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Evolution of Bindin in the Pantropical Sea Urchin Tripneustes: Comparisons to Bindin of Other Genera

https://doi.org/10.1093/molbev/msg020
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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/bf00173190openalex-snapshot
High divergence of reproductive tract proteins and their association with postzygotic reproductive isolation in Drosophila melanogaster and Drosophila virilis group species
inferredcites →https://doi.org/10.1007/bf00178874openalex-snapshot
Mammalian gene evolution: Nucleotide sequence divergence between mouse and rat
inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences
inferredcites →https://doi.org/10.1007/bf01771904openalex-snapshot
Indo-Pacific echinoids in the tropical eastern Pacific
inferredcites →https://doi.org/10.1007/bf02407308openalex-snapshot
Unbiased estimation of the rates of synonymous and nonsynonymous substitution
inferredcites →https://doi.org/10.1007/pl00000049openalex-snapshot
Positive darwinian selection on two homologous fertilization proteins: what is the selective pressure driving their divergence?
inferredcites →https://doi.org/10.1007/pl00006281openalex-snapshot
Synonymous and Nonsynonymous Substitutions in Mammalian Genes: Intragenic Correlations
inferredcites →https://doi.org/10.1007/s002390010111openalex-snapshot
Evaluation of Sequence Variation and Selection in the Bindin Locus of the Red Sea Urchin, Strongylocentrotus franciscanus
inferredcites →https://doi.org/10.1007/s002650050357openalex-snapshot
The enemies within: intergenomic conflict, interlocus contest evolution (ICE), and the intraspecific Red Queen
inferredcites →https://doi.org/10.1016/0012-1606(91)90078-hopenalex-snapshot
The sequence of the Arbacia punctulata bindin cDNA and implications for the structural basis of species-specific sperm adhesion and fertilization
inferredcites →https://doi.org/10.1016/0022-0981(81)90062-9openalex-snapshot
Reproductive periodicity of the echinoids Diadema and Echinometra on the two coasts of Panama
inferredcites →https://doi.org/10.1016/0022-0981(81)90091-5openalex-snapshot
On barriers to hybridization between Strongylocentrotus droebachiensis (O.F. Müller) and S. Pallidus (G.O. Sars)
inferredcites →https://doi.org/10.1016/0169-5347(87)90193-5openalex-snapshot
Speciation by reinforcement
inferredcites →https://doi.org/10.1016/0378-1119(90)90491-9openalex-snapshot
The ‘effective number of codons’ used in a gene
inferredcites →https://doi.org/10.1016/s0006-3495(99)76935-3openalex-snapshot
Ultrastructural Characterization of Peptide-Induced Membrane Fusion and Peptide Self-Assembly in the Lipid Bilayer
inferredcites →https://doi.org/10.1016/s0022-0981(00)00242-2openalex-snapshot
Genetic structure of populations of the red sea urchin, Strongylocentrotus franciscanus
inferredcites →https://doi.org/10.1016/s0022-0981(05)80004-8openalex-snapshot
Presence and absence of monthly reproductive rhythms among eight Caribbean echinoids off the coast of Panama
inferredcites →https://doi.org/10.1016/s0378-1119(97)00400-9openalex-snapshot
Codon bias evolution in Drosophila. Population genetics of mutation-selection drift
inferredcites →https://doi.org/10.1038/267836a0openalex-snapshot
Species specific agglutination of eggs by bindin isolated from sea urchin sperm
inferredcites →https://doi.org/10.1038/35002070openalex-snapshot
Rapid evolution of male reproductive genes in the descent of man
inferredcites →https://doi.org/10.1038/351652a0openalex-snapshot
Adaptive protein evolution at the Adh locus in Drosophila
inferredcites →https://doi.org/10.1038/sj.hdy.6886320openalex-snapshot
Reinforcement and other consequences of sympatry
inferredcites →https://doi.org/10.1046/j.1365-294x.2000.01022.xopenalex-snapshot
Dispersal barriers in tropical oceans and speciation in Atlantic and eastern Pacific sea urchins of the genus Echinometra
inferredcites →https://doi.org/10.1046/j.1440-169x.1995.00001.xopenalex-snapshot
What have we learned about sea urchin sperm bindin?
