318 related articles for article (PubMed ID: 11976733)
1. A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and beta-thalassemia compound heterozygotes.
Papadakis MN; Patrinos GP; Tsaftaridis P; Loutradi-Anagnostou A
J Mol Med (Berl); 2002 Apr; 80(4):243-7. PubMed ID: 11976733
[TBL] [Abstract][Full Text] [Related]
2. Fetal hemoglobin expression in the compound heterozygous state for -117 (G-->A) Agamma HPFH and IVS-1 nt 110 (G-->A) beta+ thalassemia: a case study.
Dedoussis GV; Sinopoulou K; Gyparaki M; Loutradis A
Eur J Haematol; 2000 Aug; 65(2):93-6. PubMed ID: 10966167
[TBL] [Abstract][Full Text] [Related]
3. Fetal hemoglobin expression in the compound heterozygous state for -117 (G-->A) Agamma HPFH and IVSII-745 (C-->G) beta+ thalassemia: a case study.
Dedoussis GV; Sinopoulou K; Gyparaki M; Loutradis A
Am J Hematol; 1999 Jun; 61(2):139-43. PubMed ID: 10367795
[TBL] [Abstract][Full Text] [Related]
4. Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population.
Lemsaddek W; Picanço I; Seuanes F; Mahmal L; Benchekroun S; Khattab M; Nogueira P; Osório-Almeida L
Am J Hematol; 2003 Jul; 73(3):161-8. PubMed ID: 12827652
[TBL] [Abstract][Full Text] [Related]
5. G gamma-196 C-->T, A gamma-201 C-->T: two novel mutations in the promoter region of the gamma-globin genes associated with nondeletional hereditary persistence of fetal hemoglobin in Greece.
Tasiopoulou M; Boussiou M; Sinopoulou K; Moraitis G; Loutradi-Anagnostou A; Karababa P
Blood Cells Mol Dis; 2008; 40(3):320-2. PubMed ID: 18096417
[TBL] [Abstract][Full Text] [Related]
6. Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
Hariharan P; Sawant M; Gorivale M; Manchanda R; Colah R; Ghosh K; Nadkarni A
Mol Biol Rep; 2017 Oct; 44(5):413-417. PubMed ID: 28879539
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Maximal gamma-globin expression in the compound heterozygous state for -175G gamma HPFH and beta degree 39 nonsense thalassaemia: a case study.
Pistidda P; Frogheri L; Guiso L; Manca L; Dore F; Mura L; Longinotti M
Eur J Haematol; 1997 May; 58(5):320-5. PubMed ID: 9222287
[TBL] [Abstract][Full Text] [Related]
9. Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotype.
Ragusa A; Amata S; Lombardo T; Castiglia L; Maier-Redelsperger M; Labie D; Bernini L
Haematologica; 2003 Oct; 88(10):1099-105. PubMed ID: 14555304
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
Fucharoen S; Pengjam Y; Surapot S; Fucharoen G; Sanchaisuriya K
Am J Hematol; 2002 Oct; 71(2):109-13. PubMed ID: 12353310
[TBL] [Abstract][Full Text] [Related]
12. High levels of human gamma-globin are expressed in adult mice carrying a transgene of the Brazilian type of hereditary persistence of fetal hemoglobin ((A)gamma -195).
da Cunha AF; Brugnerotto AF; Corat MA; Devlin EE; Gimenes AP; de Melo MB; Passos LA; Bodine D; Saad ST; Costa FF
Hemoglobin; 2009; 33(6):439-47. PubMed ID: 19958189
[TBL] [Abstract][Full Text] [Related]
13. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
Indrák K; Divoký V; Brabec V; Indráková J; Svobodová M; Huisman TH
Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
[TBL] [Abstract][Full Text] [Related]
14. Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia.
Papachatzopoulou A; Kourakli A; Makropoulou P; Kakagianne T; Sgourou A; Papadakis M; Athanassiadou A
Eur J Haematol; 2006 Apr; 76(4):322-30. PubMed ID: 16519704
[TBL] [Abstract][Full Text] [Related]
15. [Beta-thalassemia mutations and single nucleotide polymorphism at -158 of Ggamma-globin gene associated with altered levels of Hb F in beta-thalassemia heterozygotes].
Chen JF; Long GF; Lin WX; Chen P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):498-501. PubMed ID: 15476181
[TBL] [Abstract][Full Text] [Related]
16. Xmn I polymorphism associated with concomitant activation of Gγ and Aγ globin gene transcription on a β0-thalassemia chromosome.
Haj Khelil A; Morinière M; Laradi S; Khelif A; Perrin P; Ben Chibani J; Baklouti F
Blood Cells Mol Dis; 2011 Feb; 46(2):133-8. PubMed ID: 21144779
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Compound heterozygote state for GgammaAgamma(deltabeta) degrees -thalassemia and hereditary persistence of fetal hemoglobin.
Fucharoen S; Panyasai S; Surapot S; Fucharoen G; Sanchaisuriya K
Am J Hematol; 2005 Oct; 80(2):119-23. PubMed ID: 16184575
[TBL] [Abstract][Full Text] [Related]
19. The molecular basis of normal HbA2 (type 2) beta-thalassemia in Greece.
Tzetis M; Traeger-Synodinos J; Kanavakis E; Metaxotou-Mavromati A; Kattamis C
Hematol Pathol; 1994; 8(1-2):25-34. PubMed ID: 8034555
[TBL] [Abstract][Full Text] [Related]
20. Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysis.
Gottardi E; Alfarano A; Serra A; Sciarratta G; Bertero MT; Saglio G; Camaschella C
Haematologica; 1990; 75(1):17-20. PubMed ID: 1692560
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
