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Phototransduction and clock gene expression in the troglobiont beetlePtomaphagus hirtusof Mammoth cave
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cne.903280302openalex-snapshot
Visual system of a naturally microphthalmic mammal: The blind mole rat, Spalax ehrenbergi
inferredcites →https://doi.org/10.1002/jez.1401680213openalex-snapshot
Evidence of circadian rhythms in a cave crayfish
inferredcites →https://doi.org/10.1007/978-94-015-9795-1_8openalex-snapshot
Responses to light in epigean and hypogean populations of Gambusia affinis (Cyprinodontiformes: Poeciliidae)
inferredcites →https://doi.org/10.1007/978-94-015-9795-1_9openalex-snapshot
Temporal organization in locomotor activity of the hypogean loach, Nemacheilus evezardi, and its epigean ancestor
inferredcites →https://doi.org/10.1007/978-94-017-0968-2_34openalex-snapshot
Highly sensitive reactions of microphthalmic carabid beetles to light/dark cycles
inferredcites →https://doi.org/10.1007/bf00330524openalex-snapshot
Cloning and characterization of the vermilion gene of Drosophila melanogaster
inferredcites →https://doi.org/10.1007/bf00603965openalex-snapshot
Response of antennal cold receptors of the catopid beetles,Speophyes lucidulus Delar. andCholera angustata Fab. to very slowly changing temperature
inferredcites →https://doi.org/10.1007/bf00609911openalex-snapshot
Antennal warm and cold receptors of the cave beetle,Speophyes lucidulus delar., in sensilla with a lamellated dendrite
inferredcites →https://doi.org/10.1007/bf00612588openalex-snapshot
Antennal thermal receptors of the cave beetle,Speophyes lucidulus Delar
inferredcites →https://doi.org/10.1007/s00018-009-0232-yopenalex-snapshot
A comparative view of insect circadian clock systems
inferredcites →https://doi.org/10.1007/s00424-007-0251-1openalex-snapshot
Phototransduction and retinal degeneration in Drosophila
inferredcites →https://doi.org/10.1007/s004270050039openalex-snapshot
The early stages of ommatidial development in the flour beetle Tribolium castaneum (Coleoptera; Tenebrionidae)
inferredcites →https://doi.org/10.1007/s12052-008-0086-zopenalex-snapshot
Evolution of Insect Eyes: Tales of Ancient Heritage, Deconstruction, Reconstruction, Remodeling, and Recycling
inferredcites →https://doi.org/10.1016/0022-1910(85)90125-8openalex-snapshot
Circadian organization in cockroaches: Effects of temperature cycles on locomotor activity
inferredcites →https://doi.org/10.1016/0022-1910(89)90098-xopenalex-snapshot
Photoperiodic entrainment of locomotor activity in crickets (Gryllus bimaculatus) lacking the optic lobe pacemaker
inferredcites →https://doi.org/10.1016/0168-9525(90)90017-zopenalex-snapshot
The development of Drosophila melanogaster
inferredcites →https://doi.org/10.1016/0300-9629(86)90342-7openalex-snapshot
Bioenergetics of the cave cricket, Hadenoecus subterraneus
inferredcites →https://doi.org/10.1016/0896-6273(91)90295-bopenalex-snapshot
A Gβ protein in the drosophila compound eye is different from that in the brain
inferredcites →https://doi.org/10.1016/0896-6273(95)90182-5openalex-snapshot
Gqα protein function in vivo: Genetic dissection of its role in photoreceptor cell physiology
inferredcites →https://doi.org/10.1016/j.cub.2005.11.030openalex-snapshot
The two CRYs of the butterfly
inferredcites →https://doi.org/10.1016/j.devcel.2006.08.012openalex-snapshot
The Agrin/Perlecan-Related Protein Eyes Shut Is Essential for Epithelial Lumen Formation in the Drosophila Retina
inferredcites →https://doi.org/10.1016/j.ymeth.2009.03.016openalex-snapshot
RNA-Seq—quantitative measurement of expression through massively parallel RNA-sequencing
inferredcites →https://doi.org/10.1016/j.ympev.2009.10.008openalex-snapshot
