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Global Biodiversity and Phylogenetic Evaluation of Remipedia (Crustacea)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-94-011-4904-4_14openalex-snapshot
Crustacean phylogeny inferred from 18S rDNA
inferredcites →https://doi.org/10.1007/978-94-011-4904-4_7openalex-snapshot
Theories, patterns, and reality: game plan for arthropod phylogeny
inferredcites →https://doi.org/10.1007/bf00006900openalex-snapshot
Biogeographic synthesis of the insular groundwater faunas of the (sub)tropical Atlantic
inferredcites →https://doi.org/10.1007/s00427-009-0273-0openalex-snapshot
The post-embryonic development of Remipedia (Crustacea)—additional results and new insights
inferredcites →https://doi.org/10.1007/s12526-009-0019-2openalex-snapshot
The Corona lava tube, Lanzarote: geology, habitat diversity and biogeography
inferredcites →https://doi.org/10.1007/s12526-009-0021-8openalex-snapshot
A new, disjunct species of Speleonectes (Remipedia, Crustacea) from the Canary Islands
inferredcites →https://doi.org/10.1007/s12526-009-0033-4openalex-snapshot
Cryptocorynetes elmorei, a new species of Remipedia (Crustacea) from an anchialine cave on Eleuthera, Bahamas
inferredcites →https://doi.org/10.1016/0198-0254(87)96115-2openalex-snapshot
Cryptocorynetes haptodiscus new genus, new species, and Speleonectes benjamini, new species, of remipede crustaceans from anchialine caves in the Bahamas, with remarks on distribution and ecology
inferredcites →https://doi.org/10.1016/j.asd.2005.01.007openalex-snapshot
A brain atlas of Godzilliognomus frondosus Yager, 1989 (Remipedia, Godzilliidae) and comparison with the brain of Speleonectes tulumensis Yager, 1987 (Remipedia, Speleonectidae): implications for arthropod relationships
inferredcites →https://doi.org/10.1016/j.asd.2009.10.003openalex-snapshot
Arthropod phylogeny revisited, with a focus on crustacean relationships
inferredcites →https://doi.org/10.1016/j.asd.2009.11.001openalex-snapshot
Higher-level crustacean phylogeny: Consensus and conflicting hypotheses
inferredcites →https://doi.org/10.1016/j.ode.2006.07.002openalex-snapshot
Micropacteridae, a new family of Remipedia (Crustacea) from the Turks and Caicos Islands
inferredcites →https://doi.org/10.1038/23231openalex-snapshot
Chronology, causes and progression of the Messinian salinity crisis
inferredcites →https://doi.org/10.1038/35093097openalex-snapshot
Arthropod phylogeny based on eight molecular loci and morphology
inferredcites →https://doi.org/10.1038/nature08742openalex-snapshot
Arthropod relationships revealed by phylogenomic analysis of nuclear protein-coding sequences
inferredcites →https://doi.org/10.1046/j.1463-6409.2000.00027.xopenalex-snapshot
Danielopolina kornickeri sp. n. (Ostracoda, Thaumatocypridoidea) from a western Australian anchialine cave: morphology and evolution
inferredcites →https://doi.org/10.1071/it9960171openalex-snapshot
Lasionectes exleyi , sp, nov., the first remipede crustacean recorded from Australia and the Indian Ocean, with a key to the world species
inferredcites →https://doi.org/10.1073/pnas.0306212101openalex-snapshot
The brain of the Remipedia (Crustacea) and an alternative hypothesis on their phylogenetic relationships
inferredcites →https://doi.org/10.1073/pnas.41.1.61openalex-snapshot
THE CEPHALOCARIDA, A NEW SUBCLASS OF CRUSTACEA FROM LONG ISLAND SOUND
inferredcites →https://doi.org/10.1080/00222939300770491openalex-snapshot
Some remarkable distribution patterns in stygobiont Amphipoda
inferredcites →https://doi.org/10.1080/00222939600770921openalex-snapshot
The persistence of an ancient marine fauna in Mediterranean waters: new evidence from misophrioid copepods living in anchihaline caves
inferredcites →https://doi.org/10.1080/00364827.1973.10411237openalex-snapshot
A new genus and species of bottom-living calanoid (Copepoda) from Florida and Colombia
inferredcites →https://doi.org/10.1080/10635150802570791openalex-snapshot
Resolving Arthropod Phylogeny: Exploring Phylogenetic Signal within 41 kb of Protein-Coding Nuclear Gene Sequence
inferredcites →https://doi.org/10.1093/bioinformatics/17.8.754openalex-snapshot
MRBAYES: Bayesian inference of phylogenetic trees
inferredcites →https://doi.org/10.1093/molbev/msp186openalex-snapshot
Hemocyanin Suggests a Close Relationship of Remipedia and Hexapoda
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/oso/9780195172348.003.0018openalex-snapshot
Arthropod Systematics: The Comparative Study of Genomic, Anatomical, and Paleontological Information
inferredcites →https://doi.org/10.1093/oso/9780195172348.003.0020openalex-snapshot
Are the Crustaceans Monophyletic?
