Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its combinations in patients also carrying Hb constant spring (codon 142, TAA>CAA, α2) in Northern Thailand

Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its combinations in patients also carrying Hb constant spring (codon 142, TAA>CAA, α2) in Northern Thailand

The incidence of Hb Paksé (codon 142, TAA > TAT, α2) might have been underestimated due to misidentifying some cases as Hb Constant Spring (Hb CS, codon 142, TAA > CAA, α2) since both abnormal hemoglobins (Hbs) migrate to the same position on Hb electrophoresis or chromatography. Multiplex asy...

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محفوظ في:

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Pornprasert S., Panyasai S., Treesuwan K.
التنسيق:	دورية
منشور في:	2017
الوصول للمادة أونلاين:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84866606689&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/42799
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مواد مشابهة

Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its combinations in patients also carrying Hb constant spring (codon 142, TAA>CAA, α2) in Northern Thailand
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2018)

Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and Paksé (codon 142, TAA>TAT, α2) mutations in Thailand
بواسطة: Dalad Pichanun, وآخرون
منشور في: (2018)

Comparison between capillary electrophoresis and high performance liquid chromatography for detection and quantification of Hb constant spring [Hb CS; α142, Term→Gln (TAA>CAA in α2)]
بواسطة: Waneesorn J., وآخرون
منشور في: (2017)

Comparison between capillary electrophoresis and high performance liquid chromatography for detection and quantification of Hb constant spring [Hb CS; α142, Term→Gln (TAA>CAA in α2)]
بواسطة: Jarurin Waneesorn, وآخرون
منشور في: (2018)

Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-Thalassemia codon 17 (A>T) in a thai patient
بواسطة: Pornprasert S., وآخرون
منشور في: (2017)

Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-Thalassemia codon 17 (A>T) in a thai patient
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2018)

Elevated Hb A<inf>2</inf> levels in a patient with a compound heterozygosity for the (β <sup>+</sup>)-31 (A > G) and (β <sup>0</sup>) Codon 17 (A > T) mutations together with a single α-globin gene
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Elevated Hb A<inf>2</inf> levels in a patient with a compound heterozygosity for the (β <sup>+</sup>)-31 (A > G) and (β <sup>0</sup>) Codon 17 (A > T) mutations together with a single α-globin gene
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Hematological Characterizations and Molecular Diagnostic Aspects of Hb Wiangpapao [α44(CE2)Pro→Ser (α1), CCG>TCG; HBA1: c.133C>T], a New α-Globin Variant Found in a Pregnant Thai Woman
بواسطة: Panyasai S., وآخرون
منشور في: (2017)

Hematological and Molecular Characterization of Hb J-Buda [α61(E10)Lys → Asn, AAG > AAT]
بواسطة: Panyasai S., وآخرون
منشور في: (2017)

Hematological Characterizations and Molecular Diagnostic Aspects of Hb Wiangpapao [α44(CE2)Pro→Ser (α1), CCG>TCG; HBA1: c.133C>T], a New α-Globin Variant Found in a Pregnant Thai Woman
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Hematological Characterizations and Molecular Diagnostic Aspects of Hb Wiangpapao [α44(CE2)Pro→Ser (α1), CCG>TCG; HBA1: c.133C>T], a New α-Globin Variant Found in a Pregnant Thai Woman
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Hematological and Molecular Characterization of Hb J-Buda [α61(E10)Lys → Asn, AAG > AAT]
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Hb Woodville, a rare α-globin variant, caused by codon 6 mutation of the α1 gene
بواسطة: Vip Viprakasit, وآخرون
منشور في: (2018)

Co-inheritance of Hb J-Kaohsiung [β59(E3) AAG>ACG, Lys→Thr] and HbE [β26(B8) GAG>AAG, Glu→Lys] in a Thai Woman
بواسطة: Panyasai S., وآخرون
منشور في: (2017)

