Works matching AU Svasti, Saovaros
Results: 72
Impaired bone formation and osteopenia in heterozygous β knockin thalassemic mice.
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- Histochemistry & Cell Biology, 2011, v. 136, n. 1, p. 47, doi. 10.1007/s00418-011-0823-1
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- Article
The hypoferremic response to acute inflammation is maintained in thalassemia mice even under parenteral iron loading.
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- PeerJ, 2021, p. 1, doi. 10.7717/peerj.11367
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- Article
Combination of ferric ammonium citrate with cytokines involved in apoptosis and insulin secretion of human pancreatic beta cells related to diabetes in thalassemia.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.9298
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- Article
Iron homeostasis in a mouse model of thalassemia intermedia is altered between adolescence and adulthood.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.8802
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- Article
Iron induces blood-brain barrier alteration contributing to cognitive impairment in β-thalassaemia mice.
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- Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-024-84395-z
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- Article
Cognitive impairment and hippocampal neuronal damage in β-thalassaemia mice.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-60459-y
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- Article
Moringa oleifera Pod Inhibits Inflammatory Mediator Production by Lipopolysaccharide-Stimulated RAW 264.7 Murine Macrophage Cell Lines.
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- Inflammation, 2012, v. 35, n. 2, p. 445, doi. 10.1007/s10753-011-9334-4
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- Article
Development of DNA controls for detection of β‐thalassemia mutations commonly found in Asian.
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- International Journal of Laboratory Hematology, 2020, v. 42, n. 6, p. 727, doi. 10.1111/ijlh.13292
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- Article
Molecular prevalence of thalassemia and hemoglobinopathies among the Lao Loum Group in the Lao People's Democratic Republic.
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- International Journal of Laboratory Hematology, 2019, v. 41, n. 5, p. 650, doi. 10.1111/ijlh.13080
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- Article
Extracellular vesicles from thalassemia patients carry iron-containing ferritin and hemichrome that promote cardiac cell proliferation.
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- Annals of Hematology, 2021, v. 100, n. 8, p. 1929, doi. 10.1007/s00277-021-04567-z
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- Article
Elevated levels of platelet- and red cell-derived extracellular vesicles in transfusion-dependent β-thalassemia/HbE patients with pulmonary arterial hypertension.
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- Annals of Hematology, 2019, v. 98, n. 2, p. 281, doi. 10.1007/s00277-018-3518-z
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- Article
Microparticles from splenectomized β-thalassemia/HbE patients play roles on procoagulant activities with thrombotic potential.
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- 2017
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- journal article
Dysregulation of ferroportin gene expression in β(0)-thalassemia/Hb E disease.
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- 2016
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- journal article
A reduced curcuminoid analog as a novel inducer of fetal hemoglobin.
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- Annals of Hematology, 2013, v. 92, n. 3, p. 379, doi. 10.1007/s00277-012-1604-1
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- Article
Quantitative analysis of Hb Bart's in cord blood by capillary electrophoresis system.
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- Annals of Hematology, 2011, v. 90, n. 7, p. 741, doi. 10.1007/s00277-010-1137-4
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- Article
Enhanced activation of autophagy in β-thalassemia/Hb E erythroblasts during erythropoiesis.
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- Annals of Hematology, 2011, v. 90, n. 7, p. 747, doi. 10.1007/s00277-010-1152-5
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- Article
Expression of microRNA-451 in normal and thalassemic erythropoiesis.
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- Annals of Hematology, 2010, v. 89, n. 10, p. 953, doi. 10.1007/s00277-010-0980-7
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- Article
Molecular mechanism of β-thalassaemia caused by 22-bp duplication.
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- Annals of Hematology, 2008, v. 87, n. 8, p. 633, doi. 10.1007/s00277-008-0479-7
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- Article
Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease.
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- Annals of Hematology, 2008, v. 87, n. 5, p. 375, doi. 10.1007/s00277-007-0407-2
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- Article
A genome-wide association identified the common genetic variants influence disease severity in β<sup>0</sup>-thalassemia/hemoglobin E.
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- Human Genetics, 2010, v. 127, n. 3, p. 303, doi. 10.1007/s00439-009-0770-2
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- Article
Pre-Analytical Modification of Serum miRNAs: Diagnostic Reliability of Serum miRNAs in Hemolytic Diseases.
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- Journal of Clinical Medicine, 2021, v. 10, n. 21, p. 5045, doi. 10.3390/jcm10215045
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- Article
Genetic predictions of life expectancy in southern Thai patients with β<sup>0</sup>-thalassemia/Hb E.
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- Biomedical Reports, 2022, v. 16, n. 6, p. N.PAG, doi. 10.3892/br.2022.1535
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- Article
Responses of primary osteoblasts and osteoclasts from hemizygous β-globin knockout thalassemic mice with elevated plasma glucose to 1,25-dihydroxyvitamin D<sub>3</sub>.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50414-7
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- Article
Platelet proteome reveals specific proteins associated with platelet activation and the hypercoagulable state in β-thalassmia/HbE patients.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-42432-2
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- Article
Na/H exchanger 3 inhibitor diminishes hepcidin-enhanced duodenal calcium transport in hemizygous β-globin knockout thalassemic mice.
