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Hormone Signaling and Phenotypic Plasticity in Nematode Development and Evolution
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Sensory control of dauer larva formation in Caenorhabditis elegans
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Targets of TGF-β Signaling in Caenorhabditis elegans Dauer Formation
inferredcites →https://doi.org/10.1016/0010-406x(67)90334-9openalex-snapshot
Ascarosides and ascaroside esters in Ascaris lumbricoides (Nematoda)
inferredcites →https://doi.org/10.1016/0012-1606(75)90109-8openalex-snapshot
The dauerlarva, a post-embryonic developmental variant of the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0012-1606(84)90201-xopenalex-snapshot
The Caenorhabditis elegans dauer larva: Developmental effects of pheromone, food, and temperature
inferredcites →https://doi.org/10.1016/0012-1606(88)90138-8openalex-snapshot
Mutants of Caenorhabditis elegans that form dauer-like larvae
inferredcites →https://doi.org/10.1016/0012-1606(89)90214-5openalex-snapshot
Developmental regulation of energy metabolism in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0092-8674(90)90475-topenalex-snapshot
daf-1, a C. elegans gene controlling dauer larva development, encodes a novel receptor protein kinase
inferredcites →https://doi.org/10.1016/0305-0491(90)90258-uopenalex-snapshot
Intermediary metabolism in the dauer larva of the nematode Caenorhabditis elegans—II. The glyoxylate cycle and fatty-acid oxidation
inferredcites →https://doi.org/10.1016/j.cell.2006.01.037openalex-snapshot
Identification of Ligands for DAF-12 that Govern Dauer Formation and Reproduction in C. elegans
inferredcites →https://doi.org/10.1016/j.cub.2005.06.022openalex-snapshot
High Local Genetic Diversity and Low Outcrossing Rate in Caenorhabditis elegans Natural Populations
inferredcites →https://doi.org/10.1016/j.cub.2006.03.021openalex-snapshot
DAF-16/FOXO Regulates Transcription of cki-1/Cip/Kip and Repression of lin-4 during C. elegans L1 Arrest
inferredcites →https://doi.org/10.1016/j.cub.2006.10.031openalex-snapshot
Chemoattraction in Pristionchus Nematodes and Implications for Insect Recognition
inferredcites →https://doi.org/10.1016/j.cub.2007.12.048openalex-snapshot
Wnt Signaling Induces Vulva Development in the Nematode Pristionchus pacificus
inferredcites →https://doi.org/10.1016/j.cub.2008.11.063openalex-snapshot
A Conserved Endocrine Mechanism Controls the Formation of Dauer and Infective Larvae in Nematodes
inferredcites →https://doi.org/10.1016/j.cub.2010.07.009openalex-snapshot
Phenotypic Plasticity: Different Teeth for Different Feasts
inferredcites →https://doi.org/10.1016/j.cub.2010.08.014openalex-snapshot
Genetics, Chromatin Diminution, and Sex Chromosome Evolution in the Parasitic Nematode Genus Strongyloides
inferredcites →https://doi.org/10.1016/j.cub.2011.01.048openalex-snapshot
A Sensory Code for Host Seeking in Parasitic Nematodes
inferredcites →https://doi.org/10.1016/j.devcel.2006.02.008openalex-snapshot
Hormonal Control of C. elegans Dauer Formation and Life Span by a Rieske-like Oxygenase
inferredcites →https://doi.org/10.1016/j.tig.2009.03.006openalex-snapshot
How to become a parasite – lessons from the genomes of nematodes
inferredcites →https://doi.org/10.1016/j.ydbio.2010.02.022openalex-snapshot
Functional divergence of dafachronic acid pathways in the control of C. elegans development and lifespan
inferredcites →https://doi.org/10.1016/s0047-6374(03)00132-5openalex-snapshot
SAGE surveys C. elegans carbohydrate metabolism: evidence for an anaerobic shift in the long-lived dauer larva
inferredcites →https://doi.org/10.1016/s0960-9822(01)00595-4openalex-snapshot
Regulation of C. elegans DAF-16 and its human ortholog FKHRL1 by the daf-2 insulin-like signaling pathway
inferredcites →https://doi.org/10.1016/s1097-2765(00)80303-2openalex-snapshot
The C. elegans PTEN Homolog, DAF-18, Acts in the Insulin Receptor-like Metabolic Signaling Pathway
inferredcites →https://doi.org/10.1016/s1534-5807(01)00085-5openalex-snapshot
A Hormonal Signaling Pathway Influencing C. elegans Metabolism, Reproductive Development, and Life Span
