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1.
Direct cord blood LAMP colorimetric phenol red assay for detecting α0-thalassemia (SEA deletion); the validation and post-natal screening in Thailand.
Scand J Clin Lab Invest
; 83(7): 495-500, 2023 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-37933918
2.
Genetics background of ß-thalassemia (3.5 kb deletion) in Southern Thailand: Haplotype analysis using novel reverse dot blot hybridization.
Ann Hum Genet
; 85(3-4): 115-124, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33559179
3.
Molecular Spectrum of ß-Thalassemia Mutations in Central to Eastern Thailand.
Hemoglobin
; 45(2): 97-102, 2021 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-33966551
4.
A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders.
Ann Hematol
; 99(1): 23-29, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-31776727
5.
Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand.
Scand J Clin Lab Invest
; 80(7): 528-535, 2020 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-32723194
6.
Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (- -SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart's Hydrops Fetalis Syndrome in Thailand.
Hemoglobin
; 43(4-5): 236-240, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31635494
7.
Coinheritance of Hb A2-Melbourne (HBD: c.130G>A) and Hb E (HBB: c.79G>A) in Laos and Simultaneous High Resolution Melt Detection of Hb A2-Melbourne and Hb A2-Lampang (HBD: c.142G>A) in a Single Tube.
Hemoglobin
; 43(3): 214-217, 2019 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-31450984
8.
Genetic origin of α0-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart's hydrops fetalis syndrome.
J Hum Genet
; 62(8): 747-754, 2017 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-28381876
9.
Molecular analysis of haemoglobin E in Southeast Asian populations.
Ann Hum Biol
; 44(8): 747-750, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29047316
10.
Retrospective study and implementation of a low-cost LAMP-turbidimetric assay for screening α0-thalassemia (SEA deletion): preventing and controlling Hb Bart's hydrops fetalis syndrome in Thailand.
PeerJ
; 12: e17054, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38436007
11.
Molecular understanding of unusual HbE-ß+-thalassemia with Hb phenotype similar to HbE heterozygote: simple and rapid differentiation using HbE levels.
Ann Med
; 55(2): 2267054, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37816374
12.
Revisiting and updating molecular epidemiology of α-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine α-thalassemia deletion.
Sci Rep
; 13(1): 9850, 2023 06 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-37330590
13.
Loop-mediated isothermal amplification (LAMP) colorimetric phenol red assay for rapid identification of α0-thalassemia: Application to population screening and prenatal diagnosis.
PLoS One
; 17(4): e0267832, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35482800
14.
Genetic Background Studies of Eight Common Beta Thalassemia Mutations in Thailand Using ß-Globin Gene Haplotype and Phylogenetic Analysis.
Genes (Basel)
; 13(8)2022 08 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-36011295
15.
Rapid Molecular Detection for Differentiation of Homozygous HbE and ß0-Thalassemia/HbE in Samples Related With HbE >80% and Variable HbF Levels.
Lab Med
; 52(3): 232-239, 2021 May 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-32926164
16.
Rapid molecular diagnostics of large deletional ß0-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypes.
Heliyon
; 7(11): e08372, 2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-34816050
17.
Screening of (-SEA) α-thalassaemia using an immunochromatographic strip assay for the ζ-globin chain in a population with a high prevalence and heterogeneity of haemoglobinopathies.
J Clin Pathol
; 70(1): 63-68, 2017 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-27312111
18.
Characterization and identification of Prachinburi ß0 -thalassemia: A novel-60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous state.
Int J Lab Hematol
; 43(4): O200-O203, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-33734585
19.
Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis.
PLoS One
; 10(12): e0145230, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26683994
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