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Items: 1 to 50 of 80

1.

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

Phanmany S, Chanprasert S, Munkongdee T, Svasti S, Leecharoenkiat K.

Int J Lab Hematol. 2019 Jul 4. doi: 10.1111/ijlh.13080. [Epub ahead of print]

PMID:
31271507
2.

Neglected Tropical Diseases: The Potential Application to Monitoring by microRNAs in the Real World.

Chamnanchanunt S, Svasti S, Fucharoen S, Umemura T.

Microrna. 2019 Jun 19. doi: 10.2174/2211536608666190620104308. [Epub ahead of print]

PMID:
31218967
3.

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

Yatmark P, Huaijantug S, Teerapan W, Svasti S, Fucharoen S, Morales NP.

Magn Reson Imaging. 2019 May 23;61:267-272. doi: 10.1016/j.mri.2019.05.022. [Epub ahead of print]

PMID:
31128226
4.

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

Nualkaew T, Jearawiriyapaisarn N, Hongeng S, Fucharoen S, Kole R, Svasti S.

Sci Rep. 2019 May 21;9(1):7672. doi: 10.1038/s41598-019-43964-3.

5.

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

Chaichompoo P, Qillah A, Sirankapracha P, Kaewchuchuen J, Rimthong P, Paiboonsukwong K, Fucharoen S, Svasti S, Worawichawong S.

J Clin Pathol. 2019 Aug;72(8):520-524. doi: 10.1136/jclinpath-2019-205775. Epub 2019 Apr 22.

PMID:
31010830
6.

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

Chanpeng P, Svasti S, Paiboonsukwong K, Smith DR, Leecharoenkiat K.

Sci Rep. 2019 Apr 15;9(1):6059. doi: 10.1038/s41598-019-42432-2.

7.

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

Koonyosying P, Kongkarnka S, Uthaipibull C, Svasti S, Fucharoen S, Srichairatanakool S.

Biomed Pharmacother. 2018 Dec;108:1694-1702. doi: 10.1016/j.biopha.2018.10.017. Epub 2018 Oct 12.

8.

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

Manakeng K, Prasertphol P, Phongpao K, Chuncharunee S, Tanyong D, Worawichawong S, Svasti S, Chaichompoo P.

Ann Hematol. 2019 Feb;98(2):281-288. doi: 10.1007/s00277-018-3518-z. Epub 2018 Oct 18.

PMID:
30334069
9.

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

Kheansaard W, Phongpao K, Paiboonsukwong K, Pattanapanyasat K, Chaichompoo P, Svasti S.

Sci Rep. 2018 Aug 29;8(1):13033. doi: 10.1038/s41598-018-31386-6.

10.

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

Preedagasamzin S, Nualkaew T, Pongrujikorn T, Jinawath N, Kole R, Fucharoen S, Jearawiriyapaisarn N, Svasti S.

Biochem Biophys Res Commun. 2018 Apr 30;499(1):86-92. doi: 10.1016/j.bbrc.2018.03.102. Epub 2018 Mar 21.

PMID:
29550480
11.

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

Jaratsittisin J, Sornjai W, Svasti S, Fucharoen S, Roytrakul S, Smith DR.

Hematology. 2018 Aug;23(7):423-428. doi: 10.1080/10245332.2017.1405571. Epub 2017 Nov 21.

PMID:
29157161
12.

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

Kulaphisit M, Kampuansai J, Leecharoenkiat K, Wathikthinnakon M, Kangwanpong D, Munkongdee T, Svasti S, Fucharoen S, Smith DR, Lithanatudom P.

Sci Rep. 2017 Jul 5;7(1):4690. doi: 10.1038/s41598-017-04957-2.

13.

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

Pengon J, Svasti S, Kamchonwongpaisan S, Vattanaviboon P.

Hematol Oncol Stem Cell Ther. 2018 Mar;11(1):18-24. doi: 10.1016/j.hemonc.2017.05.029. Epub 2017 Jun 15.

14.

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

Leecharoenkiat K, Tanaka Y, Harada Y, Chaichompoo P, Sarakul O, Abe Y, Smith DR, Fucharoen S, Svasti S, Umemura T.

Mol Med Rep. 2017 May;15(5):2495-2502. doi: 10.3892/mmr.2017.6326. Epub 2017 Mar 15.

15.