A molecular phylogeny shows the single origin of the Pyrenean subterranean Trechini ground beetles (Coleoptera: Carabidae)
inferredcites →https://doi.org/10.1016/s0021-9258(18)82349-3openalex-snapshot
Tissue-specific expression of phospholipase C encoded by the norpA gene of Drosophila melanogaster
inferredcites →https://doi.org/10.1016/s0065-2806(08)60130-7openalex-snapshot
The Tryptophan → Ommochrome Pathway in Insects
inferredcites →https://doi.org/10.1016/s0092-8674(00)81232-5openalex-snapshot
The Drosophila Light-Activated Conductance Is Composed of the Two Channels TRP and TRPL
inferredcites →https://doi.org/10.1016/s0092-8674(88)80017-5openalex-snapshot
Isolation of a putative phospholipase c gene of drosophila, norpA, and its role in phototransduction
inferredcites →https://doi.org/10.1016/s0896-6273(00)81201-5openalex-snapshot
TRPγ, a Drosophila TRP–Related Subunit, Forms a Regulated Cation Channel with TRPL
inferredcites →https://doi.org/10.1016/s0959-4388(98)80066-4openalex-snapshot
TRP trapped in fly signaling web
inferredcites →https://doi.org/10.1023/a:1004115718597openalex-snapshot
Sub-cellular Localisation of the White/Scarlet ABC Transporter to Pigment Granule Membranes Within the Compound Eye of Drosophila Melanogaster
inferredcites →https://doi.org/10.1023/a:1011804020490openalex-snapshot
Temporal Organization in Locomotor Activity of the Hypogean Loach, Nemacheilus Evezardi, and its Epigean Ancestor
inferredcites →https://doi.org/10.1023/a:1011872509199openalex-snapshot
Responses to Light in Epigean and Hypogean Populations of Gambusia Affinis (Cyprinodontiformes: Poeciliidae)
inferredcites →https://doi.org/10.1038/370059a0openalex-snapshot
An eye-specific Gβ subunit essential for termination of the phototransduction cascade
inferredcites →https://doi.org/10.1038/nature05128openalex-snapshot
Transforming the architecture of compound eyes
inferredcites →https://doi.org/10.1038/nature06603openalex-snapshot
Preserving cell shape under environmental stress
inferredcites →https://doi.org/10.1038/nature06784openalex-snapshot
The genome of the model beetle and pest Tribolium castaneum
inferredcites →https://doi.org/10.1046/j.1365-2583.2003.00396.xopenalex-snapshot
Substitution of a non‐retinal phospholipase C in Drosophila phototransduction
inferredcites →https://doi.org/10.1071/is07034openalex-snapshot
Systematics and evolution of the Australian subterranean hydroporine diving beetles (Dytiscidae), with notes on Carabhydrus
inferredcites →https://doi.org/10.1073/pnas.0308240100openalex-snapshot
Seasonal behavior in Drosophila melanogaster requires the photoreceptors, the circadian clock, and phospholipase C
inferredcites →https://doi.org/10.1073/pnas.1013850108openalex-snapshot
Genetic basis of eye and pigment loss in the cave crustacean, Asellus aquaticus
inferredcites →https://doi.org/10.1074/jbc.270.24.14376openalex-snapshot
Multiple Subtypes of Phospholipase C Are Encoded by the norpA Gene of Drosophila melanogaster
inferredcites →https://doi.org/10.1074/jbc.273.32.20425openalex-snapshot
Rab6 Regulation of Rhodopsin Transport inDrosophila
inferredcites →https://doi.org/10.1074/jbc.274.53.37605openalex-snapshot
A Novel Gγ Isolated from Drosophila Constitutes a Visual G Protein γ Subunit of the Fly Compound Eye
inferredcites →https://doi.org/10.1074/jbc.275.4.2901openalex-snapshot
The Visual G Protein of Fly Photoreceptors Interacts with the PDZ Domain Assembled INAD Signaling Complex via Direct Binding of Activated Gαq to Phospholipase Cβ
inferredcites →https://doi.org/10.1078/0944-2006-00074openalex-snapshot
The circadian system of Drosophila melanogaster and its light input pathways
inferredcites →https://doi.org/10.1080/00222930801995762openalex-snapshot
Can we agree on an ecological classification of subterranean animals?