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040082openalex-snapshot
Maximum-likelihood estimation of phylogeny from DNA sequences when substitution rates differ over sites.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040152openalex-snapshot
A likelihood approach for comparing synonymous and nonsynonymous nucleotide substitution rates, with application to the chloroplast genome.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040153openalex-snapshot
A codon-based model of nucleotide substitution for protein-coding DNA sequences.
inferredcites →https://doi.org/10.1098/rspb.2003.2631openalex-snapshot
Phylogenetic position of the Pentastomida and (pan)crustacean relationships
inferredcites →https://doi.org/10.1098/rspb.2004.2917openalex-snapshot
Pancrustacean phylogeny: hexapods are terrestrial crustaceans and maxillopods are not monophyletic
inferredcites →https://doi.org/10.1098/rspb.2004.3042openalex-snapshot
Mitochondrial genomes suggest that hexapods and crustaceans are mutually paraphyletic
inferredcites →https://doi.org/10.1109/tac.1974.1100705openalex-snapshot
A new look at the statistical model identification
inferredcites →https://doi.org/10.1111/j.0300-3256.2004.00159.xopenalex-snapshot
Genetic exchange between anchialine cave populations by means of larval dispersal: the case of a new gastropod species Neritilia cavernicola
inferredcites →https://doi.org/10.1111/j.1096-3642.2001.tb00620.xopenalex-snapshot
New stygobiont copepods (Calanoida; Misophrioida) from Bundera Sinkhole, an anchialine cenote in north-western Australia
inferredcites →https://doi.org/10.1111/j.1469-7998.1914.tb07038.xopenalex-snapshot
Fauna of Western Australia.—II. The Phyllopoda of Western Australia.
