149 related articles for article (PubMed ID: 25694242)
1. 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]
2. 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]
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. 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]
5. 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]
6. Hemoglobins F, A
Kingchaiyaphum B; Sanchaisuriya K; Fucharoen G; Chaibunruang A; Hess SY; Hinnouho GM; Barffour MA; Wessells KR; Kounnavong S; Fucharoen S
Int J Lab Hematol; 2020 Jun; 42(3):277-283. PubMed ID: 32048804
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Mutation screening of the Krüppel-like factor 1 gene using single-strand conformational polymorphism in a cohort of Iranian β-thalassemia patients.
Zaker-Kandjani B; Namdar-Aligoodarzi P; Azarkeivan A; Najmabadi H; Banan M
Hemoglobin; 2015; 39(1):24-9. PubMed ID: 25583416
[TBL] [Abstract][Full Text] [Related]
9. Phenotypic expression of hemoglobins A₂, E and F in various hemoglobin E related disorders.
Sae-ung N; Srivorakun H; Fucharoen G; Yamsri S; Sanchaisuriya K; Fucharoen S
Blood Cells Mol Dis; 2012 Jan; 48(1):11-6. PubMed ID: 22014901
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Co-inheritance of α
Singha K; Srivorakun H; Fucharoen G; Fucharoen S
Int J Lab Hematol; 2017 Oct; 39(5):508-512. PubMed ID: 28497611
[TBL] [Abstract][Full Text] [Related]
12. The validation of an automated liquid chromatography system for the diagnosis of thalassemias and hemoglobinopathies.
Sangkitporn S; Pung-amritt P; Sangkitporn SK; Sangnoi A; Tanphaichitr VS
Southeast Asian J Trop Med Public Health; 2002 Dec; 33(4):862-8. PubMed ID: 12757240
[TBL] [Abstract][Full Text] [Related]
13. %Hb A2, %Hb F, %G gamma values and the haplotypes in the beta-globin gene cluster in Japanese adults with elevated Hb F.
Shimizu K; Keino H
Hum Hered; 1992; 42(4):222-30. PubMed ID: 1380945
[TBL] [Abstract][Full Text] [Related]
14. Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals.
Lou JW; Li DZ; Zhang Y; He Y; Sun MN; Ye WL; Liu YH
Blood Cells Mol Dis; 2014 Dec; 53(4):261-4. PubMed ID: 24857170
[TBL] [Abstract][Full Text] [Related]
15. Capillary Electrophoresis Resolves Inconclusive HPLC Analysis for Hemoglobin Variants: a Study of Two Cases.
Li Y; Tian M; Qin T; Wan L
Clin Lab; 2018 Jul; 64(7):1305-1309. PubMed ID: 30146834
[TBL] [Abstract][Full Text] [Related]
16. Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation.
Satta S; Paglietti ME; Sollaino MC; Barella S; Moi P; Desogus MF; Demartis FR; Manunza L; Origa R
Blood Cells Mol Dis; 2017 May; 64():30-32. PubMed ID: 28342932
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Comparison of Sebia Capillarys Flex capillary electrophoresis with the BioRad Variant II high pressure liquid chromatography in the evaluation of hemoglobinopathies.
Greene DN; Pyle AL; Chang JS; Hoke C; Lorey T
Clin Chim Acta; 2012 Aug; 413(15-16):1232-8. PubMed ID: 22515960
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of beta-thalassemia/Hb E by hemoglobin typing compared to DNA analysis.
Sirichotiyakul S; Saetung R; Sanguansermsri T
Hemoglobin; 2009; 33(1):17-23. PubMed ID: 19205969
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