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

Wongkummool W, Maneepitasut W, Munkongdee T, Tong-Ngam P, Tangprasittipap A, Svasti S, Kitiyanant N, Paiboonsukwong K, Fucharoen S, Tubsuwan A.

Stem Cell Res. 2017 Apr;20:84-87. doi: 10.1016/j.scr.2017.02.014. Epub 2017 Mar 7.

16.

Establishment of MUi009 - A human induced pluripotent stem cells from a 32year old male with homozygous β°-thalassemia coinherited with heterozygous α-thalassemia 2.

Wongkummool W, Maneepitasut W, Tong-Ngam P, Tangprasittipap A, Munkongdee T, Boonchuay C, Svasti S, Kitiyanant N, Paiboonsukwong K, Fucharoen S, Tubsuwan A.

Stem Cell Res. 2017 Apr;20:80-83. doi: 10.1016/j.scr.2017.02.012. Epub 2017 Mar 7.

17.

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

Siwaponanan P, Siegers JY, Ghazali R, Ng T, McColl B, Ng GZ, Sutton P, Wang N, Ooi I, Thiengtavor C, Fucharoen S, Chaichompoo P, Svasti S, Wijburg O, Vadolas J.

Blood. 2017 Jun 8;129(23):3087-3099. doi: 10.1182/blood-2016-07-730135. Epub 2017 Mar 21.

18.

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

Charoenphandhu N, Kraidith K, Lertsuwan K, Sripong C, Suntornsaratoon P, Svasti S, Krishnamra N, Wongdee K.

Mol Cell Biochem. 2017 Mar;427(1-2):201-208. doi: 10.1007/s11010-016-2911-y. Epub 2016 Dec 19.

PMID:
27995414
19.

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

Klaihmon P, Phongpao K, Kheansaard W, Noulsri E, Khuhapinant A, Fucharoen S, Morales NP, Svasti S, Pattanapanyasat K, Chaichompoo P.

Ann Hematol. 2017 Feb;96(2):189-198. doi: 10.1007/s00277-016-2885-6. Epub 2016 Nov 29.

PMID:
27900452
20.

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

Sornjai W, Lithanatudom P, Erales J, Joly P, Francina A, Hacot S, Fucharoen S, Svasti S, Diaz JJ, Mertani HC, Smith DR.

Int J Biol Macromol. 2017 Jan;94(Pt A):728-734. doi: 10.1016/j.ijbiomac.2016.10.039. Epub 2016 Oct 17.

PMID:
27765567
21.

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.

Lithanatudom P, Wipasa J, Inti P, Chawansuntati K, Svasti S, Fucharoen S, Kangwanpong D, Kampuansai J.

PLoS One. 2016 Sep 15;11(9):e0163430. doi: 10.1371/journal.pone.0163430. eCollection 2016.

22.

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

Yatmark P, Morales NP, Chaisri U, Wichaiyo S, Hemstapat W, Srichairatanakool S, Svasti S, Fucharoen S.

Exp Toxicol Pathol. 2016 Sep;68(8):427-34. doi: 10.1016/j.etp.2016.06.006. Epub 2016 Jul 9.

PMID:
27402198
23.

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

Siwaponanan P, Fucharoen S, Sirankapracha P, Winichagoon P, Umemura T, Svasti S.

Int J Hematol. 2016 Sep;104(3):338-43. doi: 10.1007/s12185-016-2032-0. Epub 2016 Jun 6.

PMID:
27272941
24.

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

Kraidith K, Svasti S, Teerapornpuntakit J, Vadolas J, Chaimana R, Lapmanee S, Suntornsaratoon P, Krishnamra N, Fucharoen S, Charoenphandhu N.

Am J Physiol Endocrinol Metab. 2016 Jul 1;311(1):E214-23. doi: 10.1152/ajpendo.00067.2016. Epub 2016 May 31.

25.

Molecular Epidemiology of Hemoglobinopathies in Cambodia.

Munkongdee T, Tanakulmas J, Butthep P, Winichagoon P, Main B, Yiannakis M, George J, Devenish R, Fucharoen S, Svasti S.

Hemoglobin. 2016 Jun;40(3):163-7. doi: 10.3109/03630269.2016.1158723.

PMID:
27117566
26.

Mitochondrial Changes in β0-Thalassemia/Hb E Disease.

