96 related articles for article (PubMed ID: 2498431)
1. Interspersion of the VHQ52 and VH7183 gene families in the NFS/N mouse.
Kleinfield RW; Weigert MG
J Immunol; 1989 Jun; 142(12):4483-92. PubMed ID: 2498431
[TBL] [Abstract][Full Text] [Related]
2. Analysis of VH gene replacement events in a B cell lymphoma.
Kleinfield RW; Weigert MG
J Immunol; 1989 Jun; 142(12):4475-82. PubMed ID: 2498430
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A single VH gene is utilized predominantly in anti-BrMRBC hybridomas derived from purified Ly-1 B cells. Definition of the VH11 family.
Hardy RR; Carmack CE; Shinton SA; Riblet RJ; Hayakawa K
J Immunol; 1989 May; 142(10):3643-51. PubMed ID: 2497178
[TBL] [Abstract][Full Text] [Related]
5. Deletional mapping of fifteen mouse VH gene families reveals a common organization for three Igh haplotypes.
Mainville CA; Sheehan KM; Klaman LD; Giorgetti CA; Press JL; Brodeur PH
J Immunol; 1996 Feb; 156(3):1038-46. PubMed ID: 8557977
[TBL] [Abstract][Full Text] [Related]
6. VH gene family repertoire of resting B cells. Preferential use of D-proximal families early in development may be due to distinct B cell subsets.
Jeong HD; Teale JM
J Immunol; 1989 Oct; 143(8):2752-60. PubMed ID: 2507637
[TBL] [Abstract][Full Text] [Related]
7. The sheep Ig variable region repertoire consists of a single VH family.
Dufour V; Malinge S; Nau F
J Immunol; 1996 Mar; 156(6):2163-70. PubMed ID: 8690905
[TBL] [Abstract][Full Text] [Related]
8. Recombination between an expressed immunoglobulin heavy-chain gene and a germline variable gene segment in a Ly 1+ B-cell lymphoma.
Kleinfield R; Hardy RR; Tarlinton D; Dangl J; Herzenberg LA; Weigert M
Nature; 1986 Aug 28-Sep 3; 322(6082):843-6. PubMed ID: 3092106
[TBL] [Abstract][Full Text] [Related]
9. Eleven MRL-lpr/lpr anti-DNA autoantibodies are encoded by genes from four VH gene families: a potentially biased usage of VH genes.
Trepicchio W; Barrett KJ
J Immunol; 1987 Apr; 138(7):2323-31. PubMed ID: 3104460
[TBL] [Abstract][Full Text] [Related]
10. Structure, map position, and evolution of two newly diverged mouse Ig VH gene families.
Tutter A; Brodeur P; Shlomchik M; Riblet R
J Immunol; 1991 Nov; 147(9):3215-23. PubMed ID: 1680926
[TBL] [Abstract][Full Text] [Related]
11. B lymphocyte selection and age-related changes in VH gene usage in mutant Alicia rabbits.
Zhu X; Boonthum A; Zhai SK; Knight KL
J Immunol; 1999 Sep; 163(6):3313-20. PubMed ID: 10477601
[TBL] [Abstract][Full Text] [Related]
12. Selective use of the VHQ52 family in functional VH to DJH rearrangements in a B precursor cell line.
Sugiyama H; Maeda T; Tani Y; Miyake S; Oka Y; Komori T; Ogawa H; Soma T; Minami Y; Sakato N
J Exp Med; 1987 Aug; 166(2):607-12. PubMed ID: 3110357
[TBL] [Abstract][Full Text] [Related]
13. Unusual immunoglobulin DNA sequences from the nonexpressed chromosome of mouse normal B lymphocytes: implications for allelic exclusion and the DNA rearrangement process.
Nottenburg C; St John T; Weissman IL
J Immunol; 1987 Sep; 139(5):1718-26. PubMed ID: 3114375
[TBL] [Abstract][Full Text] [Related]
14. Comparison of V kappa gene family expression in adult and fetal B cells.
Teale JM; Morris EG
J Immunol; 1989 Oct; 143(8):2768-72. PubMed ID: 2507639
[TBL] [Abstract][Full Text] [Related]
15. Analysis of Ig H chain gene segment utilization in human fetal liver. Revisiting the "proximal utilization hypothesis".
Pascual V; Verkruyse L; Casey ML; Capra JD
J Immunol; 1993 Oct; 151(8):4164-72. PubMed ID: 8409393
[TBL] [Abstract][Full Text] [Related]
16. Ontogeny of the heavy chain immunoglobulin repertoire in fetal liver and bone marrow.
Delassus S; Darche S; Kourilsky P; Cumano A
J Immunol; 1998 Apr; 160(7):3274-80. PubMed ID: 9531284
[TBL] [Abstract][Full Text] [Related]
17. Frequency of VH81x usage during B cell development: initial decline in usage is independent of Ig heavy chain cell surface expression.
Marshall AJ; Wu GE; Paige GJ
J Immunol; 1996 Mar; 156(6):2077-84. PubMed ID: 8690895
[TBL] [Abstract][Full Text] [Related]
18. Mouse VH7183 recombination signal sequences mediate recombination more frequently than those of VHJ558.
Connor AM; Fanning LJ; Celler JW; Hicks LK; Ramsden DA; Wu GE
J Immunol; 1995 Dec; 155(11):5268-72. PubMed ID: 7594539
[TBL] [Abstract][Full Text] [Related]
19. The utilization of individual VH exons in the primary repertoire of adult BALB/c mice.
Sheehan KM; Mainville CA; Willert S; Brodeur PH
J Immunol; 1993 Nov; 151(10):5364-75. PubMed ID: 8228231
[TBL] [Abstract][Full Text] [Related]
20. Molecular analysis of heavy and light chains used by primary and secondary anti-(T,G)-A--L antibodies produced by normal and xid mice.
Busto P; Gerstein R; Dupre L; Giorgetti CA; Selsing E; Press JL
J Immunol; 1987 Jul; 139(2):608-18. PubMed ID: 3110274
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]