BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

246 related articles for article (PubMed ID: 23234478)

  • 1. Homozygosity for the severe β(+)-thalassemia mutation [IVS-I-5 (G>C)] causes the phenotype of thalassemia trait: an extremely rare presentation.
    Bohara V; Raut L; Badarkhe G; Roy SS; Chaudhuri U
    Hemoglobin; 2013; 37(1):101-5. PubMed ID: 23234478
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Homozygosity for a rare beta 0-thalassemia mutation [frameshift codons 25/26 (+T)] causes beta-thalassemia intermedia in an Iranian family.
    Haghi M; Feizi AA; Harteveld CL; Pouladi N; Feizi MA
    Hemoglobin; 2009; 33(1):75-80. PubMed ID: 19205978
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular basis of β-thalassemia in the United Arab Emirates.
    Baysal E
    Hemoglobin; 2011; 35(5-6):581-8. PubMed ID: 22074124
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN
    Hemoglobin; 2007; 31(2):233-41. PubMed ID: 17486506
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The IVS-II-837 (T>G) appears to be a relatively common 'rare' β-globin gene mutation in β-thalassemia patients in Karnataka State, South India.
    Bashyam MD; Chaudhary AK; Bhat V
    Hemoglobin; 2012; 36(5):497-503. PubMed ID: 22734501
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Asymptomatic homozygous deletional beta(0)-thalassemia in an African individual.
    Faustino P; Reis AB; Feliciano H; Ferrão L; Pereira P; Picanço I; Miranda A; Seixas T; Romão L; Júnior EC; Lavinha J
    Am J Hematol; 2002 Jul; 70(3):232-6. PubMed ID: 12111769
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association in cis of the mutations +20 (C>T) in the 5' untranslated region and IVS-II-745 (C>G) on the β-globin gene.
    Ropero P; González FA; Cela E; Beléndez C; Cervera A; Martínez-Nieto J; de la Fuente-Gonzalo F; Vinuesa L; Villegas A; Díaz-Mediavilla J
    Hemoglobin; 2013; 37(2):112-8. PubMed ID: 23425204
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassaemia due to a homozygosity for the IVS-I-6 (T-->C) mutation.
    Efremov DG; Dimovski AJ; Baysal E; Ye Z; Adekile AD; Ribeiro ML; Schiliro G; Altay C; Gürgey A; Efremov GD
    Br J Haematol; 1994 Apr; 86(4):824-30. PubMed ID: 7522523
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Concomitant inheritance of homozygous alpha-thalassemia-2 with homozygous IVS-I-5 G-C beta gene mutation does not influence the severity of the thalassemic phenotype.
    Beris PH; Darbellay R; Beck D; Oner R
    Nouv Rev Fr Hematol (1978); 1991; 33(3):227-30. PubMed ID: 1720237
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia.
    Vinciguerra M; Passarello C; Cassarà F; Leto F; Cannata M; Calvaruso G; Di Maggio R; Renda D; Maggio A; Giambona A
    Int J Lab Hematol; 2016 Feb; 38(1):17-26. PubMed ID: 26418075
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia.
    Huang G; Jiang WL; Rong KB; Li YX; Luo XL; Meng JX; Yu XY
    Hemoglobin; 2010 Jan; 34(2):179-83. PubMed ID: 20353356
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.
    Daniel Y; Hill K; Inusa B; Thein SL; Howard J
    Hemoglobin; 2011; 35(4):406-10. PubMed ID: 21797706
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of two rare β-globin gene mutations in a patient with β-thalassemia intermedia from Azerbaijan.
    Asadov CD; Abdulalimov ER; Mammadova TA; Qafarova SN; Guliyeva YJ; Tuli A; Cürük MA
    Hemoglobin; 2013; 37(3):291-6. PubMed ID: 23510507
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
    Colah R; Nadkarni A; Gorakshakar A; Phanasgaonkar S; Surve R; Subramaniam PG; Bondge N; Pujari K; Ghosh K; Mohanty D
    Blood Cells Mol Dis; 2004; 33(2):153-7. PubMed ID: 15315795
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon gene.
    Adhiyanto C; Yamashiro Y; Hattori Y; Nitta T; Hino M; Matar M; Takagi F; Kimoto M
    Hemoglobin; 2013; 37(3):227-40. PubMed ID: 23600595
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Three new beta-thalassemia mutations with varying degrees of severity.
    Frischknecht H; Dutly F; Walker L; Nakamura-Garrett LM; Eng B; Waye JS
    Hemoglobin; 2009; 33(3):220-5. PubMed ID: 19657836
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].
    Phylipsen M; Harteveld CL; de Metz M; Gallivan MV; Arkesteijn SG; Luo HY; Chui DH; Giordano PC
    Hemoglobin; 2010; 34(5):445-50. PubMed ID: 20854118
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
    Moumni I; Zorai A; Mahjoub S; Mosbahi I; Chaouechi D; Benromdhane N; Abbes S
    Hemoglobin; 2014; 38(2):88-90. PubMed ID: 24471655
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of Iran.
    Salehi R; Fisher CA; Bignell PA; Eslami G; Old JM
    Hemoglobin; 2010; 34(1):115-20. PubMed ID: 20113296
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.