Works by Munkongdee, Thongperm

Results: 23

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

Published in:

2018

By:

Khamphikham, Pinyaphat;
Sripichai, Orapan;
Munkongdee, Thongperm;
Fucharoen, Suthat;
Tongsima, Sissades;
Smith, Duncan R.

Publication type:

journal article

Simple method for screening of alpha-thalassaemia 1 carriers.

Published in:

2009

By:

Tayapiwatana, Chatchai;
Kuntaruk, Surakit;
Tatu, Thanusak;
Chiampanichayakul, Sawitree;
Munkongdee, Thongperm;
Winichagoon, Pranee;
Fuchareon, Suthat;
Kasinrerk, Watchara

Publication type:

journal article

Association of SNP in exon 1 of HBS1L with hemoglobin F level in beta0-thalassemia/hemoglobin E.

Published in:

2008

By:

Pandit, Riyaz;
Svasti, Saovaros;
Sripichai, Orapan;
Munkongdee, Thongperm;
Triwitayakorn, Kanokporn;
Winichagoon, Pranee;
Fucharoen, Suthat;
Peerapittayamongkol, Chayanon;
Pandit, Riyaz A

Publication type:

journal article

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

Published in:

American Journal of Hematology, 2008, v. 83, n. 6, p. 482, doi. 10.1002/ajh.21130

By:

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

Publication type:

Article

Development of molecular diagnostic platform for α0‐thalassemia 44.6 kb (Chiang Rai, ‐‐CR) deletion in individuals with microcytic red blood cells across Thailand.

Published in:

Annals of Human Genetics, 2023, v. 87, n. 3, p. 137, doi. 10.1111/ahg.12496

By:

Khamphikham, Pinyaphat;
Hanmanoviriya, Oravee;
Wongpalee, Somsakul Pop;
Munkongdee, Thongperm;
Paiboonsukwong, Kittiphong;
Jopang, Yupin;
Wangchauy, Chaowanee;
Sancharernsook, Charan;
Jinorose, Nathawat;
Pornprasert, Sakorn

Publication type:

Article

Impact of the detection of ζ-globin chains and hemoglobin Bart's using immunochromatographic strip tests for α0-thalassemia (--SEA) differential diagnosis.

Published in:

PLoS ONE, 2019, v. 14, n. 10, p. 1, doi. 10.1371/journal.pone.0223996

By:

Pata, Supansa;
Laopajon, Witida;
Pongpaiboon, Matawee;
Thongkum, Weeraya;
Polpong, Nattapong;
Munkongdee, Thongperm;
Paiboonsukwong, Kittiphong;
Fucharoen, Suthat;
Tayapiwatana, Chatchai;
Kasinrerk, Watchara

Publication type:

Article

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

Published in:

British Journal of Haematology, 2011, v. 154, n. 5, p. 635, doi. 10.1111/j.1365-2141.2011.08770.x

By:

Tubsuwan, Alisa;
Munkongdee, Thongperm;
Jearawiriyapaisarn, Natee;
Boonchoy, Chanikarn;
Winichagoon, Pranee;
Fucharoen, Suthat;
Svasti, Saovaros

Publication type:

Article

Expression level of pro-apoptotic genes determine disease severity of HbE/ beta thalassemia.

Published in:

Journal of Applied Hematology, 2019, v. 10, p. S16

By:

Alsaleh, Heba;
Rasidi, Nur Natasya;
Sulong, Sarina;
Svasti, Saovaros;
Tubsuwan, Alisa;
Munkongdee, Thongperm;
Hassan, Rosline

Publication type:

Article

Identification and expression of gene loci underlying the quantitative trait loci of starch content in cassava.

