Fetal haemoglobin, sickling, and thalassaemia: a therapeutic lead?
出版信息
Br Med J. 1978 Jul 1;2(6129):3-4. doi: 10.1136/bmj.2.6129.3-a.
Abstract
摘要
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Fetal haemoglobin, sickling, and thalassaemia: a therapeutic lead?胎儿血红蛋白、镰状化与地中海贫血：一种治疗线索？
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alpha-Thalassemia and HbF concentration in sickle cell anemia.
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A new sickling disorder resulting from interaction of the genes for haemoglobin S and alpha-thalassaemia.一种由血红蛋白S基因与α地中海贫血基因相互作用导致的新型镰状细胞疾病。
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Sickle-cell thalassaemia disease in Sudanese.苏丹人中的镰状细胞地中海贫血病
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本文引用的文献
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Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia.不可逆镰状红细胞：镰状细胞贫血中血红蛋白类型异质分布的结果。
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Benign sickle-cell anaemia.
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Fetal haemoglobin in homozygous sickle cell disease.纯合子镰状细胞病中的胎儿血红蛋白
Clin Haematol. 1975 Feb;4(1):109-22.
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Switch from foetal to adult haemoglobin synthesis in normal and hypophysectomised sheep.正常和垂体切除绵羊从胎儿血红蛋白合成向成人血红蛋白合成的转变。
Nature. 1976;264(5588):799-801. doi: 10.1038/264799a0.
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Interaction of heterocellular hereditary persistence of foetal haemoglobin with beta thalassaemia and sickle cell anaemia.
Nature. 1976 Nov 18;264(5583):247-9. doi: 10.1038/264247a0.
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A physical map of the DNA regions flanking the rabbit beta-globin gene.兔β-珠蛋白基因侧翼DNA区域的物理图谱。
Cell. 1977 Oct;12(2):429-39. doi: 10.1016/0092-8674(77)90119-2.
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Heterocellular hereditary persistence of fetal haemoglobin (heterocellular HPFH) and its interaction with beta thalassaemia.
Br J Haematol. 1977 Aug;36(4):461-73. doi: 10.1111/j.1365-2141.1977.tb00986.x.
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Erythroid progenitors circulating in the blood of adult individuals produce fetal hemoglobin in culture.
Science. 1978 Mar 24;199(4335):1349-50. doi: 10.1126/science.628844.
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Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.沙特阿拉伯人镰状细胞贫血的自然病史。对270名受试者的研究。
Ann Intern Med. 1978 Jan;88(1):1-6. doi: 10.7326/0003-4819-88-1-1.
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