S. Svasti

发表

A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E

Yusuke Nakamura, Vip Viprakasit, Naoyuki Kamatani, 2009, Human Genetics.

Enhanced erythroid cell differentiation in hypoxic condition is in part contributed by miR-210.

S. Fucharoen, S. Svasti, Orawan Sarakul, 2013, Blood cells, molecules & diseases.

MRI imaging and histopathological study of brain iron overload of β-thalassemic mice.

S. Fucharoen, S. Svasti, P. Yatmark, 2019, Magnetic resonance imaging.

Anti-inflammatory activities of red curry paste extract on lipopolysaccharide-activated murine macrophage cell line.

S. Tuntipopipat, S. Svasti, Pimjai Chingsuwanrote, 2011, Nutrition.

Stir-Fry Chicken with Green Curry Suppresses Inflammatory Gene Expression by Lipopolysaccharide-Induced Murine Macrophages

S. Tuntipopipat, S. Svasti, Pimjai Chingsuwanrote, 2011 .

Hypermethylation of 28S ribosomal RNA in β-thalassemia trait carriers.

J. Erales, S. Fucharoen, Duncan R. Smith, 2017, International journal of biological macromolecules.

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

S. Fucharoen, P. Butthep, S. Svasti, 2021, PeerJ.

An in vivo model for analysis of developmental erythropoiesis and globin gene regulation

Linden J. Gearing, J. Vadolas, S. Fucharoen, 2014, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Insight into the Peopling of Mainland Southeast Asia from Thai Population Genetic Structure

V. Praphanphoj, Chumpol Ngamphiw, A. Assawamakin, 2013, PloS one.

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

J. Vadolas, S. Fucharoen, P. Sutton, 2017, Blood.

Restoration of correct βIVS2-654-globin mRNA splicing and HbA production by engineered U7 snRNA in β-thalassaemia/HbE erythroid cells

R. Kole, S. Fucharoen, S. Svasti, 2019, Scientific Reports.

Engineered U7 snRNA mediates sustained splicing correction in erythroid cells from β-thalassemia/HbE patients.

R. Kole, S. Fucharoen, N. Jinawath, 2018, Biochemical and biophysical research communications.

Elevated levels of miR-210 correlate with anemia in β-thalassemia/HbE patients

S. Fucharoen, S. Svasti, P. Winichagoon, 2016, International Journal of Hematology.

Proteomic analysis of hemoglobin H-constant spring (Hb H-CS) erythroblasts.

S. Fucharoen, Duncan R. Smith, J. Svasti, 2012, Blood cells, molecules & diseases.

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

S. Fucharoen, Duncan R. Smith, S. Svasti, 2010, Haematologica.

Impaired bone formation and osteopenia in heterozygous βIVSII-654 knockin thalassemic mice

S. Fucharoen, N. Charoenphandhu, S. Svasti, 2011, Histochemistry and Cell Biology.

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

S. Fucharoen, Duncan R. Smith, Wannapa Sornjai, 2018, Hematology.

High phosphate intake induces bone loss in nephrectomized thalassemic mice

M. Greenblatt, S. Lotinun, S. Svasti, 2022, PloS one.

Comparative Plasma Protein Profiling of Hemoglobin H Disease

S. Fucharoen, Duncan R. Smith, Wannapa Sornjai, 2014, Disease markers.

Deferiprone and efonidipine mitigated iron-overload induced neurotoxicity in wild-type and thalassemic mice.

N. Chattipakorn, S. Chattipakorn, S. Srichairatanakool, 2019, Life sciences.

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

N. Charoenphandhu, S. Svasti, N. Krishnamra, 2015, American journal of physiology. Endocrinology and metabolism.

Enhanced activation of autophagy in β-thalassemia/Hb E erythroblasts during erythropoiesis

S. Fucharoen, Duncan R. Smith, S. Svasti, 2011, Annals of Hematology.

Dengue virus infection of erythroid precursor cells is modulated by both thalassemia trait status and virus adaptation.

