Molecular basis of beta thalassemia in the south of thailand
✍ Scribed by Dr. V. Laosombat; S-P. Fucharoen; V. Panich; G. Fucharoen; M. Wongchanchailert; W. Sriroongrueng; C. Nopparatana; K. Kenpitak; M. Maipang; Y. Fukumaki
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 341 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0361-8609
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The -thalassemia syndromes are a heterogeneous group of genetic disorders characterized by reduced or absent expression of the -globin gene. To date, over 300 -thalassemia alleles have been characterized in or around the -globin region. Thalassemia major is severe anemia necessitating chronic bl
## Abstract The process of allorecognition consists of an ability to discriminate self from non‐self. This discrimination is used either to identify non‐self cells and reject them (“non‐self histocompatibility”) or to identify self cells and reject them (as in the avoidance of self‐fertilization by
Crosslinked polystyrene (XPS ) and poly(methyl methacrylate) (XPMMA) were prepared by photopolymerization of the respective monomers in the presence of reversible crosslinkers, acrylic acid anhydride (AAA), and methacrylic acid anhydride (MAA). Fracture studies on the crosslinked samples were carrie
## Abstract The chronic severe anemia of patients with β‐thalassemia major stimulates extensive erythropoiesis, which results in circulating nucleated normoblasts. We devised a dual staining flow cytometric procedure in order to analyse the cell cycle and ploidy of these normoblasts. Peripheral blo