inferredcites →https://doi.org/10.1126/science.225.4659.309openalex-snapshot
Marine Lava Cave Fauna: Composition, Biogeography, and Origins
inferredcites →https://doi.org/10.1163/156854005776759861openalex-snapshot
Danielopolina (Ostracoda, Thaumatocyprididae) on Christmas Island, Indian Ocean, a sea mount island
inferredcites →https://doi.org/10.1163/156854006777584296openalex-snapshot
Trunk segmentation patterns in Remipedia
inferredcites →https://doi.org/10.1163/156854099503861openalex-snapshot
SPELEONECTES EPILIMNIUS NEW SPECIES (REMIPEDIA, SPELEONECTIDAE) FROM SURFACE WATER OF AN ANCHIALINE CAVE ON SAN SALVADOR ISLAND, BAHAMAS
inferredcites →https://doi.org/10.1163/156854099503889openalex-snapshot
BEHAVIOR AND ECOLOGY OF SPELEONECTES EPILIMNIUS (REMIPEDIA, SPELEONECTIDAE) FROM SURFACE WATER OF AN ANCHIALINE CAVE ON SAN SALVADOR ISLAND, BAHAMAS
inferredcites →https://doi.org/10.1163/18759866-07204004openalex-snapshot
Three new sympatric species of Remipedia (Crustacea) from Great Exuma Island, Bahamas Islands
inferredcites →https://doi.org/10.1163/193724094x00722openalex-snapshot
SPELEONECTES GIRONENSIS, NEW SPECIES (REMIPEDIA: SPELEONECTIDAE), FROM ANCHIALINE CAVES IN CUBA, WITH REMARKS ON BIOGEOGRAPHY AND ECOLOGY
inferredcites →https://doi.org/10.11646/zootaxa.1543.1.3openalex-snapshot
Speleonectes emersoni, a new species of Remipedia (Crustacea) from the Dominican Republic
inferredcites →https://doi.org/10.11646/zootaxa.1565.1.1openalex-snapshot
Ostracoda (Myodocopa) from Anchialine Caves and Ocean Blue Holes
inferredcites →https://doi.org/10.11646/zootaxa.1990.1.4openalex-snapshot
First record of the thermosbaenacean genus Halosbaena from Asia: H. daitoensis sp. nov. (Peracarida: Thermosbaenacea: Halosbaenidae) from an anchialine cave of Minamidaito-jima Is., in Okinawa, southern Japan
inferredcites →https://doi.org/10.11646/zootaxa.2016.1.3openalex-snapshot
Speleonectes kakuki, a new species of Remipedia (Crustacea) from anchialine and sub-seafloor caves on Andros and Cat Island, Bahamas
inferredcites →https://doi.org/10.11646/zootaxa.2491.1.4openalex-snapshot
Godzilliognomus schrami, a new species of Remipedia (Crustacea) from Eleuthera, Bahamas
inferredcites →https://doi.org/10.11646/zootaxa.618.1.1openalex-snapshot
Kaloketos pilosus, a new genus and species of Remipedia (Crustacea) from the Turks and Caicos Islands
inferredcites →https://doi.org/10.1186/1471-2148-7-s2-s8openalex-snapshot
Phylogenetic analysis of mitochondrial protein coding genes confirms the reciprocal paraphyly of Hexapoda and Crustacea
inferredcites →https://doi.org/10.1651/07-2865r.1openalex-snapshot
Pleomothra Fragilis N. Sp. (Remipedia) from the Bahamas, with Remarks on Morphologic Reductions and Postnaupliar Development
inferredcites →https://doi.org/10.1651/c-2516openalex-snapshot
New Species of the Genus Typhlatya (Decapoda: Atyidae) from Anchialine Caves in Mexico, the Bahamas, and Honduras
inferredcites →https://doi.org/10.1651/s-2763.1openalex-snapshot
A New Remipede, Cryptocorynetes Longulus, N. Sp., from Cat Island, Bahamas
inferredcites →https://doi.org/10.1651/s-2809a.1openalex-snapshot
Behavior of Remipedia in the Laboratory, with Supporting Field Observations
inferredcites →https://doi.org/10.2307/1547965openalex-snapshot
Remipedia, A New Class of Crustacea From a Marine Cave in the Bahamas
inferredcites →https://doi.org/10.2307/1548869openalex-snapshot
Speleonectes gironensis, New Species (Remipedia: Speleonectidae), from Anchialine Caves in Cuba, with Remarks on Biogeography and Ecology
inferredcites →https://doi.org/10.4095/103962openalex-snapshot
The Arthropod Branchiocaris N. Gen., Middle Cambrian, Burgess Shale, British Columbia
inferredcites →https://doi.org/10.5281/zenodo.13483256openalex-snapshot
Lasionectes entrichoma, New Genus, New Species, (Crustacea, Remipedia) From Anchialine Caves In The Turks and-Caicos, British West indies
inferredcites →https://doi.org/10.5281/zenodo.13650909openalex-snapshot