inferredcites →https://doi.org/10.1016/s1534-5807(04)00095-4openalex-snapshot
C. elegans SGK-1 Is the Critical Component in the Akt/PKB Kinase Complex to Control Stress Response and Life Span
inferredcites →https://doi.org/10.1017/s003118200700399xopenalex-snapshot
Reproduction inStrongyloides(Nematoda): a life between sex and parthenogenesis
inferredcites →https://doi.org/10.1038/19328openalex-snapshot
Direct control of the Forkhead transcription factor AFX by protein kinase B
inferredcites →https://doi.org/10.1038/260523a0openalex-snapshot
Non-ageing developmental variant of Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/290668a0openalex-snapshot
Interacting genes in nematode dauer larva formation
inferredcites →https://doi.org/10.1038/32160openalex-snapshot
A molecular evolutionary framework for the phylum Nematoda
inferredcites →https://doi.org/10.1038/365644a0openalex-snapshot
The daf-4 gene encodes a bone morphogenetic protein receptor controlling C. elegans dauer larva development
inferredcites →https://doi.org/10.1038/366461a0openalex-snapshot
A C. elegans mutant that lives twice as long as wild type
inferredcites →https://doi.org/10.1038/382536a0openalex-snapshot
A phosphatidylinositol-3-OH kinase family member regulating longevity and diapause in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/40194openalex-snapshot
The Fork head transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in C. elegans
inferredcites →https://doi.org/10.1038/416844aopenalex-snapshot
Developmental constraints versus flexibility in morphological evolution
inferredcites →https://doi.org/10.1038/88850openalex-snapshot
Regulation of the Caenorhabditis elegans longevity protein DAF-16 by insulin/IGF-1 and germline signaling
inferredcites →https://doi.org/10.1038/nature03201openalex-snapshot
Chemical structure and biological activity of the Caenorhabditis elegans dauer-inducing pheromone
inferredcites →https://doi.org/10.1038/nature07168openalex-snapshot
A blend of small molecules regulates both mating and development in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/nature09164openalex-snapshot
Co-option of the hormone-signalling module dafachronic acid–DAF-12 in nematode evolution
inferredcites →https://doi.org/10.1038/nchembio.2007.3openalex-snapshot
Small-molecule pheromones that control dauer development in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/nrg2567openalex-snapshot
The future of evo–devo: model systems and evolutionary theory
inferredcites →https://doi.org/10.1039/b815064hopenalex-snapshot
Stereoselective synthesis of the hormonally active (25S)-Δ7-dafachronic acid, (25S)-Δ4-dafachronic acid, (25S)-dafachronic acid, and (25S)-cholestenoic acid
inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01485.xopenalex-snapshot
Molecular barcodes for soil nematode identification
inferredcites →https://doi.org/10.1046/j.1439-0469.2000.381125.xopenalex-snapshot
Comparative and functional morphology of the buccal cavity of Diplogastrina (Nematoda) and a first outline of the phylogeny of this taxon*
inferredcites →https://doi.org/10.1073/pnas.0806676105openalex-snapshot
A potent dauer pheromone component in Caenorhabditis elegans that acts synergistically with other components
inferredcites →https://doi.org/10.1073/pnas.0810338106openalex-snapshot
Biosynthesis of the Caenorhabditis elegans dauer pheromone
inferredcites →https://doi.org/10.1073/pnas.0904064106openalex-snapshot
Identification of the nuclear receptor DAF-12 as a therapeutic target in parasitic nematodes
inferredcites →https://doi.org/10.1074/jbc.m207866200openalex-snapshot
Insulin Receptor Substrate and p55 Orthologous Adaptor Proteins Function in the Caenorhabditis elegans daf-2/Insulin-like Signaling Pathway
inferredcites →https://doi.org/10.1086/381741openalex-snapshot
Trade‐offs during the Development of Primary and Secondary Sexual Traits in a Horned Beetle
inferredcites →https://doi.org/10.1093/genetics/118.1.75openalex-snapshot
A mutation in the age-1 gene in Caenorhabditis elegans lengthens life and reduces hermaphrodite fertility.
