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The Roles of Mitophagy and Autophagy in Ineffective Erythropoiesis in β-Thalassemia

International journal of molecular sciences, 2022-09, Vol.23 (18), p.10811

2022

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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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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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Pre-Analytical Modification of Serum miRNAs: Diagnostic Reliability of Serum miRNAs in Hemolytic Diseases

Journal of clinical medicine, 2021-10, Vol.10 (21), p.5045

2021

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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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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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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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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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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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Proteomic profiling of circulating β‐thalassaemia/haemoglobin E extra‐cellular vesicles reveals that association with immunoglobulin induces membrane vesiculation

British journal of haematology, 2024-05, Vol.204 (5), p.2025-2039

2024

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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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A comprehensive study of immune function and immunophenotyping of white blood cells from β‐thalassaemia/HbE patients on hydroxyurea supports the safety of the drug

British journal of haematology, 2023-02, Vol.200 (3), p.367-376

2023

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Elevated levels of circulating monocytic myeloid derived suppressor cells in splenectomised β‐thalassaemia/HbE patients

British journal of haematology, 2020-11, Vol.191 (3), p.e72-e76

2020

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Silencing of the Long Noncoding RNA MYCNOS1 Suppresses Activity of MYCN-Amplified Retinoblastoma Without RB1 Mutation

Investigative ophthalmology & visual science, 2020-12, Vol.61 (14), p.8-8

2020

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Molecular analysis of β‐thalassemia in South Vietnam

American journal of hematology, 2002-10, Vol.71 (2), p.85-88

2002

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Running exercise alleviates trabecular bone loss and osteopenia in hemizygous β-globin knockout thalassemic mice

American journal of physiology: endocrinology and metabolism, 2014-06, Vol.306 (12), p.E1406-E1417

2014

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The effect of cryopreservation media on the quality of β-thalassemia mouse spermatozoa

Open veterinary journal (Tripoli, Libya), 2022-01, Vol.12 (5), p.602-611

2022

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Bone microstructural defects and osteopenia in hemizygous βIVSII-654 knockin thalassemic mice: sex-dependent changes in bone density and osteoclast function

American journal of physiology: endocrinology and metabolism, 2015-12, Vol.309 (11), p.E936-E948

2015

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Reduced PU.1 expression underlies aberrant neutrophil maturation and function in β-thalassemia mice and patients

Blood, 2017-06, Vol.129 (23), p.3087-3099

2017

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Hepcidin and 1,25(OH)2D3 effectively restore Ca2+ transport in β-thalassemic mice: reciprocal phenomenon of Fe2+ and Ca2+ absorption

American journal of physiology: endocrinology and metabolism, 2016-07, Vol.311 (1), p.E214-E223

2016

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Pathogen-Associated Molecules from Gut Translocation Enhance Severity of Cecal Ligation and Puncture Sepsis in Iron-Overload β-Thalassemia Mice

Journal of inflammation research, 2020-01, Vol.13, p.719-735

2020

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Modulation of hepcidin expression by normal control and beta0-thalassemia/Hb E erythroblasts

Hematology (Luxembourg), 2018-08, Vol.23 (7), p.423-428

2018

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The prevalence of alpha-thalassemia amongst Tai and Mon-Khmer ethnic groups residing in northern Thailand: A population-based study

Hematology (Luxembourg), 2016-09, Vol.21 (8), p.480-485

2016

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Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of β pre-mRNA splicing determine disease severity

British journal of haematology, 2011-09, Vol.154 (5), p.635-643

2011

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The Roles of Mitophagy and Autophagy in Ineffective Erythropoiesis in β-Thalassemia

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

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

Pre-Analytical Modification of Serum miRNAs: Diagnostic Reliability of Serum miRNAs in Hemolytic Diseases

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

Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice

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

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

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

Proteomic profiling of circulating β‐thalassaemia/haemoglobin E extra‐cellular vesicles reveals that association with immunoglobulin induces membrane vesiculation

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

A comprehensive study of immune function and immunophenotyping of white blood cells from β‐thalassaemia/HbE patients on hydroxyurea supports the safety of the drug

Elevated levels of circulating monocytic myeloid derived suppressor cells in splenectomised β‐thalassaemia/HbE patients

Silencing of the Long Noncoding RNA MYCNOS1 Suppresses Activity of MYCN-Amplified Retinoblastoma Without RB1 Mutation

Molecular analysis of β‐thalassemia in South Vietnam

Running exercise alleviates trabecular bone loss and osteopenia in hemizygous β-globin knockout thalassemic mice

The effect of cryopreservation media on the quality of β-thalassemia mouse spermatozoa

Bone microstructural defects and osteopenia in hemizygous βIVSII-654 knockin thalassemic mice: sex-dependent changes in bone density and osteoclast function

Reduced PU.1 expression underlies aberrant neutrophil maturation and function in β-thalassemia mice and patients

Hepcidin and 1,25(OH)2D3 effectively restore Ca2+ transport in β-thalassemic mice: reciprocal phenomenon of Fe2+ and Ca2+ absorption

Pathogen-Associated Molecules from Gut Translocation Enhance Severity of Cecal Ligation and Puncture Sepsis in Iron-Overload β-Thalassemia Mice

Modulation of hepcidin expression by normal control and beta0-thalassemia/Hb E erythroblasts

The prevalence of alpha-thalassemia amongst Tai and Mon-Khmer ethnic groups residing in northern Thailand: A population-based study

Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of β pre-mRNA splicing determine disease severity

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