151 related articles for article (PubMed ID: 27282573)
1. Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder.
Tepakhan W; Yamsri S; Sanchaisuriya K; Fucharoen G; Xu X; Fucharoen S
Blood Cells Mol Dis; 2016 Jul; 59():85-91. PubMed ID: 27282573
[TBL] [Abstract][Full Text] [Related]
2. Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome.
Tepakhan W; Yamsri S; Fucharoen G; Sanchaisuriya K; Fucharoen S
Ann Hematol; 2015 Jul; 94(7):1093-8. PubMed ID: 25694242
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults.
Gallienne AE; Dréau HM; Schuh A; Old JM; Henderson S
Haematologica; 2012 Mar; 97(3):340-3. PubMed ID: 22102705
[TBL] [Abstract][Full Text] [Related]
6. KFL1 Gene Variants in α-Thalassemia Individuals with Increased Fetal Hemoglobin in a Chinese Population.
Jiang F; Qu YX; Chen GL; Li J; Zhou JY; Zuo LD; Liao C; Li DZ
Hemoglobin; 2018 May; 42(3):161-165. PubMed ID: 30205725
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β
Khamphikham P; Sripichai O; Munkongdee T; Fucharoen S; Tongsima S; Smith DR
Int J Hematol; 2018 Mar; 107(3):297-310. PubMed ID: 29067594
[TBL] [Abstract][Full Text] [Related]
9. Quantitative Trait Loci Influencing Hb F Levels in Southern Thai Hb E (HBB: c.79G>A) Heterozygotes.
Kesornsit A; Jeenduang N; Horpet D; Plyduang T; Nuinoon M
Hemoglobin; 2018 Jan; 42(1):23-29. PubMed ID: 29457528
[TBL] [Abstract][Full Text] [Related]
10. A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the
Yang K; Ren Q; Wu Y; Zhou Y; Yin X
Hemoglobin; 2019 Mar; 43(2):140-144. PubMed ID: 31190573
[TBL] [Abstract][Full Text] [Related]
11. Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin.
Huang J; Zhang X; Liu D; Wei X; Shang X; Xiong F; Yu L; Yin X; Xu X
Eur J Hum Genet; 2015 Oct; 23(10):1341-8. PubMed ID: 25585695
[TBL] [Abstract][Full Text] [Related]
12. Hemoglobin EE disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression.
Arong A; Srivorakun H; Chaibunruang A; Fucharoen S; Fucharoen G; Kounnavong S; Sanchaisuriya K
Int J Lab Hematol; 2023 Jun; 45(3):387-393. PubMed ID: 36597281
[TBL] [Abstract][Full Text] [Related]
13. The Impact of XmnI-HBG2, BCL11A and HBS1L-MYB Single Nucleotide Polymorphisms on Hb F Variation of Hematologically Normal Iranian Individuals.
Keyhani E; Jafari Vesiehsari M; Talebi Kakroodi S; Darabi E; Zamani F; Karimlou M; Kamali K; Neishabury M
Hemoglobin; 2016 Jun; 40(3):198-201. PubMed ID: 27117569
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Does the Novel KLF1 Gene Mutation Lead to a Delay in Fetal Hemoglobin Switch?
Hariharan P; Gorivale M; Colah R; Ghosh K; Nadkarni A
Ann Hum Genet; 2017 May; 81(3):125-128. PubMed ID: 28369821
[TBL] [Abstract][Full Text] [Related]
18. Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts.
Heshusius S; Grech L; Gillemans N; Brouwer RWW; den Dekker XT; van IJcken WFJ; Nota B; Felice AE; van Dijk TB; von Lindern M; Borg J; van den Akker E; Philipsen S
Sci Rep; 2022 Jan; 12(1):336. PubMed ID: 35013432
[TBL] [Abstract][Full Text] [Related]
19. KLF1 gene mutations in Chinese adults with increased fetal hemoglobin.
Wang T; He Y; Zhou JY; Xie XM; Li J; Li R; Liao C; Li DZ
Hemoglobin; 2013; 37(5):501-6. PubMed ID: 23806141
[TBL] [Abstract][Full Text] [Related]
20. Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran.
Hamid M; Ershadi Oskouei S; Shariati G; Babaei E; Galehdari H; Saberi A; Sedaghat A
J Pediatr Hematol Oncol; 2018 Apr; 40(3):192-195. PubMed ID: 29420372
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]