inferredcites →https://doi.org/10.1093/genetics/130.1.105openalex-snapshot
Genetic analysis of chemosensory control of dauer formation in Caenorhabditis elegans.
inferredcites →https://doi.org/10.1093/genetics/134.4.1105openalex-snapshot
Evidence for parallel processing of sensory information controlling dauer formation in Caenorhabditis elegans.
inferredcites →https://doi.org/10.1093/genetics/137.1.107openalex-snapshot
daf-2, daf-16 and daf-23: genetically interacting genes controlling Dauer formation in Caenorhabditis elegans.
inferredcites →https://doi.org/10.1093/genetics/139.1.171openalex-snapshot
Mutations affecting the chemosensory neurons of Caenorhabditis elegans.
inferredcites →https://doi.org/10.1093/genetics/141.4.1399openalex-snapshot
The age-1 and daf-2 genes function in a common pathway to control the lifespan of Caenorhabditis elegans.
inferredcites →https://doi.org/10.1093/oso/9780195122343.001.0001openalex-snapshot
Developmental Plasticity and Evolution
inferredcites →https://doi.org/10.1098/rspb.2010.2760openalex-snapshot
Natural variation in Pristionchus pacificus dauer formation reveals cross-preference rather than self-preference of nematode dauer pheromones
inferredcites →https://doi.org/10.1101/087969532.33.739openalex-snapshot
Genetic and Environmental Regulation of Dauer Larva Development
inferredcites →https://doi.org/10.1101/gad.1066503openalex-snapshot
daf-28 encodes a C. elegans insulin superfamily member that is regulated by environmental cues and acts in the DAF-2 signaling pathway
inferredcites →https://doi.org/10.1101/gad.11.20.2679openalex-snapshot
The DAF-3 Smad protein antagonizes TGF-β-related receptor signaling in the Caenorhabditis elegansdauer pathway
inferredcites →https://doi.org/10.1101/gad.12.16.2488openalex-snapshot
Caenorhabditis elegans Akt/PKB transduces insulin receptor-like signals from AGE-1 PI3 kinase to the DAF-16 transcription factor
inferredcites →https://doi.org/10.1101/gad.13.11.1438openalex-snapshot
A PDK1 homolog is necessary and sufficient to transduce AGE-1 PI3 kinase signals that regulate diapause in Caenorhabditis elegans
inferredcites →https://doi.org/10.1101/gad.14.12.1512openalex-snapshot
daf-12encodes a nuclear receptor that regulates the dauer diapause and developmental age inC. elegans
inferredcites →https://doi.org/10.1101/gr.184401openalex-snapshot
Changes in Gene Expression Associated with Developmental Arrest and Longevity in Caenorhabditis elegans
inferredcites →https://doi.org/10.1111/j.1095-8312.2010.01410.xopenalex-snapshot
Haplotype diversity of the nematode Pristionchus pacificus on Réunion in the Indian Ocean suggests multiple independent invasions
inferredcites →https://doi.org/10.1111/j.1525-142x.2008.00236.xopenalex-snapshot
Species‐specific recognition of beetle cues by the nematode Pristionchus maupasi
inferredcites →https://doi.org/10.1126/science.1176331openalex-snapshot
Two Chemoreceptors Mediate Developmental Effects of Dauer Pheromone in C. elegans
inferredcites →https://doi.org/10.1126/science.1178343openalex-snapshot
Starvation Protects Germline Stem Cells and Extends Reproductive Longevity in C. elegans
inferredcites →https://doi.org/10.1126/science.2006412openalex-snapshot
Control of Larval Development by Chemosensory Neurons in Caenorhabditis elegans
inferredcites →https://doi.org/10.1126/science.274.5291.1389openalex-snapshot
Control of C. elegans Larval Development by Neuronal Expression of a TGF-β Homolog
inferredcites →https://doi.org/10.1126/science.277.5328.942openalex-snapshot
daf-2 , an Insulin Receptor-Like Gene That Regulates Longevity and Diapause in Caenorhabditis elegans
inferredcites →https://doi.org/10.1126/science.6896933openalex-snapshot
A Pheromone Influences Larval Development in the Nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1139/z78-244openalex-snapshot
