يعرض 1 - 5 نتائج من 5 نتيجة بحث عن '"Amphai Phasit"', وقت الاستعلام: 0.36s تنقيح النتائج
  1. 1
    Academic Journal
    Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of α- and β-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis

    المؤلفون: Sitthichai Panyasai, Surada Satthakarn, Amphai Phasit

    المصدر: Heliyon, Vol 9, Iss 8, Pp e19116- (2023)

    مصطلحات موضوعية: Hb Constant Spring, Hb Paksé, Capillary electrophoresis, Efficiency, Accuracy, Science (General), Q1-390, Social sciences (General), H1-99

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S2405844023063247; https://doaj.org/toc/2405-8440

    URL الوصول: https://doaj.org/article/80de1ea391eb4a799b3457fb2a002b84

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  2. 2
    Academic Journal
    Phenotypic Expression of Known and Novel Hemoglobin A2-Variants, Hemoglobin A2-Mae Phrik [Delta 52(D3) Asp > Gly, HBD:c.158A > G], Associated with Hemoglobin E [Beta 26(B8) Glu > Lys, HBB:c.79G > A] in Thailand

    المؤلفون: Amphai Phasit, Sitthichai Panyasai, Monthon Mayoon, Niphawan Jettawan, Surada Satthakarn

    المصدر: Genes; Volume 13; Issue 6; Pages: 959

    مصطلحات موضوعية: Hb A 2 -Mae Phrik, δ-globin variant, Hb E, deletional α + -thalassemia, β-globin haplotype

    جغرافية الموضوع: agris

    وصف الملف: application/pdf

    Relation: Molecular Genetics and Genomics; https://dx.doi.org/10.3390/genes13060959

    الاتاحة: https://doi.org/10.3390/genes13060959

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  3. 3
    Association of Hb Shenyang [α26(B7)Ala→Glu, GCG>GAG, HBA2: c.80C>A (or HBA1)] with Several Types of α-Thalassemia in Thailand

    المؤلفون: Sitthichai Panyasai, Kanyakan Kongthai, Amphai Phasit

    المصدر: Hemoglobin. 44:354-360

    مصطلحات موضوعية: Hb Shenyang, Thalassemia, Biochemistry (medical), Clinical Biochemistry, medicine, Hematology, Biology, medicine.disease, Molecular biology, Genetics (clinical)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::79c915eca1996111a357acd0267d5ce3
    https://doi.org/10.1080/03630269.2020.1828096

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  4. 4
    α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [– –SEA (Southeast Asian)] Deletion in Thailand

    المؤلفون: Amphai Phasit, Sitthichai Panyasai

    المصدر: Hemoglobin. 44:264-271

    مصطلحات موضوعية: Proband, Chemistry, Thalassemia, Biochemistry (medical), Clinical Biochemistry, Haplotype, Hematology, Southeast asian, medicine.disease, Molecular biology, Abnormal hemoglobin, Hypervariable region, medicine, Globin, Hemoglobin, Genetics (clinical)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::24bcb418afa85cf4ac3c905b69e9f3a6
    https://doi.org/10.1080/03630269.2020.1797773

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  5. 5
    α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (

    المؤلفون: Sitthichai, Panyasai, Amphai, Phasit

    المصدر: Hemoglobin. 44(4)

    مصطلحات موضوعية: Erythrocyte Indices, Genotype, Hemoglobins, Abnormal, DNA Mutational Analysis, Hemoglobin A, Sequence Analysis, DNA, Thailand, Pedigree, Phenotype, Amino Acid Substitution, Haplotypes, alpha-Thalassemia, Mutation, Humans, Alleles

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::a50bd05522af0ff95da66d5d4e5a8514
    https://pubmed.ncbi.nlm.nih.gov/32727229

    View record in OpenAIRE

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