全部文献期刊学位论文会议报纸专利标准年鉴图书|学者科研项目
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作者:Supat Chamnanchanunt , Suthat Fucharoen , Tsukuru Umemura
来源:[J].Malaria Journal(IF 3.4), 2017, Vol.16 (1)Springer
摘要:Severe malaria has a poor prognosis with a morbidity rate of 80% in tropical areas. The early parasite detection is one of the effective means to prevent severe malaria of which specific treatment strategies are limited. Many clinical characteristics and laboratory testings ...
作者:... Chamnong Nopparatana , Malai Wongchanchailert , Suthat Fucharoen
来源:[J].International Journal of Hematology(IF 1.681), 2017, Vol.106 (5), pp.638-647Springer
摘要:Abnormal red blood cell (RBC) clearance in β-thalassemia is triggered by activated monocytes. Recent reports indicate that miRNA (miR-) plays a role in monocyte activation. To study phagocytic function, we co-cultured monocytes of normal, non-splenectomized and splenectomize...
作者:... Prachya Kongtawelert , Suthat Fucharoen , Somdet Srichairatanakool
来源:[J].International Journal of Hematology(IF 1.681), 2017, Vol.106 (2), pp.196-205Springer
摘要:Atonal homolog 8 (ATOH8) is defined as a positive regulator of hepcidin transcription, which links erythropoietic activity with iron-sensing molecules. In the present study, we investigated the association between hepcidin and ATOH8 expression in β-thalassemia. We found that...
作者:Suthat Fucharoen , John B Porter ...
来源:[J].Journal of Cardiovascular Magnetic Resonance, 2017, Vol.19 (1)Springer
摘要:Heart failure related to cardiac siderosis remains a major cause of death in transfusion dependent anaemias. Replacement fibrosis has been reported as causative of heart failure in siderotic cardiomyopathy in historical reports, but these findings do not accord with the reversibl...
作者:... Hoa Thi Thuy Phan , Goonnapa Fucharoen , Supan Fucharoen
来源:[J].Journal of Community Genetics, 2017, Vol.8 (3), pp.221-228Springer
摘要:Thalassemia is a genetic condition that can result in long and expensive treatments, and severe thalassemia may lead to death if left untreated. Couples contributing two genes for thalassemia place their children at particular risk for severe thalassemia. Gene frequency of t...
作者:Fucharoen Suthat , Braun Andreas
来源:[J].BMC Medical Genetics(IF 2.536), 2010, Vol.11 (1), pp.51DOAJ
摘要:Abstract Background Patients with Hb E/β0 thalassemia display remarkable variability in disease severity. To identify genetic modifiers influencing disease severity, we conducted a two-stage genome scan in groups of 207 mild and 305 severe unrelated patients from ...
作者:Suthat Fucharoen , Ryszard Kole
来源:[J].Scientific Reports(IF 2.927), 2019, Vol.9 (1), pp.1-8DOAJ
摘要:Abstract A cytosine to thymine mutation at nucleotide 654 of human β-globin intron 2 (βIVS2-654) is one of the most common mutations causing β-thalassaemia in Chinese and Southeast Asians. This mutation results in aberrant β-globin pre-mRNA splicing and prevents synthesis of...
作者:Fucharoen Supan , Perls Thomas ...
来源:[J].BMC Genetics(IF 2.808), 2008, Vol.9 (1), pp.85DOAJ
摘要:Abstract Background Imputation of missing genotypes is becoming a very popular solution for synchronizing genotype data collected with different microarray platforms but the effect of ethnic background, subject ascertainment, and amount of missing data on the accuracy of imputati...

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