BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

344 related articles for article (PubMed ID: 19650141)

  • 1. Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
    Koenig SC; Becirevic E; Hellberg MS; Li MY; So JC; Hankins JS; Ware RE; McMahon L; Steinberg MH; Luo HY; Chui DH
    Am J Hematol; 2009 Sep; 84(9):603-6. PubMed ID: 19650141
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.
    Andersson BA; Wering ME; Luo HY; Basran RK; Steinberg MH; Smith HP; Chui DH
    Eur J Haematol; 2007 Jan; 78(1):82-5. PubMed ID: 17038017
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Modification of hemoglobin H disease by sickle trait.
    Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rearrangements of the beta-globin gene cluster in apparently typical betaS haplotypes.
    Zago MA; Silva WA; Gualandro S; Yokomizu IK; Araujo AG; Tavela MH; Gerard N; Krishnamoorthy R; Elion J
    Haematologica; 2001 Feb; 86(2):142-5. PubMed ID: 11224482
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Microsatellite and single nucleotide polymorphisms in the β-globin locus control region-hypersensitive Site 2: SPECIFICITY of Tunisian βs chromosomes.
    Ben Mustapha M; Moumni I; Zorai A; Douzi K; Ghanem A; Abbes S
    Hemoglobin; 2012; 36(6):533-44. PubMed ID: 23101664
    [TBL] [Abstract][Full Text] [Related]  

  • 7. beta(S)-Globin gene cluster haplotypes in the West Bank of Palestine.
    Samarah F; Ayesh S; Athanasiou M; Christakis J; Vavatsi N
    Hemoglobin; 2009; 33(2):143-9. PubMed ID: 19373591
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Localisation of cis regulatory elements at the beta-globin locus: analysis of hybrid haplotype chromosomes.
    Ofori-Acquah SF; Lalloz MR; Layton DM
    Biochem Biophys Res Commun; 1999 Jan; 254(1):181-7. PubMed ID: 9920754
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.
    Amid A; Cheong M; Eng B; Hanna M; Hohenadel BA; Nakamura LM; Walker L; Odame I; Kirby-Allen M; Waye JS
    Haematologica; 2015 May; 100(5):e166-8. PubMed ID: 25682598
    [No Abstract]   [Full Text] [Related]  

  • 10. Analyzing 5'HS3 and 5'HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations.
    Neishabury M; Azarkeivan A; Oberkanins C; Abedini SS; Zamani S; Najmabadi H
    Blood Cells Mol Dis; 2011 Mar; 46(3):201-5. PubMed ID: 21232998
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristics.
    Kutlar F; Redding-Lallinger R; Meiler SE; Bakanay SM; Borders L; Kutlar A
    Acta Haematol; 2010; 124(2):120-4. PubMed ID: 20861612
    [TBL] [Abstract][Full Text] [Related]  

  • 12. β-globin gene cluster haplotypes in a cohort of 221 children with sickle cell anemia or Sβ⁰-thalassemia and their association with clinical and hematological features.
    Belisário AR; Martins ML; Brito AM; Rodrigues CV; Silva CM; Viana MB
    Acta Haematol; 2010; 124(3):162-70. PubMed ID: 20938172
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel large deletions in the human alpha-globin gene cluster: Clarifying the HS-40 long-range regulatory role in the native chromosome environment.
    Coelho A; Picanço I; Seuanes F; Seixas MT; Faustino P
    Blood Cells Mol Dis; 2010 Aug; 45(2):147-53. PubMed ID: 20580289
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian families.
    Voruganti I; Eng B; Waye JS
    Hemoglobin; 2009; 33(6):422-7. PubMed ID: 19958187
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H
    Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.
    Patel DK; Patel M; Mashon RS; Patel S; Dash PM; Das BS
    Hemoglobin; 2010; 34(6):604-9. PubMed ID: 21077771
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sickle cell disease caused by Hb S/Québec-CHORI: treatment with hydroxyurea and response.
    Tubman VN; Bennett CM; Luo HY; Chui DH; Heeney MM
    Pediatr Blood Cancer; 2007 Aug; 49(2):207-10. PubMed ID: 17551985
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification and molecular characterization of four new large deletions in the beta-globin gene cluster.
    Joly P; Lacan P; Garcia C; Couprie N; Francina A
    Blood Cells Mol Dis; 2009; 43(1):53-7. PubMed ID: 19269866
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel deletion/insertion caused by a replication error in the β-globin gene locus control region.
    Joly P; Lacan P; Garcia C; Meley R; Pondarré C; Francina A
    Hemoglobin; 2011; 35(4):316-22. PubMed ID: 21797698
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.