514 related articles for article (PubMed ID: 7511648)
1. Limited junctional diversity in kappa light chains. Junctional sequences from CD43+B220+ early B cell progenitors resemble those from peripheral B cells.
Victor KD; Vu K; Feeney AJ
J Immunol; 1994 Apr; 152(7):3467-75. PubMed ID: 7511648
[TBL] [Abstract][Full Text] [Related]
2. Extensive junctional diversity in Ig light chain genes from early B cell progenitors of mu MT mice.
Bentolila LA; Olson S; Marshall A; Rougeon F; Paige CJ; Doyen N; Wu GE
J Immunol; 1999 Feb; 162(4):2123-8. PubMed ID: 9973486
[TBL] [Abstract][Full Text] [Related]
3. Clonal analysis of a human antibody response. III. Nucleotide sequences of monoclonal IgM, IgG, and IgA to rabies virus reveal restricted V kappa gene utilization, junctional V kappa J kappa and V lambda J lambda diversity, and somatic hypermutation.
Ikematsu W; Kobarg J; Ikematsu H; Ichiyoshi Y; Casali P
J Immunol; 1998 Sep; 161(6):2895-905. PubMed ID: 9743351
[TBL] [Abstract][Full Text] [Related]
4. Predominance of the prototypic T15 anti-phosphorylcholine junctional sequence in neonatal pre-B cells.
Feeney AJ
J Immunol; 1991 Dec; 147(12):4343-50. PubMed ID: 1753104
[TBL] [Abstract][Full Text] [Related]
5. Evidence that the V kappa III gene usage is nonstochastic in both adult and newborn peripheral B cells and that peripheral CD5+ adult B cells are oligoclonal.
Weber JC; Blaison G; Martin T; Knapp AM; Pasquali JL
J Clin Invest; 1994 May; 93(5):2093-105. PubMed ID: 7514192
[TBL] [Abstract][Full Text] [Related]
6. Asymmetric contribution to Ig repertoire diversity by V kappa exons: differences in the utilization of V kappa 10 exons.
Fitzsimmons SP; Rotz BT; Shapiro MA
J Immunol; 1998 Sep; 161(5):2290-300. PubMed ID: 9725223
[TBL] [Abstract][Full Text] [Related]
7. Immunoglobulin gene rearrangement during pre-B cell differentiation.
Coffman RL; Weissman IL
J Mol Cell Immunol; 1983; 1(1):31-41. PubMed ID: 6336590
[TBL] [Abstract][Full Text] [Related]
8. Status of kappa L chain gene rearrangements and c-kit and IL-7 receptor expression in stromal cell-dependent pre-B cells.
Henderson AJ; Narayanan R; Collins L; Dorshkind K
J Immunol; 1992 Sep; 149(6):1973-9. PubMed ID: 1381391
[TBL] [Abstract][Full Text] [Related]
9. Extensive junctional diversity of Ig heavy chain rearrangements generated in the progeny of single fetal multipotent hematopoietic cells in the absence of selection.
Nourrit F; Doyen N; Kourilsky P; Rougeon F; Cumano A
J Immunol; 1998 May; 160(9):4254-61. PubMed ID: 9574527
[TBL] [Abstract][Full Text] [Related]
10. B cell deletion, anergy, and receptor editing in "knock in" mice targeted with a germline-encoded or somatically mutated anti-DNA heavy chain.
Pewzner-Jung Y; Friedmann D; Sonoda E; Jung S; Rajewsky K; Eilat D
J Immunol; 1998 Nov; 161(9):4634-45. PubMed ID: 9794392
[TBL] [Abstract][Full Text] [Related]
11. Kappa light chain rearrangement in mouse fetal liver.
Ramsden DA; Paige CJ; Wu GE
J Immunol; 1994 Aug; 153(3):1150-60. PubMed ID: 8027546
[TBL] [Abstract][Full Text] [Related]
12. Neonatal and adult primary B cells use the same germ-line VH and V kappa genes in their (T,G)-A-L-specific repertoire.
Borriero L; Giorgetti C; Smith G; Landry D; Selsing E; Zhukovsky E; Press JL
J Immunol; 1990 Jan; 144(2):583-92. PubMed ID: 2129539
[TBL] [Abstract][Full Text] [Related]
13. Structure of rearranged and germ-line rabbit V kappa genes indicated that the CDR3 is encoded by the V kappa gene.
Ayadi H; Cazenave PA; Marche PN
Eur J Immunol; 1990 Feb; 20(2):259-64. PubMed ID: 2107083
[TBL] [Abstract][Full Text] [Related]
14. Predominance of VH-D-JH junctions occurring at sites of short sequence homology results in limited junctional diversity in neonatal antibodies.
Feeney AJ
J Immunol; 1992 Jul; 149(1):222-9. PubMed ID: 1607655
[TBL] [Abstract][Full Text] [Related]
15. Rearrangement and selection in the developing Vkappa repertoire of the mouse: an analysis of the usage of two Vkappa gene segments.
Whitcomb EA; Brodeur PH
J Immunol; 1998 May; 160(10):4904-13. PubMed ID: 9590238
[TBL] [Abstract][Full Text] [Related]
16. Utilization of V kappa families and V kappa exons. Implications for the available B cell repertoire.
Kalled SL; Brodeur PH
J Immunol; 1991 Nov; 147(9):3194-200. PubMed ID: 1919010
[TBL] [Abstract][Full Text] [Related]
17. Constitutive expression of terminal deoxynucleotidyl transferase in transgenic mice is sufficient for N region diversity to occur at any Ig locus throughout B cell differentiation.
Bentolila LA; Wu GE; Nourrit F; Fanton d'Andon M; Rougeon F; Doyen N
J Immunol; 1997 Jan; 158(2):715-23. PubMed ID: 8992987
[TBL] [Abstract][Full Text] [Related]
18. Molecular analysis of the V kappa III-J kappa junctional diversity of polyclonal rheumatoid factors during rheumatoid arthritis frequently reveals N addition.
Martin T; Blaison G; Levallois H; Pasquali JL
Eur J Immunol; 1992 Jul; 22(7):1773-9. PubMed ID: 1339352
[TBL] [Abstract][Full Text] [Related]
19. Ig heavy chain protein controls B cell development by regulating germ-line transcription and retargeting V(D)J recombination.
Schlissel MS; Morrow T
J Immunol; 1994 Aug; 153(4):1645-57. PubMed ID: 8046237
[TBL] [Abstract][Full Text] [Related]
20. Pre-B cell receptor-mediated selection of pre-B cells synthesizing functional mu heavy chains.
Kline GH; Hartwell L; Beck-Engeser GB; Keyna U; Zaharevitz S; Klinman NR; Jäck HM
J Immunol; 1998 Aug; 161(4):1608-18. PubMed ID: 9712022
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
