854 related articles for article (PubMed ID: 28879539)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin.
Collins FS; Metherall JE; Yamakawa M; Pan J; Weissman SM; Forget BG
Nature; 1985 Jan 24-30; 313(6000):325-6. PubMed ID: 2578620
[TBL] [Abstract][Full Text] [Related]
9. A genome-editing strategy to treat β-hemoglobinopathies that recapitulates a mutation associated with a benign genetic condition.
Traxler EA; Yao Y; Wang YD; Woodard KJ; Kurita R; Nakamura Y; Hughes JR; Hardison RC; Blobel GA; Li C; Weiss MJ
Nat Med; 2016 Sep; 22(9):987-90. PubMed ID: 27525524
[TBL] [Abstract][Full Text] [Related]
10. DNA methylation patterns of β-globin cluster in β-thalassemia patients.
Bao X; Zuo Y; Chen D; Zhao C
Clin Epigenetics; 2020 Dec; 12(1):187. PubMed ID: 33272312
[TBL] [Abstract][Full Text] [Related]
11. Genetic research and clinical analysis of β-globin gene cluster deletions in the Chinese population of Fujian province: A 14-year single-center experience.
Chen M; Zhang M; Chen L; Lin N; Wang Y; Xu L; Huang H
J Clin Lab Anal; 2022 Feb; 36(2):e24181. PubMed ID: 34951062
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Structural and Functional Insights on an Uncharacterized Aγ-Globin-Gene Polymorphism Present in Four β0-Thalassemia Families with High Fetal Hemoglobin Levels.
Bianchi N; Cosenza LC; Lampronti I; Finotti A; Breveglieri G; Zuccato C; Fabbri E; Marzaro G; Chilin A; De Angelis G; Borgatti M; Gallucci C; Alfieri C; Ribersani M; Isgrò A; Marziali M; Gaziev J; Morrone A; Sodani P; Lucarelli G; Gambari R; Paciaroni K
Mol Diagn Ther; 2016 Apr; 20(2):161-73. PubMed ID: 26897028
[TBL] [Abstract][Full Text] [Related]
15. Molecular understanding of unusual HbE-β
Jomoui W; Satthakarn S; Panyasai S
Ann Med; 2023; 55(2):2267054. PubMed ID: 37816374
[TBL] [Abstract][Full Text] [Related]
16. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.
Singha K; Fucharoen G; Hama A; Fucharoen S
Clin Biochem; 2015 Jul; 48(10-11):703-8. PubMed ID: 25866400
[TBL] [Abstract][Full Text] [Related]
17. Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia.
Bao X; Zhang X; Wang L; Wang Z; Huang J; Zhang Q; Ye Y; Liu Y; Chen D; Zuo Y; Liu Q; Xu P; Huang B; Fang J; Lao J; Feng X; Li Y; Kurita R; Nakamura Y; Yu W; Ju C; Huang C; Mohandas N; Li D; Zhao C; Xu X
Am J Hum Genet; 2021 Apr; 108(4):709-721. PubMed ID: 33735615
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Original Research: Generation of non-deletional hereditary persistence of fetal hemoglobin β-globin locus yeast artificial chromosome transgenic mouse models: -175 Black HPFH and -195 Brazilian HPFH.
Braghini CA; Costa FC; Fedosyuk H; Neades RY; Novikova LV; Parker MP; Winefield RD; Peterson KR
Exp Biol Med (Maywood); 2016 Apr; 241(7):697-705. PubMed ID: 26946532
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
