G. W. van der Heijden

发表

In vivo repair of DNA damage induced by X-rays in the early stages of mouse fertilization, and the influence of maternal PARP1 ablation.

P. de Boer, R. Ranaldi, A. Derijck, 2011, Mutation research.

Silencing markers are retained on pericentric heterochromatin during murine primordial germ cell development

M. Eijpe, W. V. van Cappellen, J. Gribnau, 2017, Epigenetics & Chromatin.

Differential Expression and Sex Chromosome Association of CHD3/4 and CHD5 during Spermatogenesis

R. Moll, A. Brehm, H. Elsässer, 2014, PloS one.

Defending the genome in tudor style.

A. Bortvin, G. W. van der Heijden, 2009, Developmental cell.

The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans

M. J. Xavier, D. Conrad, J. Veltman, 2022, American journal of human genetics.

Motile human normozoospermic and oligozoospermic semen samples show a difference in double-strand DNA break incidence.

L. Ramos, P. de Boer, J. Kremer, 2007, Human reproduction.

Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failure.

M. J. Xavier, D. Conrad, J. Veltman, 2022, American journal of human genetics.

The X and Y chromosome in meiosis: how and why they keep silent.

M. Eijpe, W. Baarends, G. W. van der Heijden, 2011, Asian journal of andrology.

Parental origin of chromatin in human monopronuclear zygotes revealed by asymmetric histone methylation patterns, differs between IVF and ICSI

P. de Boer, P. Boer, G. W. Heijden, 2009, Molecular reproduction and development.

Sperm-derived histones contribute to zygotic chromatin in humans

L. Ramos, P. de Boer, J. van der Vlag, 2008, BMC Developmental Biology.

Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.

M. J. Xavier, D. Conrad, J. Veltman, 2020, American journal of human genetics.

Reduced oocyte activation and first cleavage rate after ICSI with spermatozoa from a sterile mouse chromosome mutant.

P. de Boer, F. van der Hoeven, T. Cooper, 2004, Human reproduction.

gammaH2AX signalling during sperm chromatin remodelling in the mouse zygote.

P. de Boer, M. Philippens, A. Derijck, 2006, DNA repair.

Biallelic mutations in M1AP are a frequent cause of meiotic arrest leading to male infertility

D. Conrad, J. Veltman, S. Kahraman, 2019, bioRxiv.

Incomplete meiotic sex chromosome inactivation in the domestic dog

W. V. van Cappellen, J. Laven, J. Grootegoed, 2015, BMC Genomics.

Cytoplasmic Compartmentalization of the Fetal piRNA Pathway in Mice

G. Hannon, A. Aravin, V. Vagin, 2009, PLoS genetics.

Transient relaxation of transposon silencing at the onset of mammalian meiosis

A. Bortvin, G. W. van der Heijden, 2009, Epigenetics.

Mouse maelstrom, a component of nuage, is essential for spermatogenesis and transposon repression in meiosis.

P. de Boer, M. Goodheart, A. Bortvin, 2008, Developmental cell.

A role for retrotransposon LINE-1 in fetal oocyte attrition in mice.

Kathryn A. O’Donnell, A. Bortvin, Sandra L. Martin, 2014, Developmental cell.

Meiotic failure in male mice lacking an X-linked factor.

D. Page, K. Mclaughlin, Fang Yang, 2008, Genes & development.

Transmission of modified nucleosomes from the mouse male germline to the zygote and subsequent remodeling of paternal chromatin.

L. Ramos, P. de Boer, J. van der Vlag, 2006, Developmental biology.

Transient reduction of DNA methylation at the onset of meiosis in male mice

K. Hansen, V. Gaysinskaya, A. Bortvin, 2017, Epigenetics & Chromatin.

Bodies of evidence - compartmentalization of the piRNA pathway in mouse fetal prospermatogonia.

Julio Castañeda, A. Bortvin, G. W. van der Heijden, 2010, Current opinion in cell biology.

Paternal heterochromatin formation in human embryos is H3K9/HP1 directed and primed by sperm-derived histone modifications

J. Laven, W. Baarends, A. Peters, 2014, Nature Communications.

Synaptonemal Complex Length Variation in Wild-Type Male Mice

A. Bortvin, G. W. van der Heijden, S. Malki, 2010, Genes.

DNA double-strand break repair in parental chromatin of mouse zygotes, the first cell cycle as an origin of de novo mutation.

P. de Boer, M. Philippens, A. Derijck, 2008, Human molecular genetics.

Silencing markers are retained on pericentric heterochromatin during murine primordial germ cell development

M. Eijpe, W. V. van Cappellen, J. Gribnau, 2017, Epigenetics & Chromatin.

Intracellular Detection of Cytosine Incorporation in Genomic DNA by Using 5‐Ethynyl‐2′‐Deoxycytidine

A. Bortvin, M. Greenberg, L. Guan, 2011, Chembiochem : a European journal of chemical biology.

Variant PNLDC1, Defective piRNA Processing, and Azoospermia.

D. Conrad, J. Veltman, N. Skakkebaek, 2021, The New England journal of medicine.

Incomplete nuclear transformation of human spermatozoa in oligo-astheno-teratospermia: characterization by indirect immunofluorescence of chromatin and thiol status.

L. Ramos, P. de Boer, J. Kremer, 2007, Human reproduction.

A Role for Retrotransposon LINE-1 in Fetal Oocyte Attrition in Mice.

Kathryn A. O’Donnell, A. Bortvin, Sandra L. Martin, 2019, Developmental cell.

Fen1 does not control somatic hypermutability of the (CTG) n · (CAG) n repeat in a knock‐in mouse model for DM1

M. Nelen, B. Wieringa, D. G. Wansink, 2006, FEBS letters.