inferredcites →https://doi.org/10.1073/pnas.051605998openalex-snapshot
Positive Darwinian selection drives the evolution of several female reproductive proteins in mammals
inferredcites →https://doi.org/10.1073/pnas.74.6.2456openalex-snapshot
Isolation of bindin: the protein responsible for adhesion of sperm to sea urchin eggs.
inferredcites →https://doi.org/10.1073/pnas.83.22.8634openalex-snapshot
Sequence of mRNA coding for bindin, a species-specific sea urchin sperm protein required for fertilization.
inferredcites →https://doi.org/10.1073/pnas.85.23.8998openalex-snapshot
Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer.
inferredcites →https://doi.org/10.1073/pnas.94.16.8634openalex-snapshot
Rapid evolution of sex-related genes in Chlamydomonas
inferredcites →https://doi.org/10.1073/pnas.96.22.12632openalex-snapshot
All males are not created equal: Fertility differences depend on gamete recognition polymorphisms in sea urchins
inferredcites →https://doi.org/10.1074/jbc.273.27.16748openalex-snapshot
Membrane Fusion Is Induced by a Distinct Peptide Sequence of the Sea Urchin Fertilization Protein Bindin
inferredcites →https://doi.org/10.1083/jcb.83.3.595openalex-snapshot
Species-specific sperm adhesion in sea urchins. A quantitative investigation of bindin- mediated egg agglutination
inferredcites →https://doi.org/10.1086/286044openalex-snapshot
How Often Does Sympatry Affect Sexual Isolation inDrosophila?
inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot
MODELTEST: testing the model of DNA substitution.
inferredcites →https://doi.org/10.1093/genetics/139.2.1067openalex-snapshot
Inferring weak selection from patterns of polymorphism and divergence at "silent" sites in Drosophila DNA.
inferredcites →https://doi.org/10.1093/genetics/144.3.1053openalex-snapshot
Synonymous Substitutions in the Xdh Gene of Drosophila: Heterogeneous Distribution Along the Coding Region
inferredcites →https://doi.org/10.1093/genetics/150.2.767openalex-snapshot
The Correlation Between Synonymous and Nonsynonymous Substitutions in Drosophila: Mutation, Selection or Relaxed Constraints?
inferredcites →https://doi.org/10.1093/genetics/152.2.543openalex-snapshot
Positive Selection Drives the Evolution of the Acp29AB Accessory Gland Protein in Drosophila
inferredcites →https://doi.org/10.1093/genetics/155.1.431openalex-snapshot
Codon-Substitution Models for Heterogeneous Selection Pressure at Amino Acid Sites
inferredcites →https://doi.org/10.1093/genetics/157.1.295openalex-snapshot
Substitution Rates in Drosophila Nuclear Genes: Implications for Translational Selection
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111205openalex-snapshot
CODONS: A Microcomputer Program for Codon Usage Analysis
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003813openalex-snapshot
Polymorphism in Abalone Fertilization Proteins Is Consistent with the Neutral Evolution of the Egg's Receptor for Lysin (VERL) and Positive Darwinian Selection of Sperm Lysin
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025598openalex-snapshot
Positive selection and sequence rearrangements generate extensive polymorphism in the gamete recognition protein bindin
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025791openalex-snapshot
Positive selection and the molecular evolution of a gene of male reproduction, Acp26Aa of Drosophila
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025902openalex-snapshot
The molecular evolution of sperm bindin in six species of sea urchins (Echinoida: Strongylocentrotidae)
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025914openalex-snapshot
Mitochondrial DNA and bindin gene sequence evolution among allopatric species of the sea urchin genus Arbacia
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025994openalex-snapshot
Sex-related genes, directional sexual selection, and speciation
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026168openalex-snapshot
Rapid evolution of fertilization selectivity and lysin cDNA sequences in teguline gastropods
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040003openalex-snapshot
Evolution of the Zfx and Zfy genes: rates and interdependence between the genes.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040023openalex-snapshot
Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040200openalex-snapshot
Positive selection is a general phenomenon in the evolution of abalone sperm lysin.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040410openalex-snapshot
Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040454openalex-snapshot
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040507openalex-snapshot
Phylogenetic Relationsghip, Divergence Times, and Rates of Molecular Evolution for Camarodent Sea Urchins
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040642openalex-snapshot
Strong reproductive isolation between closely related tropical sea urchins (genus Echinometra).