Khungwanmaythawee K, Sornjai W, Paemanee A, Jaratsittisin J, Fucharoen S, Svasti S, Lithanatudom P, Roytrakul S, Smith DR.

PLoS One. 2016 Apr 19;11(4):e0153831. doi: 10.1371/journal.pone.0153831. eCollection 2016.

27.

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

Lithanatudom P, Khampan P, Smith DR, Svasti S, Fucharoen S, Kangwanpong D, Kampuansai J.

Hematology. 2016 Sep;21(8):480-5. doi: 10.1080/10245332.2016.1148374. Epub 2016 Mar 4.

PMID:
27077764
28.

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.

Lithanatudom P, Wipasa J, Inti P, Chawansuntati K, Svasti S, Fucharoen S, Kangwanpong D, Kampuansai J.

PLoS One. 2016 Jan 25;11(1):e0148079. doi: 10.1371/journal.pone.0148079. eCollection 2016. Erratum in: PLoS One. 2016;11(9):e0163430.

29.

Dysregulation of ferroportin gene expression in β(0)-thalassemia/Hb E disease.

Sornjai W, Jaratsittisin J, Khungwanmaythawee K, Svasti S, Fucharoen S, Lithanatudom P, Smith DR.

Ann Hematol. 2016 Feb;95(3):387-96. doi: 10.1007/s00277-015-2572-z. Epub 2015 Dec 14.

PMID:
26666535
30.

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

Thongchote K, Svasti S, Teerapornpuntakit J, Suntornsaratoon P, Krishnamra N, Charoenphandhu N.

Am J Physiol Endocrinol Metab. 2015 Dec 1;309(11):E936-48. doi: 10.1152/ajpendo.00329.2015. Epub 2015 Oct 20.

31.

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

Yatmark P, Morales NP, Chaisri U, Wichaiyo S, Hemstapat W, Srichairatanakool S, Svasti S, Fucharoen S.

Pharmacology. 2015;96(3-4):192-9. doi: 10.1159/000438994. Epub 2015 Aug 29.

PMID:
26316149
32.

[Dysregulation of microRNA in thalassemia].

Umemura T, Svasti S.

Fukuoka Igaku Zasshi. 2015 Feb;106(2):23-32. Review. Japanese. No abstract available.

PMID:
26021126
33.

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

Chamnanchanunt S, Kuroki C, Desakorn V, Enomoto M, Thanachartwet V, Sahassananda D, Sattabongkot J, Jenwithisuk R, Fucharoen S, Svasti S, Umemura T.

Exp Parasitol. 2015 Aug;155:19-25. doi: 10.1016/j.exppara.2015.04.013. Epub 2015 Apr 22.

PMID:
25913668
34.

Accelerated telomere shortening in β-thalassemia/HbE patients.

Chaichompoo P, Pattanapanyasat K, Winichagoon P, Fucharoen S, Svasti S.

Blood Cells Mol Dis. 2015 Aug;55(2):173-9. doi: 10.1016/j.bcmd.2015.01.003. Epub 2015 Jan 17.

PMID:
25631622
35.

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

Wichaiyo S, Yatmark P, Morales Vargas RE, Sanvarinda P, Svasti S, Fucharoen S, Morales NP.

Toxicol Rep. 2015 Jan 10;2:415-422. doi: 10.1016/j.toxrep.2015.01.004. eCollection 2015.

36.

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

Sornjai W, Khungwanmaythawee K, Svasti S, Fucharoen S, Wintachai P, Yoksan S, Ubol S, Wikan N, Smith DR.

Virology. 2014 Dec;471-473:61-71. doi: 10.1016/j.virol.2014.10.004. Epub 2014 Oct 25.

37.

Comparative plasma protein profiling of hemoglobin H disease.

Leecharoenkiat K, Sornjai W, Khungwanmaythawee K, Paemanee A, Chaichana C, Roytrakul S, Fucharoen S, Svasti S, Smith DR.

Dis Markers. 2014;2014:340214. doi: 10.1155/2014/340214. Epub 2014 Jun 15.

38.

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

Yatmark P, Morales NP, Chaisri U, Wichaiyo S, Hemstapat W, Srichairatanakool S, Svasti S, Fucharoen S.

Exp Toxicol Pathol. 2014 Sep;66(7):333-43. doi: 10.1016/j.etp.2014.03.002. Epub 2014 Jun 3.

