例如，一个血红蛋白基因细胞转换并集中，将成为一个红血细胞。
A cell with its haemoglobin genes switched on to overdrive, for example, will become a red blood cell.
世界人口近5%携带血红蛋白疾患的特征基因，血红蛋白疾患主要包括镰状细胞病和地中海贫血。
Approximately 5% of the world's population carries trait genes for haemoglobin disorders, mainly, sickle-cell disease and thalassaemia.
血红蛋白疾患是遗传性血液病，由通常健康的父母所遗传的血红蛋白突变基因所导致。
Haemoglobin disorders are genetic blood diseases due to inheritance of mutant haemoglobin genes from both, generally healthy, parents.
果与电镜和流式细胞光度计的实验结果一致，表明珠蛋白基因产物血红蛋白住杂交细胞中，能够表达并成为融合细胞的标志。
Results indicated that the resultant cybrid cells are characterized by the appearance of hemoglobin and its expression might be served as a marker for the cybrids.
ALAS2基因的表达在红细胞发生过程中显著增加以满足血红蛋白合成增加时对更多血红素的需求。
ALAS2 expression is markedly increased during erythropoiesis to meet the demand for heme in hemoglobin production.
血红蛋白中遗传密码出现问题会导致世界上最常见的单基因病变。
Errors in the genetic recipe for haemoglobin give rise to the most common single-gene disorder in the world.
起病年龄、体重指数、空腹血糖、糖化血红蛋白、高密度脂蛋白和糖尿病肾病等指标是线粒体基因突变的相关因素（P<0.05）。
Onset age, body mass index, fasting blood glucose, HbA1C, high density lipoprotein-cholesterol and diabetic nephropathy could be related to occurrence of mtDNA mutations (P<0.05).
起病年龄、体重指数、空腹血糖、糖化血红蛋白、高密度脂蛋白和糖尿病肾病等指标是线粒体基因突变的相关因素（P<0.05）。
Onset age, body mass index, fasting blood glucose, HbA1C, high density lipoprotein-cholesterol and diabetic nephropathy could be related to occurrence of mtDNA mutations (P<0.05).
应用推荐