S. Yoksan, S. Fucharoen, Duncan R. Smith, 2014, Virology.

Increased oxidative metabolism is associated with erythroid precursor expansion in β0-thalassaemia/Hb E disease.

S. Fucharoen, Duncan R. Smith, C. Srisomsap, 2011, Blood cells, molecules & diseases.

Microparticles from splenectomized β-thalassemia/HbE patients play roles on procoagulant activities with thrombotic potential

E. Noulsri, S. Fucharoen, K. Pattanapanyasat, 2017, Annals of Hematology.

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

S. Srichairatanakool, N. Utama‐ang, Pimpisid Koonyosying, 2021, Molecules.

Development of DNA controls for detection of β‐thalassemia mutations commonly found in Asian

S. Fucharoen, O. Sripichai, S. Svasti, 2020, International journal of laboratory hematology.

Molecular prevalence of thalassemia and hemoglobinopathies among the Lao Loum Group in the Lao People’s Democratic Republic

S. Svasti, T. Munkongdee, S. Chanprasert, 2019, International journal of laboratory hematology.

Molecular Epidemiology of Hemoglobinopathies in Cambodia

Joby V. George, S. Fucharoen, P. Butthep, 2016, Hemoglobin.

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

S. Fucharoen, Jatupol Kampuansai, Duncan R. Smith, 2016, Hematology.

Effects of Iron Chelators on Pulmonary Iron Overload and Oxidative Stress in β-Thalassemic Mice

S. Srichairatanakool, S. Fucharoen, S. Svasti, 2015, Pharmacology.

Association of SNP in exon 1 of HBS1L with hemoglobin F level in β0-thalassemia/hemoglobin E

S. Fucharoen, K. Triwitayakorn, O. Sripichai, 2008, International journal of hematology.

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

S. Tongsima, T. Mandrup-Poulsen, S. Svasti, 2020, PeerJ.

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

R. M. Morales Vargas, S. Fucharoen, S. Svasti, 2015, Toxicology reports.

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

S. Fucharoen, P. Butthep, S. Svasti, 2020, PeerJ.

Dysregulation of ferroportin gene expression in β0-thalassemia/Hb E disease

S. Fucharoen, Duncan R. Smith, Wannapa Sornjai, 2016, Annals of Hematology.

Iron distribution and histopathological study of the effects of deferoxamine and deferiprone in the kidneys of iron overloaded β-thalassemic mice.

S. Srichairatanakool, S. Fucharoen, S. Svasti, 2016, Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie.

Lipopolysaccharide alters iron homeostasis in both wild type and β-thalassemia mice even under parenteral iron loading

S. Fucharoen, P. Butthep, S. Svasti, 2021 .

Responses of primary osteoblasts and osteoclasts from hemizygous β-globin knockout thalassemic mice with elevated plasma glucose to 1,25-dihydroxyvitamin D3

N. Charoenphandhu, S. Svasti, Kannikar Wongdee, 2019, Scientific Reports.

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

J. Vadolas, S. Fucharoen, Sarawut Lapmanee, 2016, American journal of physiology. Endocrinology and metabolism.

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

N. Charoenphandhu, S. Svasti, N. Krishnamra, 2014, American journal of physiology. Endocrinology and metabolism.

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

J. Vadolas, S. Fucharoen, K. Pattanapanyasat, 2020, British journal of haematology.

Limit of sensitivity for melting curve screening for α-thalassemia

Duncan R. Smith, S. Svasti, T. Munkongdee, 2012 .

Rapid diagnosis of alpha-thalassemia by melting curve analysis.

S. Fucharoen, S. Svasti, T. Munkongdee, 2010, The Journal of molecular diagnostics : JMD.

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

Duncan R. Smith, S. Svasti, Pornthip Chaichompoo, 2022, International journal of molecular sciences.

