Genome-wide search for disease modifier genes in [beta]-Thalassemia

by Orapan Sripichai
Published 2023

Fetal hemoglobin regulation in β-thalassemia: heterogeneity, modifiers and therapeutic approaches

by Orapan Sripichai, Suthat Fucharoen
Published 2018

Genetic polymorphisms and implications for human diseases

by Orapan Sripichai, Suthat Fucharoen
Published 2018

Impaired Terminal Erythroid Maturation in β⁰-Thalassemia/HbE Patients with Different Clinical Severity

by Thunwarat Suriyun, Pranee Winichagoon, Suthat Fucharoen, Orapan Sripichai
Published 2022

Association between SCN5A and sudden unexplained nocturnal death syndrome in Thai decedents: a case–control study

by Supawon Srettabunjong, Duangkamon Eakkunnathum, Wanna Thongnoppakhun, Orapan Sripichai
Published 2020

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

by Orapan Sripichai, Thongperm Munkongdee, Chutima Kumkhaek, Saovaros Svasti, Pranee Winichagoon, Suthat Fucharoen
Published 2018

Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β⁰-thalassemia/HbE disease

by Pinyaphat Khamphikham, Orapan Sripichai, Thongperm Munkongdee, Suthat Fucharoen, Sissades Tongsima, Duncan R. Smith
Published 2019

Lysine-specific histone demethylase 1 inhibition enhances robust fetal hemoglobin induction in human β⁰-thalassemia/hemoglobin E erythroid cells

by Woratree Kaewsakulthong, Phitchapa Pongpaksupasin, Tiwaporn Nualkaew, Suradej Hongeng, Suthat Fucharoen, Natee Jearawiriyapaisarn, Orapan Sripichai
Published 2022

Association of the Degree of Erythroid Expansion and Maturation Arrest with the Clinical Severity of β⁰-Thalassemia/Hemoglobin e Patients

by Thunwarat Suriyun, Woratree Kaewsakulthong, Pinyaphat Khamphikham, Sukanya Chumchuen, Suradej Hongeng, Suthat Fucharoen, Orapan Sripichai
Published 2022

Visual genotyping of thalassemia by using pyrrolidinyl peptide nucleic acid probes immobilized on carboxymethylcellulose-modified paper and enzyme-induced pigmentation

by Nuttapon Jirakittiwut, Thongperm Munkongdee, Kanet Wongravee, Orapan Sripichai, Suthat Fucharoen, Thanit Praneenararat, Tirayut Vilaivan
Published 2020

Down-regulation of the transcriptional repressor ZNF802 (JAZF1) reactivates fetal hemoglobin in β⁰-thalassemia/HbE

by Chokdee Wongborisuth, Sukanya Chumchuen, Orapan Sripichai, Usanarat Anurathaphan, Nuankanya Sathirapongsasuti, Duantida Songdej, Amornrat Tangprasittipap, Suradej Hongeng
Published 2022

Author Correction: Down-regulation of the transcriptional repressor ZNF802 (JAZF1) reactivates fetal hemoglobin in β⁰-thalassemia/HbE (Scientific Reports, (2022), 12, 1,...

by Chokdee Wongborisuth, Sukanya Chumchuen, Orapan Sripichai, Usanarat Anurathaphan, Nuankanya Sathirapongsasuti, Duantida Songdej, Amornrat Tangprasittipap, Suradej Hongeng
Published 2022

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

by Riyaz A. Pandit, Saovaros Svasti, Orapan Sripichai, Thongperm Munkongdee, Kanokporn Triwitayakorn, Pranee Winichagoon, Suthat Fucharoen, Chayanon Peerapittayamongkol
Published 2018

Comparison of gene expression profiles between human erythroid cells derived from fetal liver and adult peripheral blood

by Amornrat Tangprasittipap, Pavita Kaewprommal, Orapan Sripichai, Nuankanya Sathirapongsasuti, Chonthicha Satirapod, Philip J. Shaw, Jittima Piriyapongsa, Suradej Hongeng
Published 2019

Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation --^SEA/--^CR, a novel α⁰-thalassemia dele...

by Chedtapak Ruengdit, Sitthichai Panyasai, Naowarat Kunyanone, Worawich Phornsiricharoenphant, Chumpol Ngamphiw, Sissades Tongsima, Orapan Sripichai, Serge Pissard, Sakorn Pornprasert
Published 2020

Genetic analysis of candidate modifier polymorphisms in Hb E-β⁰-thalassemia patients

by Orapan Sripichai, Johanna Whitacre, Thongperm Munkongdee, Chutima Kumkhaek, Wattanan Makarasara, Pranee Winichagoon, Ken Abel, Andreas Braun, Suthat Fucharoen
Published 2018

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

by Thongperm Munkongdee, Tiwaporn Nualkaew, Nattrika Buasuwan, Nurmeeha Hinna, Kittiphong Paiboonsukwong, Orapan Sripichai, Saovaros Svasti, Pranee Winichagoon, Suthat Fucharoen, Natee Jearawiriyapaisarn
Published 2020

A scoring system for the classification of β-thalassemia/Hb E disease severity

by Orapan Sripichai, Wattanan Makarasara, Thongperm Munkongdee, Chutima Kumkhaek, Issarang Nuchprayoon, Ampaiwan Chuansumrit, Suporn Chuncharunee, Nawarat Chantrakoon, Piathip Boonmongkol, Pranee Winichagoon, Suthat Fucharoen
Published 2018

MTAP-related increased erythroblast proliferation as a mechanism of polycythaemia vera

by Chartsiam Tipgomut, Archrob Khuhapinant, Marieangela C. Wilson, Saiphon Poldee, Kate J. Heesom, Chanatip Metheetrairut, Orapan Sripichai, Chalermchai Mitrpant, Jan Frayne, Kongtana Trakarnsanga
Published 2022

UNC0638 induces high levels of fetal hemoglobin expression in β-thalassemia/HbE erythroid progenitor cells

by Tiwaporn Nualkaew, Pinyaphat Khamphikham, Phitchapa Pongpaksupasin, Woratree Kaewsakulthong, Duantida Songdej, Kittiphong Paiboonsukwong, Orapan Sripichai, James Douglas Engel, Suradej Hongeng, Suthat Fucharoen, Natee Jearawiriyapaisarn
Published 2020