656 related articles for article (PubMed ID: 9759863)
1. Differential usage of VH gene segments is mediated by cis elements.
Yu CC; Larijani M; Miljanic IN; Wu GE
J Immunol; 1998 Oct; 161(7):3444-54. PubMed ID: 9759863
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. VDJ genes in VHa2 allotype-suppressed rabbits. Limited germline VH gene usage and accumulation of somatic mutations in D regions.
Short JA; Sethupathi P; Zhai SK; Knight KL
J Immunol; 1991 Dec; 147(11):4014-8. PubMed ID: 1940383
[TBL] [Abstract][Full Text] [Related]
4. Biased VH gene usage in early lineage human B cells: evidence for preferential Ig gene rearrangement in the absence of selection.
Rao SP; Riggs JM; Friedman DF; Scully MS; LeBien TW; Silberstein LE
J Immunol; 1999 Sep; 163(5):2732-40. PubMed ID: 10453015
[TBL] [Abstract][Full Text] [Related]
5. Rearrangement of upstream DH and VH genes to a rearranged immunoglobulin variable region gene inserted into the DQ52-JH region of the immunoglobulin heavy chain locus.
Taki S; Schwenk F; Rajewsky K
Eur J Immunol; 1995 Jul; 25(7):1888-96. PubMed ID: 7621865
[TBL] [Abstract][Full Text] [Related]
6. No evidence for the use of DIR, D-D fusions, chromosome 15 open reading frames or VH replacement in the peripheral repertoire was found on application of an improved algorithm, JointML, to 6329 human immunoglobulin H rearrangements.
Ohm-Laursen L; Nielsen M; Larsen SR; Barington T
Immunology; 2006 Oct; 119(2):265-77. PubMed ID: 17005006
[TBL] [Abstract][Full Text] [Related]
7. Abbreviated junctional sequences impoverish antibody diversity in urodele amphibians.
Patel HM; Hsu E
J Immunol; 1997 Oct; 159(7):3391-9. PubMed ID: 9317138
[TBL] [Abstract][Full Text] [Related]
8. Interdependence of N nucleotide addition and recombination site choice in V(D)J rearrangement.
Kepler TB; Borrero M; Rugerio B; McCray SK; Clarke SH
J Immunol; 1996 Nov; 157(10):4451-7. PubMed ID: 8906821
[TBL] [Abstract][Full Text] [Related]
9. Analysis of direct and inverted DJH rearrangements in a human Ig heavy chain transgenic minilocus.
Tuaillon N; Miller AB; Tucker PW; Capra JD
J Immunol; 1995 Jun; 154(12):6453-65. PubMed ID: 7759881
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Deletion of the DQ52 element within the Ig heavy chain locus leads to a selective reduction in VDJ recombination and altered D gene usage.
Nitschke L; Kestler J; Tallone T; Pelkonen S; Pelkonen J
J Immunol; 2001 Feb; 166(4):2540-52. PubMed ID: 11160315
[TBL] [Abstract][Full Text] [Related]
12. Antibody repertoires generated by VH replacement and direct VH to JH joining.
Koralov SB; Novobrantseva TI; Königsmann J; Ehlich A; Rajewsky K
Immunity; 2006 Jul; 25(1):43-53. PubMed ID: 16860756
[TBL] [Abstract][Full Text] [Related]
13. Immunoglobulin variable region heptamer-nonamer recognition sequence joined to rearranged D-J segment: implications for the immunoglobulin recombinase mechanism.
Stenzel-Poore MP; Rittenberg MB
J Immunol; 1987 May; 138(9):3055-9. PubMed ID: 3106497
[TBL] [Abstract][Full Text] [Related]
14. An immunoglobulin heavy chain variable region gene is generated from three segments of DNA: VH, D and JH. 1980.
Early P; Huang H; Davis M; Calame K; Hood L
J Immunol; 2004 Dec; 173(11):6503-14. PubMed ID: 15557138
[No Abstract] [Full Text] [Related]
15. Biased utilization of DHQ52 and JH4 gene segments in a human Ig transgenic minilocus is independent of antigenic selection.
Tuaillon N; Miller AB; Longberg N; Tucker PW; Capra JD
J Immunol; 1994 Mar; 152(6):2912-20. PubMed ID: 8144892
[TBL] [Abstract][Full Text] [Related]
16. A novel VH to VHDJH joining mechanism in heavy-chain-negative (null) pre-B cells results in heavy-chain production.
Reth M; Gehrmann P; Petrac E; Wiese P
Nature; 1986 Aug 28-Sep 3; 322(6082):840-2. PubMed ID: 3092105
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. The expression of the Ig H chain repertoire in developing bone marrow B lineage cells.
Decker DJ; Boyle NE; Koziol JA; Klinman NR
J Immunol; 1991 Jan; 146(1):350-61. PubMed ID: 1898607
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
