BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

277 related articles for article (PubMed ID: 1478008)

  • 21. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
    Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalence.
    Traeger-Synodinos J; Tzetis M; Kanavakis E; Metaxotou-Mavromati A; Kattamis C
    Br J Haematol; 1991 Oct; 79(2):302-5. PubMed ID: 1720325
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.
    Chen XW; Mo QH; Li Q; Zeng R; Xu XM
    Ann Hematol; 2007 Sep; 86(9):653-7. PubMed ID: 17516066
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. [Current views of thalassemia intermedia].
    Longinotti M; Dore F; Oggiano L; Pardini S; Pistidda P; Guiso L; Frogheri L; Bonfigli S; Murineddu M; Rimini E
    Recenti Prog Med; 1992 Apr; 83(4):233-40. PubMed ID: 1626119
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Normal delta globin gene sequence in carrier of the silent-101 (C-T) beta-thalassemia mutation with normal HbA2 level.
    Ristaldi MS; Casula S; Porcu S; Cao A
    Am J Hematol; 2001 May; 67(1):58. PubMed ID: 11279661
    [No Abstract]   [Full Text] [Related]  

  • 27. 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]  

  • 28. A beta-thalassaemia phenotype not linked to the beta-globin cluster in an Italian family.
    Murru S; Loudianos G; Porcu S; Sciarratta GV; Agosti S; Parodi MI; Cao A; Pirastu M
    Br J Haematol; 1992 Jun; 81(2):283-7. PubMed ID: 1643026
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemia.
    Camaschella C; Bertero MT; Serra A; Dall'Acqua M; Gasparini P; Trento M; Vettore L; Perona G; Saglio G; Mazza U
    Br J Haematol; 1987 May; 66(1):103-7. PubMed ID: 3593644
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassaemia in the Italian population.
    Ristaldi MS; Murru S; Loudianos G; Casula L; Porcu S; Pigheddu D; Fanni B; Sciarratta GV; Agosti S; Parodi MI
    Br J Haematol; 1990 Apr; 74(4):480-6. PubMed ID: 2346726
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases.
    Colaco S; Colah R; Ghosh K; Nadkarni A
    Clin Chim Acta; 2012 Oct; 413(19-20):1705-7. PubMed ID: 22659060
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Association of alpha and beta thalassemia with alpha gene triplication in one family].
    Villegas A; Muñoz JA; Risueño CF; Castro JM; Sánchez J; Ropero P; González FA
    Med Clin (Barc); 1997 May; 108(20):781-3. PubMed ID: 9265084
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel Mediterranean "delta beta-thalassemia" determinant containing the delta (+) 27 and beta (0) 39 point mutations in cis.
    Oggiano L; Guiso L; Frogheri L; Loudianos G; Pistidda P; Rimini E; Pirastu M; Cao A; Longinotti M
    Am J Hematol; 1994 Jan; 45(1):81-4. PubMed ID: 7504402
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Beta thalassemia: molecular pathogenesis and clinical variability].
    Kulozik AE
    Klin Padiatr; 1991; 203(4):276-83. PubMed ID: 1942934
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Silent carrier beta-thalassaemia due to a severe beta-globin mutation interacting with other genetic elements.
    Rund D; Filon D; Oppenheim A; Abramov A
    Eur J Pediatr; 1993 Jul; 152(7):574-6. PubMed ID: 8354316
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian family.
    Oggiano L; Pirastu M; Moi P; Longinotti M; Perseu L; Cao A
    Br J Haematol; 1987 Oct; 67(2):225-9. PubMed ID: 3676110
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermedia.
    Galanello R; Maccioni L; Rosatelli MC; Ibba P; Nurchi AM; Cao A
    J Med Genet; 1984 Apr; 21(2):153-6. PubMed ID: 6716419
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Thalassaemia intermedia: interaction of the triple alpha-globin gene arrangement and heterozygous beta-thalassaemia.
    Kulozik AE; Thein SL; Wainscoat JS; Gale R; Kay LA; Wood JK; Weatherall DJ; Huehns ER
    Br J Haematol; 1987 May; 66(1):109-12. PubMed ID: 3593645
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular, haematological and clinical studies of the -101 C --> T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotes.
    Maragoudaki E; Kanavakis E; Traeger-Synodinos J; Vrettou C; Tzetis M; Metaxotou-Mavrommati A; Kattamis C
    Br J Haematol; 1999 Dec; 107(4):699-706. PubMed ID: 10606872
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemia.
    Camaschella C; Kattamis AC; Petroni D; Roetto A; Sivera P; Sbaiz L; Cohen A; Ohene-Frempong K; Trifillis P; Surrey S; Fortina P
    Am J Hematol; 1997 Jun; 55(2):83-8. PubMed ID: 9209003
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.