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Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 16, p. 3695, doi. 10.1093/hmg/dds200
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- Article
A new mutation identified in SPATA16 in two globozoospermic patients.
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- Journal of Assisted Reproduction & Genetics, 2016, v. 33, n. 6, p. 815, doi. 10.1007/s10815-016-0715-3
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- Article
Quantitative, titratable and high-throughput reporter assays to measure DNA double strand break repair activity in cells.
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- Nucleic Acids Research, 2024, v. 52, n. 4, p. 1736, doi. 10.1093/nar/gkad1196
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- Article
Histone H2AFX Links Meiotic Chromosome Asynapsis to Prophase I Oocyte Loss in Mammals.
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- PLoS Genetics, 2015, v. 11, n. 10, p. 1, doi. 10.1371/journal.pgen.1005462
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- Article
Silencing of X-Linked MicroRNAs by Meiotic Sex Chromosome Inactivation.
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- PLoS Genetics, 2015, v. 11, n. 10, p. 1, doi. 10.1371/journal.pgen.1005461
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- Article
The BCL-2 pathway preserves mammalian genome integrity by eliminating recombination-defective oocytes.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16441-z
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- Article