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Page 1
Genetic regulation of fetal hemoglobin across global populations.
Cato LD, Li R, Lu HY, Yu F, Wissman M, Mkumbe BS, Ekwattanakit S, Deelen P, Mwita L, Sangeda R, Suksangpleng T, Riolueang S, Bronson PG, Paul DS, Kawabata E, Astle WJ, Aguet F, Ardlie K, de Lapuente Portilla AL, Kang G, Zhang Y, Nouraie SM, Gordeuk VR, Gladwin MT, Garrett ME, Ashley-Koch A, Telen MJ, Custer B, Kelly S, Dinardo CL, Sabino EC, Loureiro P, Carneiro-Proietti AB, Maximo C; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; BIOS Consortium; Méndez A, Hammerer-Lercher A, Sheehan VA, Weiss MJ, Franke L, Nilsson B, Butterworth AS, Viprakasit V, Nkya S, Sankaran VG. Cato LD, et al. Among authors: riolueang s. medRxiv [Preprint]. 2023 Mar 28:2023.03.24.23287659. doi: 10.1101/2023.03.24.23287659. medRxiv. 2023. PMID: 36993312 Free PMC article. Preprint.
Paper-based microchip electrophoresis for point-of-care hemoglobin testing.
Hasan MN , Fraiwan A , An R , Alapan Y , Ung R , Akkus A , Xu JZ , Rezac AJ , Kocmich NJ , Creary MS , Oginni T , Olanipekun GM , Hassan-Hanga F , Jibir BW , Gambo S , Verma AK , Bharti PK , Riolueang S , Ngimhung T , Suksangpleng T , Thota P , Werner G , Shanmugam R , Das A , Viprakasit V , Piccone CM , Little JA , Obaro SK , Gurkan UA . Hasan MN , et al. Among authors: riolueang s. Analyst. 2020 Apr 7;145(7):2525-2542. doi: 10.1039/c9an02250c. Epub 2020 Mar 3. Analyst. 2020. PMID: 32123889 Free PMC article.
The origin of sickle cell disease in Thailand.
Xu JZ, Riolueang S, Glomglao W, Tachavanich K, Suksangpleng T, Ekwattanakit S, Viprakasit V. Xu JZ, et al. Among authors: riolueang s. Int J Lab Hematol. 2019 Feb;41(1):e13-e16. doi: 10.1111/ijlh.12926. Epub 2018 Sep 27. Int J Lab Hematol. 2019. PMID: 30264513 No abstract available.
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes.
Jiang Z, Luo HY, Huang S, Farrell JJ, Davis L, Théberge R, Benson KA, Riolueang S, Viprakasit V, Al-Allawi NA, Ünal S, Gümrük F, Akar N, Başak AN, Osorio L, Badens C, Pissard S, Joly P, Campbell AD, Gallagher PG, Steinberg MH, Forget BG, Chui DH. Jiang Z, et al. Among authors: riolueang s. Br J Haematol. 2016 Mar;172(6):958-65. doi: 10.1111/bjh.13909. Epub 2016 Jan 13. Br J Haematol. 2016. PMID: 26771086 Free article.
Human primary erythroid cells as a more sensitive alternative in vitro hematological model for nanotoxicity studies: Toxicological effects of silver nanoparticles.
Rujanapun N, Aueviriyavit S, Boonrungsiman S, Rosena A, Phummiratch D, Riolueang S, Chalaow N, Viprakasit V, Maniratanachote R. Rujanapun N, et al. Among authors: riolueang s. Toxicol In Vitro. 2015 Dec;29(8):1982-92. doi: 10.1016/j.tiv.2015.08.005. Epub 2015 Aug 18. Toxicol In Vitro. 2015. PMID: 26291277
Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression.
Viprakasit V, Ekwattanakit S, Riolueang S, Chalaow N, Fisher C, Lower K, Kanno H, Tachavanich K, Bejrachandra S, Saipin J, Juntharaniyom M, Sanpakit K, Tanphaichitr VS, Songdej D, Babbs C, Gibbons RJ, Philipsen S, Higgs DR. Viprakasit V, et al. Among authors: riolueang s. Blood. 2014 Mar 6;123(10):1586-95. doi: 10.1182/blood-2013-09-526087. Epub 2014 Jan 17. Blood. 2014. PMID: 24443441 Free article.
Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
Viprakasit V, Ekwattanakit S, Chalaow N, Riolueang S, Wijit S, Tanyut P, Chat-Uthai N, Tachavanich K. Viprakasit V, et al. Among authors: riolueang s. Acta Haematol. 2014;131(2):88-94. doi: 10.1159/000353119. Epub 2013 Sep 26. Acta Haematol. 2014. PMID: 24081251
12 results