239 related articles for article (PubMed ID: 27710960)
1. Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia in Northeast Thailand.
Yamsri S; Pakdee N; Fucharoen G; Sanchaisuriya K; Fucharoen S
Acta Haematol; 2016; 136(4):233-239. PubMed ID: 27710960
[TBL] [Abstract][Full Text] [Related]
2. Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis.
Pakdee N; Yamsri S; Fucharoen G; Sanchaisuriya K; Pissard S; Fucharoen S
Blood Cells Mol Dis; 2014; 53(1-2):11-5. PubMed ID: 24581976
[TBL] [Abstract][Full Text] [Related]
3. The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients.
Nguyen TK; Joly P; Bardel C; Moulsma M; Bonello-Palot N; Francina A
Blood Cells Mol Dis; 2010 Aug; 45(2):124-7. PubMed ID: 20472475
[TBL] [Abstract][Full Text] [Related]
4. Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia Disease without α-Thalassemia.
Phanrahan P; Yamsri S; Teawtrakul N; Fucharoen G; Sanchaisuriya K; Fucharoen S
Mediterr J Hematol Infect Dis; 2019; 11(1):e2019038. PubMed ID: 31308914
[TBL] [Abstract][Full Text] [Related]
5. Modifying effect of XmnI, BCL11A, and HBS1L-MYB on clinical appearances: A study on β-thalassemia and hemoglobin E/β-thalassemia patients in Indonesia.
Rujito L; Basalamah M; Siswandari W; Setyono J; Wulandari G; Mulatsih S; Sofro AS; Sadewa AH; Sutaryo S
Hematol Oncol Stem Cell Ther; 2016 Jun; 9(2):55-63. PubMed ID: 27009595
[TBL] [Abstract][Full Text] [Related]
6. Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast Thailand.
Prayalaw P; Teawtrakul N; Jetsrisuparb A; Pongudom S; Fucharoen G; Fucharoen S
Acta Haematol; 2016; 135(1):15-20. PubMed ID: 26303193
[TBL] [Abstract][Full Text] [Related]
7. Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin.
Pereira C; Relvas L; Bento C; Abade A; Ribeiro ML; Manco L
Blood Cells Mol Dis; 2015 Apr; 54(4):315-20. PubMed ID: 25842369
[TBL] [Abstract][Full Text] [Related]
8. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
Muszlak M; Pissard S; Badens C; Chamouine A; Maillard O; Thuret I
Hemoglobin; 2015; 39(3):156-61. PubMed ID: 25806420
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. The associations of SEA-alpha thalassemia 1, XmnI-Ggamma polymorphism and beta-globin gene mutations with the clinical severity of beta-thalassemia syndrome in northern Thailand.
Tatu T; Sritong W; Sa-Nguansermsri T
J Med Assoc Thai; 2014 Mar; 97(3):300-7. PubMed ID: 25123009
[TBL] [Abstract][Full Text] [Related]
11. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
Charoenkwan P; Teerachaimahit P; Sanguansermsri T
Hemoglobin; 2014; 38(5):335-8. PubMed ID: 25238043
[TBL] [Abstract][Full Text] [Related]
12. A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders.
Jomoui W; Tepakhan W; Yamsri S; Srivorakun H; Fucharoen G; Fucharoen S
Ann Hematol; 2020 Jan; 99(1):23-29. PubMed ID: 31776727
[TBL] [Abstract][Full Text] [Related]
13. Essential genetic modifiers and their measurable impact in a community-recruited population analysis for non-severe hemoglobin E/β-thalassemia prenatal genetic counseling.
Wong P; Chitsobhak T; Jittasathian S; Sirichantharawat C; Cherdchoo N; Prangcharoen W; Jongautchariyakul P; Jampachaisri K; Tapprom A; Deoisares R; Chumnumsiriwath P
Blood Cells Mol Dis; 2023 Nov; 103():102765. PubMed ID: 37353362
[TBL] [Abstract][Full Text] [Related]
14. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand.
Nuntakarn L; Fucharoen S; Fucharoen G; Sanchaisuriya K; Jetsrisuparb A; Wiangnon S
Blood Cells Mol Dis; 2009; 42(1):32-5. PubMed ID: 18951049
[TBL] [Abstract][Full Text] [Related]
15. A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations.
Yamsri S; Singha K; Prajantasen T; Taweenan W; Fucharoen G; Sanchaisuriya K; Fucharoen S
Blood Cells Mol Dis; 2015 Feb; 54(2):164-9. PubMed ID: 25471338
[TBL] [Abstract][Full Text] [Related]
16. The association of HBG2, BCL11A, and HBS1L-MYB polymorphisms to thalidomide response in Chinese β-thalassemia patients.
Yang K; Wu Y; Ma Y; Xiao J; Zhou Y; Yin X
Blood Cells Mol Dis; 2020 Sep; 84():102442. PubMed ID: 32387854
[TBL] [Abstract][Full Text] [Related]
17. Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous β-Thalassemia 3.5 kb Deletions.
Tepakhan W; Kanjanaopas S; Srewaradachpisal K
Hemoglobin; 2020 Sep; 44(5):338-343. PubMed ID: 32878504
[TBL] [Abstract][Full Text] [Related]
18. Common fetal hemoglobin variants in Lebanese patients bearing the codon 29 beta gene mutation associated with different thalassemia phenotypes.
Brancaleoni V; Moukhadder HM; Consonni D; Koussa S; Di Pierro E; Cappellini MD; Taher A
Ann Hematol; 2019 Apr; 98(4):833-840. PubMed ID: 30506348
[TBL] [Abstract][Full Text] [Related]
19. Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion.
Danjou F; Anni F; Perseu L; Satta S; Dessì C; Lai ME; Fortina P; Devoto M; Galanello R
Haematologica; 2012 Jul; 97(7):989-93. PubMed ID: 22271886
[TBL] [Abstract][Full Text] [Related]
20. Correlations between Multiple SNPs and HbF Levels in β-Thalassemia Carriers.
Xu Q; Huang L; Jin T; Han Y; Liu J; Zhang W; Biao Y; An B; Huang S
Clin Lab; 2023 Sep; 69(9):. PubMed ID: 37702677
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]