The Fauna Of Atlantic Marine Caves - Evidence Of Dispersal By Sea floor Spreading While Maintaining Ties To Deep Waters
inferredcites →https://doi.org/10.5281/zenodo.15145663openalex-snapshot
Table 1 in A new Gammarus species from Xinjiang Uygur Autonomous Region (China) with a key to Xinjiang freshwater gammarids (Crustacea, Amphipoda, Gammaridae)
inferredcites →https://doi.org/10.5479/si.00810282.131openalex-snapshot
Two new caridean shrimps, one representing a new family, from marine pools on Ascension Island (Crustacea: Decapoda: Natantia)
inferredcites →https://doi.org/10.5479/si.00810282.219openalex-snapshot
Phylogeny, ontogeny & morphology of living and fossil Thaumatocypridacea (Myodocopa: Ostracoda)
inferredcites →https://doi.org/10.5479/si.00963801.108-3398.137openalex-snapshot
A Review of the Copepod Genus Ridgewayia (Calanoida) with Descriptions of New Species from the Dry Tortugas, Florida
inferredcites →https://doi.org/10.5479/si.00963801.76-2806.1openalex-snapshot
New Lower and Middle Cambrian Crustacea
inferredcites →https://doi.org/10.5962/bhl.title.106607openalex-snapshot
Analyse de la nature : or, Tableau de l'univers et des corps organises /
inferredcites →https://doi.org/10.5962/bhl.title.130093openalex-snapshot
Le regne animal distribue d'apres son organisation, pour servir de base a l'histoire naturelle des animaux et d'introduction a l'anatomie comparee
inferredcites →https://doi.org/10.5962/bhl.title.15764openalex-snapshot
Histoire naturelle, générale et particulière des crustacés et des insectes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5852/ejt.2017.316zenodo-depositor-declared
Xibalbanus cozumelensis, a new species of Remipedia (Crustacea) from Cozumel, Mexico, and a molecular phylogeny of Xibalbanus on the Yucatán Peninsula
inferred← citeshttps://doi.org/10.1002/aqc.2350openalex-snapshot
Conservation status of the inland aquatic crustaceans in the Yucatan Peninsula, Mexico: shortcomings of a protection strategy
inferred← citeshttps://doi.org/10.1007/978-3-662-54512-6_3openalex-snapshot
Diversity and the Phylogenetic Age of Cave Species
inferred← citeshttps://doi.org/10.1007/978-4-431-56432-4_22openalex-snapshot
Copepod Biodiversity in Japan: Recent Advances in Japanese Copepodology
inferred← citeshttps://doi.org/10.1007/978-981-97-1817-7_2openalex-snapshot
Introduction to Heteroptera
inferred← citeshttps://doi.org/10.1007/978-981-99-1470-8_2-1openalex-snapshot
Introduction to Heteroptera
inferred← citeshttps://doi.org/10.1007/s12526-016-0586-yopenalex-snapshot
Distribution of meiofaunal abundances in a marine cave complex with secondary openings and freshwater filtrations
inferred← citeshttps://doi.org/10.1007/s13127-014-0167-5openalex-snapshot
How might sea level change affect arthropod biodiversity in anchialine caves: a comparison of Remipedia and Atyidae taxa (Arthropoda: Altocrustacea)
inferred← citeshttps://doi.org/10.1016/b978-0-12-819119-4.00020-2openalex-snapshot
Phylogenies reveal speciation dynamics
inferred← citeshttps://doi.org/10.1016/bs.amb.2026.07.001openalex-snapshot
Marine benthic invertebrate biodiversity in South Africa: Advances and gaps in taxonomic and genetic knowledge
inferred← citeshttps://doi.org/10.1016/j.cub.2012.09.012openalex-snapshot
Mitogenomic Phylogenetic Analysis Supports Continental-Scale Vicariance in Subterranean Thalassoid Crustaceans
inferred← citeshttps://doi.org/10.1016/j.dsr2.2025.105508openalex-snapshot
Species richness patterns of brachyuran crabs in the Persian Gulf and the Gulf of Oman
inferred← citeshttps://doi.org/10.1016/j.earscirev.2015.02.003openalex-snapshot
The fossil record and palaeoenvironmental significance of marine arthropod zooplankton
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2020.102692openalex-snapshot
Global biodiversity and biogeography of mangrove crabs: Temperature, the key driver of latitudinal gradients of species richness
inferred← citeshttps://doi.org/10.1016/j.pocean.2019.102199openalex-snapshot
