BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 7510147)

  • 1. Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification.
    Craig JE; Barnetson RA; Prior J; Raven JL; Thein SL
    Blood; 1994 Mar; 83(6):1673-82. PubMed ID: 7510147
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterization and PCR detection of a deletional HPFH: application to rapid prenatal diagnosis for compound heterozygotes of this defect with beta-thalassemia in a Chinese family.
    Xu XM; Li ZQ; Liu ZY; Zhong XL; Zhao YZ; Mo QH
    Am J Hematol; 2000 Nov; 65(3):183-8. PubMed ID: 11074532
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genotypic-phenotypic heterogeneity of δβ-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India.
    Hariharan P; Kishnani P; Sawant P; Gorivale M; Mehta P; Kargutkar N; Colah R; Nadkarni A
    Ann Hematol; 2020 Jul; 99(7):1475-1483. PubMed ID: 32524201
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Eastern European (delta beta) zero-thalassemia: molecular characterization of a novel 9.1-kb deletion resulting in high levels of fetal hemoglobin in the adult.
    Palena A; Blau A; Stamatoyannopoulos G; Anagnou NP
    Blood; 1994 Jun; 83(12):3738-45. PubMed ID: 7515720
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
    Fornari TA; Lanaro C; Albuquerque DM; Ferreira R; Costa FF
    Exp Biol Med (Maywood); 2017 Feb; 242(3):267-274. PubMed ID: 27591578
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?
    Ottolenghi S; Giglioni B; Taramelli R; Comi P; Mazza U; Saglio G; Camaschella C; Izzo P; Cao A; Galanello R; Gimferrer E; Baiget M; Gianni AM
    Proc Natl Acad Sci U S A; 1982 Apr; 79(7):2347-51. PubMed ID: 6179097
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular characterization of hereditary persistence of fetal hemoglobin in the Karen people of Thailand.
    Trachoo O; Sura T; Sakuntabhai A; Singhasivanon P; Krudsood S; Phimpraphi W; Krasaesub S; Chanjarunee S; Looareesuwan S
    Hemoglobin; 2003 May; 27(2):97-104. PubMed ID: 12779271
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3' end of the beta-globin gene cluster.
    Kosteas T; Palena A; Anagnou NP
    Hum Genet; 1997 Sep; 100(3-4):441-5. PubMed ID: 9272169
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex.
    Thein SL; Weatherall DJ
    Prog Clin Biol Res; 1989; 316B():97-111. PubMed ID: 2482508
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nucleotide sequence of the Belgian G gamma+(A gamma delta beta)0-thalassemia deletion breakpoint suggests a common mechanism for a number of such recombination events.
    Fodde R; Losekoot M; Casula L; Bernini LF
    Genomics; 1990 Dec; 8(4):732-5. PubMed ID: 2276746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
    Carrocini GC; Ondei LS; Zamaro PJ; Bonini-Domingos CR
    Genet Mol Res; 2011 Dec; 10(4):3213-9. PubMed ID: 22194178
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant.
    Losekoot M; Fodde R; Gerritsen EJ; van de Kuit I; Schreuder A; Giordano PC; Vossen JM; Bernini LF
    Blood; 1991 Feb; 77(4):861-7. PubMed ID: 1704267
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection and characterisation of beta-globin gene cluster deletions in Chinese using multiplex ligation-dependent probe amplification.
    So CC; So AC; Chan AY; Tsang ST; Ma ES; Chan LC
    J Clin Pathol; 2009 Dec; 62(12):1107-11. PubMed ID: 19946097
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N; Fucharoen S; Fuchareon G; Siriratmanawong N
    Eur J Haematol; 2014 Jan; 92(1):73-9. PubMed ID: 24112054
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China.
    Jiang F; Zuo L; Li D; Li J; Tang X; Chen G; Zhou J; Lu H; Liao C
    BMC Med Genet; 2020 Feb; 21(1):43. PubMed ID: 32111191
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction.
    Vives-Corrons JL; Pujades MA; Miguel-García A; Miguel-Sosa A; Cambiazzo S
    Blood; 1992 Sep; 80(6):1582-5. PubMed ID: 1520881
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster.
    Feingold EA; Forget BG
    Blood; 1989 Nov; 74(6):2178-86. PubMed ID: 2478223
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel deletion of approximately 27 kb including the beta-globin gene and the locus control region 3'HS-1 regulatory sequence: beta zero-thalassemia or hereditary persistence of fetal hemoglobin?
    Dimovski AJ; Divoky V; Adekile AD; Baysal E; Wilson JB; Prior JF; Raven JL; Huisman TH
    Blood; 1994 Feb; 83(3):822-7. PubMed ID: 7507736
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
    Panyasai S; Fucharoen S; Surapot S; Fucharoen G; Sanchaisuriya K
    Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.