Works matching IS 00166731 AND DT 2023 AND VI 224 AND IP 4
Results: 24
daf-42 is an evolutionarily young gene essential for dauer development in Caenorhabditis elegans.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad097
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Highlighting rare disease research with a GENETICS and G3 series on genetic models of rare diseases.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad121
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The effects of inversion polymorphisms on patterns of neutral genetic diversity.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad116
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How flower development genes were identified using forward genetic screens in Arabidopsis thaliana.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad102
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Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad115
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- Article
A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad110
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An angiotensin converting enzyme homolog is required for volatile pheromone detection, odorant binding protein secretion and normal courtship behavior in Drosophila melanogaster.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad109
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Reduced histone gene copy number disrupts Drosophila Polycomb function.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad106
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Natural variation in codon bias and mRNA folding strength interact synergistically to modify protein expression in Saccharomyces cerevisiae.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad113
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Permissiveness and competition within and between Neurospora crassa syncytia.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad112
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A dual, catalytic role for the fission yeast Ccr4-Not complex in gene silencing and heterochromatin spreading.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad108
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Sensitized piRNA reporter identifies multiple RNA processing factors involved in piRNA-mediated gene silencing.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad095
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- Article
Context-dependent role of Pho binding sites in Polycomb complex recruitment in Drosophila.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad096
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- Article
Demographic history inference and the polyploid continuum.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad107
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- Article
Transcriptome profiling of the Caenorhabditis elegans intestine reveals that ELT-2 negatively and positively regulates intestinal gene expression within the context of a gene regulatory network.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad088
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A primary microcephaly-associated sas-6 mutation perturbs centrosome duplication, dendrite morphogenesis, and ciliogenesis in Caenorhabditis elegans.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad105
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Mob4 is essential for spermatogenesis in Drosophila melanogaster.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad104
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Linking genetic and environmental factors through marker effect networks to understand trait plasticity.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad103
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Learning and memory using Drosophila melanogaster: a focus on advances made in the fifth decade of research.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad085
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Impact of pathogen genetics on clinical phenotypes in a population of Talaromyces marneffei from Vietnam.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad100
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Rare disease research resources at the Rat Genome Database.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad078
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A Twist-Box domain of the C. elegans Twist homolog, HLH-8, plays a complex role in transcriptional regulation.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad066
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Genetic and genomic analyses of Drosophila melanogaster models of chromatin modification disorders.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad061
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Developmental expression of the Sturge-Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesis.
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- Genetics, 2023, v. 224, n. 4, p. 1, doi. 10.1093/genetics/iyad077
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