PubRank

Saovaros Svasti

Author PubWeight™ 24.48‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. Hum Genet 2010 1.75
2 Restoration of human beta-globin gene expression in murine and human IVS2-654 thalassemic erythroid cells by free uptake of antisense oligonucleotides. Mol Pharmacol 2002 1.02
3 UGT1A6 genotype-related pharmacokinetics of deferiprone (L1) in healthy volunteers. Br J Clin Pharmacol 2008 0.90
4 Eryngium foetidum suppresses inflammatory mediators produced by macrophages. Asian Pac J Cancer Prev 2012 0.89
5 Increased erythropoiesis of beta-thalassaemia/Hb E proerythroblasts is mediated by high basal levels of ERK1/2 activation. Br J Haematol 2009 0.87
6 Increased oxidative metabolism is associated with erythroid precursor expansion in β0-thalassaemia/Hb E disease. Blood Cells Mol Dis 2011 0.86
7 Enhanced activation of autophagy in β-thalassemia/Hb E erythroblasts during erythropoiesis. Ann Hematol 2011 0.84
8 Moringa oleifera pod inhibits inflammatory mediator production by lipopolysaccharide-stimulated RAW 264.7 murine macrophage cell lines. Inflammation 2012 0.84
9 Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study. BMC Med Genet 2010 0.84
10 Impaired bone formation and osteopenia in heterozygous β(IVSII-654) knockin thalassemic mice. Histochem Cell Biol 2011 0.84
11 Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease. Ann Hematol 2007 0.83
12 Association of SNP in exon 1 of HBS1L with hemoglobin F level in beta0-thalassemia/hemoglobin E. Int J Hematol 2008 0.83
13 A mechanism of ineffective erythropoiesis in β-thalassemia/Hb E disease. Haematologica 2009 0.82
14 Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure. PLoS One 2013 0.82
15 Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice. Haematologica 2009 0.81
16 Enhanced erythroid cell differentiation in hypoxic condition is in part contributed by miR-210. Blood Cells Mol Dis 2013 0.79
17 Rapid diagnosis of alpha-thalassemia by melting curve analysis. J Mol Diagn 2010 0.79
18 Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of β(E) pre-mRNA splicing determine disease severity. Br J Haematol 2011 0.79
19 Anti-inflammatory activities of red curry paste extract on lipopolysaccharide-activated murine macrophage cell line. Nutrition 2010 0.79
20 An in vivo model for analysis of developmental erythropoiesis and globin gene regulation. FASEB J 2014 0.78
21 Quantitative analysis of Hb Bart's in cord blood by capillary electrophoresis system. Ann Hematol 2010 0.78
22 Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and Paksé (codon 142, TAA>TAT, α2) mutations in Thailand. Hemoglobin 2010 0.78
23 Rapid diagnosis of thalassemias and other hemoglobinopathies by capillary electrophoresis system. Transl Res 2008 0.77
24 Proteomic analysis of hemoglobin H-constant spring (Hb H-CS) erythroblasts. Blood Cells Mol Dis 2011 0.77
25 Cardiomyocyte ultrastructural damage in β-thalassaemic mice. Int J Exp Pathol 2013 0.76
26 Hb Siam [alpha15(A13)Gly-->Arg (alpha1) (GGT-->CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect. Hemoglobin 2002 0.76
27 Clinical severity of β-thalassaemia/Hb E disease is associated with differential activities of the calpain-calpastatin proteolytic system. PLoS One 2012 0.75
28 A reduced curcuminoid analog as a novel inducer of fetal hemoglobin. Ann Hematol 2012 0.75
29 Correction: Hemoglobin E Prevalence among Ethnic Groups Residing in Malaria-Endemic Areas of Northern Thailand and Its Lack of Association with Plasmodium falciparum Invasion In Vitro. PLoS One 2016 0.75
30 Effect of human beta-globin bacterial artificial chromosome transgenesis on embryo cryopreservation in mouse models. Reprod Fertil Dev 2010 0.75
31 Phenotypic comparison of four thalassemia model mice reconstructed from cryo-banked embryos. Acta Biol Hung 2013 0.75
32 Expression of betaE and gamma-globin genes in infants heterozygous for hemoglobin E and double heterozygous for hemoglobin E and alpha-thalassemia. Haematologica 2007 0.75
33 [Dysregulation of microRNA in thalassemia]. Fukuoka Igaku Zasshi 2015 0.75
34 Effects of Iron Chelators on Pulmonary Iron Overload and Oxidative Stress in β-Thalassemic Mice. Pharmacology 2015 0.75
35 Double heterozygosity for Hb Pyrgos [beta83(EF7)Gly-->Asp] and Hb E [beta26(B8)Glu-->Lys] found in association with alpha-thalassemia. Hemoglobin 2002 0.75
36 1,25-Dihydroxyvitamin D3 -induced intestinal calcium transport is impaired in β-globin knockout thalassemic mice. Cell Biochem Funct 2013 0.75
37 Labdane diterpenes from the aerial parts of Curcuma comosa enhance fetal hemoglobin production in an erythroid cell line. J Nat Prod 2010 0.75