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Willy M. Baarends

Researcher at Erasmus University Rotterdam

Publications -  83
Citations -  6112

Willy M. Baarends is an academic researcher from Erasmus University Rotterdam. The author has contributed to research in topics: Meiosis & Chromatin. The author has an hindex of 36, co-authored 78 publications receiving 5587 citations. Previous affiliations of Willy M. Baarends include Erasmus University Medical Center.

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Anti-müllerian hormone and anti-müllerian hormone type II receptor messenger ribonucleic acid expression in rat ovaries during postnatal development, the estrous cycle, and gonadotropin-induced follicle growth.

TL;DR: The results indicate that FSH and estrogens may play a role in the down-regulation of AMH and AMHRII mRNA expression in vivo when small antral follicles differentiate into large antRAL follicles.
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Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formation

TL;DR: It is proposed that SYCP1 has a coordinating role, and ensures formation of crossovers in meiotic chromosome behavior and recombination, and Unexpectedly, Sycp1(-/-) spermatocytes did not form XY bodies.
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Chromatin dynamics during spermiogenesis.

TL;DR: This review highlights the current knowledge on post-meiotic chromatin reorganization and reveals for the first time intriguing parallels in this process in Drosophila and mammals and illustrates the possible mechanisms that lead from a histone-based chromatin to a mainly protamine-based structure during spermatid differentiation.
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Inactivation of the HR6B Ubiquitin-Conjugating DNA Repair Enzyme in Mice Causes Male Sterility Associated with Chromatin Modification

TL;DR: The phenotype of the first animal mutant in the ubiquitin pathway is reported: inactivation of the hHR6B-homologous gene in mice causes male infertility, and this findings provide a parallel between yeast sporulation and mammalian spermatogenesis and strongly implicate h HR6-dependent ubiquitination in chromatin remodeling.
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Targeted inactivation of mouse RAD52 reduces homologous recombination but not resistance to ionizing radiation.

TL;DR: Results show that, as in S. cerevisiae, MmRAD52 is involved in recombination, although the repair of DNA damage is not affected upon inactivation, indicating that Mm RAD52 may be involved in certain types of DSB repair processes and not in others.