Endemicity and community composition of marine species along the NW Pacific and the adjacent Arctic Ocean
inferred← citeshttps://doi.org/10.1016/j.toxicon.2018.11.433openalex-snapshot
Arthropod venoms: Biochemistry, ecology and evolution
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.04.014openalex-snapshot
Dark offshoot: Phylogenomic data sheds light on the evolutionary history of a new species of cave brittle star
inferred← citeshttps://doi.org/10.1038/s41586-026-10961-2openalex-snapshot
Amphibious stem-insect sheds light on colonization of land
inferred← citeshttps://doi.org/10.1038/s41598-019-45813-9openalex-snapshot
Latitudinal and bathymetrical species richness patterns in the NW Pacific and adjacent Arctic Ocean
inferred← citeshttps://doi.org/10.1071/sb16051openalex-snapshot
Biogeographic relationships between Macaronesia and the Americas
inferred← citeshttps://doi.org/10.1073/pnas.2408775121openalex-snapshot
Revisiting the four Hexapoda classes: Protura as the sister group to all other hexapods
inferred← citeshttps://doi.org/10.1080/14772000.2016.1249112openalex-snapshot
Taxonomic, phylogenetic and ecological diversity of Niphargus (Amphipoda: Crustacea) in the Hölloch cave system (Switzerland)
inferred← citeshttps://doi.org/10.1080/14772019.2022.2109216openalex-snapshot
Description of Acheronauta gen. nov., a possible mandibulate from the Silurian Waukesha Lagerstätte, Wisconsin, USA
inferred← citeshttps://doi.org/10.1088/1748-3190/aab460openalex-snapshot
Locomotion of arthropods in aquatic environment and their applications in robotics
inferred← citeshttps://doi.org/10.1093/molbev/mst199openalex-snapshot
The First Venomous Crustacean Revealed by Transcriptomics and Functional Morphology: Remipede Venom Glands Express a Unique Toxin Cocktail Dominated by Enzymes and a Neurotoxin
inferred← citeshttps://doi.org/10.1093/oso/9780190637842.003.0002openalex-snapshot
The Fossil Record of the Pancrustacea
inferred← citeshttps://doi.org/10.1093/oso/9780190637842.003.0004openalex-snapshot
The Pancrustacean Conundrum: A Conflicted Phylogeny with Emphasis on Crustacea
inferred← citeshttps://doi.org/10.1093/oso/9780190637842.003.0006openalex-snapshot
Biogeography of the Oceans
inferred← citeshttps://doi.org/10.1093/oso/9780190688554.003.0008openalex-snapshot
Hermaphroditism and Gonochorism
inferred← citeshttps://doi.org/10.1111/brv.12376openalex-snapshot
Tethyan changes shaped aquatic diversification
inferred← citeshttps://doi.org/10.1111/jbi.12903openalex-snapshot
Bimodal latitudinal species richness and high endemicity of razor clams (Mollusca)
inferred← citeshttps://doi.org/10.1126/science.1206375openalex-snapshot
The Cambrian Conundrum: Early Divergence and Later Ecological Success in the Early History of Animals
inferred← citeshttps://doi.org/10.1163/15685403-00003376openalex-snapshot
Chemosynthetic ectosymbiosis reported in the predatory anchialine cave endemic, Xibalbanus tulumensis (Yager, 1987) (Remipedia)
inferred← citeshttps://doi.org/10.1163/1937240x-00002132openalex-snapshot
Godzillius fuchsi, a new species of Remipedia (Godzilliidae) from Abaco Island, Bahamas
inferred← citeshttps://doi.org/10.1163/1937240x-00002179openalex-snapshot
Phylogenetic analysis and systematic revision of Remipedia (Nectiopoda) from Bayesian analysis of molecular data
inferred← citeshttps://doi.org/10.1163/1937240x-00002238openalex-snapshot
Arthropods host intracellular chemosynthetic symbionts, too: cave study reveals an unusual form of symbiosis
inferred← citeshttps://doi.org/10.1186/1471-2148-12-168openalex-snapshot
Serotonin immunoreactive interneurons in the brain of the Remipedia: new insights into the phylogenetic affinities of an enigmatic crustacean taxon
inferred← citeshttps://doi.org/10.1186/1471-2148-13-119openalex-snapshot
Serotonin-immunoreactive neurons in the ventral nerve cord of Remipedia (Crustacea): support for a sister group relationship of Remipedia and Hexapoda?