Complex Interaction of Hb Q-Thailand (HBA1: c.223G>C) with β-Thalassemia/Hb E (HBB: c.79G>A) Disease
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Co-inheritance of Hb J-Kaohsiung [β59(E3) AAG>ACG, Lys→Thr] and HbE [β26(B8) GAG>AAG, Glu→Lys] in a Thai Woman
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Co-inheritance of Hb J-Kaohsiung [β59(E3) AAG>ACG, Lys→Thr] and HbE [β26(B8) GAG>AAG, Glu→Lys] in a Thai Woman
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Hb Agenogi [β 90(F6)Glu→Lys (G AG> A AG) HBB: C.271G>A)] in a Pregnant Thai Woman
بواسطة: Panyasai S., وآخرون
منشور في: (2017)

Hb Agenogi [β 90(F6)Glu→Lys (G AG> A AG) HBB: C.271G>A)] in a Pregnant Thai Woman
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Comparison of capillary electrophoregram among heterozygous Hb Hope, Hb Hope/α-thalassemia-1 SEA type deletion and Hb Hope/β0- thalassemia
بواسطة: Pornprasert S., وآخرون
منشور في: (2017)

Detection of coinherited Hb H-constant spring/Paksé disease and Hb e by capillary electrophoresis and high performance liquid chromatography
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2018)

Detection of coinherited Hb H-constant spring/Paksé disease and Hb e by capillary electrophoresis and high performance liquid chromatography
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2018)

A formula to identify potential cases of β-thalassemia/HbE disease among patients with absent HbA, HbE >75% and HbF between 5 and 15%
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2019)

Comparison of capillary electrophoregram among heterozygous Hb Hope, Hb Hope/α-thalassemia-1 SEA type deletion and Hb Hope/β0- thalassemia
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2018)

Detection of Hb Constant Spring (HBA2: C.427T>C) Heterozygotes in Combination with β-Thalassemia or Hb e Trait by Capillary Electrophoresis
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2018)

Detection of Hb Constant Spring (HBA2: C.427T>C) Heterozygotes in Combination with β-Thalassemia or Hb e Trait by Capillary Electrophoresis
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2018)

Quenching of the relaxation pathway in the Weyl semimetal TaAs
بواسطة: Liu, Jiayun, وآخرون
منشور في: (2021)

Hb A2/E levels found in co-inheritance with the α-thalassemia-1- SEA/ type deletion and either Hb e or β-thalassemia
بواسطة: Pornprasert S., وآخرون
منشور في: (2017)

A rare association of α<sup>0</sup>-thalassemia (--<sup>SEA</sup>) and an initiation codon mutation (ATG→A-G) of the α2 gene causes Hb H disease in Thailand
بواسطة: Vip Viprakasit, وآخرون
منشور في: (2018)

Proficiency Testing Program for Hb E (HBB: c.79G>A) Screening in Thailand Using Lyophilized Hb E Control Materials
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2020)

Hb A2/E levels found in co-inheritance with the α-thalassemia-1- SEA/ type deletion and either Hb e or β-thalassemia
بواسطة: Sakorn Pornprasert, وآخرون
منشور في: (2018)

Association of Hb A<inf>2</inf> Variants with Several Forms of α- and β-Thalassemia in Thailand
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2020)

Hemoglobin J-Singapore [α79(EF8)Ala→Gly, GCG>GGG] in a pregnant Thai woman
بواسطة: Sitthichai Panyasai, وآخرون
منشور في: (2018)

Non-saturating quantum magnetization in Weyl semimetal TaAs
بواسطة: Zhang, C.-L., وآخرون
منشور في: (2022)

Association of estrogen receptor-alpha single-nucleotide polymorphism (codon 594 G-->A) and Thai patients affected by knee osteoarthritis.
بواسطة: Tulyapruek Tawonsawatruk, وآخرون
منشور في: (2018)

Image-based tissue informatics - TAA induced hepatotoxicity model
بواسطة: SHAO LIN
منشور في: (2010)

Detection of Co-inheritance of Hb Hope and Hb Constant Spring in Three Thai Samples by Capillary Electrophoresis
بواسطة: Panyasai S., وآخرون
منشور في: (2017)

Hemoglobin vancouver [α<inf>2</inf>β<inf>2</inf> 73(E17) Asp→ Tyr]: Its structure and function
بواسطة: R. T. Jones, وآخرون
منشور في: (2018)

Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA<inf>2</inf> Levels on Capillary Electrophoresis
بواسطة: Panyasai S., وآخرون
منشور في: (2017)