Published in:

Journal of Crop Improvement, 2024, v. 38, n. 4, p. 368, doi. 10.1080/15427528.2024.2353094

By:

Sawangsalee, Kanlayanee;
Sraphet, Supajit;
Srisawad, Nattaya;
Munkongdee, Thongperm;
Svasti, Saovaros;
Bumrung, Saowaree;
Smith, Duncan R.;
Triwitayakorn, Kanokporn

Publication type:

Article

Genetic Analysis of Candidate Modifier Polymorphisms in Hb E-β0-Thalassemia Patients.

Published in:

Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 433, doi. 10.1196/annals.1345.066

By:

SRIPICHAI, ORAPAN;
WHITACRE, JOHANNA;
MUNKONGDEE, THONGPERM;
KUMKHAEK, CHUTIMA;
MAKARASARA, WATTANAN;
WINICHAGOON, PRANEE;
ABEL, KEN;
BRAUN, ANDREAS;
FUCHAROEN, SUTHAT

Publication type:

Article

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

Published in:

Human Genetics, 2010, v. 127, n. 3, p. 303, doi. 10.1007/s00439-009-0770-2

By:

Nuinoon, Manit;
Makarasara, Wattanan;
Mushiroda, Taisei;
Setianingsih, Iswari;
Wahidiyat, Pustika Amalia;
Sripichai, Orapan;
Kumasaka, Natsuhiko;
Takahashi, Atsushi;
Svasti, Saovaros;
Munkongdee, Thongperm;
Mahasirimongkol, Surakameth;
Peerapittayamongkol, Chayanon;
Viprakasit, Vip;
Kamatani, Naoyuki;
Winichagoon, Pranee;
Kubo, Michiaki;
Nakamura, Yusuke;
Fucharoen, Suthat

Publication type:

Article

Molecular Epidemiology of Hemoglobinopathies in Cambodia.

Published in:

Hemoglobin, 2016, v. 40, n. 3, p. 163, doi. 10.3109/03630269.2016.1158723

By:

Munkongdee, Thongperm;
Tanakulmas, Jatuporn;
Butthep, Punnee;
Winichagoon, Pranee;
Main, Barbara;
Yiannakis, Miriam;
George, Joby;
Devenish, Robyn;
Fucharoen, Suthat;
Svasti, Saovaros

Publication type:

Article

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

Published in:

Hemoglobin, 2010, v. 34, n. 6, p. 582, doi. 10.3109/03630269.2010.526914

By:

Pichanun, Dalad;
Munkongdee, Thongperm;
Klamchuen, Sumonmaln;
Butthep, Punnee;
Winichagoon, Pranee;
Fucharoen, Suthat;
Svasti, Saovaros

Publication type:

Article

Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-36676-2

By:

Chumworathayee, Worakawee;
Munkongdee, Thongperm;
Buasuwan, Nattrika;
Chaichompoo, Pornthip;
Svasti, Saovaros

Publication type:

Article

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

Published in:

Microchimica Acta, 2020, v. 187, n. 4, p. 1, doi. 10.1007/s00604-020-4197-8

By:

Jirakittiwut, Nuttapon;
Munkongdee, Thongperm;
Wongravee, Kanet;
Sripichai, Orapan;
Fucharoen, Suthat;
Praneenararat, Thanit;
Vilaivan, Tirayut

Publication type:

Article

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

Published in:

International Journal of Laboratory Hematology, 2020, v. 42, n. 6, p. 727, doi. 10.1111/ijlh.13292

By:

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

Publication type:

Article

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

Published in:

International Journal of Laboratory Hematology, 2019, v. 41, n. 5, p. 650, doi. 10.1111/ijlh.13080

By:

Phanmany, Sayphonh;
Chanprasert, Supantitra;
Munkongdee, Thongperm;
Svasti, Saovaros;
Leecharoenkiat, Kamonlak

Publication type:

Article

Predictive SNPs for β0-thalassemia/HbE disease severity.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-89641-2

By:

Munkongdee, Thongperm;
Tongsima, Sissades;
Ngamphiw, Chumpol;
Wangkumhang, Pongsakorn;
Peerapittayamongkol, Chayanon;
Hashim, Hafizah Binti;
Fucharoen, Suthat;
Svasti, Saovaros

