BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 3463933)

  • 1. Globin gene transcripts can utilize histone gene 3' end processing signals.
    Whitelaw E; Coates A; Proudfoot NJ
    Nucleic Acids Res; 1986 Sep; 14(17):7059-70. PubMed ID: 3463933
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Alpha-thalassaemia caused by a poly(A) site mutation reveals that transcriptional termination is linked to 3' end processing in the human alpha 2 globin gene.
    Whitelaw E; Proudfoot N
    EMBO J; 1986 Nov; 5(11):2915-22. PubMed ID: 3024968
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Introns in histone genes alter the distribution of 3' ends.
    Pandey NB; Chodchoy N; Liu TJ; Marzluff WF
    Nucleic Acids Res; 1990 Jun; 18(11):3161-70. PubMed ID: 2356116
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 3' RNA processing efficiency plays a primary role in generating termination-competent RNA polymerase II elongation complexes.
    Edwalds-Gilbert G; Prescott J; Falck-Pedersen E
    Mol Cell Biol; 1993 Jun; 13(6):3472-80. PubMed ID: 7684499
    [TBL] [Abstract][Full Text] [Related]  

  • 5. RNA processing of beta-globin transcripts containing 5' flanking and structural gene sequences.
    Winicov I
    Nucleic Acids Res; 1988 Jan; 16(2):593-607. PubMed ID: 2829132
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Thalassemia due to a mutation in the cleavage-polyadenylation signal of the human beta-globin gene.
    Orkin SH; Cheng TC; Antonarakis SE; Kazazian HH
    EMBO J; 1985 Feb; 4(2):453-6. PubMed ID: 4018033
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Coupling of replication type histone mRNA levels to DNA synthesis requires the stem-loop sequence at the 3' end of the mRNA.
    Levine BJ; Chodchoy N; Marzluff WF; Skoultchi AI
    Proc Natl Acad Sci U S A; 1987 Sep; 84(17):6189-93. PubMed ID: 2888112
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Definition of an efficient synthetic poly(A) site.
    Levitt N; Briggs D; Gil A; Proudfoot NJ
    Genes Dev; 1989 Jul; 3(7):1019-25. PubMed ID: 2570734
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 3' Processing and termination of mouse histone transcripts synthesized in vitro by RNA polymerase II.
    Gu X; Marzluff WF
    Nucleic Acids Res; 1996 Oct; 24(19):3797-805. PubMed ID: 8871561
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Polyadenylation and U7 snRNP-mediated cleavage: alternative modes of RNA 3' processing in two avian histone H1 genes.
    Kirsh AL; Groudine M; Challoner PB
    Genes Dev; 1989 Dec; 3(12B):2172-9. PubMed ID: 2576416
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sequence divergence in the 3' untranslated regions of human zeta- and alpha-globin mRNAs mediates a difference in their stabilities and contributes to efficient alpha-to-zeta gene development switching.
    Russell JE; Morales J; Makeyev AV; Liebhaber SA
    Mol Cell Biol; 1998 Apr; 18(4):2173-83. PubMed ID: 9528789
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A chimeric mouse histone H4 gene containing either an intron or poly(A) addition signal behaves like a basal histone.
    Seiler-Tuyns A; Paterson BM
    Nucleic Acids Res; 1986 Nov; 14(22):8845-62. PubMed ID: 3024121
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Occlusion of the HIV poly(A) site.
    Weichs an der Glon C; Monks J; Proudfoot NJ
    Genes Dev; 1991 Feb; 5(2):244-53. PubMed ID: 1995416
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regulation of histone and beta A-globin gene expression during differentiation of chicken erythroid cells.
    Affolter M; Côté J; Renaud J; Ruiz-Carrillo A
    Mol Cell Biol; 1987 Oct; 7(10):3663-72. PubMed ID: 3119991
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Polyadenylation of the Xenopus beta 1 globin mRNA at a downstream minor site in the absence of the major site and utilization of an AAUACA polyadenylation signal.
    Mason PJ; Jones MB; Elkington JA; Williams JG
    EMBO J; 1985 Jan; 4(1):205-11. PubMed ID: 2862026
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The gene for theta-globin is transcribed in human fetal erythroid tissues.
    Leung S; Proudfoot NJ; Whitelaw E
    Nature; 1987 Oct 8-14; 329(6139):551-4. PubMed ID: 3657976
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Beta-globin gene promoter generates 5' truncated transcripts in the embryonic/fetal erythroid environment.
    Khazaie K; Gounari F; Antoniou M; deBoer E; Grosveld F
    Nucleic Acids Res; 1986 Sep; 14(18):7199-212. PubMed ID: 2429259
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Efficient 3'-end formation of human beta-globin mRNA in vivo requires sequences within the last intron but occurs independently of the splicing reaction.
    Antoniou M; Geraghty F; Hurst J; Grosveld F
    Nucleic Acids Res; 1998 Feb; 26(3):721-9. PubMed ID: 9443963
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The complete nucleotide sequence of the duck alpha A-globin gene.
    Erbil C; Niessing J
    Gene; 1982 Dec; 20(2):211-7. PubMed ID: 7166233
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two mutations in the beta-globin polyadenylylation signal reveal extended transcripts and new RNA polyadenylylation sites.
    Rund D; Dowling C; Najjar K; Rachmilewitz EA; Kazazian HH; Oppenheim A
    Proc Natl Acad Sci U S A; 1992 May; 89(10):4324-8. PubMed ID: 1374896
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.