inferred← citeshttps://doi.org/10.1186/s12915-024-01955-5openalex-snapshot
Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.1371/journal.pone.0044083openalex-snapshot
The First Record of a Trans-Oceanic Sister-Group Relationship between Obligate Vertebrate Troglobites
inferred← citeshttps://doi.org/10.1371/journal.pone.0051629openalex-snapshot
Global Coordination and Standardisation in Marine Biodiversity through the World Register of Marine Species (WoRMS) and Related Databases
inferred← citeshttps://doi.org/10.1371/journal.pone.0202909openalex-snapshot
Ecological patterns in anchialine caves
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3741593/v1openalex-snapshot
Global Distribution and Biodiversity of Brachyuran Crabs in the Persian Gulf
inferred← citeshttps://doi.org/10.25148/etd.fidc008966openalex-snapshot
Phylogenetic and Transcriptomic Analyses of Vision in Two Cave Adapted Crustaceans, Asellus aquaticus (Isopoda: Asellidae) and Niphargus hrabei (Amphipoda: Niphargidae).
inferred← citeshttps://doi.org/10.3390/d17020077openalex-snapshot
Toward an Integrative Overview of Stygobiotic Crustaceans for Aquifer Delimitation in the Yucatan Peninsula, Mexico
inferred← citeshttps://doi.org/10.3390/toxins9080234openalex-snapshot
Venomics of Remipede Crustaceans Reveals Novel Peptide Diversity and Illuminates the Venom’s Biological Role
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.26755303openalex-snapshot
Additional file 1 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755306openalex-snapshot
Additional file 2 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755309openalex-snapshot
Additional file 3 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755315openalex-snapshot
Additional file 4 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755318openalex-snapshot
Additional file 5 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755321openalex-snapshot
Additional file 6 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755324openalex-snapshot
Additional file 7 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755327openalex-snapshot
Additional file 8 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755330openalex-snapshot
Additional file 9 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755333openalex-snapshot
Additional file 10 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755336openalex-snapshot
Additional file 11 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755339openalex-snapshot
Additional file 12 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755342openalex-snapshot
Additional file 13 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755345openalex-snapshot
Additional file 14 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755348openalex-snapshot
Additional file 15 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755351openalex-snapshot
Additional file 16 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755354openalex-snapshot
Additional file 17 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755357openalex-snapshot
Additional file 18 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755360openalex-snapshot
Additional file 19 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755363openalex-snapshot
Additional file 20 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755366openalex-snapshot
Additional file 21 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755369openalex-snapshot
Additional file 22 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755372openalex-snapshot
Additional file 23 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755375openalex-snapshot
Additional file 24 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755378openalex-snapshot
Additional file 25 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
inferred← citeshttps://doi.org/10.6084/m9.figshare.26755381openalex-snapshot
Additional file 26 of Diversely evolved xibalbin variants from remipede venom inhibit potassium channels and activate PKA-II and Erk1/2 signaling
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