157 related articles for article (PubMed ID: 7660070)
21. Relative contribution of T and B cells to hypermutation and selection of the antibody repertoire in germinal centers of aged mice.
Yang X; Stedra J; Cerny J
J Exp Med; 1996 Mar; 183(3):959-70. PubMed ID: 8642299
[TBL] [Abstract][Full Text] [Related]
22. Limited heterogeneity of T-cell receptor V beta gene expression in the early stage of insulitis in NOD mice.
Drexler K; Burtles S; Hurtenbach U
Immunol Lett; 1993 Aug; 37(2-3):187-96. PubMed ID: 8258459
[TBL] [Abstract][Full Text] [Related]
23. Herpes simplex virus type 1 infection in mice with severe combined immunodeficiency (SCID).
Minagawa H; Sakuma S; Mohri S; Mori R; Watanabe T
Arch Virol; 1988; 103(1-2):73-82. PubMed ID: 2850780
[TBL] [Abstract][Full Text] [Related]
24. Restricted heterogeneity in T-cell antigen receptor V beta gene usage in the lymph nodes and arthritic joints of mice.
Haqqi TM; Anderson GD; Banerjee S; David CS
Proc Natl Acad Sci U S A; 1992 Feb; 89(4):1253-5. PubMed ID: 1311091
[TBL] [Abstract][Full Text] [Related]
25. A role for T lymphocytes in preventing experimental herpes simplex virus type 1-induced retinitis.
Whittum-Hudson J; Farazdaghi M; Prendergast RA
Invest Ophthalmol Vis Sci; 1985 Nov; 26(11):1524-32. PubMed ID: 3877027
[TBL] [Abstract][Full Text] [Related]
26. T lymphocytes infiltrating sites of tumor rejection and progression display identical V beta usage but different cytotoxic activities.
Kurt RA; Park JA; Panelli MC; Schluter SF; Marchalonis JJ; Carolus B; Akporiaye ET
J Immunol; 1995 Apr; 154(8):3969-74. PubMed ID: 7706735
[TBL] [Abstract][Full Text] [Related]
27. Differential expression of VH gene families in peripheral B cell repertoires of newborn or adult immunoglobulin H chain congenic mice.
Viale AC; Coutinho A; Freitas AA
J Exp Med; 1992 Jun; 175(6):1449-56. PubMed ID: 1588274
[TBL] [Abstract][Full Text] [Related]
28. Usage of T cell receptor beta-chain variable gene is highly restricted at the site of inflammation in murine autoimmune uveitis.
Rao NA; Naidu YM; Bell R; Lindsey JW; Pararajasegaram G; Sun Y; Steinman L
J Immunol; 1993 Jun; 150(12):5716-21. PubMed ID: 8390540
[TBL] [Abstract][Full Text] [Related]
29. The Ig VH repertoire of fetal liver-derived pre-B cells is influenced by the expression of a gene linked to X-linked immune deficiency.
Osman GE; Brodeur PH; Rosenberg N; Wortis HH
J Immunol; 1992 Mar; 148(6):1928-33. PubMed ID: 1541830
[TBL] [Abstract][Full Text] [Related]
30. Stochastic pairing of heavy-chain and kappa light-chain variable gene families occurs in polyclonally activated B cells.
Kaushik A; Schulze DH; Bonilla FA; Bona C; Kelsoe G
Proc Natl Acad Sci U S A; 1990 Jul; 87(13):4932-6. PubMed ID: 2114644
[TBL] [Abstract][Full Text] [Related]
31. Biased expression of JH-proximal VH genes occurs in the newly generated repertoire of neonatal and adult mice.
Malynn BA; Yancopoulos GD; Barth JE; Bona CA; Alt FW
J Exp Med; 1990 Mar; 171(3):843-59. PubMed ID: 2261012
[TBL] [Abstract][Full Text] [Related]
32. Use of the V delta 1 variable region in the functional T-cell receptor alpha chain of a WT31+ cytotoxic T lymphocyte clone which specifically recognizes HLA-A2 molecule.
Castelli C; Mazzocchi A; Salvi S; Anichini A; Sensi M
Scand J Immunol; 1992 Apr; 35(4):487-94. PubMed ID: 1313600
[TBL] [Abstract][Full Text] [Related]
33. Analysis of T cell antigen receptor (TCR) expression by human peripheral blood CD4-8- alpha/beta T cells demonstrates preferential use of several V beta genes and an invariant TCR alpha chain.
Porcelli S; Yockey CE; Brenner MB; Balk SP
J Exp Med; 1993 Jul; 178(1):1-16. PubMed ID: 8391057
[TBL] [Abstract][Full Text] [Related]
34. Immune or normal gamma delta T cells that assist alpha beta T cells in elicitation of contact sensitivity preferentially use V gamma 5 and V delta 4 variable region gene segments.
Ptak W; Szczepanik M; Ramabhadran R; Askenase PW
J Immunol; 1996 Feb; 156(3):976-86. PubMed ID: 8558025
[TBL] [Abstract][Full Text] [Related]
35. Restricted alpha/beta receptor gene usage of idiotype-specific major histocompatibility complex-restricted T cells: selection for CDR3-related sequences.
Snodgrass HR; Fisher AM; Bruyns E; Bogen B
Eur J Immunol; 1992 Aug; 22(8):2169-72. PubMed ID: 1379189
[TBL] [Abstract][Full Text] [Related]
36. Molecular analysis of the T-cell receptor V beta 5 and V beta 8 repertoire in pancreatic lesions of autoimmune diabetic NOD mice.
Berschick P; Fehsel K; Weltzien HU; Kolb H
J Autoimmun; 1993 Aug; 6(4):405-22. PubMed ID: 8216686
[TBL] [Abstract][Full Text] [Related]
37. Gene-targeted deletion and replacement mutations of the T-cell receptor beta-chain enhancer: the role of enhancer elements in controlling V(D)J recombination accessibility.
Bories JC; Demengeot J; Davidson L; Alt FW
Proc Natl Acad Sci U S A; 1996 Jul; 93(15):7871-6. PubMed ID: 8755569
[TBL] [Abstract][Full Text] [Related]
38. Virus infection expands a biased subset of T cells that bind tetrameric class I peptide complexes.
Coles RM; Jones CM; Brooks AG; Cameron PU; Heath WR; Carbone FR
Eur J Immunol; 2003 Jun; 33(6):1557-67. PubMed ID: 12778473
[TBL] [Abstract][Full Text] [Related]
39. [Analyses of the rearrangement of T-cell receptor- and immunoglobulin genes in the diagnosis of lymphoproliferative disorders].
Griesser DH
Veroff Pathol; 1995; 144():1-109. PubMed ID: 7856305
[TBL] [Abstract][Full Text] [Related]
40. Junctional diversity in the absence of N regions. Neonatal T cell receptor beta chain junctional sequences are more heterogeneous than neonatal T cell receptor gamma delta or IgH junctions.
Feeney AJ
J Immunol; 1993 Sep; 151(6):3094-9. PubMed ID: 8397251
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]