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]