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040690openalex-snapshot
Comparison of the bindin proteins of Strongylocentrotus franciscanus, S. purpuratus, and Lytechinus variegatus: sequences involved in the species specificity of fertilization.
inferredcites →https://doi.org/10.1098/rspb.2001.1780openalex-snapshot
Sexual selection at the protein level drives the extraordinary divergence of sex–related genes during sympatric speciation
inferredcites →https://doi.org/10.1098/rstb.1992.0155openalex-snapshot
Comparative variation of morphological and molecular evolution through geologic time: 28 S ribosomal RNA versus morphology in echinoids
inferredcites →https://doi.org/10.1111/j.1096-0031.1989.tb00567.xopenalex-snapshot
RNA SEQUENCE DATA IN PHYLOGENETIC RECONSTRUCTION: TESTING THE LIMITS OF ITS RESOLUTION
inferredcites →https://doi.org/10.1111/j.1558-5646.1984.tb00382.xopenalex-snapshot
POSSIBLE PREZYGOTIC REPRODUCTIVE ISOLATION IN SEA URCHINS SEPARATED BY THE ISTHMUS OF PANAMA
inferredcites →https://doi.org/10.1111/j.1558-5646.1990.tb03815.xopenalex-snapshot
GAMETIC INCOMPATIBILITY BETWEEN SPECIES OF THE SEA URCHIN ECHINOMETRA ON THE TWO SIDES OF THE ISTHMUS OF PANAMA
inferredcites →https://doi.org/10.1111/j.1558-5646.1990.tb05208.xopenalex-snapshot
MITOCHONDRIAL DNA DIVERSITY IN THE SEA URCHINS STRONGYLOCENTROTUS PURPURATUS AND S. DROEBACHIENSIS
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb01474.xopenalex-snapshot
SPECIATION AND POPULATION GENETIC STRUCTURE IN TROPICAL PACIFIC SEA URCHINS
inferredcites →https://doi.org/10.1111/j.1558-5646.1999.tb05374.xopenalex-snapshot
PHYLOGEOGRAPHY OF THE PANTROPICAL SEA URCHINEUCIDARISIN RELATION TO LAND BARRIERS AND OCEAN CURRENTS
inferredcites →https://doi.org/10.1385/0-89603-383-x:61openalex-snapshot
Using Rapid Amplification of cDNA Ends (RACE) to Obtain Full-Length cDNAs
inferredcites →https://doi.org/10.1515/9780295743240openalex-snapshot
Reproduction and Development of Marine Invertebrates of the Northern Pacific Coast
inferredcites →https://doi.org/10.1554/0014-3820(2001)055[0955:psasit]2.0.co;2openalex-snapshot
POPULATION STRUCTURE AND SPECIATION IN TROPICAL SEAS: GLOBAL PHYLOGEOGRAPHY OF THE SEA URCHIN DIADEMA
inferredcites →https://doi.org/10.2307/1542162openalex-snapshot
Fertilization Between Closely Related Sea Urchins Is Blocked by Incompatibilities During Sperm-Egg Attachment and Early Stages of Fusion
inferredcites →https://doi.org/10.2307/3226854openalex-snapshot
Reproductive Isolation? Interannual Variability in the Timing of Reproduction in Sympatric Sea Urchins, Genus Pseudechinus

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Searchin' for Urchins: Utilising Museum Collections and Citizen Science to Assess Species on the Move in the Genus Tripneustes
inferred← citeshttps://doi.org/10.5852/ejt.2024.949.2641zenodo-depositor-declared
Understanding the color variability and resolving taxonomic confusion in the sea cucumber Isostichopus badionotus (Echinodermata, Holothuroidea): a revision of the genus Isostichopus
inferred← citeshttps://doi.org/10.1002/ece3.1042openalex-snapshot
Selection and demographic history shape the molecular evolution of the gamete compatibility protein bindin in P isaster sea stars
