Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Wanicha Tepakhan"'
Autor:
Wanicha Tepakhan, Sataron Kanjanaopas, Korntip Sreworadechpisal, Tipparat Penglong, Pornpun Sripornsawan, Chaowanee Wangchauy, Chadaporn Nokkong, Chulalak Kongkan, Saristha Buathong
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract Data on hemoglobin (Hb) variants in southern Thailand are lacking. This study aimed to reassess the frequency of Hb variants and the clinical aspects of compound heterozygous Hb variant with other hemoglobinopathies. We enrolled 13,391 parti
Externí odkaz:
https://doaj.org/article/45d889cec6dd478c8e6e3fe3084bf6db
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract α-thalassemia is an inherited blood disorder that is most frequently found in Southeast Asian populations. In Thailand, molecular characterization can diagnose most patients with α-thalassemia; however, several atypical patients are also o
Externí odkaz:
https://doaj.org/article/448416539ab94f028f87d0d713a4cb4e
Autor:
Chayada Soontornpanawet, Kritsada Singha, Hataichanok Srivorakun, Wanicha Tepakhan, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
PeerJ, Vol 11, p e15308 (2023)
Background β0-thalassemia deletion removing 5´β-globin promoter usually presents phenotype with high hemoglobin (Hb) A2 and Hb F levels. We report the molecular characteristics and phenotype-genotype correlation in a large cohort of the β0-thalas
Externí odkaz:
https://doaj.org/article/47bd68c5bc5f4225b0178f6ffe7f917e
Autor:
Korntip Srewaradachpisal, Wanicha Tepakhan, Sataron Kanjanaopas, Chawadee Nopparatana, Malai Wongchanchailert, Chamnong Nopparatana
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 38, Iss 3, Pp 221-229 (2020)
Objective: The aim of this study was to characterize unknown β-globin gene mutations in individuals who attended Songklanagarind Hospital for thalassemia screening and genetic counseling. Material and Methods: β-thalassemia mutations in individuals
Externí odkaz:
https://doaj.org/article/4026707a92314b8299dcca2669e741ce
Autor:
Wanicha Tepakhan, Wittaya Jomoui
Publikováno v:
Heliyon, Vol 7, Iss 11, Pp e08372- (2021)
Background: β-thalassemia is an inherited disorder that is reported worldwide. Two common β0-thalassemia mutations (3.5 kb and 45 kb deletions) are prevalent in Southeast Asia and Thailand. Identification of these defects is essential to population
Externí odkaz:
https://doaj.org/article/8aec7bcf5ada485ba55aa0cad2b54634
Autor:
Rossarin Karnpean, Wanicha Tepakhan, Prame Suankul, Sitthikorn Thingphom, Apichaya Poonsawat, Naritthakarn Thanunchaikunlanun, Rotsakorn Ruangsanngamsiri, Wittaya Jomoui
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1384
Single nucleotide polymorphisms are informative for haplotype analysis associated with genetic background and clinical linkage studies of β-thalassemia mutations. Hence, the aim of this study was to investigate five polymorphisms (codon 2 (C/T), IVS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6302daf155d7a18076bc90a244c4fc46
https://pubmed.ncbi.nlm.nih.gov/36011295
https://pubmed.ncbi.nlm.nih.gov/36011295
Autor:
Wanicha Tepakhan, Putita Wongsariya, Pitchaya Wongsariya, Prapaporn Panichchob, Pinnaree Wongwattanasanti, Wittaya Jomoui, Pooncharus Iamdeelert
Publikováno v:
Hemoglobin. 45:97-102
The aim of this study was to determine the molecular spectrum of β-thalassemia (β-thal) mutations in eastern Thailand. We identified β-thal mutations using allele specific-polymerase chain reaction (ASPCR) and direct DNA sequencing. We found 18 di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b751e36cfefb11db218c495ca197ce6a
https://doi.org/10.1080/03630269.2021.1924193
https://doi.org/10.1080/03630269.2021.1924193
Publikováno v:
Annals of Human Genetics. 85:115-124
β-thalassemia (β-thal) (3.5 kb deletion or NC_000011.10:g.5224302-5227791del3490bp) is a common mutation in southern Thailand. This study aimed to determine genetic diversity in subjects with β-thal (3.5 kb deletion) alleles and to ascertain the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b1312f11a175b2ce78f1cd848daf300
https://doi.org/10.1111/ahg.12416
https://doi.org/10.1111/ahg.12416
Autor:
Chayada Soontornpanawet, Kritsada Singha, Hataichanok Srivorakun, Wanicha Tepakhan, Goonnapa Fucharoen, Supan Fucharoen
Publikováno v:
PeerJ; May2023, p1-18, 18p
Autor:
Wittaya Jomoui, Wanicha Tepakhan
Publikováno v:
Heliyon, Vol 7, Iss 11, Pp e08372-(2021)
Heliyon
Heliyon
Background β-thalassemia is an inherited disorder that is reported worldwide. Two common β0-thalassemia mutations (3.5 kb and 45 kb deletions) are prevalent in Southeast Asia and Thailand. Identification of these defects is essential to population
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f180145b1c0b97e570bd5bd2efcb7872
http://www.sciencedirect.com/science/article/pii/S2405844021024750
http://www.sciencedirect.com/science/article/pii/S2405844021024750