inferredcites →https://doi.org/10.1080/09291010412331335742openalex-snapshot
About the Existence of Circadian Activity in Cave Crayfish
inferredcites →https://doi.org/10.1081/cbi-100102111openalex-snapshot
PRESENCE OF CIRCADIAN RHYTHMS IN THE LOCOMOTOR ACTIVITY OF A CAVE-DWELLING MILLIPEDEGLYPHIULUS CAVERNICOLUS SULU(CAMBALIDAE, SPIROSTREPTIDA)
inferredcites →https://doi.org/10.1093/bioinformatics/18.3.502openalex-snapshot
TREE-PUZZLE: maximum likelihood phylogenetic analysis using quartets and parallel computing
inferredcites →https://doi.org/10.1093/genetics/12.2.198openalex-snapshot
DEVELOPMENT IN DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1093/genetics/160.1.225openalex-snapshot
Cloning and Characterization of the Tribolium castaneum Eye-Color Genes Encoding Tryptophan Oxygenase and Kynurenine 3-Monooxygenase
inferredcites →https://doi.org/10.1093/molbev/msm011openalex-snapshot
Insect Cryptochromes: Gene Duplication and Loss Define Diverse Ways to Construct Insect Circadian Clocks
inferredcites →https://doi.org/10.1093/molbev/msp039openalex-snapshot
Molecular Evolution of the Drosophila Retinome: Exceptional Gene Gain in the Higher Diptera
inferredcites →https://doi.org/10.1093/molbev/msp188openalex-snapshot
Benchmarking Next-Generation Transcriptome Sequencing for Functional and Evolutionary Genomics
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003851openalex-snapshot
A General Empirical Model of Protein Evolution Derived from Multiple Protein Families Using a Maximum-Likelihood Approach
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026334openalex-snapshot
Selection of Conserved Blocks from Multiple Alignments for Their Use in Phylogenetic Analysis
inferredcites →https://doi.org/10.1098/rsbl.2005.0358openalex-snapshot
Regressive evolution of an eye pigment gene in independently evolved eyeless subterranean diving beetles
inferredcites →https://doi.org/10.1101/gr.107854.110openalex-snapshot
The Drosophila melanogaster transcriptome by paired-end RNA sequencing
inferredcites →https://doi.org/10.1101/gr.8.3.175openalex-snapshot
Base-Calling of Automated Sequencer Traces Using Phred. I. Accuracy Assessment
inferredcites →https://doi.org/10.1101/gr.8.3.186openalex-snapshot
Base-Calling of Automated Sequencer Traces Using Phred. II. Error Probabilities
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb01523.xopenalex-snapshot
EVOLUTION OF SUBTERRANEAN DIVING BEETLES (COLEOPTERA: DYTISCIDAE HYDROPORINI, BIDESSINI) IN THE ARID ZONE OF AUSTRALIA
inferredcites →https://doi.org/10.1111/j.1365-2583.2009.00931.xopenalex-snapshot
Identification and characterization of circadian clock genes in the pea aphid Acyrthosiphon pisum
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04759.xopenalex-snapshot
Evolution in caves: Darwin’s ‘wrecks of ancient life’ in the molecular era
inferredcites →https://doi.org/10.1111/j.1558-5646.1986.tb00569.xopenalex-snapshot
EVOLUTION OF ADULT MORPHOLOGY AND LIFE-HISTORY CHARACTERS IN CAVERNICOLOUSPTOMAPHAGUSBEETLES
inferredcites →https://doi.org/10.1126/science.1158395openalex-snapshot
Phylogeny-Aware Gap Placement Prevents Errors in Sequence Alignment and Evolutionary Analysis
inferredcites →https://doi.org/10.1126/science.1158441openalex-snapshot
The Transcriptional Landscape of the Yeast Genome Defined by RNA Sequencing
inferredcites →https://doi.org/10.1126/science.1179217openalex-snapshot
Arrhythmically Singing Crickets: Thermoperiodic Reentrainment After Bilobectomy
inferredcites →https://doi.org/10.1126/science.8235618openalex-snapshot