inferred← citeshttps://doi.org/10.1002/jez.b.23004openalex-snapshot
Molecular mechanisms and evolution of fertilization proteins
inferred← citeshttps://doi.org/10.1007/978-1-4020-8278-8_39openalex-snapshot
Echinoderms
inferred← citeshttps://doi.org/10.1007/978-3-319-17894-3_1openalex-snapshot
Cryptic Female Choice and Other Types of Post-copulatory Sexual Selection
inferred← citeshttps://doi.org/10.1007/978-3-642-20051-9_4openalex-snapshot
Echinoderm Diversity in Panama: 144 Years of Research Across the Isthmus
inferred← citeshttps://doi.org/10.1007/978-94-017-7499-4_16openalex-snapshot
Gene Flow in Coral Reef Organisms of the Tropical Eastern Pacific
inferred← citeshttps://doi.org/10.1007/s00239-009-9219-4openalex-snapshot
Characterization of the Sperm Molecule Bindin in the Sea Urchin Genus Paracentrotus
inferred← citeshttps://doi.org/10.1007/s00339-011-6495-9openalex-snapshot
Dispersion of laser droplets using H+ ions and annealing effect on pulsed laser deposited nickel ferrite thin films
inferred← citeshttps://doi.org/10.1007/s13127-012-0087-1openalex-snapshot
Phylogeny of Cidaroida (Echinodermata: Echinoidea) based on mitochondrial and nuclear markers
inferred← citeshttps://doi.org/10.1016/b978-0-12-372568-4.00009-4openalex-snapshot
Sperm and speciation
inferred← citeshttps://doi.org/10.1016/b978-0-12-396491-5.00032-0openalex-snapshot
Tripneustes
inferred← citeshttps://doi.org/10.1016/b978-0-12-819570-3.00037-8openalex-snapshot
Tripneustes
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.10.005openalex-snapshot
Species-specific mechanisms during fertilization
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2004.09.006openalex-snapshot
Interaction of the fusogenic peptide B18 in its amyloid-state with lipid membranes studied by solid state NMR
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.07.028openalex-snapshot
Do genes lie? Mitochondrial capture masks the Red Sea collector urchin’s true identity (Echinodermata: Echinoidea: Tripneustes)
inferred← citeshttps://doi.org/10.1016/s0074-7696(05)43002-8openalex-snapshot
Calcium Channels and Ca2+ Fluctuations in Sperm Physiology
inferred← citeshttps://doi.org/10.1016/s0091-679x(04)74021-2openalex-snapshot
Sea Urchin Spermatozoa
inferred← citeshttps://doi.org/10.1016/s0167-9309(07)80088-3openalex-snapshot
Chapter 24 Ecology of Tripneustes
inferred← citeshttps://doi.org/10.1038/s41598-017-06183-2openalex-snapshot
Cryptic speciation in pan-tropical sea urchins: a case study of an edge-of-range population of Tripneustes from the Kermadec Islands
inferred← citeshttps://doi.org/10.1038/s41598-020-66390-2openalex-snapshot
Slow evolution under purifying selection in the gamete recognition protein bindin of the sea urchin Diadema
inferred← citeshttps://doi.org/10.1071/is23038openalex-snapshot
Hidden in plain sight: Tripneustes kermadecensis (Echinodermata: Echinoidea) is a junior synonym of the eastern Australian sea urchin Evechinus australiae described in 1878
inferred← citeshttps://doi.org/10.1073/pnas.0501806102openalex-snapshot
Evolutionary animation: How do molecular phylogenies compare to Mayr's reconstruction of speciation patterns in the sea?