Responses of dauerlarvae of Caenorhabditis elegans (Nematoda: Rhabditidae) to thermal stress and oxygen deprivation
inferredcites →https://doi.org/10.1210/me.2008-0415openalex-snapshot
Synthesis and Activity of Dafachronic Acid Ligands for the C. elegans DAF-12 Nuclear Hormone Receptor
inferredcites →https://doi.org/10.1242/dev.00363openalex-snapshot
Global analysis of dauer gene expression inCaenorhabditis elegans
inferredcites →https://doi.org/10.1242/dev.01068openalex-snapshot
Hormonal signals produced by DAF-9/cytochrome P450 regulate C. elegans dauer diapause in response to environmental cues
inferredcites →https://doi.org/10.1242/dev.01069openalex-snapshot
Intercellular signaling of reproductive development by theC. elegansDAF-9 cytochrome P450
inferredcites →https://doi.org/10.1242/dev.01408openalex-snapshot
NCR-1 and NCR-2, the C. elegans homologs of the human Niemann-Pick type C1 disease protein, function upstream of DAF-9 in the dauer formation pathways
inferredcites →https://doi.org/10.1242/dev.016972openalex-snapshot
Genetic identification of HSD-1, a conserved steroidogenic enzyme that directs larval development inCaenorhabditis elegans
inferredcites →https://doi.org/10.1242/dev.058909openalex-snapshot
Pristionchus pacificus daf-16is essential for dauer formation but dispensable for mouth form dimorphism
inferredcites →https://doi.org/10.1242/dev.125.7.1191openalex-snapshot
daf-12 regulates developmental age and the dauer alternative in Caenorhabditis elegans
inferredcites →https://doi.org/10.1242/dev.129.1.221openalex-snapshot
DAF-9, a cytochrome P450 regulatingC. eleganslarval development and adult longevity
inferredcites →https://doi.org/10.1371/journal.pbio.0020280openalex-snapshot
Sterol-Derived Hormone(s) Controls Entry into Diapause in Caenorhabditis elegans by Consecutive Activation of DAF-12 and DAF-16
inferredcites →https://doi.org/10.1515/9781400840809openalex-snapshot
Evolutionary Ecology of Parasites
inferredcites →https://doi.org/10.1645/ge-2319.1openalex-snapshot
Quantitative Assessment of the Nematode Fauna Present on Geotrupes Dung Beetles Reveals Species-Rich Communities with a Heterogeneous Distribution
inferredcites →https://doi.org/10.2108/zsj.24.883openalex-snapshot
The Nematode Pristionchus pacificus (Nematoda: Diplogastridae) Is Associated with the Oriental Beetle Exomala orientalis (Coleoptera: Scarabaeidae) in Japan
inferredcites →https://doi.org/10.5860/choice.36-4478openalex-snapshot
Phenotypic evolution: a reaction norm perspective
inferredcites →https://doi.org/10.5860/choice.41-0308openalex-snapshot
Developmental plasticity and evolution
inferredcites →https://doi.org/10.5860/choice.46-5590openalex-snapshot
Ecological developmental biology: integrating epigenetics, medicine, and evolution
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Starvation resistance in the nematode Pristionchus pacificus requires a conserved supplementary nuclear receptor
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Intersectional roles of trait covariation and phenotypic plasticity in the coloration and behavior of an African cichlid
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Feeding plasticity in the nematode Pristionchus pacificus is influenced by sex and social context and is linked to developmental speed
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Three new species ofPristionchus(Nematoda: Diplogastridae) show morphological divergence through evolutionary intermediates of a novel feeding-structure polymorphism
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Toward a Synthesis of Developmental Biology with Evolutionary Theory and Ecology
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Diplogasteroides nix n. sp. (Nematoda: Diplogastridae), a cryptic species related to D. andrassyi, isolated from Monochamus urussovii (Coleoptera: Cerambycidae) from Hokkaido, Japan, with remarks on body surface structures
