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 *

114 related articles for article (PubMed ID: 2582366)

  • 1. A beta zero-thalassemic beta-globin RNA that is labile in bone marrow cells is relatively stable in HeLa cells.
    Maquat LE; Kinniburgh AJ
    Nucleic Acids Res; 1985 Apr; 13(8):2855-67. PubMed ID: 2582366
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel metabolism of several beta zero-thalassemic beta-globin mRNAs in the erythroid tissues of transgenic mice.
    Lim S; Mullins JJ; Chen CM; Gross KW; Maquat LE
    EMBO J; 1989 Sep; 8(9):2613-9. PubMed ID: 2573525
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Processing of human beta-globin mRNA precursor to mRNA is defective in three patients with beta+-thalassemia.
    Maquat LE; Kinniburgh AJ; Beach LR; Honig GR; Lazerson J; Ershler WB; Ross J
    Proc Natl Acad Sci U S A; 1980 Jul; 77(7):4287-91. PubMed ID: 6933479
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Equal stabilities of normal beta globin and nontranslatable beta0 -39 thalassemic transcripts in cell-free extracts.
    Stolle CA; Payne MS; Benz EJ
    Blood; 1987 Jul; 70(1):293-300. PubMed ID: 3593968
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Human beta-globin mRNAs that harbor a nonsense codon are degraded in murine erythroid tissues to intermediates lacking regions of exon I or exons I and II that have a cap-like structure at the 5' termini.
    Lim SK; Maquat LE
    EMBO J; 1992 Sep; 11(9):3271-8. PubMed ID: 1324170
    [TBL] [Abstract][Full Text] [Related]  

  • 6. mRNA-deficient beta o-thalassemia results from a single nucleotide deletion.
    Kinniburgh AJ; Maquat LE; Schedl T; Rachmilewitz E; Ross J
    Nucleic Acids Res; 1982 Sep; 10(18):5421-7. PubMed ID: 6292840
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Beta + thalassemia: aberrant splicing results from a single point mutation in an intron.
    Busslinger M; Moschonas N; Flavell RA
    Cell; 1981 Dec; 27(2 Pt 1):289-98. PubMed ID: 6895866
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nonsense codons in human beta-globin mRNA result in the production of mRNA degradation products.
    Lim SK; Sigmund CD; Gross KW; Maquat LE
    Mol Cell Biol; 1992 Mar; 12(3):1149-61. PubMed ID: 1545796
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Heterogeneity of globin protein synthesis in bone marrow cells of patients with homozygous beta-thalassemia from Tadzhikistan].
    Nasyrova FIu; Mirakilova AM; Ryzhova IB; Sabzanova RB; Limborskaia SA
    Mol Gen Mikrobiol Virusol; 1988 Oct; (10):34-40. PubMed ID: 2976480
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular defects in beta-thalassemia.
    Nienhuis AW; Ley T; Pepe G; Tam J; Kantor J
    Birth Defects Orig Artic Ser; 1982; 18(7):69-79. PubMed ID: 6186315
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Heterogeneity of beta-thalassemia in Azerbaidzhan.
    Dergunova LV; Ryskov AP; Slominsky PA; Rustamov RS; Limborska SA
    Haematologia (Budap); 1984; 17(4):473-81. PubMed ID: 6241915
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unstable beta-globin mRNA in mRNA-deficient beta o thalassemia.
    Maquat LE; Kinniburgh AJ; Rachmilewitz EA; Ross J
    Cell; 1981 Dec; 27(3 Pt 2):543-53. PubMed ID: 6101206
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A single-base change at a splice site in a beta 0-thalassemic gene causes abnormal RNA splicing.
    Treisman R; Proudfoot NJ; Shander M; Maniatis T
    Cell; 1982 Jul; 29(3):903-11. PubMed ID: 7151176
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Base substitution in an intervening sequence of a beta+-thalassemic human globin gene.
    Spritz RA; Jagadeeswaran P; Choudary PV; Biro PA; Elder JT; deRiel JK; Manley JL; Gefter ML; Forget BG; Weissman SM
    Proc Natl Acad Sci U S A; 1981 Apr; 78(4):2455-9. PubMed ID: 6264477
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Beta O-39 thalassemia gene: a premature termination codon causes beta-mRNA deficiency without affecting cytoplasmic beta-mRNA stability.
    Humphries RK; Ley TJ; Anagnou NP; Baur AW; Nienhuis AW
    Blood; 1984 Jul; 64(1):23-32. PubMed ID: 6733274
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Abnormal RNA splicing causes one form of alpha thalassemia.
    Felber BK; Orkin SH; Hamer DH
    Cell; 1982 Jul; 29(3):895-902. PubMed ID: 7151175
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Relative stability of alpha- and beta-globin messenger RNAs in homozygous beta+ thalassemia.
    Nienhuis AW; Turner P; Benz EJ
    Proc Natl Acad Sci U S A; 1977 Sep; 74(9):3960-4. PubMed ID: 71735
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reversal of aberrant splicing of beta-thalassemia allele by antisense RNA in vitro and in vivo.
    Zeng Y; Gu X; Chen Y; Gong L; Ren Z; Huang S
    Chin Med J (Engl); 1999 Feb; 112(2):107-11. PubMed ID: 11593572
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RNA processing errors in patients with beta-thalassemia.
    Ley TJ; Anagnou NP; Pepe G; Nienhuis AW
    Proc Natl Acad Sci U S A; 1982 Aug; 79(15):4775-9. PubMed ID: 6956887
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Base substitution at position -88 in a beta-thalassemic globin gene. Further evidence for the role of distal promoter element ACACCC.
    Orkin SH; Antonarakis SE; Kazazian HH
    J Biol Chem; 1984 Jul; 259(14):8679-81. PubMed ID: 6086605
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.