Na+/H+ exchanger 3 inhibitor diminishes hepcidin-enhanced duodenal calcium transport in hemizygous β-globin knockout thalassemic mice

N. Charoenphandhu, S. Svasti, Kannikar Wongdee, 2017, Molecular and Cellular Biochemistry.

Clinical Severity of β-thalassaemia/Hb E Disease Is Associated with Differential Activities of the Calpain-Calpastatin Proteolytic System

G. Katzenmeier, S. Fucharoen, E. Melloni, 2012, PloS one.

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

J. Vadolas, S. Fucharoen, Duncan R. Smith, 2022, Scientific Reports.

Impaired neutrophil extracellular trap formation in β-thalassaemia/HbE

J. Vadolas, S. Fucharoen, K. Pattanapanyasat, 2022, Scientific Reports.

Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemia.

S. Kamchonwongpaisan, S. Svasti, P. Vattanaviboon, 2017, Hematology/oncology and stem cell therapy.

Accelerated telomere shortening in β-thalassemia/HbE patients.

S. Fucharoen, K. Pattanapanyasat, S. Svasti, 2015, Blood cells, molecules & diseases.

Molecular mechanism of β-thalassaemia caused by 22-bp duplication

S. Fucharoen, S. Svasti, P. Winichagoon, 2008, Annals of Hematology.

Mitochondrial Changes in β0-Thalassemia/Hb E Disease

S. Fucharoen, Duncan R. Smith, Wannapa Sornjai, 2016, PloS one.

Iron distribution and histopathological characterization of the liver and heart of β-thalassemic mice with parenteral iron overload: Effects of deferoxamine and deferiprone.

S. Srichairatanakool, S. Fucharoen, S. Svasti, 2014, Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie.

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

J. Vadolas, A. Suksamrarn, S. Svasti, 2021, Scientific Reports.

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

C. Saisawang, Duangnate Rojanaporn, Rossukon Kaewkhaw, 2020, Investigative ophthalmology & visual science.

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

S. Srichairatanakool, S. Fucharoen, Pimpisid Koonyosying, 2022, Frontiers in Physiology.

Cardiomyocyte ultrastructural damage in β‐thalassaemic mice

S. Fucharoen, P. Butthep, S. Svasti, 2013, International journal of experimental pathology.

Increased susceptibility to dextran sulfate-induced mucositis of iron-overload β-thalassemia mice, another endogenous cause of septicemia in thalassemia

S. Fucharoen, N. Somboonna, S. Svasti, 2021, Clinical science.

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

S. Fucharoen, S. Svasti, A. Leelahavanichkul, 2020, Journal of inflammation research.

Gut leakage enhances sepsis susceptibility in iron-overloaded β-thalassemia mice through macrophage hyper-inflammatory responses.

S. Fucharoen, N. Somboonna, S. Svasti, 2020, American journal of physiology. Gastrointestinal and liver physiology.

1,25‐Dihydroxyvitamin D3‐induced intestinal calcium transport is impaired in β‐globin knockout thalassemic mice

P. Khuituan, N. Charoenphandhu, S. Svasti, 2013, Cell biochemistry and function.

Labdane diterpenes from the aerial parts of Curcuma comosa enhance fetal hemoglobin production in an erythroid cell line.

J. Vadolas, S. Fucharoen, A. Suksamrarn, 2010, Journal of natural products.

Increased erythropoiesis of β‐thalassaemia/Hb E proerythroblasts is mediated by high basal levels of ERK1/2 activation

S. Fucharoen, Duncan R. Smith, S. Svasti, 2009, British journal of haematology.

Quercetin analogs with high fetal hemoglobin-inducing activity

A. Suksamrarn, S. Svasti, Waraluck Chaichompoo, 2019, Medicinal Chemistry Research.

Restoration of human beta-globin gene expression in murine and human IVS2-654 thalassemic erythroid cells by free uptake of antisense oligonucleotides.

