BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 8972854)

  • 1. B-lineage regulated polyadenylation occurs on weak poly(A) sites regardless of sequence composition at the cleavage and downstream regions.
    Matis SA; Martincic K; Milcarek C
    Nucleic Acids Res; 1996 Dec; 24(23):4684-92. PubMed ID: 8972854
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Plasma cell-regulated polyadenylation at the Ig gamma 2b secretion-specific poly(A) site.
    Lassman CR; Matis S; Hall BL; Toppmeyer DL; Milcarek C
    J Immunol; 1992 Feb; 148(4):1251-60. PubMed ID: 1346622
    [TBL] [Abstract][Full Text] [Related]  

  • 3. B-cell and plasma-cell splicing differences: a potential role in regulated immunoglobulin RNA processing.
    Bruce SR; Dingle RW; Peterson ML
    RNA; 2003 Oct; 9(10):1264-73. PubMed ID: 13130140
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The regulated production of mu m and mu s mRNA is dependent on the relative efficiencies of mu s poly(A) site usage and the c mu 4-to-M1 splice.
    Peterson ML; Perry RP
    Mol Cell Biol; 1989 Feb; 9(2):726-38. PubMed ID: 2565533
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inducible nuclear factors binding the IgM heavy chain pre-mRNA secretory poly(A) site.
    Phillips C; Schimpl A; Dietrich-Goetz W; Clements JB; Virtanen A
    Eur J Immunol; 1996 Dec; 26(12):3144-52. PubMed ID: 8977316
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An RNA polymerase pause site is associated with the immunoglobulin mus poly(A) site.
    Peterson ML; Bertolino S; Davis F
    Mol Cell Biol; 2002 Aug; 22(15):5606-15. PubMed ID: 12101252
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The binding of a subunit of the general polyadenylation factor cleavage-polyadenylation specificity factor (CPSF) to polyadenylation sites changes during B cell development.
    Edwalds-Gilbert G; Milcarek C
    Nucleic Acids Symp Ser; 1995; (33):229-33. PubMed ID: 8643379
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exon size affects competition between splicing and cleavage-polyadenylation in the immunoglobulin mu gene.
    Peterson ML; Bryman MB; Peiter M; Cowan C
    Mol Cell Biol; 1994 Jan; 14(1):77-86. PubMed ID: 7903422
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Definition of essential sequences and functional equivalence of elements downstream of the adenovirus E2A and the early simian virus 40 polyadenylation sites.
    Hart RP; McDevitt MA; Ali H; Nevins JR
    Mol Cell Biol; 1985 Nov; 5(11):2975-83. PubMed ID: 3018490
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The 3'-untranslated region of membrane exon 2 from the gamma 2a immunoglobulin gene contributes to efficient transcription termination.
    Flaspohler JA; Boczkowski D; Hall BL; Milcarek C
    J Biol Chem; 1995 May; 270(20):11903-11. PubMed ID: 7744841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis of two mRNAs by utilization of alternate polyadenylation sites: expression of SV40-mouse immunoglobulin mu chain gene recombinants in Cos monkey cells.
    Nishikura K; Vuocolo GA
    EMBO J; 1984 Apr; 3(4):689-99. PubMed ID: 6327285
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myelomas and lymphomas expressing the Ig gamma 2a H chain gene have similar transcription termination regions.
    Flaspohler JA; Milcarek C
    J Immunol; 1990 Apr; 144(7):2802-10. PubMed ID: 2108214
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Regulation of poly(A) site use during mouse B-cell development involves a change in the binding of a general polyadenylation factor in a B-cell stage-specific manner.
    Edwalds-Gilbert G; Milcarek C
    Mol Cell Biol; 1995 Nov; 15(11):6420-9. PubMed ID: 7565794
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regulated immunoglobulin (Ig) RNA processing does not require specific cis-acting sequences: non-Ig RNA can be alternatively processed in B cells and plasma cells.
    Peterson ML
    Mol Cell Biol; 1994 Dec; 14(12):7891-8. PubMed ID: 7969129
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Alternative processing of IgA pre-mRNA responds like IgM to alterations in the efficiency of the competing splice and cleavage-polyadenylation reactions.
    Seipelt RL; Peterson ML
    Mol Immunol; 1995 Mar; 32(4):277-85. PubMed ID: 7723773
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Polyadenylation at a cryptic site in the pBR322 portion of pSV2-neo: prevention of its utilization by the SV40 late poly(A) signal.
    Kessler MM; Westhafer MA; Carson DD; Nordstrom JL
    Nucleic Acids Res; 1987 Jan; 15(2):631-42. PubMed ID: 3029687
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The developmentally regulated shift from membrane to secreted mu mRNA production is accompanied by an increase in cleavage-polyadenylation efficiency but no measurable change in splicing efficiency.
    Peterson ML; Gimmi ER; Perry RP
    Mol Cell Biol; 1991 Apr; 11(4):2324-7. PubMed ID: 1826045
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Balanced efficiencies of splicing and cleavage-polyadenylation are required for mu-s and mu-m mRNA regulation.
    Peterson ML
    Gene Expr; 1992; 2(4):319-27. PubMed ID: 1361868
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Regulated expression of the mouse gamma 2b Ig H chain gene is influenced by polyA site order and strength.
    Lassman CR; Milcarek C
    J Immunol; 1992 Apr; 148(8):2578-85. PubMed ID: 1560212
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiple features contribute to the use of the immunoglobulin M secretion-specific poly(A) signal but are not required for developmental regulation.
    Peterson ML; Bingham GL; Cowan C
    Mol Cell Biol; 2006 Sep; 26(18):6762-71. PubMed ID: 16943419
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.