52 results on '"Fucharoen, Suthat"'
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2. Increased autophagy leads to decreased apoptosis during β-thalassaemic mouse and patient erythropoiesis
3. Impaired neutrophil extracellular trap formation in β-thalassaemia/HbE
4. Predictive SNPs for β0-thalassemia/HbE disease severity
5. UNC0638 induces high levels of fetal hemoglobin expression in β-thalassemia/HbE erythroid progenitor cells
6. Visual genotyping of thalassemia by using pyrrolidinyl peptide nucleic acid probes immobilized on carboxymethylcellulose-modified paper and enzyme-induced pigmentation
7. Immunostick Test for Detecting ζ-Globin Chains and Screening of the Southeast Asian α-Thalassemia 1 Deletion
8. miR-144 regulates oxidative stress tolerance of thalassemic erythroid cell via targeting NRF2
9. Restoration of correct βIVS2-654-globin mRNA splicing and HbA production by engineered U7 snRNA in β-thalassaemia/HbE erythroid cells
10. Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β0-thalassemia/HbE disease
11. Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder
12. Circulating microRNAs in malaria infection: bench to bedside
13. MiR-155 enhances phagocytic activity of β-thalassemia/HbE monocytes via targeting of BACH1
14. A comprehensive ethnic-based analysis of alpha thalassaemia allelle frequency in northern Thailand
15. Hepcidin suppression in β-thalassemia is associated with the down-regulation of atonal homolog 8
16. Post-mortem study of the association between cardiac iron and fibrosis in transfusion dependent anaemia
17. Characterising private and shared signatures of positive selection in 37 Asian populations
18. Microparticles from splenectomized β-thalassemia/HbE patients play roles on procoagulant activities with thrombotic potential
19. Elevated levels of miR-210 correlate with anemia in β-thalassemia/HbE patients
20. Dysregulation of ferroportin gene expression in β0-thalassemia/Hb E disease
21. Calibration of myocardial T2 and T1 against iron concentration
22. Phenotypic comparison of four thalassemia model mice reconstructed from cryo-banked embryos
23. Differential plasma proteome profiles of mild versus severe β-thalassemia/Hb E
24. A reduced curcuminoid analog as a novel inducer of fetal hemoglobin
25. Mitochondrial calcium uniporter blocker prevents cardiac mitochondrial dysfunction induced by iron overload in thalassemic mice
26. Platelet activation and platelet–leukocyte interaction in β-thalassemia/hemoglobin E patients with marked nucleated erythrocytosis
27. Impaired bone formation and osteopenia in heterozygous βIVSII-654 knockin thalassemic mice
28. Enhanced activation of autophagy in β-thalassemia/Hb E erythroblasts during erythropoiesis
29. Pharmacokinetics of Deferiprone in Patients with β-Thalassaemia
30. Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system
31. Molecular basis and hematological features of hemoglobin variants in Southern Thailand
32. Expression of microRNA-451 in normal and thalassemic erythropoiesis
33. Genetic modifiers of Hb E/β0 thalassemia identified by a two-stage genome-wide association study
34. A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E
35. pHCR: a Parallel Haplotype Configuration Reduction algorithm for haplotype interaction analysis
36. Can we measure iron overload in the heart using in vivo MRI T2*?
37. Calibration of myocardial iron concentration against T2-star Cardiovascular Magnetic Resonance
38. Association of SNP in exon 1 of HBS1L with hemoglobin F level in β0-thalassemia/hemoglobin E
39. Molecular mechanism of β-thalassaemia caused by 22-bp duplication
40. Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease
41. High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin
42. Chicken Egg Yolk Antibodies Specific for the γ Chain of Human Hemoglobin for Diagnosis of Thalassemia
43. Molecular Mechanism of High Hemoglobin F Production in Southeast Asian-Type Hereditary Persistence of Fetal Hemoglobin
44. Hydroxyurea responses and fetal hemoglobin induction in β-thalassemia/HbE patients’ peripheral blood erythroid cell culture
45. Noninvasive Prenatal Diagnosis for Hemoglobin Bart's Hydrops Fetalis
46. The Signaling Pathways of Erythropoietin and Interferon-γ Differ in Preventing the Apoptosis of Mature Erythroid Progenitor Cells
47. Prevalence and Clinical Significance of Hepatitis C Virus Infection in Thai Patients with Thalassemia
48. Insertion of Modifications in the Beta-Globin Locus Using GET Recombination with Single-Stranded Oligonucleotides and Denatured PCR Fragments
49. Thalassemia and abnormal hemoglobin
50. Liver injury due to iron overload in thalassemia: histopathologic and ultrastructural studies
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