R. Kole, S. Fucharoen, H. Sierakowska, 2002, Molecular pharmacology.

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

S. Svasti, K. Buranaamnuay, C. Changsangfa, 2022, Open veterinary journal.

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

S. Fucharoen, Jatupol Kampuansai, Duncan R. Smith, 2017, Scientific Reports.

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

S. Fucharoen, Duncan R. Smith, S. Svasti, 2017, Molecular medicine reports.

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

J. Vadolas, S. Fucharoen, G. Grigoriadis, 2021, Molecular therapy : the journal of the American Society of Gene Therapy.

Genetic mModifiers of Hb E / β 0 Thalassemia Identified by a Two-Stage Genome-Wide Association Study

K. Abel, L. Farrer, A. Braun, 2010 .

Genetic modifiers of Hb E/β0 thalassemia identified by a two-stage genome-wide association study

K. Abel, L. Farrer, A. Braun, 2010, BMC Medical Genetics.

Expression of βE and γ-globin genes in infants heterozygous for hemoglobin E and double heterozygous for hemoglobin E and α-thalassemia

S. Fucharoen, S. Svasti, P. Winichagoon, 2007 .

Genetic predictions of life expectancy in southern Thai patients with β0-thalassemia/Hb E

S. Fucharoen, Manit Nuinoon, S. Svasti, 2022, Biomedical reports.

Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice

J. Vadolas, S. Fucharoen, S. Svasti, 2009, Haematologica.

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

S. Fucharoen, S. Svasti, T. Munkongdee, 2011, British journal of haematology.

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

S. Fucharoen, Jatupol Kampuansai, D. Kangwanpong, 2016, PloS one.

Molecular Screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and PAKSÉ (codon 142, TAA>TAT, α2) Mutations in Thailand

S. Fucharoen, P. Butthep, S. Svasti, 2010, Hemoglobin.

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

Duncan R. Smith, S. Svasti, K. Paiboonsukwong, 2019, Scientific Reports.

7 Genomic Study in β-Thalassemia

S. Fucharoen, Manit Nuinoon, O. Sripichai, 2018 .

Genomic Study in β-Thalassemia

S. Fucharoen, Manit Nuinoon, O. Sripichai, 2011 .

UGT1A6 genotype-related pharmacokinetics of deferiprone (L1) in healthy volunteers.

S. Fucharoen, P. Wilairat, S. Svasti, 2008, British journal of clinical pharmacology.

Extracellular vesicles from thalassemia patients carry iron-containing ferritin and hemichrome that promote cardiac cell proliferation

K. Pattanapanyasat, S. Svasti, A. Khuhapinant, 2021, Annals of Hematology.

Construction of thalassemic mouse induced pluripotent stem cells for disease modeling

S. Svasti, Natee Jearawiriyapaisarn, A. Tubsuwan, 2015 .

Expression of microRNA-451 in normal and thalassemic erythropoiesis

S. Fucharoen, S. Svasti, P. Winichagoon, 2010, Annals of Hematology.

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

S. Fucharoen, Kenichi Sato, S. Svasti, 2021, Journal of clinical medicine.

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

S. Srichairatanakool, S. Fucharoen, Pimpisid Koonyosying, 2018, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Eryngium foetidum suppresses inflammatory mediators produced by macrophages.

S. Tuntipopipat, S. Svasti, Pimjai Chingsuwanrote, 2012, Asian Pacific journal of cancer prevention : APJCP.

Rapid diagnosis of thalassemias and other hemoglobinopathies by capillary electrophoresis system.

S. Fucharoen, S. Svasti, T. Munkongdee, 2008, Translational research : the journal of laboratory and clinical medicine.

Hb SIAM [α15(A13)Gly → Arg (α1) (GGT → CGT)] IS A TYPICAL α CHAIN HEMOGLOBINOPATHY WITHOUT AN α-THALASSEMIC EFFECT

P. Wilairat, S. Fucharoen, C. Srisomsap, 2002 .

Abnormal red blood cell morphological changes in thalassaemia associated with iron overload and oxidative stress

S. Fucharoen, S. Svasti, K. Paiboonsukwong, 2019, Journal of Clinical Pathology.

Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease.

