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The immunologic V-gene repertoire in mammals
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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/eji.200425574openalex-snapshot
High variability in complementarity‐determining regions compensates for a low number of V gene families in the λ light chain locus of the platypus
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05092.xopenalex-snapshot
Immunoglobulin VH clan and family identity predicts variable domain structure and may influence antigen binding.
inferredcites →https://doi.org/10.1006/jmbi.1996.0127openalex-snapshot
The Imprint of Somatic Hypermutation on the Repertoire of Human Germline V Genes
inferredcites →https://doi.org/10.1007/bf00188428openalex-snapshot
Evolution of immunoglobulin heavy chain variable region genes: a VH family can last for 150?200 million years or longer
inferredcites →https://doi.org/10.1007/bf00191221openalex-snapshot
Evolution of V genes: DNA sequence structure of functional germline genes and pseudogenes
inferredcites →https://doi.org/10.1007/s00251-004-0706-xopenalex-snapshot
Evolution of the variable gene segments and recombination signal sequences of the human T-cell receptor ?/? locus
inferredcites →https://doi.org/10.1007/s00251-008-0349-4openalex-snapshot
Evolutionary history of an MHC gene in two leporid species: characterisation of Mhc-DQA in the European brown hare and comparison with the European rabbit
inferredcites →https://doi.org/10.1007/s00251-010-0425-4openalex-snapshot
Immunoglobulin heavy chain diversity in Pteropid bats: evidence for a diverse and highly specific antigen binding repertoire
inferredcites →https://doi.org/10.1007/s00251-013-0715-8openalex-snapshot
An automated algorithm for extracting functional immunologic V-genes from genomes in jawed vertebrates
inferredcites →https://doi.org/10.1007/s002510050220openalex-snapshot
Characterization of horse ( Equus caballus ) immunoglobulin mu chain-encoding genes
inferredcites →https://doi.org/10.1016/b978-0-12-637150-5.50025-0openalex-snapshot
THE ORGANIZATION OF IMMUNOGLOBULIN GENES
inferredcites →https://doi.org/10.1016/j.dci.2005.06.010openalex-snapshot
Antibody repertoire development in camelids
inferredcites →https://doi.org/10.1016/j.dci.2005.10.002openalex-snapshot
TCR gamma chain diversity in the spleen of the duckbill platypus (Ornithorhynchus anatinus)
inferredcites →https://doi.org/10.1016/j.dci.2010.06.004openalex-snapshot
The little brown bat, M. lucifugus, displays a highly diverse VH, DH and JH repertoire but little evidence of somatic hypermutation
inferredcites →https://doi.org/10.1016/j.dci.2012.02.006openalex-snapshot
The bovine genomic DNA sequence data reveal three IGHV subgroups, only one of which is functionally expressed
inferredcites →https://doi.org/10.1016/j.molimm.2009.05.025openalex-snapshot
The immunoglobulin heavy chain locus in the platypus (Ornithorhynchus anatinus)
inferredcites →https://doi.org/10.1016/j.vetimm.2008.10.299openalex-snapshot
Camelid immunoglobulins and nanobody technology
inferredcites →https://doi.org/10.1016/j.vetimm.2010.04.011openalex-snapshot
Molecular characterization of the VH repertoire in Canis familiaris
inferredcites →https://doi.org/10.1016/j.ympev.2011.11.008openalex-snapshot
Molecular phylogenetics unveils the ancient evolutionary origins of the enigmatic fairy armadillos
inferredcites →https://doi.org/10.1016/s0145-305x(02)00008-3openalex-snapshot
Cloning of the IgM heavy chain of the bottlenose dolphin (Tursiops truncatus), and initial analysis of VH gene usage
inferredcites →https://doi.org/10.1016/s1055-7903(03)00111-8openalex-snapshot
Molecular systematics of armadillos (Xenarthra, Dasypodidae): contribution of maximum likelihood and Bayesian analyses of mitochondrial and nuclear genes
inferredcites →https://doi.org/10.1038/334395a0openalex-snapshot
T-cell antigen receptor genes and T-cell recognition
inferredcites →https://doi.org/10.1038/363446a0openalex-snapshot
Naturally occurring antibodies devoid of light chains
inferredcites →https://doi.org/10.1038/ncomms2192openalex-snapshot
Genome sequences of wild and domestic bactrian camels
inferredcites →https://doi.org/10.1038/nri1245openalex-snapshot
T-cell-antigen recognition and the immunological synapse
inferredcites →https://doi.org/10.1038/nri889openalex-snapshot
Comparative analyses of immunoglobulin genes: surprises and portents
inferredcites →https://doi.org/10.1046/j.1365-2567.2003.01695.xopenalex-snapshot
Genomic structure around joining segments and constant regions of swine T‐cell receptor α/δ (TRA/TRD) locus
inferredcites →https://doi.org/10.1073/pnas.0511344103openalex-snapshot
Evolution of the mammalian placenta revealed by phylogenetic analysis
inferredcites →https://doi.org/10.1073/pnas.0609106104openalex-snapshot
A unique T cell receptor discovered in marsupials
inferredcites →https://doi.org/10.1073/pnas.73.10.3628openalex-snapshot
Evidence for somatic rearrangement of immunoglobulin genes coding for variable and constant regions.
