BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

311 related articles for article (PubMed ID: 8257991)

  • 1. Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletion.
    Eng B; Chui DH; Saunderson J; Olivieri NF; Waye JS
    Hum Mutat; 1993; 2(5):375-9. PubMed ID: 8257991
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family.
    Yi P; Yu F; Huang S; Zhong C; Li Q; Yang Y; Zhang W; Xiao C; Xu X
    Blood Cells Mol Dis; 2008; 41(1):56-9. PubMed ID: 18381244
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spectrum of beta-thalassemia mutations and their association with allelic sequence polymorphisms at the beta-globin gene cluster in an Eastern Indian population.
    Kukreti R; Dash D; E VK; Chakravarty S; Das SK; De M; Talukder G
    Am J Hematol; 2002 Aug; 70(4):269-77. PubMed ID: 12210807
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.
    Feriotto G; Salvatori F; Finotti A; Breveglieri G; Venturi M; Zuccato C; Bianchi N; Borgatti M; Lampronti I; Mancini I; Massei F; Favre C; Gambari R
    Acta Haematol; 2008; 119(1):28-37. PubMed ID: 18230963
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The spectrum of beta-thalassemia mutations in southern Thailand.
    Nopparatana C; Panich V; Saechan V; Sriroongrueng V; Nopparatana C; Rungjeadpha J; Pornpatkul M; Laosombat V; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():229-34. PubMed ID: 8629112
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two new beta0-thalassemic mutations: a deletion (-CC) at codon 142 or overlapping codons 142-143, and an insertion (+T) at codon 45 or overlapping codons 44-45/45-46 of the beta-globin gene.
    Lacan P; Aubry M; Couprie N; Francina A
    Hemoglobin; 2007; 31(2):159-65. PubMed ID: 17486497
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A second observation of the rare frameshift mutation in the β-globin gene: codon 46 (+A) (Hbb:c.138_139insA).
    Ghedira ES; Dupin-Deguine D; Duffilot D; Lemetayer N; Faubert E; Pissard S
    Hemoglobin; 2011; 35(2):157-61. PubMed ID: 21417574
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM; El-Khatib FF; Ayesh S
    Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G; Das R; Awasthi A; Ahluwalia J; Marwaha RK
    Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Most frequent beta-thalassemia mutations in the Argentinian population].
    Varela V; Abreu S; Rossetti LC; Targovnik H
    Sangre (Barc); 1996 Apr; 41(2):137-40. PubMed ID: 9045354
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel frameshift mutation (+G) at codons 15/16 in a beta0 thalassaemia gene results in a significant reduction of beta globin mRNA values.
    Mo QH; Li XR; Li CF; He YL; Xu XM
    J Clin Pathol; 2005 Sep; 58(9):923-6. PubMed ID: 16126871
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian proband.
    Jain PK; Dozy AM; Verma IC; Chehab FF
    Hum Mutat; 1994; 3(4):397-8. PubMed ID: 8081396
    [No Abstract]   [Full Text] [Related]  

  • 13. Dominantly Inherited beta-Thalassemia.
    Efremov GD
    Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis.
    Peng CT; Wu JY; Tsai CH; Tsai FJ; Chang JG
    J Hum Genet; 1998; 43(4):237-41. PubMed ID: 9852674
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular nature of beta-thalassemia in Tajikistan: a four base pair deletion in codons 41-42 of the beta-globin gene].
    Kolesnikova TN; Surin VL; Moliaka IuK; Luk'ianenko AV; Tagiev AF; Asanov AIu; Bobokhodzhaev ZM; Solov'ev GIa
    Genetika; 1992 Nov; 28(11):28-33. PubMed ID: 1286798
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel beta-Thalassemic allele due to a two nucleotide deletion: beta76 (-GC).
    Foulon K; Rochette J; Cadet E
    Hemoglobin; 2007; 31(1):31-7. PubMed ID: 17365003
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel beta-thalassemia mutation (G-->A) at the initiation codon of the beta-globin gene.
    Saba L; Meloni A; Sardu R; Travi M; Primignani P; Rosatelli MC; Cao A
    Hum Mutat; 1992; 1(5):420-2. PubMed ID: 1301952
    [No Abstract]   [Full Text] [Related]  

  • 18. A novel beta-thalassemia mutation: frameshift at codon 59 detected in an Italian carrier.
    Meloni A; Demurtas M; Moi L; Faà V; Cao A; Rosatelli MC
    Hum Mutat; 1994; 3(3):309-11. PubMed ID: 8019567
    [No Abstract]   [Full Text] [Related]  

  • 19. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).
    Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH
    J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Japanese beta zero-thalassemia: molecular characterization of a novel insertion causing a stop codon.
    Oshima K; Harano T; Harano K
    Am J Hematol; 1996 May; 52(1):39-41. PubMed ID: 8638609
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.