Association of UGT1A1*6, UGT1A1*28, or ABCC2 c.3972C>T genetic polymorphisms with irinotecan-induced toxicity in Asian cancer patients: Meta-analysis

بواسطة Chalirmporn Atasilp, Mohitosh Biswas, Pimonpan Jinda, Nutthan Nuntharadthanaphong, Jiratha Rachanakul, Yaowaluck Hongkaew, Natchaya Vanwong, Surasak Saokaew, Chonlaphat Sukasem
منشور في 2022

Allele frequencies of single nucleotide polymorphisms of clinically important drug-metabolizing enzymes CYP2C9, CYP2C19, and CYP3A4 in a Thai population

بواسطة Rattanaporn Sukprasong, Sumonrat Chuwongwattana, Napatrupron Koomdee, Thawinee Jantararoungtong, Santirhat Prommas, Pimonpan Jinda, Jiratha Rachanakul, Nutthan Nuntharadthanaphong, Nutcha Jongjitsook, Apichaya Puangpetch, Chonlaphat Sukasem
منشور في 2022

Implementation of HLA-B*15:02 Genotyping as Standard-of-Care for Reducing Carbamazepine/Oxcarbazepine Induced Cutaneous Adverse Drug Reactions in Thailand

بواسطة Kanyawan Tiwattanon, Shobana John, Napatrupron Koomdee, Pimonpan Jinda, Jiratha Rachanakul, Thawinee Jantararoungtong, Nutthan Nuntharadthanaphong, Chiraphat Kloypan, Mohitosh Biswas, Apisit Boongird, Chonlaphat Sukasem
منشور في 2022

Tpmt*3c as a predictor of 6-mercaptopurine-induced myelotoxicity in thai children with acute lymphoblastic leukemia

بواسطة Thawinee Jantararoungtong, Supaporn Wiwattanakul, Rawiporn Tiyasirichokchai, Santirhat Prommas, Rattanaporn Sukprasong, Napatrupron Koomdee, Pimonpan Jinda, Jiratha Rachanakul, Nutthan Nuntharadthanaphong, Samart Pakakasama, Usanarat Anurathapan, Suradej Hongeng, Chonlaphat Sukasem
منشور في 2022

Evolution of HLA-B Pharmacogenomics and the Importance of PGx Data Integration in Health Care System: A 10 Years Retrospective Study in Thailand

بواسطة Napatrupron Koomdee, Chiraphat Kloypan, Pimonpan Jinda, Jiratha Rachanakul, Thawinee Jantararoungtong, Rattanaporn Sukprasong, Santirhat Prommas, Nutthan Nuntharadthanaphong, Apichaya Puangpetch, Maliheh Ershadian, Shobana John, Mohitosh Biswas, Chonlaphat Sukasem
منشور في 2022

Risperidone plasma concentrations are associated with hyperprolactinemia in autism spectrum disorder children: The impact of CYP2D6 polymorphisms

بواسطة Monpat Chamnanphon, Natchaya Vanwong, Santirhat Prommas, Napatrupron Koomdee, Rattanaporn Sukprasong, Jiratha Rachanakul, Nutthan Nuntharadthanaphong, Yaowaluck Hongkaew, Shobana John, Nattawat Ngamsamut, Nopphadol Nuntamool, Penkhae Limsila, Chonlaphat Sukasem
منشور في 2022