inferredcites →https://doi.org/10.1073/pnas.94.15.7799openalex-snapshot
Evolution by the birth-and-death process in multigene families of the vertebrate immune system
inferredcites →https://doi.org/10.1073/pnas.97.21.11415openalex-snapshot
Evolution of the recombination signal sequences in the Ig heavy-chain variable region locus of mammals
inferredcites →https://doi.org/10.1084/jem.61.5.643openalex-snapshot
STUDIES ON THE SENSITIZATION OF ANIMALS WITH SIMPLE CHEMICAL COMPOUNDS
inferredcites →https://doi.org/10.1093/bioinformatics/btm404openalex-snapshot
Clustal W and Clustal X version 2.0
inferredcites →https://doi.org/10.1093/intimm/1.5.540openalex-snapshot
A large proportion of bovine T cells express the γδ T cell receptor and show a distinct tissue distribution and surface phenotype
inferredcites →https://doi.org/10.1093/molbev/msm201openalex-snapshot
Retroposed Elements and Their Flanking Regions Resolve the Evolutionary History of Xenarthran Mammals (Armadillos, Anteaters, and Sloths)
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
inferredcites →https://doi.org/10.1093/molbev/mst116openalex-snapshot
Less Is More in Mammalian Phylogenomics: AT-Rich Genes Minimize Tree Conflicts and Unravel the Root of Placental Mammals
inferredcites →https://doi.org/10.1093/molbev/mst117openalex-snapshot
Heterogeneous Models Place the Root of the Placental Mammal Phylogeny
inferredcites →https://doi.org/10.1093/molbev/mst118openalex-snapshot
Making the Impossible Possible: Rooting the Tree of Placental Mammals
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003989openalex-snapshot
Molecular Phylogeny of Living Xenarthrans and the Impact of Character and Taxon Sampling on the Placental Tree Rooting
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040127openalex-snapshot
Divergent evolution and evolution by the birth-and-death process in the immunoglobulin VH gene family.
inferredcites →https://doi.org/10.1098/rspb.2012.0683openalex-snapshot
Phylogenomic datasets provide both precision and accuracy in estimating the timescale of placental mammal phylogeny
inferredcites →https://doi.org/10.1101/gr.125864.111openalex-snapshot
Ultraconserved elements are novel phylogenomic markers that resolve placental mammal phylogeny when combined with species-tree analysis
inferredcites →https://doi.org/10.1101/gr.5918807openalex-snapshot
Using genomic data to unravel the root of the placental mammal phylogeny
inferredcites →https://doi.org/10.1101/sqb.1978.042.01.094openalex-snapshot
Organization of Immunoglobulin Genes
inferredcites →https://doi.org/10.1126/science.1211028openalex-snapshot
Impacts of the Cretaceous Terrestrial Revolution and KPg Extinction on Mammal Diversification
inferredcites →https://doi.org/10.1126/science.1229237openalex-snapshot
The Placental Mammal Ancestor and the Post–K-Pg Radiation of Placentals
inferredcites →https://doi.org/10.1186/1471-2164-9-111openalex-snapshot
Comparative genomic analysis and evolution of the T cell receptor loci in the opossum Monodelphis domestica
inferredcites →https://doi.org/10.1371/journal.pone.0010720openalex-snapshot
Sequencing, Analysis, and Annotation of Expressed Sequence Tags for Camelus dromedarius
inferredcites →https://doi.org/10.4049/jimmunol.0903616openalex-snapshot
Antibody Repertoire Development in Fetal and Neonatal Piglets. XI. The Relationship of Variable Heavy Chain Gene Usage and the Genomic Organization of the Variable Heavy Chain Locus
inferredcites →https://doi.org/10.4049/jimmunol.1101113openalex-snapshot
Platypus TCRμ Provides Insight into the Origins and Evolution of a Uniquely Mammalian TCR Locus
inferredcites →https://doi.org/10.4049/jimmunol.1200212openalex-snapshot
Evidence of IgY Subclass Diversification in Snakes: Evolutionary Implications
inferredcites →https://doi.org/10.4049/jimmunol.156.6.2163openalex-snapshot
The sheep Ig variable region repertoire consists of a single VH family
inferredcites →https://doi.org/10.4049/jimmunol.160.1.259openalex-snapshot
VH Repertoire of a Marsupial ( Monodelphis domestica )
inferredcites →https://doi.org/10.4049/jimmunol.174.9.5665openalex-snapshot
Unusually Similar Patterns of Antibody V Segment Diversity in Distantly Related Marsupials,
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/b978-0-323-95219-4.00010-1openalex-snapshot
The Afrotheria: Elephants, manatees, and their relatives
inferred← citeshttps://doi.org/10.1016/b978-0-323-95219-4.00023-xopenalex-snapshot
Four other orders: the Xenarthra, the Scandentia, the Eulipotyphla, and the Pholidota
inferred← citeshttps://doi.org/10.1016/j.biologicals.2017.01.004openalex-snapshot
Comparative analysis of the feline immunoglobulin repertoire
inferred← citeshttps://doi.org/10.1016/j.imbio.2018.07.005openalex-snapshot
Immunoglobulin heavy chain variable region analysis in dairy goats
inferred← citeshttps://doi.org/10.1016/j.molimm.2018.04.011openalex-snapshot
Genomic organization and adaptive evolution of IGHC genes in marine mammals
inferred← citeshttps://doi.org/10.1073/pnas.2501637122openalex-snapshot
Cross-reactive sarbecovirus antibodies induced by mosaic RBD nanoparticles
inferred← citeshttps://doi.org/10.1101/2020.10.24.353342openalex-snapshot
Immunoglobulins, MHC and T Cell receptors genes in Cetaceans
inferred← citeshttps://doi.org/10.1186/s12864-019-6431-5openalex-snapshot
Topology and expressed repertoire of the Felis catus T cell receptor loci
inferred← citeshttps://doi.org/10.1371/journal.pone.0233794openalex-snapshot
Sequencing B cell receptors from ferrets (Mustela putorius furo)
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