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1
Genome destabilization by homologous recombination in the germ line.
Nat Rev Mol Cell Biol. 2010 Mar;11(3):182-95. doi: 10.1038/nrm2849. Epub 2010 Feb 18.
2
Mechanisms of germ line genome instability.
Semin Cell Dev Biol. 2016 Jun;54:177-87. doi: 10.1016/j.semcdb.2016.02.019. Epub 2016 Feb 12.
6
DNA double-strand breaks in meiosis: checking their formation, processing and repair.
DNA Repair (Amst). 2009 Sep 2;8(9):1127-38. doi: 10.1016/j.dnarep.2009.04.005. Epub 2009 May 22.
7
Protection of repetitive DNA borders from self-induced meiotic instability.
Nature. 2011 Aug 7;477(7362):115-9. doi: 10.1038/nature10331.
8
Competitive repair by naturally dispersed repetitive DNA during non-allelic homologous recombination.
PLoS Genet. 2010 Dec 2;6(12):e1001228. doi: 10.1371/journal.pgen.1001228.
10
Double-stranded DNA breaks and gene functions in recombination and meiosis.
Cell Res. 2006 May;16(5):402-12. doi: 10.1038/sj.cr.7310052.

引用本文的文献

2
Light-controlled Spo11-less meiotic DNA breaks by MagTAQing lead to chromosomal aberrations.
Nucleic Acids Res. 2025 Apr 10;53(7). doi: 10.1093/nar/gkaf206.
3
Genetic diversity and regulatory features of human-specific duplications.
bioRxiv. 2025 Mar 17:2025.03.14.643395. doi: 10.1101/2025.03.14.643395.
5
Intercellular bridges are essential for transposon repression and meiosis in the male germline.
Nat Commun. 2025 Feb 10;16(1):1488. doi: 10.1038/s41467-025-56742-9.
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Transcription near arrested DNA replication forks triggers ribosomal DNA copy number changes.
Nucleic Acids Res. 2025 Jan 24;53(3). doi: 10.1093/nar/gkaf014.
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Mechanisms of tandem duplication in the cancer genome.
DNA Repair (Amst). 2025 Jan;145:103802. doi: 10.1016/j.dnarep.2024.103802. Epub 2024 Dec 25.
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Keeping it safe: control of meiotic chromosome breakage.
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Global diversity, recurrent evolution, and recent selection on amylase structural haplotypes in humans.
bioRxiv. 2024 Jun 13:2024.02.07.579378. doi: 10.1101/2024.02.07.579378.

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1
Drive against hotspot motifs in primates implicates the PRDM9 gene in meiotic recombination.
Science. 2010 Feb 12;327(5967):876-9. doi: 10.1126/science.1182363. Epub 2009 Dec 31.
2
PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice.
Science. 2010 Feb 12;327(5967):836-40. doi: 10.1126/science.1183439. Epub 2009 Dec 31.
3
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes.
Nat Genet. 2009 Dec;41(12):1269-71. doi: 10.1038/ng.481. Epub 2009 Nov 8.
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Copy number variation in human health, disease, and evolution.
Annu Rev Genomics Hum Genet. 2009;10:451-81. doi: 10.1146/annurev.genom.9.081307.164217.
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Distinct histone modifications define initiation and repair of meiotic recombination in the mouse.
EMBO J. 2009 Sep 2;28(17):2616-24. doi: 10.1038/emboj.2009.207. Epub 2009 Jul 30.
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Histone H3 lysine 4 trimethylation marks meiotic recombination initiation sites.
EMBO J. 2009 Jan 21;28(2):99-111. doi: 10.1038/emboj.2008.257. Epub 2008 Dec 11.
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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
N Engl J Med. 2008 Oct 16;359(16):1685-99. doi: 10.1056/NEJMoa0805384. Epub 2008 Sep 10.

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