| P50 | author | Jerzy K Kulski | Q56605742 |
| P2093 | author name string | Hidetoshi Inoko | |
| | Takashi Shiina | |
| | Sakae Kohara | |
| | Tatsuya Anzai | |
| P2860 | cites work | Nothing in Biology Makes Sense except in the Light of Evolution | Q22064567 |
| | Complete sequence and gene map of a human major histocompatibility complex. The MHC sequencing consortium | Q22122334 |
| | Association of tapasin and COPI provides a mechanism for the retrograde transport of major histocompatibility complex (MHC) class I molecules from the Golgi complex to the endoplasmic reticulum | Q24292421 |
| | Assembly and function of the two ABC transporter proteins encoded in the human major histocompatibility complex | Q24305117 |
| | A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis | Q24310146 |
| | A gene outside the human MHC related to classical HLA class I genes | Q24320252 |
| | A critical role for tapasin in the assembly and function of multimeric MHC class I-TAP complexes | Q24336286 |
| | Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complex | Q24561711 |
| | A second lineage of mammalian major histocompatibility complex class I genes | Q24561936 |
| | The bromodomain: a conserved sequence found in human, Drosophila and yeast proteins | Q24604489 |
| | Complete amino acid sequence of human plasma Zn-alpha 2-glycoprotein and its homology to histocompatibility antigens | Q24655693 |
| | A new polymorphic and multicopy MHC gene family related to nonmammalian class I | Q28114893 |
| | CIZ, a zinc finger protein that interacts with p130(cas) and activates the expression of matrix metalloproteinases | Q28144485 |
| | Yesterday's polyploids and the mystery of diploidization | Q28186761 |
| | A second susceptibility gene for developing rheumatoid arthritis in the human MHC is localized within a 70-kb interval telomeric of the TNF genes in the HLA class III region | Q28199794 |
| | The cluster of BTN genes in the extended major histocompatibility complex | Q28199806 |
| | The chicken B locus is a minimal essential major histocompatibility complex. | Q40915352 |
| | Transposition mediated by RAG1 and RAG2 and its implications for the evolution of the immune system | Q41011364 |
| | Chicken MHC molecules, disease resistance and the evolutionary origin of birds | Q41231484 |
| | The origin of interspersed repeats in the human genome | Q41312150 |
| | Invited anniversary review: HLA associated diseases | Q41451348 |
| | Differences in the central major histocompatibility complex between humans and chimpanzees. Implications for development of autoimmunity and acquired immune deficiency syndrome | Q41530553 |
| | Birth of the major histocompatibility complex | Q41728577 |
| | Unusual MHC-like molecules: CD1, Fc receptor, the hemochromatosis gene product, and viral homologs | Q41729813 |
| | The critical region for Behçet disease in the human major histocompatibility complex is reduced to a 46-kb segment centromeric of HLA-B, by association analysis using refined microsatellite mapping | Q42014366 |
| | Butyrophilin is expressed in mammary epithelial cells from a single-sized messenger RNA as a type I membrane glycoprotein | Q42060995 |
| | Songbird genomics: analysis of 45 kb upstream of a polymorphic Mhc class II gene in red-winged blackbirds (Agelaius phoeniceus). | Q42655444 |
| | Sequence of the pig major histocompatibility region containing the classical class I genes | Q42662812 |
| | Sexual preference of apparent gene conversion events in MHC genes of mice | Q42668375 |
| | The evolution of MHC diversity by segmental duplication and transposition of retroelements. | Q42669974 |
| | Phylogenetic tests of the hypothesis of block duplication of homologous genes on human chromosomes 6, 9, and 1. | Q42680427 |
| | Shared regulatory elements in the promoters of MHC class I and class II genes | Q42681020 |
| | Nonlinkage of major histocompatibility complex class I and class II loci in bony fishes | Q43445868 |
| | Proteasome, transporter associated with antigen processing, and class I genes in the nurse shark Ginglymostoma cirratum: evidence for a stable class I region and MHC haplotype lineages | Q43845872 |
| | Histocompatibility reaction in tissue and cells of the marine sponge Suberites domuncula in vitro and in vivo: central role of the allograft inflammatory factor 1. | Q43971507 |
| | Heat-shock proteins as activators of the innate immune system | Q77689830 |
| | Phylogenetic analysis of primate MIC (PERB11) sequences suggests that the representation of the gene family differs in different primates: comparison of MIC (PERB11) and C4 | Q77758618 |