inferred← citeshttps://doi.org/10.1073/pnas.0901217106openalex-snapshot
Postcopulatory sexual selection: Darwin's omission and its consequences
inferred← citeshttps://doi.org/10.1086/bblv224n3p166openalex-snapshot
Sexual Selection and the Evolution of Egg-Sperm Interactions in Broadcast-Spawning Invertebrates
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199642274.003.0014openalex-snapshot
Rates of sea urchin bindin evolution
inferred← citeshttps://doi.org/10.1093/icb/icae069openalex-snapshot
Introgression of the Gamete Recognition Molecule, Bindin, in the Sea Urchin Diadema
inferred← citeshttps://doi.org/10.1093/icb/icr039openalex-snapshot
Speciation Genes in Free-Spawning Marine Invertebrates
inferred← citeshttps://doi.org/10.1093/molbev/msg021openalex-snapshot
Positive Selection on an Acrosomal Sperm Protein, M7 Lysin, in Three Species of the Mussel Genus Mytilus
inferred← citeshttps://doi.org/10.1093/molbev/msh071openalex-snapshot
Adaptive Evolution of Sperm Bindin Tracks Egg Incompatibility in Neotropical Sea Urchins of the Genus Echinometra
inferred← citeshttps://doi.org/10.1093/molbev/msi219openalex-snapshot
Lineage-Specific Differences in Evolutionary Mode in a Salamander Courtship Pheromone
inferred← citeshttps://doi.org/10.1093/molbev/msl062openalex-snapshot
Geographic Variation and Positive Selection on M7 Lysin, an Acrosomal Sperm Protein in Mussels (Mytilus spp.)
inferred← citeshttps://doi.org/10.1093/molbev/msp122openalex-snapshot
Lack of Character Displacement in the Male Recognition Molecule, Bindin, in Altantic Sea Urchins of the Genus Echinometra
inferred← citeshttps://doi.org/10.1093/molbev/mst165openalex-snapshot
Adaptive Evolution of M3 Lysin—A Candidate Gamete Recognition Protein in the Mytilus edulis Species Complex
inferred← citeshttps://doi.org/10.1098/rsos.140538openalex-snapshot
Pre-zygotic isolation in the macroalgal genusFucusfrom four contact zones spanning 100–10 000 years: a tale of reinforcement?
inferred← citeshttps://doi.org/10.1101/cshperspect.a002931openalex-snapshot
Selection in the Rapid Evolution of Gamete Recognition Proteins in Marine Invertebrates
inferred← citeshttps://doi.org/10.1111/ede.12108openalex-snapshot
Evolution of gamete attraction molecules: evidence for purifying selection in speract and its receptor, in the pantropical sea urchin Diadema
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2003.tb00241.xopenalex-snapshot
ADAPTIVE EVOLUTION OF BINDIN IN THE GENUS HELIOCIDARIS IS CORRELATED WITH THE SHIFT TO DIRECT DEVELOPMENT
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2003.tb00382.xopenalex-snapshot
PHYLOGEOGRAPHY OF THE PANTROPICAL SEA URCHIN TRIPNEUSTES: CONTRASTING PATTERNS OF POPULATION STRUCTURE BETWEEN OCEANS
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2004.tb01702.xopenalex-snapshot
SPECIATION ON THE COASTS OF THE NEW WORLD: PHYLOGEOGRAPHY AND THE EVOLUTION OF BINDIN IN THE SEA URCHIN GENUS LYTECHINUS
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2004.tb01723.xopenalex-snapshot
SEXUAL CONFLICT AND PROTEIN POLYMORPHISM
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2005.tb00949.xopenalex-snapshot
SEA URCHIN BINDIN DIVERGENCE PREDICTS GAMETE COMPATIBILITY
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2009.04094.xopenalex-snapshot
Multiple gene genealogies reveal asymmetrical hybridization and introgression among strongylocentrotid sea urchins
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05303.xopenalex-snapshot
Phylogeography and bindin evolution in Arbacia, a sea urchin genus with an unusual distribution
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05336.xopenalex-snapshot
Positive Darwinian selection in gamete recognition proteins of Strongylocentrotus sea urchins
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2008.01017.xopenalex-snapshot
Egg and sperm recognition systems during fertilization
