| The distribution of HLA haplotypes in the ethnic groups that make up the Brazilian Bone Marrow Volunteer Donor Registry (REDOME) |
29 |
| A genomic perspective on HLA evolution |
26 |
| Prolonged stable disease in a uveal melanoma patient with germline MBD4 nonsense mutation treated with pembrolizumab and ipilimumab |
13 |
| PD-1 and cancer: molecular mechanisms and polymorphisms |
10 |
| Improved peptide-MHC class II interaction prediction through integration of eluted ligand and peptide affinity data |
10 |
| Genetics of antigen processing and presentation |
8 |
| Class II MHC antigen processing in immune tolerance and inflammation |
8 |
| On being the right size: antibody repertoire formation in the mouse and human |
7 |
| Class I transactivator, NLRC5: a central player in the MHC class I pathway and cancer immune surveillance |
7 |
| A genome-wide association study for mastitis resistance in phenotypically well-characterized Holstein dairy cattle using a selective genotyping approach |
6 |
| HLA-G peptide preferences change in transformed cells: impact on the binding motif |
6 |
| Comprehensive annotation and evolutionary insights into the canine (Canis lupus familiaris) antigen receptor loci |
5 |
| Exploring the etiopathogenesis of systemic lupus erythematosus: a genetic perspective |
5 |
| A personal retrospective on the mechanisms of antigen processing |
5 |
| Contribution of the plasma and lymph Degradome and Peptidome to the MHC Ligandome |
5 |
| Ancient features of the MHC class II presentation pathway, and a model for the possible origin of MHC molecules |
5 |
| Nomenclature for the KIR of non-human species |
5 |
| Two class I genes of the chicken MHC have different functions: BF1 is recognized by NK cells while BF2 is recognized by CTLs |
5 |
| Limited MHC class II gene polymorphism in the West African chimpanzee is distributed maximally by haplotype diversity |
5 |
| How does the immune system learn to distinguish between good and evil? The first definitive studies of T cell central tolerance and positive selection |
5 |
| MHC genotyping from rhesus macaque exome sequences |
5 |
| IPD-MHC: nomenclature requirements for the non-human major histocompatibility complex in the next-generation sequencing era |
5 |
| Comparative MHC nomenclature: report from the ISAG/IUIS-VIC committee 2018 |
5 |
| HLA class I alterations in breast carcinoma are associated with a high frequency of the loss of heterozygosity at chromosomes 6 and 15 |
5 |
| MHC haplotype diversity in Persian Arabian horses determined using polymorphic microsatellites |
5 |
| Cetacea are natural knockouts for IL20 |
4 |
| miR-455-5p downregulation promotes inflammation pathways in the relapse phase of relapsing-remitting multiple sclerosis disease |
4 |
| Signatures of historical selection on MHC reveal different selection patterns in the moor frog (Rana arvalis) |
4 |
| A Chinese DADA2 patient: report of two novel mutations and successful HSCT |
4 |
| Identification of novel polymorphisms and two distinct haplotype structures in dog leukocyte antigen class I genes: DLA- DLA-12 and DLA-64 |
3 |
| On the feasibility of mining CD8+T cell receptor patterns underlying immunogenic peptide recognition |
3 |
| Inferring the evolution of the major histocompatibility complex of wild pigs and peccaries using hybridisation DNA capture-based sequencing |
3 |
| Susceptibility to mycobacterial disease due to mutations in IL-12R beta 1 in three Iranian patients |
3 |
| Methylation of H3K27 and H3K4 in key gene promoter regions of thymus in RA mice is involved in the abnormal development and differentiation of iNKT cells |
3 |
| Conservation of sequence motifs suggests that the nonclassical MHC class I lineages CD1/PROCR and UT were established before the emergence of tetrapod species |
3 |
| MHC class I diversity of olive baboons (Papio anubis) unravelled by next-generation sequencing |
3 |
| The expression profile of the ubiquitin-like modifier FAT10 in immune cells suggests cell type-specific functions |
3 |
| Determining Mhc-DRB profiles in wild populations of three congeneric true lemur species by noninvasive methods |
3 |
| Genomic convergence of locus-based GWAS meta-analysis identifies AXIN1 as a novel Parkinson's gene |
3 |
| What to do with HLA-DO/H-2O two decades later? |
3 |
| HLA-F*01:01 presents peptides with N-terminal flexibility and a preferred length of 16 residues |
3 |
| Characterisation of MHC class I genes in the koala |
3 |
| Identification and expression analysis of a TLR11 family gene in the sea urchin Strongylocentrotus intermedius |
3 |
| Did cis- and trans-defensins derive from a common ancestor? |
2 |
| Genetic variants of tumor necrosis factor-alpha-308G/A (rs1800629) but not Toll-interacting proteins or vitamin D receptor genes enhances susceptibility and severity of malaria infection |
2 |
| On the role of the immunoproteasome in transplant rejection |
2 |
| Analysis of NOD-like receptor NLRP1 in multiple sclerosis families |
2 |
| Immune biomarkers for predicting response to adoptive cell transfer as cancer treatment |
2 |
| Specificity of inhibitory KIRs enables NK cells to detect changes in an altered peptide environment |
2 |
| Low genetic variation in the MHC class II DRB gene and MHC-linked microsatellites in endangered island populations of the leopard cat (Prionailurus bengalensis) in Japan |
2 |
