| scholarly article | Q13442814 |
| P50 | author | Victor Rutten | Q44744721 |
| Dirk M Zajonc | Q47292428 | ||
| Johannes A. Lenstra | Q47891658 | ||
| Ildiko Van Rhijn | Q48067147 | ||
| Milana Troskie | Q55201035 | ||
| Peter Reinink | Q55506880 | ||
| Darshana Morar-Leather | Q57440081 | ||
| Lonneke Vervelde | Q59687989 | ||
| Willem van Eden | Q62042571 | ||
| P2093 | author name string | Roel Hermsen | |
| Nico J Schoemaker | |||
| Axel Fun | |||
| Frank A Looringh van Beeck | |||
| Marielle J Laven | |||
| P2860 | cites work | Structure and function of a potent agonist for the semi-invariant natural killer T cell receptor | Q24672186 |
| SWISS-MODEL: An automated protein homology-modeling server | Q24672647 | ||
| CD1d-lipid-antigen recognition by the semi-invariant NKT T-cell receptor | Q27646101 | ||
| Reorganization of genera in the families Rickettsiaceae and Anaplasmataceae in the order Rickettsiales: unification of some species of Ehrlichia with Anaplasma, Cowdria with Ehrlichia and Ehrlichia with Neorickettsia, descriptions of six new species | Q28213820 | ||
| CD1d-restricted and TCR-mediated activation of valpha14 NKT cells by glycosylceramides | Q28254991 | ||
| NKT cells derive from double-positive thymocytes that are positively selected by CD1d | Q28508188 | ||
| Characterization of two avian MHC-like genes reveals an ancient origin of the CD1 family | Q28769641 | ||
| A molecular timescale for vertebrate evolution | Q29547791 | ||
| Conservation of a CD1 multigene family in the guinea pig. | Q30809453 | ||
| Two CD1 genes map to the chicken MHC, indicating that CD1 genes are ancient and likely to have been present in the primordial MHC. | Q33853815 | ||
| The bovine CD1 family contains group 1 CD1 proteins, but no functional CD1d | Q34508804 | ||
| A structural basis for selection and cross-species reactivity of the semi-invariant NKT cell receptor in CD1d/glycolipid recognition. | Q36228473 | ||
| Prevention of autoimmunity by targeting a distinct, noninvariant CD1d-reactive T cell population reactive to sulfatide | Q36399392 | ||
| CD1d-restricted T cell activation by nonlipidic small molecules | Q37535060 | ||
| Natural killer T cells recognize diacylglycerol antigens from pathogenic bacteria | Q38466705 | ||
| A critical tyrosine residue in the cytoplasmic tail is important for CD1d internalization but not for its basolateral sorting in MDCK cells | Q40974118 | ||
| Mouse CD1 is distinct from and co-exists with TL in the same thymus | Q41092898 | ||
| Distinct subsets of CD1d-restricted T cells recognize self-antigens loaded in different cellular compartments | Q41785389 | ||
| The crystal structure of human CD1d with and without alpha-galactosylceramide | Q42661990 | ||
| Structural analysis of the rat homologue of CD1. Evidence for evolutionary conservation of the CD1D class and widespread transcription by rat cells. | Q42674339 | ||
| Role of CD1d in coxsackievirus B3-induced myocarditis. | Q43834892 | ||
| Recognition of bacterial glycosphingolipids by natural killer T cells | Q44582192 | ||
| Activation of a nonclassical NKT cell subset in a transgenic mouse model of hepatitis B virus infection | Q45732782 | ||
| Analysis of evolutionary conservation in CD1d molecules among primates | Q46394661 | ||
| Amino-terminal sequencing of sheep CD1 antigens and identification of a sheep CD1D gene | Q47993293 | ||
| Analysis of the genomic structure of the porcine CD1 gene cluster | Q48083399 | ||
| Chicken CD1 genes are located in the MHC: CD1 and endothelial protein C receptor genes constitute a distinct subfamily of class-I-like genes that predates the emergence of mammals | Q48123513 | ||