Dependence of Calmodulin Localization in the Retina on the NINAC Unconventional Myosin
inferredcites →https://doi.org/10.1139/z84-103openalex-snapshot
The distribution and evolution of cavernicolous Ptomaphagus beetles in the southeastern United States (Coleoptera; Leiodidae; Cholevinae) with new species and records
inferredcites →https://doi.org/10.1146/annurev-genet-102108-134216openalex-snapshot
Regressive Evolution in Astyanax Cavefish
inferredcites →https://doi.org/10.1146/annurev-genet-102209-163432openalex-snapshot
Circadian Control of Global Gene Expression Patterns
inferredcites →https://doi.org/10.1146/annurev-physiol-021909-135815openalex-snapshot
Circadian Organization of Behavior and Physiology in Drosophila
inferredcites →https://doi.org/10.1159/000329850openalex-snapshot
Drosophila as a Developmental Paradigm of Regressive Brain Evolution: Proof of Principle in the Visual System
inferredcites →https://doi.org/10.1177/0748730403256997openalex-snapshot
Cryptochrome, Compound Eyes, Hofbauer-Buchner Eyelets, and Ocelli Play Different Roles in the Entrainment and Masking Pathway of the Locomotor Activity Rhythm in the Fruit Fly Drosophila Melanogaster
inferredcites →https://doi.org/10.1177/0748730406295754openalex-snapshot
Hofbauer-Buchner Eyelet Affects Circadian Photosensitivity and Coordinates TIM and PER Expression in Drosophila Clock Neurons
inferredcites →https://doi.org/10.1177/0748730409348551openalex-snapshot
Synergic Entrainment of Drosophila’s Circadian Clock by Light and Temperature
inferredcites →https://doi.org/10.1177/074873049701200407openalex-snapshot
Circadian Patterns of Locomotor Activity and Body Temperature in Blind Mole-Rats, Spalax ehrenbergi
inferredcites →https://doi.org/10.1186/1471-2148-10-29openalex-snapshot
Ancient origin of a Western Mediterranean radiation of subterranean beetles
inferredcites →https://doi.org/10.1186/1742-9994-4-24openalex-snapshot
Genomic and gene regulatory signatures of cryptozoic adaptation: Loss of blue sensitive photoreceptors through expansion of long wavelength-opsin expression in the red flour beetle Tribolium castaneum
inferredcites →https://doi.org/10.1371/journal.pbio.1000503openalex-snapshot
Genome-Wide Analysis of Light- and Temperature-Entrained Circadian Transcripts in Caenorhabditis elegans
inferredcites →https://doi.org/10.1515/znc-1982-11-1227openalex-snapshot
Exogenous and Endogenous Control of Swimming Activity in Astyanax mexicanus (Characidae, Pisces) by Direct Light Response and by a Circadian Oscillator I. Analyses of the Time-Control Systems of an Epigean River Population
inferredcites →https://doi.org/10.1515/znc-1982-11-1228openalex-snapshot
Exogenous and Endogenous Control of Swimming Activity in Astyanax mexicanus (Characidae, Pisces) by Direct Light Response and by a Circadian Oscillator II. Features of Time-Controlled Behaviour of a Cave Population and their Comparison to a Epigean Ancestral Form
inferredcites →https://doi.org/10.1523/jneurosci.22-21-09255.2002openalex-snapshot
The Extraretinal Eyelet ofDrosophila: Development, Ultrastructure, and Putative Circadian Function
inferredcites →https://doi.org/10.2307/1445255openalex-snapshot
Ontogenetic Change in Phototactic Responses of Surface and Cave Populations of Astyanax fasciatus (Pisces: Characidae)
inferredcites →https://doi.org/10.2307/2426293openalex-snapshot
Long-Term Effects of Weather on the Cricket (Hadenoecus subterraneus, Orthoptera, Rhaphidophoridae) Guano Community in Mammoth Cave National Park
inferredcites →https://doi.org/10.3389/neuro.03.002.2009openalex-snapshot
Drosophila Photoreceptors and Signaling Mechanisms
