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Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at Gγ-globin gene promoter

Scientific reports, 2021-04, Vol.11 (1), p.8552-8552, Article 8552

2021

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Predictive SNPs for β0-thalassemia/HbE disease severity

Scientific reports, 2021-05, Vol.11 (1), p.10352-10352, Article 10352

2021

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Mild-intensity physical activity prevents cardiac and osseous iron deposition without affecting bone mechanical property or porosity in thalassemic mice

Scientific reports, 2022-04, Vol.12 (1), p.5959-5959, Article 5959

2022

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Author Correction: An association between fibroblast growth factor 21 and cognitive impairment in iron-overload thalassemia

Scientific reports, 2023-02, Vol.13 (1), p.1851-2, Article 1851

2023

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Antioxidant Effects of Anthocyanin-Rich Riceberry™ Rice Flour Prepared Using Dielectric Barrier Discharge Plasma Technology on Iron-Induced Oxidative Stress in Mice

Molecules (Basel, Switzerland), 2021-08, Vol.26 (16), p.4978

2021

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Effects of green tea extract treatment on erythropoiesis and iron parameters in iron-overloaded β-thalassemic mice

Frontiers in physiology, 2022-12, Vol.13, p.1053060-1053060

2022

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Platelet proteome reveals specific proteins associated with platelet activation and the hypercoagulable state in β-thalassmia/HbE patients

Scientific reports, 2019-04, Vol.9 (1), p.6059-6059, Article 6059

2019

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Nephrectomy Does not Exacerbate Cancellous Bone loss in Thalassemic Mice

Scientific reports, 2020-05, Vol.10 (1), p.7786-7786, Article 7786

2020

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Iron homeostasis in a mouse model of thalassemia intermedia is altered between adolescence and adulthood

PeerJ (San Francisco, CA), 2020-03, Vol.8, p.e8802-e8802, Article e8802

2020

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The hypoferremic response to acute inflammation is maintained in thalassemia mice even under parenteral iron loading

PeerJ (San Francisco, CA), 2021-04, Vol.9, p.e11367-e11367, Article e11367

2021

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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, 2016-01, Vol.11 (1), p.e0148079-e0148079

2016

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Combination of ferric ammonium citrate with cytokines involved in apoptosis and insulin secretion of human pancreatic beta cells related to diabetes in thalassemia

PeerJ (San Francisco, CA), 2020-06, Vol.8, p.e9298-e9298, Article e9298

2020

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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, 2016-09, Vol.11 (9), p.e0163430-e0163430

2016

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Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure

PloS one, 2013-11, Vol.8 (11), p.e79522-e79522

2013

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RNA repair restores hemoglobin expression in IVS2-654 thalassemic mice

Proceedings of the National Academy of Sciences - PNAS, 2009-01, Vol.106 (4), p.1205-1210

2009

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Mitochondrial Changes in β0-Thalassemia/Hb E Disease

PloS one, 2016, Vol.11 (4), p.e0153831-e0153831

2016

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A mechanism of ineffective erythropoiesis in β-thalassemia/Hb E disease

Haematologica (Roma), 2010-05, Vol.95 (5), p.716-723

2010

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Establishment of MUi009 – A human induced pluripotent stem cells from a 32 year old male with homozygous β°-thalassemia coinherited with heterozygous α-thalassemia 2

Stem cell research, 2017-04, Vol.20 (C), p.80-83

2017

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Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice

Haematologica (Roma), 2009-09, Vol.94 (9), p.1211-1219

2009

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Gut leakage enhances sepsis susceptibility in iron-overloaded β-thalassemia mice through macrophage hyperinflammatory responses

American journal of physiology: Gastrointestinal and liver physiology, 2020-05, Vol.318 (5), p.G966-G979

2020

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Derivation of the human induced pluripotent stem cell line MUi017-A from a patient with homozygous Hemoglobin Constant Spring

Stem cell research, 2017-04, Vol.20 (C), p.84-87

2017

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Plasma microRNA-451 as a novel hemolytic marker for β0-thalassemia/HbE disease

Molecular medicine reports, 2017-05, Vol.15 (5), p.2495-2502

2017

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Effect of iron overload on furin expression in wild-type and β-thalassemic mice

Toxicology reports, 2015-01, Vol.2 (C), p.415-422

2015

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Dasatinib induces loss of vascular integrity and promotes cutaneous wound repair in mice

Journal of thrombosis and haemostasis, 2021-12, Vol.19 (12), p.3154-3167

2021

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Green tea extract modulates oxidative tissue injury in beta-thalassemic mice by chelation of redox iron and inhibition of lipid peroxidation

Biomedicine & pharmacotherapy, 2018-12, Vol.108, p.1694-1702

2018

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Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at Gγ-globin gene promoter

Predictive SNPs for β0-thalassemia/HbE disease severity

Mild-intensity physical activity prevents cardiac and osseous iron deposition without affecting bone mechanical property or porosity in thalassemic mice

Author Correction: An association between fibroblast growth factor 21 and cognitive impairment in iron-overload thalassemia

Antioxidant Effects of Anthocyanin-Rich Riceberry™ Rice Flour Prepared Using Dielectric Barrier Discharge Plasma Technology on Iron-Induced Oxidative Stress in Mice

Effects of green tea extract treatment on erythropoiesis and iron parameters in iron-overloaded β-thalassemic mice

Platelet proteome reveals specific proteins associated with platelet activation and the hypercoagulable state in β-thalassmia/HbE patients

Nephrectomy Does not Exacerbate Cancellous Bone loss in Thalassemic Mice

Iron homeostasis in a mouse model of thalassemia intermedia is altered between adolescence and adulthood

The hypoferremic response to acute inflammation is maintained in thalassemia mice even under parenteral iron loading

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

Combination of ferric ammonium citrate with cytokines involved in apoptosis and insulin secretion of human pancreatic beta cells related to diabetes in thalassemia

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

Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure

RNA repair restores hemoglobin expression in IVS2-654 thalassemic mice

Mitochondrial Changes in β0-Thalassemia/Hb E Disease

A mechanism of ineffective erythropoiesis in β-thalassemia/Hb E disease

Establishment of MUi009 – A human induced pluripotent stem cells from a 32 year old male with homozygous β°-thalassemia coinherited with heterozygous α-thalassemia 2

Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice

Gut leakage enhances sepsis susceptibility in iron-overloaded β-thalassemia mice through macrophage hyperinflammatory responses

Derivation of the human induced pluripotent stem cell line MUi017-A from a patient with homozygous Hemoglobin Constant Spring

Plasma microRNA-451 as a novel hemolytic marker for β0-thalassemia/HbE disease

Effect of iron overload on furin expression in wild-type and β-thalassemic mice

Dasatinib induces loss of vascular integrity and promotes cutaneous wound repair in mice

Green tea extract modulates oxidative tissue injury in beta-thalassemic mice by chelation of redox iron and inhibition of lipid peroxidation

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