148 related articles for article (PubMed ID: 19050890)
1. The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter.
Chassanidis C; Kalamaras A; Phylactides M; Pourfarzad F; Likousi S; Maroulis V; Papadakis MN; Vamvakopoulos NK; Aleporou-Marinou V; Patrinos GP; Kollia P
Ann Hematol; 2009 Jun; 88(6):549-55. PubMed ID: 19050890
[TBL] [Abstract][Full Text] [Related]
2. Functional Analysis of an (A)γ-Globin Gene Promoter Variant (HBG1: g.-225_-222delAGCA) Underlines Its Role in Increasing Fetal Hemoglobin Levels Under Erythropoietic Stress.
Ugrin M; Stojiljkovic M; Zukic B; Klaassen K; Katsila T; Vasiljevic J; Dokmanovic L; Janic D; Patrinos GP; Pavlovic S
Hemoglobin; 2016; 40(1):48-52. PubMed ID: 26575252
[TBL] [Abstract][Full Text] [Related]
3. Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobin.
Toma S; Tenorio M; Oakley M; Thein SL; Clark BE
Hemoglobin; 2014; 38(1):67-9. PubMed ID: 24144231
[TBL] [Abstract][Full Text] [Related]
4. Identical mutations in the paralogous human γ-globin genes leading to hemoglobin variants and nondeletional hereditary persistence of fetal hemoglobin.
Papachatzopoulou A; Patrinos GP
Hemoglobin; 2011; 35(2):135-41. PubMed ID: 21417570
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin.
Radmilovic M; Zukic B; Petrovic MS; Bartsakoulia M; Stankovic B; Kotur N; Dokmanovic L; Georgitsi M; Patrinos GP; Pavlovic S
Ann Hematol; 2013 Jan; 92(1):53-8. PubMed ID: 23161389
[TBL] [Abstract][Full Text] [Related]
7. A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F.
Chen Z; Luo HY; Basran RK; Hsu TH; Mang DW; Nuntakarn L; Rosenfield CG; Patrinos GP; Hardison RC; Steinberg MH; Chui DH
Mol Cell Biol; 2008 Jul; 28(13):4386-93. PubMed ID: 18443038
[TBL] [Abstract][Full Text] [Related]
8. A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobin.
Zertal-Zidani S; Merghoub T; Ducrocq R; Gerard N; Satta D; Krishnamoorthy R
Hemoglobin; 1999 May; 23(2):159-69. PubMed ID: 10335983
[TBL] [Abstract][Full Text] [Related]
9. A novel C-T transition within the distal CCAAT motif of the G gamma-globin gene in the Japanese HPFH: implication of factor binding in elevated fetal globin expression.
Fucharoen S; Shimizu K; Fukumaki Y
Nucleic Acids Res; 1990 Sep; 18(17):5245-53. PubMed ID: 1698280
[TBL] [Abstract][Full Text] [Related]
10. G gamma A gamma (beta+) hereditary persistence of fetal hemoglobin: the G gamma -158 C-->T mutation in cis to the -175 T-->C mutation of the A gamma-globin gene results in increased G gamma-globin synthesis.
Coleman MB; Adams JG; Steinberg MH; Plonczynski MW; Harrell AH; Castro O; Winter WP
Am J Hematol; 1993 Feb; 42(2):186-90. PubMed ID: 7679879
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Ggamma -37 (A-->T): a new nondeletional hereditary persistence of fetal hemoglobin determinant associated with the rare codon 91 (+T) delta0-thalassemia.
Bouva MJ; Harteveld CL; Bakker-Verweij G; van Delft P; Giordano PC
Hemoglobin; 2006; 30(3):371-7. PubMed ID: 16840228
[TBL] [Abstract][Full Text] [Related]
14. Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the beta-globin gene cluster.
Lee ST; Yoo EH; Kim JY; Kim JW; Ki CS
Br J Haematol; 2010 Jan; 148(1):154-60. PubMed ID: 19807730
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. The relationship between the variations in Gγ and Aγ promotors and the Hereditary Persistence of Fetal Hemoglobin (HPFH).
Aydin M; Rencuzogullari E; Dalyan A; Bayram S; Genc A
Cell Mol Biol (Noisy-le-grand); 2018 Jan; 64(1):32-39. PubMed ID: 29412791
[TBL] [Abstract][Full Text] [Related]
18. The Australian type of nondeletional G gamma-HPFH has a C-->G substitution at nucleotide -114 of the G gamma gene.
Motum PI; Deng ZM; Huong L; Trent RJ
Br J Haematol; 1994 Jan; 86(1):219-21. PubMed ID: 7516698
[TBL] [Abstract][Full Text] [Related]
19. Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.
Akinbami AO; Campbell AD; Han ZJ; Luo HY; Chui DH; Steinberg MH
Hemoglobin; 2016; 40(1):64-5. PubMed ID: 26372199
[TBL] [Abstract][Full Text] [Related]
20. DNA sequences regulating human globin gene transcription in nondeletional hereditary persistence of fetal hemoglobin.
Ottolenghi S; Mantovani R; Nicolis S; Ronchi A; Giglioni B
Hemoglobin; 1989; 13(6):523-41. PubMed ID: 2481658
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
