These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 2443439)

  • 1. One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population.
    Efremov GD; Gjorgovski I; Stojanovski N; Diaz-Chico JC; Harano T; Kutlar F; Huisman TH
    Hum Genet; 1987 Oct; 77(2):132-6. PubMed ID: 2443439
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal gamma-gene expression in association with beta thalassemia and linkage relationship with the beta-globin gene cluster.
    Giampaolo A; Mavilio F; Sposi NM; Carè A; Massa A; Cianetti L; Petrini M; Russo R; Cappellini MD; Marinucci M
    Hum Genet; 1984; 66(2-3):151-6. PubMed ID: 6201431
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A frequent A gamma-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with beta-thalassemia.
    Ottolenghi S; Camaschella C; Comi P; Giglioni B; Longinotti M; Oggiano L; Dore F; Sciarratta G; Ivaldi G; Saglio G
    Hum Genet; 1988 May; 79(1):13-7. PubMed ID: 2452784
    [TBL] [Abstract][Full Text] [Related]  

  • 5. G gamma A gamma(delta beta)zero-thalassaemia and a new form of gamma globin gene triplication identified in the Yugoslavian population.
    Efremov GD; Filipce V; Gjorgovski I; Juricic D; Stojanovski N; Harano T; Nakatsuji T; Kutlar A; Kutlar F; Bakioglu I
    Br J Haematol; 1986 May; 63(1):17-28. PubMed ID: 2423109
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population.
    Collins FS; Boehm CD; Waber PG; Stoeckert CJ; Weissman SM; Forget BG; Kazazian HH
    Blood; 1984 Dec; 64(6):1292-6. PubMed ID: 6208955
    [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. Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.
    Indrak K; Indrakova J; Kutlar F; Pospisilova D; Sulovska I; Baysal E; Huisman TH
    Ann Hematol; 1991 Aug; 63(2):111-5. PubMed ID: 1716997
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Delta beta thalassemia and hereditary persistence of fetal hemoglobin.
    Bollekens JA; Forget BG
    Hematol Oncol Clin North Am; 1991 Jun; 5(3):399-422. PubMed ID: 1713909
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the beta globin gene complex.
    Donald JA; Lammi A; Trent RJ
    Hum Genet; 1988 Sep; 80(1):69-74. PubMed ID: 2458313
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Biosynthetic studies and gamma-chain composition in the Greek type of hereditary persistence of fetal hemoglobin and in its association with beta-thalassemia.
    Camaschella C; Ciocca-Vasino MA; Guerrasio A; Balegno G; Barberis E; Delponte D; Saglio G
    Acta Haematol; 1979; 61(5):272-7. PubMed ID: 111454
    [TBL] [Abstract][Full Text] [Related]  

  • 13. beta Thalassemia associated with increased HB F production. Evidence for the existence of a heterocellular hereditary persistence of fetal hemoglobin (HPFH) determinant linked to beta thalassemia in a southern Italian population.
    Marinucci M; Mavilio F; Giuliani A; Gabbianelli M; Tentori L; Tentori L; Zorini CO; Lamberti E; Palazzolo A; Lanzo D
    Hemoglobin; 1981; 5(1):1-17. PubMed ID: 6162827
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.
    Labie D; Pagnier J; Lapoumeroulie C; Rouabhi F; Dunda-Belkhodja O; Chardin P; Beldjord C; Wajcman H; Fabry ME; Nagel RL
    Proc Natl Acad Sci U S A; 1985 Apr; 82(7):2111-4. PubMed ID: 2580306
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.
    Amato A; Cappabianca MP; Perri M; Zaghis I; Grisanti P; Ponzini D; Di Biagio P
    Int J Lab Hematol; 2014 Feb; 36(1):13-9. PubMed ID: 23621512
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Restriction endonuclease mapping of gamma-delta-beta-globin region in G gamma (beta)+ HPFH and a Chinese A gamma HPFH variant.
    Farquhar M; Gelinas R; Tatsis B; Murray J; Yagi M; Mueller R; Stamatoyannopoulos G
    Am J Hum Genet; 1983 Jul; 35(4):611-20. PubMed ID: 6192712
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.
    Collins FS; Stoeckert CJ; Serjeant GR; Forget BG; Weissman SM
    Proc Natl Acad Sci U S A; 1984 Aug; 81(15):4894-8. PubMed ID: 6205403
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fetal hemoglobin levels and beta (s) globin haplotypes in an Indian populations with sickle cell disease.
    Kulozik AE; Kar BC; Satapathy RK; Serjeant BE; Serjeant GR; Weatherall DJ
    Blood; 1987 Jun; 69(6):1742-6. PubMed ID: 2437982
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects.
    Cianetti L; Care A; Sposi NM; Giampaolo A; Calandrini M; Petrini M; Massa A; Marinucci M; Mavilio F; Ceccanti M
    J Med Genet; 1984 Aug; 21(4):263-7. PubMed ID: 6208362
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.