170 related articles for article (PubMed ID: 25690802)
1. 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]
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. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. Analysis of the Genotypes in a Chinese Population with Increased Hb A
Jiang F; Chen GL; Li J; Zhou JY; Liao C; Li DZ
Hemoglobin; 2018 May; 42(3):154-158. PubMed ID: 30277083
[TBL] [Abstract][Full Text] [Related]
11. A stepwise haematological screening and whole-exome sequencing reveal multiple mutations from SUPT5H causing an elevation of Hb A
Lou J; Ye Y; Sun M; Zhao Y; Fu Y; Liu Y
Int J Lab Hematol; 2023 Feb; 45(1):90-95. PubMed ID: 36054783
[TBL] [Abstract][Full Text] [Related]
12. Whole exome sequencing and rare variant association study to identify genetic modifiers,
Hantaweepant C; Suktitipat B; Pithukpakorn M; Chinthammitr Y; Limwongse C; Tansiri N; Sawatnatee S; Takpradit C; Rotchanapanya W; Pongudom S; Charoenprasert K; Paiboonsukwong K; Thamprasert W; Nolwachai N; Rattanasawat W; Sae-Aeng B; Khorwanichakij N; Saetow P; Saengboon S; Kamjornpreecha K; Pholmoo W; Dujjawan B; Siritanaratkul N
Hematology; 2023 Dec; 28(1):2187155. PubMed ID: 36939018
[TBL] [Abstract][Full Text] [Related]
13. A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (
Hasan KN; Sufian A; Mazumder AK; Khaleque MA; Rahman M; Akhteruzzaman S
Hemoglobin; 2019 May; 43(3):162-165. PubMed ID: 31339392
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)].
Yan JM; Zhou JY; Xie XM; Li J; Li DZ
Hemoglobin; 2016 Jun; 40(3):213-4. PubMed ID: 27117573
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. KLF1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of β-thalassemia.
Liu D; Zhang X; Yu L; Cai R; Ma X; Zheng C; Zhou Y; Liu Q; Wei X; Lin L; Yan T; Huang J; Mohandas N; An X; Xu X
Blood; 2014 Jul; 124(5):803-11. PubMed ID: 24829204
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A
Satthakarn S; Panyasai S; Pornprasert S
Hemoglobin; 2020 Sep; 44(5):349-353. PubMed ID: 33023363
[TBL] [Abstract][Full Text] [Related]
20. Mutational spectrum of delta-globin gene in the Portuguese population.
Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]