inferredcites →https://doi.org/10.3897/asp.64.e31652openalex-snapshot
Insect interordinal relationships: Evidence from the visual system
inferredcites →https://doi.org/10.5038/1827-806x.7.1.2openalex-snapshot
The life cycle of a Kentucky cave beetle, Ptomaphagus hirtus, (Coleoptera; Leiodidae; Catopinae)
inferredcites →https://doi.org/10.5860/choice.47-1398openalex-snapshot
The biology of caves and other subterranean habitats
inferredcites →https://doi.org/10.5962/bhl.part.29561openalex-snapshot
Beschreibung einiger neuer in der Mammuth-Höhle in Kentucky aufgefundener Gattungen von Gliedertieren
inferredcites →https://doi.org/10.5962/bhl.title.51841openalex-snapshot
The cave fauna of North America, with remarks on the anatomy of the brain and origin of the blind species
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/asp.81.e98166zenodo-depositor-declared
New insights into the evolution of the surface antennal sensory equipment in free-living and cave-dwelling beetles (Leiodidae: Leptodirini)
inferred← citeshttps://doi.org/10.1002/ece3.70877openalex-snapshot
Molecular Insights Into the Sensory Adaption of the Cave‐Dwelling Leech Sinospelaeobdella wulingensis to the Karst Cave Environment
inferred← citeshttps://doi.org/10.1002/ece3.71584openalex-snapshot
Light in the Darkness: Responses to Light and Diel Activity Rhythm in an Eyeless Cave Flatworm ( Dendrocoelum italicum )
inferred← citeshttps://doi.org/10.1002/ece3.72260openalex-snapshot
Transcriptomic Analysis and Comparative Analysis of Gene Families Related to Environmental Adaptation in Two Grylloblattodea Species: Galloisiana sinensis and Grylloprimevala jilina
inferred← citeshttps://doi.org/10.1002/wdev.61openalex-snapshot
Evolution and development in cave animals: from fish to crustaceans
inferred← citeshttps://doi.org/10.1007/978-1-4614-4355-1_4openalex-snapshot
The Evolution of Invertebrate Photopigments and Photoreceptors
inferred← citeshttps://doi.org/10.1007/978-3-030-26827-5_10openalex-snapshot
Changing Perspectives on Subterranean Habitats
inferred← citeshttps://doi.org/10.1007/s00114-015-1329-9openalex-snapshot
Light triggers habitat choice of eyeless subterranean but not of eyed surface amphipods
inferred← citeshttps://doi.org/10.1007/s00360-016-1000-6openalex-snapshot
Life in a dark biosphere: a review of circadian physiology in “arrhythmic” environments
inferred← citeshttps://doi.org/10.1016/j.cois.2014.12.006openalex-snapshot
Circadian molecular clockworks in non-model insects
inferred← citeshttps://doi.org/10.1016/j.cois.2017.09.007openalex-snapshot
Retinal perception and ecological significance of color vision in insects
inferred← citeshttps://doi.org/10.1016/j.gde.2016.06.004openalex-snapshot
Emerging developmental genetic model systems in holometabolous insects
inferred← citeshttps://doi.org/10.1016/j.ympev.2022.107522openalex-snapshot
Parallel decay of vision genes in subterranean water beetles
inferred← citeshttps://doi.org/10.1038/s41467-023-39603-1openalex-snapshot
Parallel and convergent genomic changes underlie independent subterranean colonization across beetles
inferred← citeshttps://doi.org/10.1038/s41467-024-54478-6openalex-snapshot
Reduced adult stem cell fate specification led to eye reduction in cave planarians
inferred← citeshttps://doi.org/10.1038/s41598-018-28098-2openalex-snapshot
Hypothesis on monochromatic vision in scorpionflies questioned by new transcriptomic data
inferred← citeshttps://doi.org/10.1038/s41598-018-34405-8openalex-snapshot
Embryonic origin and genetic basis of cave associated phenotypes in the isopod crustacean Asellus aquaticus
