BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 27086429)

  • 1. GENETIC FACTORS INFLUENCING HEMOGLOBIN F LEVEL IN β-THALASSEMIA/HB E DISEASE.
    Ruangrai W; Jindadamrongwech S
    Southeast Asian J Trop Med Public Health; 2016 Jan; 47(1):84-91. PubMed ID: 27086429
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Implication of globin gene expression, hemoglobin F and hemoglobin E levels on β-thalassemia/Hb E disease severity.
    Siriworadechkul S; Jindadamrongwech S; Chuncharunee S; Aupparakkitanon S
    Ann Clin Lab Sci; 2014; 44(4):437-42. PubMed ID: 25361929
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels.
    Vrettou C; Kanavakis E; Traeger-Synodinos J; Metaxotou-Mavrommati A; Basiakos I; Maragoudaki E; Stamoulakatou A; Papassotiriou I; Kattamis C
    Hemoglobin; 2000 Aug; 24(3):203-20. PubMed ID: 10975440
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of SNP in exon 1 of HBS1L with hemoglobin F level in beta0-thalassemia/hemoglobin E.
    Pandit RA; Svasti S; Sripichai O; Munkongdee T; Triwitayakorn K; Winichagoon P; Fucharoen S; Peerapittayamongkol C
    Int J Hematol; 2008 Nov; 88(4):357-361. PubMed ID: 18839276
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Variation and heritability of Hb F and F-cells among beta-thalassemia heterozygotes in Hong Kong.
    Gibney GT; Panhuysen CI; So JC; Ma ES; Ha SY; Li CK; Lee AC; Li CK; Yuen HL; Lau YL; Johnson DM; Farrell JJ; Bisbee AB; Farrer LA; Steinberg MH; Chan LC; Chui DH
    Am J Hematol; 2008 Jun; 83(6):458-64. PubMed ID: 18266208
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Molecular basis of a high Hb A
    Soontornpanawet C; Singha K; Srivorakun H; Tepakhan W; Fucharoen G; Fucharoen S
    PeerJ; 2023; 11():e15308. PubMed ID: 37159832
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Regulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for β-Globin Chain Deficiency?
    Jiang F; Li J; Zhou JY; Liao C; Li DZ
    Hemoglobin; 2019 Jan; 43(1):73-75. PubMed ID: 31104519
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Analysis of clinical phenotype and genotype of unstable Hemoglobin Rush].
    Ge S; Yang B; Yi W; Huang K; Liu H; Huang X; Chu J; Yang Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):15-20. PubMed ID: 28186586
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Beta-thalassemia mutations and single nucleotide polymorphism at -158 of Ggamma-globin gene associated with altered levels of Hb F in beta-thalassemia heterozygotes].
    Chen JF; Long GF; Lin WX; Chen P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):498-501. PubMed ID: 15476181
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular basis of thalassemia intermedia in Iran.
    Akbari MT; Izadi P; Izadyar M; Kyriacou K; Kleanthous M
    Hemoglobin; 2008; 32(5):462-70. PubMed ID: 18932071
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hemoglobin F and hemoglobin E/beta-thalassemia.
    Rees DC
    J Pediatr Hematol Oncol; 2000; 22(6):567-72. PubMed ID: 11132232
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New Insights on β-Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G>A) Patients with High Levels of Hb F.
    Ghoti H; Fibach E; Rachmilewitz EA; Jeadi H; Filon D
    Hemoglobin; 2017 Mar; 41(2):144-146. PubMed ID: 28670942
    [TBL] [Abstract][Full Text] [Related]  

  • 17. %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]  

  • 18. Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster.
    Manco L; Santos R; Rocha C; Relvas L; Bento C; Maia T; Gomes V; Amorim A; Prata MJ
    Hemoglobin; 2022 May; 46(3):168-175. PubMed ID: 35635444
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of XmnIgG Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients.
    Motovali-Bashi M; Ghasemi T
    Iran Biomed J; 2015; 19(3):177-82. PubMed ID: 26024726
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Beta-thalassaemia-87 C-->G: relationship of the Hb F modulation and polymorphisms in compound heterozygous patients.
    De Angioletti M; Lacerra G; Pagano L; Alessi M; D'Avino R; Manca L; Carestia C
    Br J Haematol; 2004 Sep; 126(5):743-9. PubMed ID: 15327529
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.