BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 6310991)

  • 1. beta-Thalassemia due to a deletion of the nucleotide which is substituted in the beta S-globin gene.
    Kazazian HH; Orkin SH; Boehm CD; Sexton JP; Antonarakis SE
    Am J Hum Genet; 1983 Sep; 35(5):1028-33. PubMed ID: 6310991
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A beta-thalassemia lesion abolishes the same Mst II site as the sickle mutation.
    Chang JC; Alberti A; Kan YW
    Nucleic Acids Res; 1983 Nov; 11(22):7789-94. PubMed ID: 6316272
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the beta-globin gene.
    Kazazian HH; Dowling CE; Hurwitz RL; Coleman M; Stopeck A; Adams JG
    Blood; 1992 Jun; 79(11):3014-8. PubMed ID: 1586746
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia.
    Orkin SH; Old JM; Weatherall DJ; Nathan DG
    Proc Natl Acad Sci U S A; 1979 May; 76(5):2400-4. PubMed ID: 287080
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gene analysis in delta beta and delta (0) thalassemia.
    Baird M; Driscoll MC; Ben-Bassat I; Ohta Y; Nakamura F; Bloom A; Bank A
    J Biol Chem; 1984 Jan; 259(1):512-5. PubMed ID: 6323412
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The beta-globin gene in Sardinian delta beta 0-thalassemia carries a C----T nonsense mutation at codon 39.
    Guida S; Giglioni B; Comi P; Ottolenghi S; Camaschella C; Saglio G
    EMBO J; 1984 Apr; 3(4):785-7. PubMed ID: 6327288
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Molecular nature of deletion in beta 0-thalassemia, established using a method of amplification of genomic DNA in vitro].
    Shvarts EI; Gol'tsov AA; Kaboev OK; Bakhlanova IN; Alekseev AN
    Bioorg Khim; 1989 Apr; 15(4):556-9. PubMed ID: 2546567
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of beta-thalassemia mutations among the Japanese.
    Hattori Y; Yamane A; Yamashiro Y; Matsuno Y; Yamamoto K; Yamamoto K; Ohba Y; Miyaji T
    Hemoglobin; 1989; 13(7-8):657-70. PubMed ID: 2634667
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nonsense and frameshift mutations in beta 0-thalassemia detected in cloned beta-globin genes.
    Orkin SH; Goff SC
    J Biol Chem; 1981 Oct; 256(19):9782-4. PubMed ID: 6985481
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two cloned beta thalassemia genes are associated with amber mutations at codon 39.
    Pergolizzi R; Spritz RA; Spence S; Goossens M; Kan YW; Bank A
    Nucleic Acids Res; 1981 Dec; 9(24):7065-72. PubMed ID: 6278453
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cloning and direct examination of a structurally abnormal human beta 0-thalassemia globin gene.
    Orkin SH; Kolodner R; Michelson A; Husson R
    Proc Natl Acad Sci U S A; 1980 Jun; 77(6):3558-62. PubMed ID: 6251466
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A single nucleotide deletion in codon 123 of the beta-globin gene causes an inclusion body beta-thalassaemia trait: a novel elongated globin chain beta Makabe.
    Fucharoen S; Kobayashi Y; Fucharoen G; Ohba Y; Miyazono K; Fukumaki Y; Takaku F
    Br J Haematol; 1990 Jul; 75(3):393-9. PubMed ID: 2167124
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of globin gene structure in patients with beta thalassemia by restriction endonuclease mapping.
    Tam JW; Kaufman RE; Nienhuis AW
    Hemoglobin; 1981; 5(3):209-15. PubMed ID: 6164667
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Beta+-thalassemia in cis of a sickle cell gene: occurrence of a promoter mutation on a beta s chromosome.
    Baklouti F; Ouazana R; Gonnet C; Lapillonne A; Delaunay J; Godet J
    Blood; 1989 Oct; 74(5):1817-22. PubMed ID: 2790205
    [TBL] [Abstract][Full Text] [Related]  

  • 16. "Silent" nucleotide substitution in codon 24 of a beta+ thalassemia globin gene activates splice site in coding sequence RNA.
    Humphries RK; Ley T; Goldsmith ME; Kantor JA; Cline AC; Nienhuis AW
    Prog Clin Biol Res; 1983; 134():123-6. PubMed ID: 6664994
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene.
    Sanguansermsri T; Pape M; Laig M; Hundrieser J; Flatz G
    Hemoglobin; 1990; 14(2):157-68. PubMed ID: 2272839
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel ochre mutation in the beta-thalassemia gene of a Thai. Identification by direct cloning of the entire beta-globin gene amplified using polymerase chain reactions.
    Fucharoen S; Fucharoen G; Fucharoen P; Fukumaki Y
    J Biol Chem; 1989 May; 264(14):7780-3. PubMed ID: 2542242
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.
    Coleman MB; Adams JG; Plonczynski MW; Harrell AH; Walker AM; Fairbanks V; Steinberg MH
    Am J Med Sci; 1992 Aug; 304(2):73-8. PubMed ID: 1380206
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Heterogeneity of DNA deletion in gamma delta beta-thalassemia.
    Orkin SH; Goff SC; Nathan DG
    J Clin Invest; 1981 Mar; 67(3):878-84. PubMed ID: 6162860
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.