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Khanita Nuamsee

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Recent Articles
1.
Aiemongkot S, Ruschadaariyachat S, Changsangfa C, Nuamsee K, Viwatpinyo K, Chaichompoo P, et al.
Sci Rep . 2025 Feb; 15(1):4903. PMID: 39929883
Heterozygous β-globin gene knockout thalassemia (BKO) mice derived from C57BL/6 wild-type (WT) mice have phenotypic of β-thalassemia (BT) and have been widely used for studying this disease except reproductive disorders....
2.
Phongpao K, Pholngam N, Chokchaichamnankit D, Nuamsee K, Praneetponkang R, Ounjai P, et al.
Br J Haematol . 2024 Apr; 204(5):2025-2039. PMID: 38613149
Splenectomised β-thalassaemia/haemoglobin E (HbE) patients have increased levels of circulating microparticles or medium extra-cellular vesicles (mEVs). The splenectomised mEVs play important roles in thromboembolic complications in patients since they can...
3.
Phannasil P, Sukhuma C, Nauphar D, Nuamsee K, Svasti S
Blood Cells Mol Dis . 2023 Jul; 103:102781. PMID: 37478523
Ineffective erythropoiesis is the main cause of anemia in β-thalassemia. The crucial hallmark of ineffective erythropoiesis is the high proliferation of erythroblast. microRNA (miR/miRNA) involves several biological processes, including cell...
4.
Nuamsee K, Chuprajob T, Pabuprapap W, Jintaridth P, Munkongdee T, Phannasil P, et al.
Sci Rep . 2021 Apr; 11(1):8552. PMID: 33879818
The reactivation of γ-globin chain synthesis to combine with excess free α-globin chains and form fetal hemoglobin (HbF) is an important alternative treatment for β-thalassemia. We had reported HbF induction...