PMID:
24907196
39.

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

Thongchote K, Svasti S, Teerapornpuntakit J, Krishnamra N, Charoenphandhu N.

Am J Physiol Endocrinol Metab. 2014 Jun 15;306(12):E1406-17. doi: 10.1152/ajpendo.00111.2014. Epub 2014 Apr 29.

40.

In vitro delivery of curcumin with cholesterol-based cationic liposomes.

Apiratikul N, Penglong T, Suksen K, Svasti S, Chairoungdua A, Yingyongnarongkula B.

Bioorg Khim. 2013 Jul-Aug;39(4):497-503.

PMID:
24707732
41.

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

McColl B, Kao BR, Lourthai P, Chan K, Wardan H, Roosjen M, Delagneau O, Gearing LJ, Blewitt ME, Svasti S, Fucharoen S, Vadolas J.

FASEB J. 2014 May;28(5):2306-17. doi: 10.1096/fj.13-246637. Epub 2014 Jan 17.

PMID:
24443374
42.

Phenotypic comparison of four thalassemia model mice reconstructed from cryo-banked embryos.

Boonkusol D, Dinnyés A, Sa-Ardrit M, Svasti S, Faisaikarm T, Vadolas J, Fucharoen S, Kitiyanant Y.

Acta Biol Hung. 2013 Dec;64(4):453-61. doi: 10.1556/ABiol.64.2013.4.5.

PMID:
24275591
43.

Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure.

Wangkumhang P, Shaw PJ, Chaichoompu K, Ngamphiw C, Assawamakin A, Nuinoon M, Sripichai O, Svasti S, Fucharoen S, Praphanphoj V, Tongsima S.

PLoS One. 2013 Nov 4;8(11):e79522. doi: 10.1371/journal.pone.0079522. eCollection 2013.

44.

Cardiomyocyte ultrastructural damage in β-thalassaemic mice.

Sanyear C, Butthep P, Nithipongvanich R, Sirankapracha P, Winichagoon P, Fucharoen S, Svasti S.

Int J Exp Pathol. 2013 Oct;94(5):336-42. doi: 10.1111/iep.12044.

45.

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

Sarakul O, Vattanaviboon P, Tanaka Y, Fucharoen S, Abe Y, Svasti S, Umemura T.

Blood Cells Mol Dis. 2013 Aug;51(2):98-103. doi: 10.1016/j.bcmd.2013.03.005. Epub 2013 Apr 24.

PMID:
23623309
46.

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

Charoenphandhu N, Kraidith K, Teerapornpuntakit J, Thongchote K, Khuituan P, Svasti S, Krishnamra N.

Cell Biochem Funct. 2013 Dec;31(8):685-91. doi: 10.1002/cbf.2956. Epub 2013 Feb 1.

PMID:
23371483
47.

A reduced curcuminoid analog as a novel inducer of fetal hemoglobin.

Chaneiam N, Changtam C, Mungkongdee T, Suthatvoravut U, Winichagoon P, Vadolas J, Suksamrarn A, Fucharoen S, Svasti S.

Ann Hematol. 2013 Mar;92(3):379-86. doi: 10.1007/s00277-012-1604-1. Epub 2012 Oct 19.

PMID:
23079892
48.

Clinical severity of β-thalassaemia/Hb E disease is associated with differential activities of the calpain-calpastatin proteolytic system.

Sukati S, Svasti S, Stifanese R, Averna M, Panutdaporn N, Penglong T, Melloni E, Fucharoen S, Katzenmeier G.

PLoS One. 2012;7(5):e37133. doi: 10.1371/journal.pone.0037133. Epub 2012 May 16.

49.

Eryngium foetidum suppresses inflammatory mediators produced by macrophages.

Mekhora C, Muangnoi C, Chingsuwanrote P, Dawilai S, Svasti S, Chasri K, Tuntipopipat S.

Asian Pac J Cancer Prev. 2012;13(2):653-64.

50.

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

Sriiam S, Leecharoenkiat A, Lithanatudom P, Wannatung T, Svasti S, Fucharoen S, Svasti J, Chokchaichamnankit D, Srisomsap C, Smith DR.

Blood Cells Mol Dis. 2012 Feb 15;48(2):77-85. doi: 10.1016/j.bcmd.2011.11.004. Epub 2011 Dec 7.

PMID:
22154201

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