| | What brought the adaptive immune system to vertebrates?--The jaw hypothesis and the seahorse | Q77894089 |
| | What sharks can tell us about the evolution of MHC genes | Q77894128 |
| | Chromosome loss is the most frequent mechanism contributing to HLA haplotype loss in human tumors | Q78132614 |
| | [Iso-leuko-antibodies] | Q78362821 |
| | QUOD ERAT FACIENDUM: sequence analysis of the H2-D and H2-Q regions of 129/SvJ mice | Q78398498 |
| | Genomic organization of the mammalian MHC. | Q35034055 |
| | Major histocompatibility complex gene mapping in the amphibian Xenopus implies a primordial organization | Q36158881 |
| | Molecular dynamics of MHC genesis unraveled by sequence analysis of the 1,796,938-bp HLA class I region | Q36670403 |
| | Directed integration of the physical and genetic linkage maps of swine chromosome 7 reveals that the SLA spans the centromere | Q36794859 |
| | Occupancy of upstream regulatory sites in vivo coincides with major histocompatibility complex class I gene expression in mouse tissues | Q36821964 |
| | Chicken major histocompatibility complex-encoded B-G antigens are found on many cell types that are important for the immune system. | Q37402918 |
| | Evolutionary significance of the HL-A system | Q39867389 |
| | Pathogen-based models favoring MHC genetic diversity | Q40413338 |
| | Hormones and the physiological architecture of life history evolution | Q40514596 |
| | "Both man & bird & beast": comparative organization of MHC genes | Q40560177 |
| | The association between HLA-A alleles and young Alu dimorphisms near the HLA-J, -H, and -F genes in workshop cell lines and Japanese and Australian populations. | Q40682909 |
| | Composite origin of major histocompatibility complex genes | Q40719931 |
| | Alu polymorphism within the MICB gene and association with HLA-B alleles | Q40748454 |
| | Structure and biology of complement protein C3, a connecting link between innate and acquired immunity | Q28202590 |
| | Nucleotide sequence of the MHC class I genomic region of a teleost, the medaka (Oryzias latipes) | Q28203570 |
| | Is tapasin a modified Mhc class I molecule? | Q28203580 |
| | Leukocyte Ig-like receptor complex (LRC) in mice and men | Q28212193 |
| | Human natural killer cells: their origin, receptors and function | Q28216090 |
| | A cluster of ten novel MHC class I related genes on human chromosome 6q24.2-q25.3 | Q28217434 |
| | A proteasome-related gene between the two ABC transporter loci in the class II region of the human MHC | Q28235385 |
| | Second proteasome-related gene in the human MHC class II region | Q28235438 |
| | In search of the 'missing self': MHC molecules and NK cell recognition | Q28250846 |
| | Nucleotide sequencing analysis of the 146-kilobase segment around the IkBL and MICA genes at the centromeric end of the HLA class I region | Q28263097 |
| | A novel, mitogen-activated nuclear kinase is related to a Drosophila developmental regulator | Q28275590 |
| | An Fc receptor structurally related to MHC class I antigens | Q28569860 |
| | Primitive synteny of vertebrate major histocompatibility complex class I and class II genes | Q28776594 |
| | A molecular timescale for vertebrate evolution | Q29547791 |
| | Interspersed repeats and other mementos of transposable elements in mammalian genomes | Q29615764 |
| | Pattern of nucleotide substitution at major histocompatibility complex class I loci reveals overdominant selection | Q29616615 |
| | On the total number of genes and their length distribution in complete microbial genomes | Q30002407 |
| | Gene organization of the quail major histocompatibility complex (MhcCoja) class I gene region | Q30630450 |
| | Multiple class I loci expressed by the quail Mhc. | Q30630505 |
| | Physical map and expression profile of genes of the telomeric class I gene region of the rat MHC. | Q30657373 |
| | Spatial arrangement of pig MHC class I sequences | Q30780106 |
| | A BAC contig of approximately 400 kb contains the classical class I major histocompatibility complex (MHC) genes of cattle. | Q30811813 |
| | Molecular and functional characterization of genes encoding horse MHC class I antigens | Q30818347 |
| | Molecular cloning and linkage analysis of complement C3 and C4 genes of the Japanese medaka fish | Q30837208 |
| | SNP profile within the human major histocompatibility complex reveals an extreme and interrupted level of nucleotide diversity. | Q30947228 |
| | Comparative feline genomics: a BAC/PAC contig map of the major histocompatibility complex class II region | Q30979114 |
| | Characterization of the MHC class I region of the Japanese pufferfish (Fugu rubripes). | Q30982116 |