Publication type:

Article

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

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-87738-2

By:

Nuamsee, Khanita;
Chuprajob, Thipphawan;
Pabuprapap, Wachirachai;
Jintaridth, Pornrutsami;
Munkongdee, Thongperm;
Phannasil, Phatchariya;
Vadolas, Jim;
Chaichompoo, Pornthip;
Suksamrarn, Apichart;
Svasti, Saovaros

Publication type:

Article

Molecular analysis of β-thalassemia in South Vietnam.

Published in:

American Journal of Hematology, 2002, v. 71, n. 2, p. 85, doi. 10.1002/ajh.10193

By:

Svasti, M.L. Saovaros;
Hieu, Tran Minh;
Munkongdee, Thongperm;
Winichagoon, Pranee;
Van Be, Tran;
Van Binh, Tran;
Fucharoen, Suthat

Publication type:

Article

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

Published in:

Annals of Hematology, 2011, v. 90, n. 7, p. 741, doi. 10.1007/s00277-010-1137-4

By:

Munkongdee, Thongperm;
Pichanun, Dalad;
Butthep, Punnee;
Klamchuen, Sumonmaln;
Chalermpolprapa, Veeradet;
Winichagoon, Pranee;
Svasti, Saovaros;
Fucharoen, Suthat

Publication type:

Article

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

Published in:

Annals of Hematology, 2008, v. 87, n. 5, p. 375, doi. 10.1007/s00277-007-0407-2

By:

Sripichai, Orapan;
Munkongdee, Thongperm;
Kumkhaek, Chutima;
Svasti, Saovaros;
Winichagoon, Pranee;
Fucharoen, Suthat

Publication type:

Article

Immunostick Test for Detecting ζ-Globin Chains and Screening of the Southeast Asian α-Thalassemia 1 Deletion.

Published in:

Biological Procedures Online, 2019, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12575-019-0104-2

By:

Pata, Supansa;
Pongpaiboon, Matawee;
Laopajon, Witida;
Munkongdee, Thongperm;
Paiboonsukwong, Kittiphong;
Pornpresert, Sakorn;
Fucharoen, Suthat;
Kasinrerk, Watchara

Publication type:

Article

Works by Munkongdee, Thongperm

Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β<sup>0</sup>-thalassemia/HbE disease.

Simple method for screening of alpha-thalassaemia 1 carriers.

Association of SNP in exon 1 of HBS1L with hemoglobin F level in beta0-thalassemia/hemoglobin E.

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

Development of molecular diagnostic platform for α<sup>0</sup>‐thalassemia 44.6 kb (Chiang Rai, ‐‐<sup>CR</sup>) deletion in individuals with microcytic red blood cells across Thailand.

Impact of the detection of ζ-globin chains and hemoglobin Bart's using immunochromatographic strip tests for α<sup>0</sup>-thalassemia (--<sup>SEA</sup>) differential diagnosis.

Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of β<sup>E</sup> pre-mRNA splicing determine disease severity.

Expression level of pro-apoptotic genes determine disease severity of HbE/ beta thalassemia.

Identification and expression of gene loci underlying the quantitative trait loci of starch content in cassava.

Genetic Analysis of Candidate Modifier Polymorphisms in Hb E-β<sup>0</sup>-Thalassemia Patients.

A genome-wide association identified the common genetic variants influence disease severity in β<sup>0</sup>-thalassemia/hemoglobin E.

Molecular Epidemiology of Hemoglobinopathies in Cambodia.

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

Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification.

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

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

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

Predictive SNPs for β0-thalassemia/HbE disease severity.

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

Molecular analysis of β-thalassemia in South Vietnam.

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

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

Immunostick Test for Detecting ζ-Globin Chains and Screening of the Southeast Asian α-Thalassemia 1 Deletion.