βサラセミア
WordNet
- an inherited form of anemia caused by faulty synthesis of hemoglobin (同)thalassaemia, Mediterranean_anemia, Mediterranean anaemia
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Japanese Journal
- SSA法(Sequence-Specific Amplification)によるβ-サラセミア遺伝子変異の簡易・迅速解析
- Development of a fibrous DNA chip for cost-effective β-thalassemia genotyping
- SUZUKI Wakako,OSAKA Takashi,SEKIZAWA Akihiko,KITAGAWA Michihiro,HONMA Ikuo
- International journal of hematology 96(3), 301-307, 2012-09-01
- NAID 10031121257
- Generation of Human β-thalassemia Induced Pluripotent Stem Cells from Amniotic Fluid Cells Using a Single Excisable Lentiviral Stem Cell Cassette
- FAN Yong,LUO Yumei,CHEN Xinjie [他],LI Qing,SUN Xiaofang
- The Journal of reproduction and development 58(4), 404-409, 2012-08-01
- … Here, we show that amniotic fluid cells from the prenatal diagnosis of a β-thalassemia patient can be efficiently reprogrammed using a doxycycline (DOX)-inducible humanized version of the single lentiviral "stem cell cassette" vector flanked by loxP sites, which can be excised with Cre recombinase. …
- NAID 10031066784
Related Links
- Standard therapy for TM: transfusion. Transfusion is the main stay of therapy in β-thalassemia, typically initiated in the first 2 years of life in patients with TM. Transfusion in TM corrects anemia, suppresses EMH, inhibits increased ...
- Figure 1 Cellular mechanisms by which decreased iron uptake into erythroid precursors may promote survival and differentiation. (A) In β-thalassemia, a relative excess of α-globin synthesis leads to formation of hemichromes (α-globin ...
- Signs and symptoms The clinical picture of the thalassemias varies widely, depending on the severity of the condition and the age at diagnosis. In the more severe forms of the disease (eg, β-thalassemia major ...
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- 英
- beta-thalassemia, beta thalassemia, β-thalassemia, β thalassemia .beta-thalassaemia
- 同
- β-サラセミア、ベータサラセミア
- 関
- β地中海貧血症、サラセミア