inferred← citeshttps://doi.org/10.1038/srep45188openalex-snapshot
Transcriptome analysis of molecular mechanisms responsible for light-stress response in Mythimna separata (Walker)
inferred← citeshttps://doi.org/10.1080/07420528.2024.2348010openalex-snapshot
The ticking clock in the dark: Review of biological rhythms in cave invertebrates
inferred← citeshttps://doi.org/10.1080/07420528.2024.2391865openalex-snapshot
Divergent patterns of locomotor activity in cave isopods (Oniscidea: Styloniscidae) in Neotropics
inferred← citeshttps://doi.org/10.1080/07420528.2025.2596773openalex-snapshot
Oscillating in darkness: Circadian rhythms of cave-dwelling scorpions
inferred← citeshttps://doi.org/10.1093/biolinnean/blab088openalex-snapshot
The eyes have it: dim-light activity is associated with the morphology of eyes but not antennae across insect orders
inferred← citeshttps://doi.org/10.1093/gbe/evz150openalex-snapshot
Evolution of Phototransduction Genes in Lepidoptera
inferred← citeshttps://doi.org/10.1093/icb/ict058openalex-snapshot
Biological Clocks and Visual Systems in Cave-Adapted Animals at the Dawn of Speleogenomics
inferred← citeshttps://doi.org/10.1093/icb/ict060openalex-snapshot
The Evolution of Complexity in the Visual Systems of Stomatopods: Insights from Transcriptomics
inferred← citeshttps://doi.org/10.1093/icb/icy029openalex-snapshot
Phototransduction Gene Expression and Evolution in Cave and Surface Crayfishes
inferred← citeshttps://doi.org/10.1093/icb/icy035openalex-snapshot
Massive Parallel Regression: A Précis of Genetic Mechanisms for Vision Loss in Diving Beetles
inferred← citeshttps://doi.org/10.1093/icb/icy047openalex-snapshot
The Kingdom of the Blind: Disentangling Fundamental Drivers in the Evolution of Eye Loss
inferred← citeshttps://doi.org/10.1093/icb/icy082openalex-snapshot
Evolution in the Dark: Unifying our Understanding of Eye Loss
inferred← citeshttps://doi.org/10.1093/jeb/voaf071openalex-snapshot
Trends in loss and retention of vision-related genes are similar between two trechine beetles independently colonizing caves
inferred← citeshttps://doi.org/10.1093/molbev/msac067openalex-snapshot
Multiple Mechanisms of Photoreceptor Spectral Tuning inHeliconiusButterflies
inferred← citeshttps://doi.org/10.1093/molbev/msv197openalex-snapshot
Transcriptome-Wide Differential Gene Expression inBicyclus anynanaButterflies: Female Vision-Related Genes Are More Plastic
inferred← citeshttps://doi.org/10.1093/molbev/msy106openalex-snapshot
The Evolution of Gene Expression Underlying Vision Loss in Cave Animals
inferred← citeshttps://doi.org/10.1098/rsos.140386openalex-snapshot
Opsin transcripts of predatory diving beetles: a comparison of surface and subterranean photic niches
inferred← citeshttps://doi.org/10.1111/aen.12264openalex-snapshot
Consequences of evolutionary transitions in changing photic environments
inferred← citeshttps://doi.org/10.1111/aen.12330openalex-snapshot
How blind are they? Phototactic responses in stygobiont diving beetles (Coleoptera: Dytiscidae) from calcrete aquifers of Western Australia
inferred← citeshttps://doi.org/10.1111/evo.14135openalex-snapshot
Evidence for speciation underground in diving beetles (Dytiscidae) from a subterranean archipelago
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2012.01964.xopenalex-snapshot
Convergence and divergence in the subterranean realm: a reassessment
inferred← citeshttps://doi.org/10.1111/j.1469-7998.2012.00976.xopenalex-snapshot
Salamanders breeding in subterranean habitats: local adaptations or behavioural plasticity?
