These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
118 related articles for article (PubMed ID: 8370399)
1. The evolutionary origin of the major histocompatibility complex: polymorphism of class II alpha chain genes in the cartilaginous fish. Kasahara M; McKinney EC; Flajnik MF; Ishibashi T Eur J Immunol; 1993 Sep; 23(9):2160-5. PubMed ID: 8370399 [TBL] [Abstract][Full Text] [Related]
2. Cloning, distribution and up-regulation of the teleost fish MHC class II alpha suggests a role for granulocytes as antigen-presenting cells. Cuesta A; Angeles Esteban M; Meseguer J Mol Immunol; 2006 Mar; 43(8):1275-85. PubMed ID: 16168483 [TBL] [Abstract][Full Text] [Related]
3. [Cloning of Xenopus laevis major histocompatibility complex class II beta-chain genes]. Sato K; Katagiri M Hokkaido Igaku Zasshi; 1994 Mar; 69(2):202-16. PubMed ID: 8157247 [TBL] [Abstract][Full Text] [Related]
4. Evolution of the MHC: isolation of class II beta-chain cDNA clones from the amphibian Xenopus laevis. Sato K; Flajnik MF; Du Pasquier L; Katagiri M; Kasahara M J Immunol; 1993 Apr; 150(7):2831-43. PubMed ID: 8454860 [TBL] [Abstract][Full Text] [Related]
5. Isolation, polymorphism and expression study of two distinct major histocompatibility complex class II B genes from half-smooth tongue sole (Cynoglossus semilaevis). Li C; Yu Y; Sun Y; Li S; Zhong Q; Wang X; Wang Z; Qi J; Zhang Q Int J Immunogenet; 2010 Jun; 37(3):185-97. PubMed ID: 20345861 [TBL] [Abstract][Full Text] [Related]
6. Characterization of genetic polymorphism of novel MHC B-LB II alleles in Chinese indigenous chickens. Xu R; Li K; Chen G; Xu H; Qiang B; Li C; Liu B J Genet Genomics; 2007 Feb; 34(2):109-18. PubMed ID: 17469783 [TBL] [Abstract][Full Text] [Related]
7. Identification of class I genes in cartilaginous fish, the most ancient group of vertebrates displaying an adaptive immune response. Bartl S; Baish MA; Flajnik MF; Ohta Y J Immunol; 1997 Dec; 159(12):6097-104. PubMed ID: 9550410 [TBL] [Abstract][Full Text] [Related]
8. The importance of dominant negative effects of amino acid side chain substitution in peptide-MHC molecule interactions and T cell recognition. Boehncke WH; Takeshita T; Pendleton CD; Houghten RA; Sadegh-Nasseri S; Racioppi L; Berzofsky JA; Germain RN J Immunol; 1993 Jan; 150(2):331-41. PubMed ID: 8093457 [TBL] [Abstract][Full Text] [Related]
9. Functional mapping of MHC class II polymorphic residues. The alpha-chain controls the specificity for binding an Ad-versus an A k-restricted peptide and the beta-chain region 65-67 controls T cell recognition but not peptide binding. Lee JM; McKean DJ; Watts TH J Immunol; 1991 May; 146(9):2952-9. PubMed ID: 1849939 [TBL] [Abstract][Full Text] [Related]
10. Patterns of polymorphism in the MHC class II of a non-passerine bird, the great snipe (Gallinago media). Ekblom R; Grahn M; Höglund J Immunogenetics; 2003 Jan; 54(10):734-41. PubMed ID: 12557060 [TBL] [Abstract][Full Text] [Related]
11. The origin of MHC class II gene polymorphism within the genus Mus. McConnell TJ; Talbot WS; McIndoe RA; Wakeland EK Nature; 1988 Apr; 332(6165):651-4. PubMed ID: 2895893 [TBL] [Abstract][Full Text] [Related]
12. Evolution of the major histocompatibility complex: isolation of class II A cDNA clones from the cartilaginous fish. Kasahara M; Vazquez M; Sato K; McKinney EC; Flajnik MF Proc Natl Acad Sci U S A; 1992 Aug; 89(15):6688-92. PubMed ID: 1495958 [TBL] [Abstract][Full Text] [Related]
13. Nature and origin of polymorphism in feline MHC class II DRA and DRB genes. Yuhki N; O'Brien SJ J Immunol; 1997 Mar; 158(6):2822-33. PubMed ID: 9058818 [TBL] [Abstract][Full Text] [Related]
14. Interaction between certain major histocompatibility complex class II and T-cell receptor V beta alleles promotes the antibody production to extractable nuclear antigen-related peptides. Youinou P; Semana G; Muller S; Piette JC; Guillevin L; Jouquan J; Salmon D; Salmon J; Genetet B; Bach JF Hum Immunol; 1997 Jan; 52(1):12-21. PubMed ID: 9021405 [TBL] [Abstract][Full Text] [Related]
15. Isolation of low molecular mass polypeptide complementary DNA clones from primitive vertebrates. Implications for the origin of MHC class I-restricted antigen presentation. Kandil E; Namikawa C; Nonaka M; Greenberg AS; Flajnik MF; Ishibashi T; Kasahara M J Immunol; 1996 Jun; 156(11):4245-53. PubMed ID: 8666794 [TBL] [Abstract][Full Text] [Related]
16. I-Ak polymorphisms define a functionally dominant region for the presentation of hen egg lysozyme peptides. Rosloniec EF; Vitez LJ; Beck BN; Buerstedde JM; McKean DJ; Landais D; Benoist C; Mathis D; Freed JH J Immunol; 1989 Jul; 143(1):50-8. PubMed ID: 2786533 [TBL] [Abstract][Full Text] [Related]
17. Molecular cloning, genomic structure, polymorphism and expression analysis of major histocompatibility complex class IIA and IIB genes of half-smooth tongue sole (Cynoglossus semilaevis). Xu TJ; Chen SL; Ji XS; Sha ZX Fish Shellfish Immunol; 2009 Aug; 27(2):192-201. PubMed ID: 19442741 [TBL] [Abstract][Full Text] [Related]
18. Evolution of Mhc class II B genes in Darwin's finches and their closest relatives: birth of a new gene. Sato A; Mayer WE; Tichy H; Grant PR; Grant BR; Klein J Immunogenetics; 2001 Dec; 53(9):792-801. PubMed ID: 11862412 [TBL] [Abstract][Full Text] [Related]
20. Gene duplication and evidence for balancing selection acting on MHC class II DAA gene of the half-smooth tongue sole (Cynoglossus semilaevis). Xu TJ; Sun YN; Wang RX Mar Genomics; 2010 Jun; 3(2):117-23. PubMed ID: 21798205 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]