255 related articles for article (PubMed ID: 31190573)
1. 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]
2.
Tamaddoni A; Khabaz Astaneh S; Tabaripour R; Akhavan-Niaki H
Hemoglobin; 2019 Jan; 43(1):12-17. PubMed ID: 30747024
[TBL] [Abstract][Full Text] [Related]
3. Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene.
Chen M; Ye YP; Liao L; Deng XL; Qiu YL; Lin FQ
Hematology; 2020 Dec; 25(1):438-445. PubMed ID: 33210974
[No 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 new Krüppel-like factor 1 mutation (c.947G > A or p.C316Y) in humans causes β-thalassemia minor.
Nitta T; Kawano F; Yamashiro Y; Takagi F; Murata T; Tanaka T; Ferania M; Adhiyanto C; Hattori Y
Hemoglobin; 2015; 39(2):121-6. PubMed ID: 25690802
[TBL] [Abstract][Full Text] [Related]
6. A
Xie XM; Liu YN; Li J; Jiang F; Li DZ
Hemoglobin; 2019 Mar; 43(2):137-139. PubMed ID: 31111750
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype.
Gallagher PG; Maksimova Y; Schulz VP; Forget BG
Hemoglobin; 2016 Sep; 40(5):361-364. PubMed ID: 27821015
[TBL] [Abstract][Full Text] [Related]
10. Molecular characterization of thalassemia intermedia associated with HPFH-6/beta-thalassemia and HPFH-6/Hb E in Thai patients.
Fucharoen S; Fucharoen G; Sanchaisuriya K; Surapot S
Acta Haematol; 2002; 108(3):157-61. PubMed ID: 12373089
[TBL] [Abstract][Full Text] [Related]
11. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.
Panyasai S; Jaiping K; Pornprasert S
Hemoglobin; 2015; 39(4):292-5. PubMed ID: 26029792
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of a β-thalassemia intermedia patient presenting inferior vena cava thrombosis: interaction of the β-globin erythroid Krüppel-like factor binding site mutation with Hb E and α(+)-thalassemia.
Prajantasen T; Teawtrakul N; Fucharoen G; Fucharoen S
Hemoglobin; 2014; 38(6):451-3. PubMed ID: 25370867
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Hereditary spherocytosis caused by copy number variation in SPTB gene identified through targeted next-generation sequencing.
Jang W; Kim J; Chae H; Kim M; Koh KN; Park CJ; Kim Y
Int J Hematol; 2019 Aug; 110(2):250-254. PubMed ID: 30903564
[TBL] [Abstract][Full Text] [Related]
15. Homozygous KLF1 mutation c.901C>T (p.Arg301Cys) resulting in mild thalassemia intermedia in an Indian: A next-generation sequencing diagnosis.
Rani N; Jamwal M; Kaur J; Sharma P; Malhotra P; Maitra A; Singh R; Das R
Blood Cells Mol Dis; 2018 Sep; 72():19-21. PubMed ID: 29980343
[No Abstract] [Full Text] [Related]
16. A novel mutation in the erythroid transcription factor KLF1 is likely responsible for ameliorating β-thalassemia major.
Fanis P; Kousiappa I; Phylactides M; Kyrri A; Hadjigavriel M; Christou S; Sitarou M; Kleanthous M
Hum Mutat; 2019 Oct; 40(10):1768-1780. PubMed ID: 31115947
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. The Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of β-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey.
Genc A; Tastemir Korkmaz D; Bayram S; Rencuzogullari E
Hemoglobin; 2020 Jul; 44(4):231-239. PubMed ID: 32674697
[TBL] [Abstract][Full Text] [Related]
19. Contrasting co-inheritance of alpha and beta mutations in delta beta thalassemia and hereditary persistence of fetal hemoglobin: a study from India.
Pandey H; Ranjan R; Singh K; Sharma A; Kishor K; Seth T; Saxena R
Hematology; 2018 Oct; 23(9):692-696. PubMed ID: 29621931
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia.
Huang G; Jiang WL; Rong KB; Li YX; Luo XL; Meng JX; Yu XY
Hemoglobin; 2010 Jan; 34(2):179-83. PubMed ID: 20353356
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