inferred← citeshttps://doi.org/10.1111/jzo.13223openalex-snapshot
We prefer night‐time, they prefer daytime: Biological rhythm variability in cave‐dwelling whip spiders (Amblypygi: Charontidae) in the Neotropics
inferred← citeshttps://doi.org/10.1111/mec.15570openalex-snapshot
Illuminating the impact of diel vertical migration on visual gene expression in deep‐sea shrimp
inferred← citeshttps://doi.org/10.1111/mec.17323openalex-snapshot
Identification, expression analysis, and functional verification of three opsin genes related to the phototactic behaviour of Ostrinia furnacalis
inferred← citeshttps://doi.org/10.1111/syen.12487openalex-snapshot
Digging deep: a revised phylogeny of Australian burrowing cockroaches (Blaberidae: Panesthiinae, Geoscapheinae) confirms extensive nonmonophyly and provides insights into biogeography and evolution of burrowing
inferred← citeshttps://doi.org/10.1126/sciadv.adj0348openalex-snapshot
Eyeless cave-dwellingLeptonetelaspiders still rely on light
inferred← citeshttps://doi.org/10.1126/sciadv.adr2802openalex-snapshot
Blue light restores functional circadian clocks in eyeless cave spiders
inferred← citeshttps://doi.org/10.1186/1471-2148-13-89openalex-snapshot
Parallel reduction in expression, but no loss of functional constraint, in two opsin paralogs within cave populations of Gammarus minus (Crustacea: Amphipoda)
inferred← citeshttps://doi.org/10.1186/s12859-014-0350-xopenalex-snapshot
Using phylogenetically-informed annotation (PIA) to search for light-interacting genes in transcriptomes from non-model organisms
inferred← citeshttps://doi.org/10.1186/s40851-023-00208-7openalex-snapshot
Photoreceptor genes in a trechine beetle, Trechiama kuznetsovi, living in the upper hypogean zone
inferred← citeshttps://doi.org/10.1371/journal.pone.0055659openalex-snapshot
An Integrated Transcriptome-Wide Analysis of Cave and Surface Dwelling Astyanax mexicanus
inferred← citeshttps://doi.org/10.1371/journal.pone.0140484openalex-snapshot
A Transcriptomic Analysis of Cave, Surface, and Hybrid Isopod Crustaceans of the Species Asellus aquaticus
inferred← citeshttps://doi.org/10.1371/journal.pone.0170424openalex-snapshot
First Insights into the Subterranean Crustacean Bathynellacea Transcriptome: Transcriptionally Reduced Opsin Repertoire and Evidence of Conserved Homeostasis Regulatory Mechanisms
inferred← citeshttps://doi.org/10.1590/1519-6984.297366openalex-snapshot
Development, survival and morphometric parameters of boll weevil reared in different photoperiods
inferred← citeshttps://doi.org/10.1649/0010-065x-71.2.211openalex-snapshot
An Annotated Catalog of the Leiodidae (Coleoptera) of the Nearctic Region (Continental North America North of Mexico)
inferred← citeshttps://doi.org/10.3390/d13080373openalex-snapshot
Mammoth Cave: A Hotspot of Subterranean Biodiversity in the United States
inferred← citeshttps://doi.org/10.3390/genes11010042openalex-snapshot
Developmental Transcriptomic Analysis of the Cave-Dwelling Crustacean, Asellus aquaticus
inferred← citeshttps://doi.org/10.3390/insects14010072openalex-snapshot