inferred← citeshttps://doi.org/10.1111/j.1471-8286.2007.01755.xopenalex-snapshot
Eleven new microsatellite markers for the tropical sea urchin Tripneustes gratilla and cross‐amplification in Tripneustes ventricosa
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ADAPTIVE GAMETE-RECOGNITION DIVERGENCE IN A HYBRIDIZING MYTILUS POPULATION
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INTROGRESSION DESPITE SUBSTANTIAL DIVERGENCE IN A BROADCAST SPAWNING MARINE INVERTEBRATE
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2012.01606.xopenalex-snapshot
LOW RATES OF BINDIN CODON EVOLUTION IN LECITHOTROPHIC HELIOCIDARIS SEA URCHINS
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NATURAL HYBRIDIZATION IN THE SEA URCHIN GENUS PSEUDOBOLETIA BETWEEN SPECIES WITHOUT APPARENT BARRIERS TO GAMETE RECOGNITION
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2012.01700.xopenalex-snapshot
MORE THAN BINDIN DIVERGENCE: REPRODUCTIVE ISOLATION BETWEEN SYMPATRIC SUBSPECIES OF A SEA URCHIN BY ASYNCHRONOUS SPAWNING
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2012.00272.xopenalex-snapshot
Morphology and gametic compatibility of color morphs of P aracentrotus gaimardi ( E chinodermata: E chinoidea)
inferred← citeshttps://doi.org/10.1186/s12862-025-02421-8openalex-snapshot
The sandfish identity: phylogeographic reconstructions uncover a species complex within the Indo-Pacific distribution of Holothuria (Metriatyla) scabra
inferred← citeshttps://doi.org/10.1186/s12863-016-0374-5openalex-snapshot
DNA polymorphism and selection at the bindin locus in three Strongylocentrotus sp. (Echinoidea)
inferred← citeshttps://doi.org/10.13057/oceanlife/o010101openalex-snapshot
Review: Biology of the commercially used sea urchin Tripneustes gratilla (Linnaeus, 1758) (Echinoidea: Echinodermata)
inferred← citeshttps://doi.org/10.1387/ijdb.072521kzopenalex-snapshot
The evolution of sea urchin sperm bindin
inferred← citeshttps://doi.org/10.1387/ijdb.082577ltopenalex-snapshot
Causes and consequences of the evolution of reproductive proteins
inferred← citeshttps://doi.org/10.1387/ijdb.082581ssopenalex-snapshot
Oyster sperm bindin is a combinatorial fucose lectin with remarkable intra-species diversity
inferred← citeshttps://doi.org/10.15517/rbt.v53i3.26773openalex-snapshot
Echinoids of the Pacific waters of Panama: status of knowledge and new records.
inferred← citeshttps://doi.org/10.15517/rbt.v60i3.28410openalex-snapshot
Bibliografía sobre investigaciones marinas, oceanográficas, geológicas y atmosféricas en el Parque Nacional Isla del Coco y aguas adyacentes, Pacífico de Costa Rica
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Echinoderm research perspectives: A Central American bibliometric review
inferred← citeshttps://doi.org/10.2307/1543440openalex-snapshot
250 Million Years of Bindin Evolution
inferred← citeshttps://doi.org/10.2307/3593129openalex-snapshot
Gamete Compatibility and Sperm Competition Affect Paternity and Hybridization Between SympatricAsteriasSea Stars
inferred← citeshttps://doi.org/10.4061/2011/595121openalex-snapshot
Is Speciation Accompanied by Rapid Evolution? Insights from Comparing Reproductive and Nonreproductive Transcriptomes inDrosophila
inferred← citeshttps://doi.org/10.70675/03d033c0za51dz4d96z9a7czeda70ab94f0bopenalex-snapshot
Histoire évolutive, structures génétique, morphologique et écologique comparées dans un complexe d'espèces jumelles : Echinocardium cordatum (Echinoidea, Irregularia)
inferred← citeshttps://doi.org/10.70675/6bac8de3z0b88z4e0dzbec7za7f96e119214openalex-snapshot
Divergence évolutive et isolement reproducteur chez les ascidies du genre Ciona, introduites et indigènes en Europe
inferred← citeshttps://doi.org/10.7150/jgen.27864openalex-snapshot
De novo male gonad transcriptome draft for the marine mussel Perumytilus purpuratus with a focus on its reproductive-related proteins
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