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Characterization of a novel deletion causing (??)0?thalassemia in a Thai family.
- Published in:
- American Journal of Hematology, 2007, v. 82, n. 2, p. 155, doi. 10.1002/ajh.20781
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- Publication type:
- Article
Molecular analysis of β-thalassemia in South Vietnam.
- Published in:
- American Journal of Hematology, 2002, v. 71, n. 2, p. 85, doi. 10.1002/ajh.10193
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- Publication type:
- Article
A genome-wide association identified the common genetic variants influence disease severity in β<sup>0</sup>-thalassemia/hemoglobin E.
- Published in:
- Human Genetics, 2010, v. 127, n. 3, p. 303, doi. 10.1007/s00439-009-0770-2
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- Publication type:
- Article
The effect of cryopreservation media on the quality of ß-thalassemia mouse spermatozoa.
- Published in:
- Open Veterinary Journal, 2022, v. 12, n. 5, p. 602, doi. 10.5455/OVJ.2022.v12.i5.2
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- Publication type:
- Article
An in vivo model for analysis of developmental erythropoiesis and globin gene regulation.
- Published in:
- FASEB Journal, 2014, v. 28, n. 5, p. 2306, doi. 10.1096/fj.13-246637
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- Publication type:
- Article
Antioxidant Effects of Anthocyanin-Rich Riceberry™ Rice Flour Prepared Using Dielectric Barrier Discharge Plasma Technology on Iron-Induced Oxidative Stress in Mice.
- Published in:
- Molecules, 2021, v. 26, n. 16, p. 4978, doi. 10.3390/molecules26164978
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- Publication type:
- Article
Platelet proteome reveals specific proteins associated with platelet activation and the hypercoagulable state in β-thalassmia/HbE patients.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-42432-2
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- Publication type:
- Article
Microparticles from β-thalassaemia/HbE patients induce endothelial cell dysfunction.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-31386-6
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- Publication type:
- Article
Effects of green tea extract treatment on erythropoiesis and iron parameters in iron-overloaded β-thalassemic mice.
- Published in:
- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.1053060
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- Publication type:
- Article
High phosphate intake induces bone loss in nephrectomized thalassemic mice.
- Published in:
- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0268732
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- Publication type:
- Article
Moringa oleifera Pod Inhibits Inflammatory Mediator Production by Lipopolysaccharide-Stimulated RAW 264.7 Murine Macrophage Cell Lines.
- Published in:
- Inflammation, 2012, v. 35, n. 2, p. 445, doi. 10.1007/s10753-011-9334-4
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- Publication type:
- Article
The Roles of Mitophagy and Autophagy in Ineffective Erythropoiesis in β-Thalassemia.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 18, p. N.PAG, doi. 10.3390/ijms231810811
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- Publication type:
- Article
1,25-Dihydroxyvitamin D<sub>3</sub>-induced intestinal calcium transport is impaired in β-globin knockout thalassemic mice.
- Published in:
- Cell Biochemistry & Function, 2013, v. 31, n. 8, p. 685, doi. 10.1002/cbf.2956
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- Publication type:
- Article
Cardiomyocyte ultrastructural damage in β-thalassaemic mice.
- Published in:
- International Journal of Experimental Pathology, 2013, v. 94, n. 5, p. 336, doi. 10.1111/iep.12044
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- Publication type:
- Article
Na/H exchanger 3 inhibitor diminishes hepcidin-enhanced duodenal calcium transport in hemizygous β-globin knockout thalassemic mice.
- Published in:
- Molecular & Cellular Biochemistry, 2017, v. 427, n. 1/2, p. 201, doi. 10.1007/s11010-016-2911-y
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- Publication type:
- Article
Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of β<sup>E</sup> pre-mRNA splicing determine disease severity.
- Published in:
- British Journal of Haematology, 2011, v. 154, n. 5, p. 635, doi. 10.1111/j.1365-2141.2011.08770.x
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- Publication type:
- Article
Increased erythropoiesis of β-thalassaemia/Hb E proerythroblasts is mediated by high basal levels of ERK1/2 activation.
- Published in:
- British Journal of Haematology, 2009, v. 146, n. 5, p. 557, doi. 10.1111/j.1365-2141.2009.07794.x
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- Publication type:
- Article
Genetic predictions of life expectancy in southern Thai patients with β<sup>0</sup>-thalassemia/Hb E.
- Published in:
- Biomedical Reports, 2022, v. 16, n. 6, p. N.PAG, doi. 10.3892/br.2022.1535
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- Publication type:
- Article
Nephrectomy Does not Exacerbate Cancellous Bone loss in Thalassemic Mice.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-64681-2
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- Publication type:
- 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>.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50414-7
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- Publication type:
- Article
Insight into the Peopling of Mainland Southeast Asia from Thai Population Genetic Structure.
- Published in:
- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0079522
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- Publication type:
- Article
Clinical Severity of ß-thalassaemia/Hb E Disease Is Associated with Differential Activities of the Calpain-Calpastatin Proteolytic System.
- Published in:
- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037133
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- Publication type:
- Article
Proteomic profiling of circulating β‐thalassaemia/haemoglobin E extra‐cellular vesicles reveals that association with immunoglobulin induces membrane vesiculation.
- Published in:
- British Journal of Haematology, 2024, v. 204, n. 5, p. 2025, doi. 10.1111/bjh.19454
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- Publication type:
- 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.