An LW-Opsin Mutation Changes the Gene Expression of the Phototransduction Pathway: A Cryptochrome1 Mutation Enhances the Phototaxis of Male Plutella xylostella (Lepidoptera: Plutellidae)
inferred← citeshttps://doi.org/10.3390/insects15120966openalex-snapshot
Transcriptomic Characterization of Phototransduction Genes of the Asian Citrus Psyllid Diaphorina citri Kuwayama
inferred← citeshttps://doi.org/10.3897/subtbiol.29.31377openalex-snapshot
Mitochondrial sequence data indicate “Vicariance by Erosion” as a mechanism of species diversification in North American Ptomaphagus (Coleoptera, Leiodidae, Cholevinae) cave beetles
inferred← citeshttps://doi.org/10.3897/subtbiol.45.100717openalex-snapshot
Evidence of ancestral nocturnality, locomotor clock regression, and cave zone-adjusted sleep duration modes in a cave beetle
inferred← citeshttps://doi.org/10.3897/subtbiol.46.105707openalex-snapshot
Eye convergence is evoked during larval prey capture (LPC) without visual stimulus and in blind cavefish
inferred← citeshttps://doi.org/10.3897/zookeys.748.24964openalex-snapshot
Ptomaphaginus troglodytes sp. n., the first anophthalmic species of Ptomaphaginina from China (Coleoptera, Leiodidae, Cholevinae, Ptomaphagini)
inferred← citeshttps://doi.org/10.3897/zookeys.749.24964openalex-snapshot
Ptomaphaginus troglodytes sp. n., the first anophthalmic species of Ptomaphaginina from China (Coleoptera, Leiodidae, Cholevinae, Ptomaphagini)
inferred← citeshttps://doi.org/10.4039/tce.2018.38openalex-snapshot
The light at the end of the tunnel: photosensitivity in larvae of the mountain pine beetle (Coleoptera: Curculionidae: Scolytinae)
inferred← citeshttps://doi.org/10.4039/tce.2019.18openalex-snapshot
Shedding new light upon circadian emergence rhythmicity in the mountain pine beetle (Coleoptera: Curculionidae: Scolytinae)
inferred← citeshttps://doi.org/10.5038/1827-806x.45.2.1954openalex-snapshot
Life in the Underworld: Anchialine cave biology in the era of speleogenomics
inferred← citeshttps://doi.org/10.6084/m9.figshare.26589006openalex-snapshot
Additional file 1 of Photoreceptor genes in a trechine beetle, Trechiama kuznetsovi, living in the upper hypogean zone
inferred← citeshttps://doi.org/10.6084/m9.figshare.26589009openalex-snapshot
Additional file 2 of Photoreceptor genes in a trechine beetle, Trechiama kuznetsovi, living in the upper hypogean zone
inferred← citeshttps://doi.org/10.6084/m9.figshare.26589012openalex-snapshot
Additional file 3 of Photoreceptor genes in a trechine beetle, Trechiama kuznetsovi, living in the upper hypogean zone
inferred← citeshttps://doi.org/10.6084/m9.figshare.26589015openalex-snapshot
Additional file 4 of Photoreceptor genes in a trechine beetle, Trechiama kuznetsovi, living in the upper hypogean zone
inferred← citeshttps://doi.org/10.70675/428a7961z0409z47adzaabbz52baacd50dc3openalex-snapshot
Origine des variations de taux d’évolution moléculaire inter-spécifiques : apport d’un modèle génomique en milieu souterrain
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