, Vol.9 (5-6), p.374-384

2010

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The epigenetic control of transposable elements and imprinted genes in newborns is affected by the mode of conception: ART versus spontaneous conception without underlying infertility

Human reproduction (Oxford), 2018-02, Vol.33 (2), p.331-340

2018

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Small-RNA Perspective on Gametogenesis, Fertilization, and Early Zygotic Development

Science (American Association for the Advancement of Science), 2010-10, Vol.330 (6004), p.617-622

2010

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Transposon silencing and imprint establishment in mammalian germ cells

Cold Spring Harbor Symposia on Quantitative Biology, 2004, Vol.69, p.381-388

2004

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Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L

Nature, 2004-09, Vol.431 (7004), p.96-99

2004

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DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

Human mutation, 2005-01, Vol.25 (1), p.56-63

2005

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Origins of extreme sexual dimorphism in genomic imprinting

Cytogenetic and genome research, 2006-03, Vol.113 (1-4), p.36-40

2006

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Delayed and incomplete reprogramming of chromosome methylation patterns in bovine cloned embryos

Current biology, 2001-10, Vol.11 (19), p.1542-1546

2001

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MIWI2 Is Essential for Spermatogenesis and Repression of Transposons in the Mouse Male Germline

Developmental cell, 2007-04, Vol.12 (4), p.503-514

2007

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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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Sex-specific promoters regulate Dnmt3L expression in mouse germ cells

Human reproduction (Oxford), 2007-02, Vol.22 (2), p.457-467

2007

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Germline correction of an epimutation related to Silver-Russell syndrome

Human molecular genetics, 2015-06, Vol.24 (12), p.3314-3321

2015

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Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing

Genome Research, 2008-08, Vol.18 (8), p.1270-1281

2008

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Identification of the Control Region for Tissue-Specific Imprinting of the Stimulatory G Protein α-Subunit

Proceedings of the National Academy of Sciences - PNAS, 2005-04, Vol.102 (15), p.5513-5518

2005

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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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Genetics and epigenetics of hydatidiform moles

Nature genetics, 2006-03, Vol.38 (3), p.274-276

2006

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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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Direct analysis of chromosome methylation

Methods in molecular biology (Clifton, N.J.), 2001, Vol.181, p.229

2001

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Do assisted reproductive technologies and in vitro embryo culture influence the epigenetic control of imprinted genes and transposable elements in children?

Human reproduction (Oxford), 2021-02, Vol.36 (2), p.479-492

2021

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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

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Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis

Cytogenetics and cell genetics, 1997-01, Vol.77 (3-4), p.308

1997

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Abnormal methylation does not prevent X inactivation in ICF patients

Cytogenetics and cell genetics, 1999-01, Vol.84 (3-4), p.245

1999

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Transposable elements in the mammalian germline: a comfortable niche or a deadly trap?

Dnmt3L and the Establishment of Maternal Genomic Imprints

Do assisted reproductive technologies and in vitro embryo culture influence the epigenetic control of imprinted genes and transposable elements in children?

Identification and resolution of artifacts in the interpretation of imprinted gene expression

The epigenetic control of transposable elements and imprinted genes in newborns is affected by the mode of conception: ART versus spontaneous conception without underlying infertility

Small-RNA Perspective on Gametogenesis, Fertilization, and Early Zygotic Development

Transposon silencing and imprint establishment in mammalian germ cells

Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

Origins of extreme sexual dimorphism in genomic imprinting

Delayed and incomplete reprogramming of chromosome methylation patterns in bovine cloned embryos

MIWI2 Is Essential for Spermatogenesis and Repression of Transposons in the Mouse Male Germline

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

Sex-specific promoters regulate Dnmt3L expression in mouse germ cells

Germline correction of an epimutation related to Silver-Russell syndrome

Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing

Identification of the Control Region for Tissue-Specific Imprinting of the Stimulatory G Protein α-Subunit

Chromosome methylation patterns during mammalian preimplantation development

Genetics and epigenetics of hydatidiform moles

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

Direct analysis of chromosome methylation

Do assisted reproductive technologies and in vitro embryo culture influence the epigenetic control of imprinted genes and transposable elements in children?

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

Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis

Abnormal methylation does not prevent X inactivation in ICF patients

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