333 related articles for article (PubMed ID: 8426111)
1. High-frequency representation of a single VH gene in the expressed human B cell repertoire.
Stewart AK; Huang C; Stollar BD; Schwartz RS
J Exp Med; 1993 Feb; 177(2):409-18. PubMed ID: 8426111
[TBL] [Abstract][Full Text] [Related]
2. Ig lambda and heavy chain gene usage in early untreated systemic lupus erythematosus suggests intensive B cell stimulation.
Dörner T; Farner NL; Lipsky PE
J Immunol; 1999 Jul; 163(2):1027-36. PubMed ID: 10395701
[TBL] [Abstract][Full Text] [Related]
3. Relationship of human variable region heavy chain germ-line genes to genes encoding anti-DNA autoantibodies.
Dersimonian H; Schwartz RS; Barrett KJ; Stollar BD
J Immunol; 1987 Oct; 139(7):2496-501. PubMed ID: 3116084
[TBL] [Abstract][Full Text] [Related]
4. Restricted use of fetal VH3 immunoglobulin genes by unselected B cells in the adult. Predominance of 56p1-like VH genes in common variable immunodeficiency.
Braun J; Berberian L; King L; Sanz I; Govan HL
J Clin Invest; 1992 May; 89(5):1395-402. PubMed ID: 1569182
[TBL] [Abstract][Full Text] [Related]
5. Somatic diversification and selection of immunoglobulin heavy and light chain variable region genes in IgG+ CD5+ chronic lymphocytic leukemia B cells.
Hashimoto S; Dono M; Wakai M; Allen SL; Lichtman SM; Schulman P; Vinciguerra VP; Ferrarini M; Silver J; Chiorazzi N
J Exp Med; 1995 Apr; 181(4):1507-17. PubMed ID: 7535340
[TBL] [Abstract][Full Text] [Related]
6. VH-gene representation in autoantibodies reflects the normal human B-cell repertoire.
Stewart AK; Huang C; Long AA; Stollar BD; Schwartz RS
Immunol Rev; 1992 Aug; 128():101-22. PubMed ID: 1427920
[TBL] [Abstract][Full Text] [Related]
7. Evidence for the overexpression of the VH4-34 (VH4.21) Ig gene segment in the normal adult human peripheral blood B cell repertoire.
Kraj P; Friedman DF; Stevenson F; Silberstein LE
J Immunol; 1995 Jun; 154(12):6406-20. PubMed ID: 7759877
[TBL] [Abstract][Full Text] [Related]
8. Human immunoglobulin heavy-chain minilocus recombination in transgenic mice: gene-segment use in mu and gamma transcripts.
Tuaillon N; Taylor LD; Lonberg N; Tucker PW; Capra JD
Proc Natl Acad Sci U S A; 1993 Apr; 90(8):3720-4. PubMed ID: 8475122
[TBL] [Abstract][Full Text] [Related]
9. Restriction fragment length polymorphisms and single germline coding region sequence in VH18/2, a duplicated gene encoding autoantibody.
Rubinstein DB; Symann M; Stewart AK; Guillaume T
Mol Immunol; 1993 Mar; 30(4):403-12. PubMed ID: 8096063
[TBL] [Abstract][Full Text] [Related]
10. Selective activation of VH3A10+ rheumatoid factor producing B cells by staphylococcal enterotoxin D.
Xie C; Brühl H; He X; Weyand CM; Goronzy JJ
Int Immunol; 1995 Mar; 7(3):425-34. PubMed ID: 7794822
[TBL] [Abstract][Full Text] [Related]
11. Clonal analysis of a human antibody response. II. Sequences of the VH genes of human IgM, IgG, and IgA to rabies virus reveal preferential utilization of VHIII segments and somatic hypermutation.
Ikematsu H; Harindranath N; Ueki Y; Notkins AL; Casali P
J Immunol; 1993 Feb; 150(4):1325-37. PubMed ID: 8432980
[TBL] [Abstract][Full Text] [Related]
12. Antibody repertoire development in fetal and neonatal piglets. I. Four VH genes account for 80 percent of VH usage during 84 days of fetal life.
Sun J; Hayward C; Shinde R; Christenson R; Ford SP; Butler JE
J Immunol; 1998 Nov; 161(9):5070-8. PubMed ID: 9794445
[TBL] [Abstract][Full Text] [Related]
13. Analysis of the genes encoding the variable regions of human IgG rheumatoid factor.
Ezaki I; Shingu M; Hashimoto M; Isayama T; Tohmatsu J; Kanda H; Nobunaga M; Watanabe T
J Rheumatol; 1994 Nov; 21(11):2005-10. PubMed ID: 7869301
[TBL] [Abstract][Full Text] [Related]
14. Analysis of the human VH gene repertoire. Differential effects of selection and somatic hypermutation on human peripheral CD5(+)/IgM+ and CD5(-)/IgM+ B cells.
Brezinschek HP; Foster SJ; Brezinschek RI; Dörner T; Domiati-Saad R; Lipsky PE
J Clin Invest; 1997 May; 99(10):2488-501. PubMed ID: 9153293
[TBL] [Abstract][Full Text] [Related]
15. The repertoire of human germline VH sequences reveals about fifty groups of VH segments with different hypervariable loops.
Tomlinson IM; Walter G; Marks JD; Llewelyn MB; Winter G
J Mol Biol; 1992 Oct; 227(3):776-98. PubMed ID: 1404388
[TBL] [Abstract][Full Text] [Related]
16. Diversification, not use, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome.
Haire RN; Buell RD; Litman RT; Ohta Y; Fu SM; Honjo T; Matsuda F; de la Morena M; Carro J; Good RA
J Exp Med; 1993 Sep; 178(3):825-34. PubMed ID: 8350056
[TBL] [Abstract][Full Text] [Related]
17. Individual VH genes detected with oligonucleotide probes from the complementarity-determining regions.
Guillaume T; Rubinstein DB; Young F; Tucker L; Logtenberg T; Schwartz RS; Barrett KJ
J Immunol; 1990 Sep; 145(6):1934-45. PubMed ID: 2118157
[TBL] [Abstract][Full Text] [Related]
18. V region diversity in human anti-insulin antibodies. Preferential use of a VHIII gene subset.
Thomas JW
J Immunol; 1993 Feb; 150(4):1375-82. PubMed ID: 8432983
[TBL] [Abstract][Full Text] [Related]
19. Human rheumatoid factors with restrictive specificity for rabbit immunoglobulin G: auto- and multi-reactivity, diverse VH gene segment usage and preferential usage of V lambda IIIb.
Fang Q; Kannapell CC; Gaskin F; Solomon A; Koopman WJ; Fu SM
J Exp Med; 1994 May; 179(5):1445-56. PubMed ID: 7545920
[TBL] [Abstract][Full Text] [Related]
20. By-passing immunisation. Human antibodies from synthetic repertoires of germline VH gene segments rearranged in vitro.
Hoogenboom HR; Winter G
J Mol Biol; 1992 Sep; 227(2):381-8. PubMed ID: 1404359
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