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- Molecular & Cellular Biochemistry, 2017, v. 427, n. 1/2, p. 201, doi. 10.1007/s11010-016-2911-y
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- Article
Modulation of hepcidin expression by normal control and beta0-thalassemia/Hb E erythroblasts.
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- Hematology, 2018, v. 23, n. 7, p. 423, doi. 10.1080/10245332.2017.1405571
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- Article
The prevalence of alpha-thalassemia amongst Tai and Mon-Khmer ethnic groups residing in northern Thailand: A population-based study.
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- Hematology, 2016, v. 21, n. 8, p. 480, doi. 10.1080/10245332.2016.1148374
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- Article
Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-36676-2
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- Article
Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of β<sup>E</sup> pre-mRNA splicing determine disease severity.
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- British Journal of Haematology, 2011, v. 154, n. 5, p. 635, doi. 10.1111/j.1365-2141.2011.08770.x
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- Article
Increased erythropoiesis of β-thalassaemia/Hb E proerythroblasts is mediated by high basal levels of ERK1/2 activation.
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- British Journal of Haematology, 2009, v. 146, n. 5, p. 557, doi. 10.1111/j.1365-2141.2009.07794.x
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- Article
Molecular Epidemiology of Hemoglobinopathies in Cambodia.
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- Hemoglobin, 2016, v. 40, n. 3, p. 163, doi. 10.3109/03630269.2016.1158723
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- Article
Molecular Screening of the Hbs Constant Spring (codon 142, TAA> CAA, α2) and PAKSÉ (codon 142, TA A>TA T, α2) Mutations in Thailand.
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- Hemoglobin, 2010, v. 34, n. 6, p. 582, doi. 10.3109/03630269.2010.526914
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- Article
Male reproductive phenotype alterations in heterozygous β-globin gene knockout thalassemia (BKO) mice as a model for β-thalassemia patients.
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- Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-87619-y
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- Article
UGT1A6 genotype-related pharmacokinetics of deferiprone (L1) in healthy volunteers.
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- British Journal of Clinical Pharmacology, 2008, v. 65, n. 6, p. 908, doi. 10.1111/j.1365-2125.2008.03103.x
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- Article
Pathogen-Associated Molecules from Gut Translocation Enhance Severity of Cecal Ligation and Puncture Sepsis in Iron-Overload β-Thalassemia Mice.
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- Journal of Inflammation Research, 2020, p. 719, doi. 10.2147/JIR.S273329
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- Article
Mitochondrial Changes in β<sup>0</sup>-Thalassemia/Hb E Disease.
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- PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0153831
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- Article
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.
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- PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0148079
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- Article
Association of SNP in exon 1 of HBS1L with hemoglobin F level in beta0-thalassemia/hemoglobin E.
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- 2008
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- Publication type:
- journal article
Increased susceptibility to dextran sulfate-induced mucositis of iron-overload β-thalassemia mice, another endogenous cause of septicemia in thalassemia.
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- Clinical Science, 2021, v. 135, n. 12, p. 1467, doi. 10.1042/CS20210328
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- Article
Mild-intensity physical activity prevents cardiac and osseous iron deposition without affecting bone mechanical property or porosity in thalassemic mice.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-09997-x
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- Article
Impaired neutrophil extracellular trap formation in β-thalassaemia/HbE.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-06036-7
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- Article
Cardiomyocyte ultrastructural damage in β-thalassaemic mice.
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- International Journal of Experimental Pathology, 2013, v. 94, n. 5, p. 336, doi. 10.1111/iep.12044
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- Article
Proteomic profiling of circulating β‐thalassaemia/haemoglobin E extra‐cellular vesicles reveals that association with immunoglobulin induces membrane vesiculation.
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- British Journal of Haematology, 2024, v. 204, n. 5, p. 2025, doi. 10.1111/bjh.19454
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- Article
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.
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- British Journal of Haematology, 2023, v. 200, n. 3, p. 367, doi. 10.1111/bjh.18508
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- Article
Elevated levels of circulating monocytic myeloid derived suppressor cells in splenectomised β‐thalassaemia/HbE patients.
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- British Journal of Haematology, 2020, v. 191, n. 3, p. e72, doi. 10.1111/bjh.17012
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- Article
Increased ferritin levels in non‐transfusion‐dependent β°‐thalassaemia/HbE are associated with reduced CXCR2 expression and neutrophil migration.
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- British Journal of Haematology, 2020, v. 189, n. 1, p. 187, doi. 10.1111/bjh.16295
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- Article
An in vivo model for analysis of developmental erythropoiesis and globin gene regulation.
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- FASEB Journal, 2014, v. 28, n. 5, p. 2306, doi. 10.1096/fj.13-246637
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- Article
Characterization of a novel deletion causing (??)0?thalassemia in a Thai family.
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- American Journal of Hematology, 2007, v. 82, n. 2, p. 155, doi. 10.1002/ajh.20781
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- Article
Molecular analysis of β-thalassemia in South Vietnam.
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- American Journal of Hematology, 2002, v. 71, n. 2, p. 85, doi. 10.1002/ajh.10193
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- Article
The effect of cryopreservation media on the quality of ß-thalassemia mouse spermatozoa.
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- Open Veterinary Journal, 2022, v. 12, n. 5, p. 602, doi. 10.5455/OVJ.2022.v12.i5.2
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- Article