S. Fucharoen, O. Sripichai, S. Svasti, 2008, Annals of hematology.

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

J. Vadolas, S. Fucharoen, K. Pattanapanyasat, 2022, British journal of haematology.

Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease

S. Fucharoen, O. Sripichai, S. Svasti, 2008, Annals of Hematology.

Increased ferritin levels in non‐transfusion‐dependent β°‐thalassaemia/HbE are associated with reduced CXCR2 expression and neutrophil migration

J. Vadolas, S. Fucharoen, K. Pattanapanyasat, 2019, British journal of haematology.

Characterization of a novel deletion causing (δβ)0‐thalassemia in a Thai family

S. Fucharoen, S. Svasti, P. Winichagoon, 2007 .

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

S. Svasti, N. P. Morales, Surasak Wichaiyo, 2021, Journal of thrombosis and haemostasis : JTH.

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

S. Fucharoen, S. Svasti, T. Munkongdee, 2017, Stem cell research.

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

S. Fucharoen, Jatupol Kampuansai, D. Kangwanpong, 2016, PloS one.

Downregulation of plasma miR-451 and miR-16 in Plasmodium vivax infection.

J. Sattabongkot, S. Fucharoen, S. Svasti, 2015, Experimental parasitology.

Microparticles from β-thalassaemia/HbE patients induce endothelial cell dysfunction

K. Pattanapanyasat, S. Svasti, K. Paiboonsukwong, 2018, Scientific Reports.

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

N. Chattipakorn, S. Chattipakorn, A. Tantiworawit, 2021, Scientific Reports.

Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system

S. Fucharoen, P. Butthep, S. Svasti, 2011, Annals of Hematology.

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

C. Rojviriya, N. Charoenphandhu, S. Svasti, 2022, Scientific Reports.

Nephrectomy Does not Exacerbate Cancellous Bone loss in Thalassemic Mice

S. Lotinun, S. Svasti, N. Krishnamra, 2020, Scientific Reports.

Elevated levels of platelet- and red cell-derived extracellular vesicles in transfusion-dependent β-thalassemia/HbE patients with pulmonary arterial hypertension

S. Chuncharunee, S. Svasti, S. Worawichawong, 2018, Annals of Hematology.

ASSOCIATION OF Hb HOPE [β136(H14)Gly → Asp] AND Hb H DISEASE

S. Fucharoen, C. Srisomsap, S. Svasti, 2001 .

Moringa oleifera Pod Inhibits Inflammatory Mediator Production by Lipopolysaccharide-Stimulated RAW 264.7 Murine Macrophage Cell Lines

S. Tuntipopipat, S. Svasti, Pimjai Chingsuwanrote, 2012, Inflammation.

In vitro delivery of curcumin with cholesterol-based cationic liposomes

B. Yingyongnarongkul, N. Apiratikul, K. Suksen, 2013, Russian Journal of Bioorganic Chemistry.

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

Duncan R. Smith, S. Svasti, K. Paiboonsukwong, 2019, Scientific Reports.

Microparticles from β-thalassaemia/HbE patients induce endothelial cell dysfunction

K. Pattanapanyasat, S. Svasti, K. Paiboonsukwong, 2018, Scientific Reports.

Nephrectomy Does not Exacerbate Cancellous Bone loss in Thalassemic Mice

S. Lotinun, S. Svasti, N. Krishnamra, 2020, Scientific Reports.

A reduced curcuminoid analog as a novel inducer of fetal hemoglobin

J. Vadolas, S. Fucharoen, A. Suksamrarn, 2013, Annals of Hematology.

RNA repair restores hemoglobin expression in IVS2–654 thalassemic mice

R. Kole, H. Moulton, N. Maeda, 2009, Proceedings of the National Academy of Sciences.

Up-regulation of microRNA 101-3p during erythropoiesis in β-thalassemia/HbE.

S. Svasti, D. Nauphar, Phatchariya Phannasil, 2023, Blood cells, molecules & diseases.

Predictive SNPs for β0-thalassemia/HbE disease severity

S. Tongsima, S. Fucharoen, Pongsakorn Wangkumhang, 2021, Scientific Reports.

Dasatinib Ointment Promotes Healing of Murine Excisional Skin Wound.

S. Svasti, N. P. Morales, Surasak Wichaiyo, 2023, ACS pharmacology & translational science.

hypoxiaafter exercise training in normoxia and chronic Skeletal muscle capillarity and angiogenic mRNA

A. Goldberg, A. Ryan, J. González‐Gallego, 2015 .