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Pristionchus pacificus : a nematode model for comparative and evolutionary biology
inferred← citeshttps://doi.org/10.1186/1471-2164-13-254openalex-snapshot
Divergent gene expression in the conserved dauer stage of the nematodes Pristionchus pacificus and Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1186/s12864-015-1654-6openalex-snapshot
Partial depletion of yolk during zebrafish embryogenesis changes the dynamics of methionine cycle and metabolic genes
inferred← citeshttps://doi.org/10.1186/s13071-019-3537-1openalex-snapshot
An appraisal of natural products active against parasitic nematodes of animals
inferred← citeshttps://doi.org/10.1186/s40851-024-00227-yopenalex-snapshot
Starvation resistance in the nematode Pristionchus pacificus requires a conserved supplementary nuclear receptor
inferred← citeshttps://doi.org/10.1242/bio.20148888openalex-snapshot
Natural variation in cold tolerance in the nematodePristionchus pacificus: the role of genotype and environment
inferred← citeshttps://doi.org/10.1242/dev.200623openalex-snapshot
Nutritional control of developmental processes
inferred← citeshttps://doi.org/10.1242/jeb.251636openalex-snapshot
Visual environment shapes the social dynamics of coloration and competition in an African cichlid fish
inferred← citeshttps://doi.org/10.1371/journal.pbio.1001307openalex-snapshot
Steroids as Central Regulators of Organismal Development and Lifespan
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005146openalex-snapshot
The Orphan Gene dauerless Regulates Dauer Development and Intraspecific Competition in Nematodes by Copy Number Variation
inferred← citeshttps://doi.org/10.1371/journal.pone.0077079openalex-snapshot
Assaying Environmental Nickel Toxicity Using Model Nematodes
inferred← citeshttps://doi.org/10.1371/journal.pone.0267398openalex-snapshot
Ecdysteroid responses to urban heat island conditions during development of the western black widow spider (Latrodectus hesperus)
inferred← citeshttps://doi.org/10.1534/g3.115.018812openalex-snapshot
No Significant Increase in the Δ4- and Δ7-Dafachronic Acid Concentration in the Long-Livedglp-1Mutant, nor in the Mutants Defective in Dauer Formation
inferred← citeshttps://doi.org/10.1534/g3.117.042390openalex-snapshot
The Genetic Architecture of Ovariole Number inDrosophila melanogaster: Genes with Major, Quantitative, and Pleiotropic Effects
inferred← citeshttps://doi.org/10.1645/17-30openalex-snapshot
Reproductive Plasticity in the Nematode Gyrinicola batrachiensis: Does an Intermediate Reproductive Strategy Exist in Sexually Reproducing, Didelphic Pinworms?
inferred← citeshttps://doi.org/10.2174/138920291505141106102854openalex-snapshot
Modeling Expression Plasticity of Genes that Differentiate Drug-sensitive from Drug-resistant Cells to Chemotherapeutic Treatment
inferred← citeshttps://doi.org/10.3389/fevo.2016.00023openalex-snapshot
Stochastic and Conditional Regulation of Nematode Mouth-Form Dimorphisms
inferred← citeshttps://doi.org/10.3389/fevo.2021.752695openalex-snapshot
Nematode Interactions on Beetle Hosts Indicate a Role of Mouth-Form Plasticity in Resource Competition
inferred← citeshttps://doi.org/10.3390/ijms20163898openalex-snapshot
Ascaroside Pheromones: Chemical Biology and Pleiotropic Neuronal Functions
inferred← citeshttps://doi.org/10.5204/thesis.eprints.129180openalex-snapshot
Molecular Insights into the Evolution of Novel Genes
inferred← citeshttps://doi.org/10.5846/stxb201112241967openalex-snapshot
Research progress on chemical communication of development and host-finding of nematodes
inferred← citeshttps://doi.org/10.6084/m9.figshare.25406001openalex-snapshot
Additional file 1 of Starvation resistance in the nematode Pristionchus pacificus requires a conserved supplementary nuclear receptor
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