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1
Widespread genetic incompatibility in C. elegans maintained by balancing selection.
Science. 2008 Feb 1;319(5863):589-94. doi: 10.1126/science.1151107. Epub 2008 Jan 10.
2
A novel sperm-delivered toxin causes late-stage embryo lethality and transmission ratio distortion in C. elegans.
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3
Natural variation in a chloride channel subunit confers avermectin resistance in C. elegans.
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The opportunity for balancing selection in experimental populations of Caenorhabditis elegans.
Evolution. 2013 Jan;67(1):142-56. doi: 10.1111/j.1558-5646.2012.01744.x. Epub 2012 Aug 20.
6
Diversity and linkage of genes in the self-incompatibility gene family in Arabidopsis lyrata.
Genetics. 2003 Aug;164(4):1519-35. doi: 10.1093/genetics/164.4.1519.
9
The Caenorhabditis elegans NR4A nuclear receptor is required for spermatheca morphogenesis.
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10
Temporal dynamics and linkage disequilibrium in natural Caenorhabditis elegans populations.
Genetics. 2007 Jun;176(2):999-1011. doi: 10.1534/genetics.106.067223. Epub 2007 Apr 3.

引用本文的文献

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Phenotypic tolerance for rDNA copy number variation within the natural range of C. elegans.
PLoS Genet. 2025 Jul 2;21(7):e1011759. doi: 10.1371/journal.pgen.1011759. eCollection 2025 Jul.
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An animal toxin-antidote system kills cells by creating a novel cation channel.
PLoS Biol. 2025 May 27;23(5):e3003182. doi: 10.1371/journal.pbio.3003182. eCollection 2025 May.
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Divergent toxin alleles are suppressed by distinct mechanisms.
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A newborn F-box gene blocks gene flow by selectively degrading phosphoglucomutase in species hybrids.
Proc Natl Acad Sci U S A. 2024 Nov 12;121(46):e2418037121. doi: 10.1073/pnas.2418037121. Epub 2024 Nov 8.
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eQTL mapping in transgenic alpha-synuclein carrying Caenorhabditis elegans recombinant inbred lines.
Hum Mol Genet. 2024 Dec 6;33(24):2123-2132. doi: 10.1093/hmg/ddae148.
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Tools and methods for cell ablation and cell inhibition in Caenorhabditis elegans.
Genetics. 2025 Jan 8;229(1):1-48. doi: 10.1093/genetics/iyae119.
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Parental-effect gene-drive elements under partial selfing, or why do genomes have hyperdivergent regions?
bioRxiv. 2024 Jul 24:2024.07.23.604817. doi: 10.1101/2024.07.23.604817.
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Mechanism of an animal toxin-antidote system.
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THE SEX-RATIO TRAIT IN DROSOPHILA SIMULANS: GEOGRAPHICAL DISTRIBUTION OF DISTORTION AND RESISTANCE.
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Asymmetric cell division and axis formation in the embryo.
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Temporal dynamics and linkage disequilibrium in natural Caenorhabditis elegans populations.
Genetics. 2007 Jun;176(2):999-1011. doi: 10.1534/genetics.106.067223. Epub 2007 Apr 3.
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The Caenorhabditis elegans cell-cycle regulator ZYG-11 defines a conserved family of CUL-2 complex components.
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A conserved role for a GATA transcription factor in regulating epithelial innate immune responses.
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Adaptive evolution in two large families of ubiquitin-ligase adapters in nematodes and plants.
Genome Res. 2006 Aug;16(8):1017-30. doi: 10.1101/gr.5089806. Epub 2006 Jul 6.
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Balancing selection and its effects on sequences in nearby genome regions.
PLoS Genet. 2006 Apr;2(4):e64. doi: 10.1371/journal.pgen.0020064.
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Analysis of homologous gene clusters in Caenorhabditis elegans reveals striking regional cluster domains.
Genetics. 2006 Jan;172(1):127-43. doi: 10.1534/genetics.104.040030. Epub 2005 Nov 15.
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Nucleotide polymorphism and linkage disequilibrium in wild populations of the partial selfer Caenorhabditis elegans.
Genetics. 2006 Jan;172(1):171-84. doi: 10.1534/genetics.105.048207. Epub 2005 Nov 4.

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