| The rabbit CD1 and the evolutionary conservation of the CD1 gene family | Q48308062 | ||
| Impaired NK1+ T cell development and early IL-4 production in CD1-deficient mice. | Q52525223 | ||
| Germline-encoded recognition of diverse glycolipids by natural killer T cells | Q56917232 | ||
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | pig | Q787 |
| P304 | page(s) | 1424-31 | |
| P577 | publication date | 2009-04-01 | |
| P1433 | published in | Molecular Immunology | Q6895954 |
| P1476 | title | Functional CD1d and/or NKT cell invariant chain transcript in horse, pig, African elephant and guinea pig, but not in ruminants | |
| P478 | volume | 46 |
| Q40739722 | Adjuvant effects of invariant NKT cell ligand potentiates the innate and adaptive immunity to an inactivated H1N1 swine influenza virus vaccine in pigs |
| Q41639759 | Adjuvant effects of therapeutic glycolipids administered to a cohort of NKT cell-diverse pigs |
| Q33695019 | CD1: A Singed Cat of the Three Antigen Presentation Systems. |
| Q26797242 | Coevolution of T-cell receptors with MHC and non-MHC ligands |
| Q42787200 | Direct identification of rat iNKT cells reveals remarkable similarities to human iNKT cells and a profound deficiency in LEW rats |
| Q35670019 | Functional invariant NKT cells in pig lungs regulate the airway hyperreactivity: a potential animal model |
| Q48343602 | Harnessing Invariant NKT Cells to Improve Influenza Vaccines: A Pig Perspective |
| Q39077547 | Highly purified mycobacterial phosphatidylinositol mannosides drive cell-mediated responses and activate NKT cells in cattle. |
| Q50940046 | Identification of invariant natural killer T cells in porcine peripheral blood. |
| Q38590013 | Lipid and small-molecule display by CD1 and MR1. |
| Q35104853 | Low cross-reactivity of T-cell responses against lipids from Mycobacterium bovis and M. avium paratuberculosis during natural infection |
| Q28596919 | Mammalian CD1 and MR1 genes |
| Q90265871 | Mucosal-Associated Invariant T Cells Expressing the TRAV1-TRAJ33 Chain Are Present in Pigs |
| Q37545341 | Natural killer T cells and the regulation of asthma |
| Q38629327 | Natural killer cells in host defense against veterinary pathogens |
| Q91689733 | Next Generation Sequencing of the Pig αβ TCR Repertoire Identifies the Porcine Invariant NKT Cell Receptor |
| Q41893247 | Polymorphisms in the CD1d promoter that regulate CD1d gene expression are associated with impaired NKT cell development |
| Q30408873 | Raising the roof: the preferential pharmacological stimulation of Th1 and th2 responses mediated by NKT cells |
| Q26801636 | Role of Group 1 CD1-Restricted T Cells in Infectious Disease |
| Q38243971 | Role of host- and pathogen-associated lipids in directing the immune response in mycobacterial infections, with emphasis on Mycobacterium avium subsp. paratuberculosis |
| Q28711641 | Serodiagnosis of tuberculosis in Asian elephants (Elephas maximus) in Southern India: a latent class analysis |
| Q43782153 | Tandem repeats modify the structure of the canine CD1D gene. |
| Q92247727 | The T cell receptor (TRA) locus in the rabbit (Oryctolagus cuniculus): Genomic features and consequences for invariant T cells |
| Q34741552 | The Vγ9Vδ2 T Cell Antigen Receptor and Butyrophilin-3 A1: Models of Interaction, the Possibility of Co-Evolution, and the Case of Dendritic Epidermal T Cells |
| Q36749511 | The bovine CD1D gene has an unusual gene structure and is expressed but cannot present α-galactosylceramide with a C26 fatty acid |
| Q42084713 | The bovine T cell receptor alpha/delta locus contains over 400 V genes and encodes V genes without CDR2. |
| Q37525591 | The evolved functions of CD1 during infection |
Search more.