| | Organization of the canine major histocompatibility complex: current perspectives | Q31905980 |
| | The complete genomic sequence of 424,015 bp at the centromeric end of the HLA class I region: gene content and polymorphism | Q32046274 |
| | Virtual reality in the MHC. | Q33630594 |
| | The chromosomal duplication model of the major histocompatibility complex | Q33630600 |
| | The MHC big bang | Q33630607 |
| | Insight into the primordial MHC from studies in ectothermic vertebrates | Q33630619 |
| | Allorecognition in colonial tunicates: protection against predatory cell lineages? | Q33630625 |
| | Toward an evolutionary genomics of the avian Mhc. | Q33630643 |
| | Comparative genome organization of the major histocompatibility complex: lessons from the Felidae | Q33630648 |
| | Comparative organization and function of the major histocompatibility complex of domesticated cattle | Q33630652 |
| | The major histocompatibility complex in swine | Q33630668 |
| | Genome sequencing analysis of the 1.8 Mb entire human MHC class I region | Q33630672 |
| | Sequence organisation of the class II region of the human MHC. | Q33630677 |
| | The mouse major histocompatibility complex: some assembly required. | Q33630683 |
| | Genomics of the major histocompatibility complex: haplotypes, duplication, retroviruses and disease | Q33630704 |
| | Major histocompatibility complex class II polymorphisms in primates | Q33630724 |
| | The CD1 system: antigen-presenting molecules for T cell recognition of lipids and glycolipids | Q33652486 |
| | Evolution of the innate and adaptive immune systems: relationships between potential immune molecules in the lowest metazoan phylum (Porifera) and those in vertebrates | Q33779800 |
| | Characterization of a murine cytomegalovirus class I major histocompatibility complex (MHC) homolog: comparison to MHC molecules and to the human cytomegalovirus MHC homolog. | Q33782034 |
| | Gene duplication and the uniqueness of vertebrate genomes circa 1970-1999. | Q33794254 |
| | Nucleotide substitution at major histocompatibility complex class II loci: evidence for overdominant selection | Q33835136 |
| | Association analysis using refined microsatellite markers localizes a susceptibility locus for psoriasis vulgaris within a 111 kb segment telomeric to the HLA-C gene | Q33878843 |
| | The inhibitory receptor LIR-1 uses a common binding interaction to recognize class I MHC molecules and the viral homolog UL18. | Q33883093 |
| | BTL-II: a polymorphic locus with homology to the butyrophilin gene family, located at the border of the major histocompatibility complex class II and class III regions in human and mouse. | Q33901322 |
| | The human and mouse MHC class III region: a parade of 21 genes at the centromeric segment | Q33953177 |
| | The mouse as a model for the effects of MHC genes on human disease | Q33953182 |
| | Chromatin-immune connections: regulation of MHC and other genes | Q34038513 |
| | How genomic and developmental dynamics affect evolutionary processes | Q34085679 |
| | Comparative genomics of the MHC: glimpses into the evolution of the adaptive immune system | Q34092192 |
| | Paternally inherited HLA alleles are associated with women's choice of male odor | Q34110163 |
| | Evidence of en bloc duplication in vertebrate genomes | Q34124854 |
| | Evolution of the complement system | Q34129355 |
| | The simple chicken major histocompatibility complex: life and death in the face of pathogens and vaccines. | Q34143973 |
| | Fine localization of a major disease-susceptibility locus for diffuse panbronchiolitis | Q34145079 |
| | A novel family of human major histocompatibility complex-related genes not mapping to chromosome 6. | Q34165704 |
| | TNF-alpha and IL-12: a balancing act in macrophage functioning | Q34184417 |
| | Divergent and convergent evolution of NK-cell receptors | Q34207553 |
| | The major histocompatibility complex of the rat (Rattus norvegicus). | Q34422446 |
| | Genomic and funtional aspects of the rat MHC, the RT1 complex | Q34579737 |
| | Cytokines as a link between innate and adaptive antitumor immunity. | Q34581798 |
| | Genomic anatomy of a premier major histocompatibility complex paralogous region on chromosome 1q21-q22 | Q35033356 |
| | Coevolution of PERB11 (MIC) and HLA class I genes with HERV-16 and retroelements by extended genomic duplication. | Q44969144 |
| | The MHC class I homolog encoded by human cytomegalovirus binds endogenous peptides | Q45992897 |
| | A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes | Q46815882 |
| | Fugu orthologues of human major histocompatibility complex genes: a genome survey | Q47428040 |
