Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Thanet Prajantasen"'
Publikováno v:
Songklanakarin Journal of Science and Technology (SJST), Vol 42, Iss 5, Pp 1021-1026 (2020)
Fucosyltransferase 2 gene (FUT2) gene plays an important role in control of enzymes that secrete blood type antigen substances. The mutation of FUT2 at nucleotide position 385 from A to T (A385T) combined with secretor phenotype is associated with
Externí odkaz:
https://doaj.org/article/118f5f3c8e024a598639c1abbe973521
Publikováno v:
Biochemistry and Biophysics Reports, Vol 26, Iss , Pp 101002- (2021)
miR-21 expression stimulates osteoclast cells in the context of osteoclastogenesis. A previous report showed that NFκB-miR-21 pathway could serve as an innovative alternative to devise therapeutics for healing diabetic ulcers. Furthermore, our study
Externí odkaz:
https://doaj.org/article/1c42c644fe72404eb90f8e6f51520de7
Autor:
Sukanya Binlee, Patcharawadee Prayalaw, Supang Nongnuan, Thanet Prajantasen, Sitthichai Panyasai
Publikováno v:
Genetic Testing and Molecular Biomarkers. 25:426-433
Background: Delta-chain (δ-chain) variants are a group of rare hemoglobin (Hb) variants resulting from mutations within the δ-globin gene. Although quantification of Hb A2 levels is a useful screen...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94492975d05e3715e3c35aea1a69d445
https://doi.org/10.1089/gtmb.2020.0291
https://doi.org/10.1089/gtmb.2020.0291
Publikováno v:
Biochemistry and Biophysics Reports
Biochemistry and Biophysics Reports, Vol 26, Iss, Pp 101002-(2021)
Biochemistry and Biophysics Reports, Vol 26, Iss, Pp 101002-(2021)
miR-21 expression stimulates osteoclast cells in the context of osteoclastogenesis. A previous report showed that NFκB-miR-21 pathway could serve as an innovative alternative to devise therapeutics for healing diabetic ulcers. Furthermore, our study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14251d14069479ece62dbc948380027e
https://doi.org/10.1016/j.bbrep.2021.101002
https://doi.org/10.1016/j.bbrep.2021.101002
A large cohort of β+-thalassemia in Thailand: Molecular, hematological and diagnostic considerations
Autor:
Supawadee Yamsri, Thanet Prajantasen, Wachiraporn Taweenan, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen, Kritsada Singha
Publikováno v:
Blood Cells, Molecules, and Diseases. 54:164-169
We report the molecular and hematological characteristics associated with a large cohort of β(+)-thalassemia in Thailand. Study was done on 21,068 unrelated subjects referred to our center in northeast Thailand for hemoglobinopathies investigation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea85ebaaa5f2d4fcbc4bf07ab625b97d
https://doi.org/10.1016/j.bcmd.2014.11.008
https://doi.org/10.1016/j.bcmd.2014.11.008
Autor:
Nirut Siriratmanawong, Charnchai Pinmuang-ngam, Supan Fucharoen, Goonnapa Fucharoen, Thanet Prajantasen
Publikováno v:
Molecular Biology Reports. 40:3173-3179
We have developed methods based on PCR and denaturing high performance liquid chromatography (DHPLC) for rapid identifications of common β-thalassemia mutations found in Thailand. The β-globin gene was separately amplified by PCR on four different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc4f58ed97382ec72ebf80ac020b25d6
https://doi.org/10.1007/s11033-012-2391-4
https://doi.org/10.1007/s11033-012-2391-4
Publikováno v:
Hemoglobin. 38:451-453
The molecular basis and hematological phenotype of adult Thai β-thalassemia intermedia (β-TI) patients encountered with inferior vena cava (IVC) thrombosis were investigated. Hematological and molecular analysis revealed a trait previously not desc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e403128229017bef9df01c1a7a24ff3a
https://doi.org/10.3109/03630269.2014.974608
https://doi.org/10.3109/03630269.2014.974608
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 441
Background High resolution melting (HRM) analysis is a powerful technology for scanning sequence alteration. We have applied this HRM assay to screen common β-thalassemia mutations found among Southeast Asian population. Methods Known DNA samples wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2435cdb4170a59f9ba8ff3ae00d5fe45
https://pubmed.ncbi.nlm.nih.gov/25526804
https://pubmed.ncbi.nlm.nih.gov/25526804