These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 17292963)

  • 1. Homology-directed recombination in IgH variable region genes from human neonates, infants and adults: implications for junctional diversity.
    Bauer K; Hummel M; Berek C; Paar C; Rosenberger C; Kerzel S; Versmold H; Zemlin M
    Mol Immunol; 2007 Apr; 44(11):2969-77. PubMed ID: 17292963
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Ig VH, DH, and JH germ-line gene segments linked by overlapping cosmid clones of rabbit DNA.
    Becker RS; Zhai SK; Currier SJ; Knight KL
    J Immunol; 1989 Feb; 142(4):1351-5. PubMed ID: 2492580
    [TBL] [Abstract][Full Text] [Related]  

  • 4. At least five DH genes of human immunoglobulin heavy chains are encoded in 9-kilobase DNA fragments.
    Ichihara Y; Abe M; Yasui H; Matsuoka H; Kurosawa Y
    Eur J Immunol; 1988 Apr; 18(4):649-52. PubMed ID: 3130268
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of homology-directed recombination in VDJ junctions from cytoplasmic Ig- pre-B cells of newborn mice.
    Chukwuocha RU; Nadel B; Feeney AJ
    J Immunol; 1995 Feb; 154(3):1246-55. PubMed ID: 7822793
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Abnormal recombination of Igh D and J gene segments in transformed pre-B cells of scid mice.
    Kim MG; Schuler W; Bosma MJ; Marcu KB
    J Immunol; 1988 Aug; 141(4):1341-7. PubMed ID: 3135329
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Extent to which homology can constrain coding exon junctional diversity in V(D)J recombination.
    Gerstein RM; Lieber MR
    Nature; 1993 Jun; 363(6430):625-7. PubMed ID: 8510753
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cloning of a human immunoglobulin gene fragment containing both VH-D and D-JH rearrangements: implication for VH-D as an intermediate to VH-D-JH formation.
    Shin EK; Matsuda F; Fujikura J; Akamizu T; Sugawa H; Mori T; Honjo T
    Eur J Immunol; 1993 Sep; 23(9):2365-7. PubMed ID: 8370413
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Use of UITma DNA polymerase improves the PCR detection of rearranged immunoglobulin heavy chain CDR3 junctions.
    Linke B; Bolz I; Pott C; Hiddemann W; Kneba M
    Leukemia; 1995 Dec; 9(12):2133-7. PubMed ID: 8609729
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. N sequences, P nucleotides and short sequence homologies at junctional sites in VH to VHDJH and VHDJH to JH joining.
    Komori T; Sugiyama H
    Mol Immunol; 1993 Nov; 30(16):1393-8. PubMed ID: 8232324
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Preferential usage of JH2 in D-J joinings with DQ52 is determined by the primary DNA sequence and is largely dependent on recombination signal sequences.
    Suzuki H; Shiku H
    Eur J Immunol; 1992 Sep; 22(9):2225-30. PubMed ID: 1516615
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evolution of specific antigen recognition: size reduction and restricted length distribution of the CDRH3 regions in the rainbow trout.
    Roman T; De Guerra A; Charlemagne J
    Eur J Immunol; 1995 Jan; 25(1):269-73. PubMed ID: 7843242
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The pattern of joining (JH) gene usage in the human IgH chain is established predominantly at the B precursor cell stage.
    Wasserman R; Ito Y; Galili N; Yamada M; Reichard BA; Shane S; Lange B; Rovera G
    J Immunol; 1992 Jul; 149(2):511-6. PubMed ID: 1624797
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Direct in vivo VH to JH rearrangement violating the 12/23 rule.
    Koralov SB; Novobrantseva TI; Hochedlinger K; Jaenisch R; Rajewsky K
    J Exp Med; 2005 Feb; 201(3):341-8. PubMed ID: 15699070
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Germ-line sequence of the DH segment employed in Ars-A antibodies: implications for the generation of junctional diversity.
    Landolfi NF; Capra JD; Tucker PW
    J Immunol; 1986 Jul; 137(1):362-5. PubMed ID: 3011910
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel VHDJH to JH joining that induces H chain production in an Ig-null immature B cell line.
    Komori T; Sugiyama H; Kishimoto S
    J Immunol; 1989 Aug; 143(3):1040-5. PubMed ID: 2501385
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Major reorganization of immunoglobulin VH segmental elements during vertebrate evolution.
    Hinds KR; Litman GW
    Nature; 1986 Apr 10-16; 320(6062):546-9. PubMed ID: 3083268
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.