- Published in:
- British Journal of Haematology, 2023, v. 200, n. 3, p. 367, doi. 10.1111/bjh.18508
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- Publication type:
- Article
Elevated levels of circulating monocytic myeloid derived suppressor cells in splenectomised β‐thalassaemia/HbE patients.
- Published in:
- British Journal of Haematology, 2020, v. 191, n. 3, p. e72, doi. 10.1111/bjh.17012
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- Publication type:
- Article
Increased ferritin levels in non‐transfusion‐dependent β°‐thalassaemia/HbE are associated with reduced CXCR2 expression and neutrophil migration.
- Published in:
- British Journal of Haematology, 2020, v. 189, n. 1, p. 187, doi. 10.1111/bjh.16295
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- Publication type:
- Article
The hypoferremic response to acute inflammation is maintained in thalassemia mice even under parenteral iron loading.
- Published in:
- PeerJ, 2021, p. 1, doi. 10.7717/peerj.11367
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- Publication type:
- Article
Combination of ferric ammonium citrate with cytokines involved in apoptosis and insulin secretion of human pancreatic beta cells related to diabetes in thalassemia.
- Published in:
- PeerJ, 2020, p. 1, doi. 10.7717/peerj.9298
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- Publication type:
- Article
Iron homeostasis in a mouse model of thalassemia intermedia is altered between adolescence and adulthood.
- Published in:
- PeerJ, 2020, p. 1, doi. 10.7717/peerj.8802
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- Publication type:
- Article
Expression level of pro-apoptotic genes determine disease severity of HbE/ beta thalassemia.
- Published in:
- Journal of Applied Hematology, 2019, v. 10, p. S16
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- Publication type:
- Article
Predictive SNPs for β0-thalassemia/HbE disease severity.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-89641-2
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- Publication type:
- Article
Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at Gγ-globin gene promoter.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-87738-2
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- Publication type:
- Article
An association between fibroblast growth factor 21 and cognitive impairment in iron-overload thalassemia.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-87597-x
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- Publication type:
- Article
UGT1A6 genotype-related pharmacokinetics of deferiprone (L1) in healthy volunteers.
- Published in:
- 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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- Publication type:
- Article
Pathogen-Associated Molecules from Gut Translocation Enhance Severity of Cecal Ligation and Puncture Sepsis in Iron-Overload β-Thalassemia Mice.
- Published in:
- Journal of Inflammation Research, 2020, p. 719, doi. 10.2147/JIR.S273329
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- Publication type:
- Article
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.
- Published in:
- 2016
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- Publication type:
- Correction Notice
Elevated levels of miR-210 correlate with anemia in β-thalassemia/HbE patients.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Association of SNP in exon 1 of HBS1L with hemoglobin F level in beta0-thalassemia/hemoglobin E.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Genetic modifiers of Hb E/β<sup>0</sup> thalassemia identified by a two-stage genome-wide association study.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 51, doi. 10.1186/1471-2350-11-51
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- Publication type:
- Article
Effects of Iron Chelators on Pulmonary Iron Overload and Oxidative Stress in β-Thalassemic Mice.
- Published in:
- Pharmacology, 2015, v. 96, n. 3/4, p. 192, doi. 10.1159/000438994
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- Publication type:
- Article
Comparative Plasma Protein Profiling of Hemoglobin H Disease.
- Published in:
- Disease Markers, 2014, p. 1, doi. 10.1155/2014/340214
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- Publication type:
- Article
Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-36676-2
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- Publication type:
- Article
Author Correction: An association between fibroblast growth factor 21 and cognitive impairment in iron-overload thalassemia.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-28995-1
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- Publication type:
- Article
Development of DNA controls for detection of β‐thalassemia mutations commonly found in Asian.
- Published in:
- International Journal of Laboratory Hematology, 2020, v. 42, n. 6, p. 727, doi. 10.1111/ijlh.13292
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- Publication type:
- Article
Molecular prevalence of thalassemia and hemoglobinopathies among the Lao Loum Group in the Lao People's Democratic Republic.
- Published in:
- International Journal of Laboratory Hematology, 2019, v. 41, n. 5, p. 650, doi. 10.1111/ijlh.13080
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- Publication type:
- Article
Pre-Analytical Modification of Serum miRNAs: Diagnostic Reliability of Serum miRNAs in Hemolytic Diseases.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 21, p. 5045, doi. 10.3390/jcm10215045
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- Publication type:
- Article
Mild-intensity physical activity prevents cardiac and osseous iron deposition without affecting bone mechanical property or porosity in thalassemic mice.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-09997-x
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- Publication type:
- Article
Impaired neutrophil extracellular trap formation in β-thalassaemia/HbE.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-06036-7
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- Publication type:
- Article
Extracellular vesicles from thalassemia patients carry iron-containing ferritin and hemichrome that promote cardiac cell proliferation.
- Published in:
- Annals of Hematology, 2021, v. 100, n. 8, p. 1929, doi. 10.1007/s00277-021-04567-z
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- Publication type:
- Article
Elevated levels of platelet- and red cell-derived extracellular vesicles in transfusion-dependent β-thalassemia/HbE patients with pulmonary arterial hypertension.
- Published in:
- Annals of Hematology, 2019, v. 98, n. 2, p. 281, doi. 10.1007/s00277-018-3518-z
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- Publication type:
- Article