| | At least one class I gene in restriction fragment pattern-Y (Rfp-Y), the second MHC gene cluster in the chicken, is transcribed, polymorphic, and shows divergent specialization in antigen binding region. | Q47582627 |
| | A contig map of the Mhc class I genomic region in the zebrafish reveals ancient synteny | Q47675078 |
| | Growing up with dinosaurs: molecular dates and the mammalian radiation | Q47718506 |
| | Comparison between two human endogenous retrovirus (HERV)-rich regions within the major histocompatibility complex | Q47719397 |
| | The immunogenetics of human infectious diseases. | Q47830930 |
| | Promoter structures suggest independent translocations of ancestral rat RT1.A and mouse H2-K class I genes | Q47832702 |
| | Physical mapping and evolution of the centromeric class I gene-containing region of the rat MHC. | Q47832760 |
| | Heat shock proteins come of age: primitive functions acquire new roles in an adaptive world | Q47877336 |
| | Cloning and sequence analysis of the H2-K2(b) gene reveals that it is a pseudogene | Q47916764 |
| | Linkage of RXRB-like genes to class I and not to class II Mhc genes in the zebrafish | Q47949902 |
| | MIC-A polymorphism in Japanese and a MIC-A-MIC-B null haplotype. | Q47955791 |
| | A radiation hybrid map of BTA23: identification of a chromosomal rearrangement leading to separation of the cattle MHC class II subregions | Q48011447 |
| | A first map of the porcine major histocompatibility complex class I region. | Q48039500 |
| | The mouse HFE gene | Q48040844 |
| | Linkage of TATA-binding protein and proteasome subunit C5 genes in mice and humans reveals synteny conserved between mammals and invertebrates | Q48045952 |
| | Nucleotide sequence analysis of the HLA class I region spanning the 237-kb segment around the HLA-B and -C genes | Q48049782 |
| | Phylogenetic analysis of penguin ( Spheniscidae) species based on sequence variation in MHC class II genes. | Q48323556 |
| | Heat shock protein 70 family: multiple sequence comparisons, function, and evolution. | Q52232632 |
| | Genomic and phylogenetic analysis of the human CD1 and HLA class I multicopy genes. | Q52544409 |
| | Churchill and the immune system of ectothermic vertebrates | Q58424608 |
| | Which came first, MHC class I or class II? | Q58424635 |
| | Organization and evolution of the class I gene family in the major histocompatibility complex of the C57BL/10 mouse | Q59063646 |
| | The evolutionary dynamics of repetitive DNA in eukaryotes | Q59090793 |
| | Class I gene contraction within the HLA-A subregion of the human MHC | Q67525516 |
| | Evolutionary relationships of the classes of major histocompatibility complex genes | Q70550067 |
| | Tissue rejection: the price of sexual acceptance? | Q71233711 |
| | Mapping of the genetically independent chicken major histocompatibility complexes B@ and RFP-Y@ to the same microchromosome by two-color fluorescent in situ hybridization | Q71973832 |
| | Evolution of MHC genetic diversity: a tale of incest, pestilence and sexual preference | Q72278928 |
| | Extensive nucleotide variability within a 370 kb sequence from the central region of the major histocompatibility complex | Q73203519 |
| | Localization of a non-melanoma skin cancer susceptibility region within the major histocompatibility complex by association analysis using microsatellite markers | Q73268471 |
| | Large-scale comparative mapping of the MHC class I region of predominant haplotypes in Japanese | Q73363123 |
| | Wide distribution of the MICA-MICB null haplotype in East Asians | Q73420335 |
| | Sequence of the swine major histocompatibility complex region containing all non-classical class I genes | Q73420363 |
| | Retrotransposons as epigenetic mediators of phenotypic variation in mammals | Q73695300 |
| | Using alu J elements as molecular clocks to trace the evolutionary relationships between duplicated HLA class I genomic segments | Q73843880 |
| | Duplication and polymorphism in the MHC: Alu generated diversity and polymorphism within the PERB11 gene family | Q74010582 |
| | HLA and AIDS: a cautionary tale | Q74446693 |
| | Evolution of the Mhc class I region: the framework hypothesis | Q74609041 |
| | Molecular evolution. Genome duplications: the stuff of evolution? | Q77375510 |
| | Wisdom through immunogenetics | Q77571334 |
| P921 | main subject | shark | Q7372 |
| | biodiversity | Q47041 |
| P304 | page(s) | 95-122 | |
| P577 | publication date | 2002-12-01 | |
| P1433 | published in | Immunological Reviews | Q15724582 |
| P1476 | title | Comparative genomic analysis of the MHC: the evolution of class I duplication blocks, diversity and complexity from shark to man | |
| P478 | volume | 190 | |