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Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification

Scientific reports, 2023-06, Vol.13 (1), p.9612-9612, Article 9612

2023

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Impaired neutrophil extracellular trap formation in β-thalassaemia/HbE

Scientific reports, 2022-02, Vol.12 (1), p.1967-1967, Article 1967

2022

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

Scientific reports, 2021-04, Vol.11 (1), p.8057-10, Article 8057

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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High phosphate intake induces bone loss in nephrectomized thalassemic mice

PloS one, 2022-05, Vol.17 (5), p.e0268732-e0268732

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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Increased autophagy leads to decreased apoptosis during β-thalassaemic mouse and patient erythropoiesis

Scientific reports, 2022-11, Vol.12 (1), p.18628-18628, Article 18628

2022

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Restoration of correct β IVS2-654 -globin mRNA splicing and HbA production by engineered U7 snRNA in β-thalassaemia/HbE erythroid cells

Scientific reports, 2019-05, Vol.9 (1), p.7672-7672, Article 7672

2019

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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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A comprehensive ethnic-based analysis of alpha thalassaemia allelle frequency in northern Thailand

Scientific reports, 2017-07, Vol.7 (1), p.4690-9, Article 4690

2017

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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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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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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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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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Coordinated β-globin expression and α2-globin reduction in a multiplex lentiviral gene therapy vector for β-thalassemia

Molecular therapy, 2021-09, Vol.29 (9), p.2841-2853

2021

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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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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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Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification

Impaired neutrophil extracellular trap formation in β-thalassaemia/HbE

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

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

High phosphate intake induces bone loss in nephrectomized thalassemic mice

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

Increased autophagy leads to decreased apoptosis during β-thalassaemic mouse and patient erythropoiesis

Restoration of correct β IVS2-654 -globin mRNA splicing and HbA production by engineered U7 snRNA in β-thalassaemia/HbE erythroid cells

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

A comprehensive ethnic-based analysis of alpha thalassaemia allelle frequency in northern Thailand

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

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

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

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

Coordinated β-globin expression and α2-globin reduction in a multiplex lentiviral gene therapy vector for β-thalassemia

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

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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