Zobrazeno 1 - 10
of 51
pro vyhledávání: '"C, Nopparatana"'
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 26, Iss 3, Pp 275-282 (2008)
A simplified hemolysate-preparation reagent was composed of 1 g of ethylenediamine tetraacetic acid and 0.1 g of saponin dissolved in 500 ml of distilled water. The hemolysate was prepared by adding equal volumes of the reagent into normal-saline-was
Externí odkaz:
https://doaj.org/article/c3104afc4c5248f69edb996a7ed52b44
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 26, Iss 3, Pp 283-291 (2008)
Reticulocytes are young non-nucleated red cells which retain RNA within the cell. The reticulocyte count is useful to indicate marrow erythropoietic activity and also to classify the causes of anemia disease. The conventional method for enumerating p
Externí odkaz:
https://doaj.org/article/5d9048d69b19439d9e4d40c2a23a4007
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Autor:
P, Winichagoon, V, Saechan, R, Sripanich, C, Nopparatana, S, Kanokpongsakdi, A, Maggio, S, Fucharoen
Publikováno v:
Prenatal diagnosis. 19(5)
Thalassaemia is the most common genetic disease and is a public health problem of Thailand. Prevention and control of beta-thalassaemia diseases need accurate diagnosis of carriers and proper genetic counselling. Prenatal diagnosis is needed to preve
Publikováno v:
American journal of hematology. 61(1)
We identified and characterized a novel beta(0)-thalassemia mutation due to partial deletion of the 5' end beta-globin gene including the mRNA cap site and a part of exon 1. The deletion was precisely 105 basepair (bp) in length extending from positi
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 28
A total of 50 patients and relatives were studied comprising 12 cases of compound heterozygosity of beta-Malay and beta + thalassemia, 10 cases of compound heterozygosity of beta-Malay and beta degree thalassemia, 10 cases of beta-Malay and HbE and 1
Autor:
W, Sriroongrueng, E, Schleiemacher, V, Panich, C, Nopparatana, V, Saechan, V, Laosombat, M, Pornpatkul, Y, Fukumaki
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 28
beta-Thalassemia mutations in 221 chromosomes of unrelated southern Thai patients were analyzed. Using dot blot hybridization of PCR amplified DNA with 15 allele specific oligonucleotide probes for beta-thalassemia mutations 196/221 (89%) of the alle
Autor:
C, Nopparatana, V, Panich, V, Saechan, V, Sriroongrueng, J, Rungjeadpha, M, Pornpatkul, V, Laosombat, Y, Fukumaki
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 26
Beta-thalassemia mutations in 282 alleles of 253 unrelated individuals originating from various provinces in the south of Thailand were characterized by dot blot hybridization, specific PCR-amplification and direct DNA sequencing. It was possible to