有几种版本的结合珠蛋白基因。
珠蛋白基因的程序性表达是组织发育时期专一性的。
The programmed expression of globin genes is tissue and developmental stage specific.
在珠蛋白链的研究中，该方法具有简单、灵敏等优点。
In general, this method is comparatively simple and sensitive for analysis of the human globin chains in he-malysates.
平阳霉素；pva颗粒；贫血，珠蛋白生成障碍性；婴幼儿。
Pingyangmycin; PVA granules; Anemia, Disorder of globin generation; Infant.
前者表现为血红蛋白分子的珠蛋白肽链结构异常，如镰刀状贫血；
The former is categorized by globin structural abnormality, like sickle cell disease;
结论触珠蛋白有可能成为白血病干细胞移植治疗疗效评价及疗程监测的标志物。
Conclusion The haptoglobin may be a potential biomarker for monitoring prognosis in patients with leukemia treated by stem cell transplantation.
测定116例珠蛋白生成障碍性贫血、37例缺铁性贫血患者及45例正常人的FEP水平。
Free erythrocyte Protoporphyrin (FEP) were determined in 116 thalassemia patients, 37 iron deficiency anemia patients and 45 normal subjects.
本文报告了从利凡诺-硫酸铵法生产人血免疫球蛋白的废渣中，制备结合珠蛋白的一种简易方法。
A simpler method for preparing haptoglobin from the waste residue of Rivanol - ammonium sulphate fractionation of human serum during the production of human immunoglobulin is described.
这个案件被170个人抱怨，他们的孩子，遭受血友病和血液疾病珠蛋白生成障碍性贫血的痛苦。
The case followed complaints by families of some 170 people, many of them children, suffering from haemophilia and the blood disease thalassemia.
随着镰珠蛋白中氧的去除，红细胞变形成镰状，红细胞膜受到破坏，破裂的可能性增加，从而导致贫血。
With the removal of oxygen from sickle hemoglobin, the red blood cell deforms into a sickled shape. This sickling damages the RBC membrane and increases the likelihood of rupture and anemia.
虽然对于珠蛋白基因表达调控及开关的研究已取得许多进展，但至今对于调节这些开关的决定性调节因子仍不明确。
Although advance has been made in the study on control of globin gene expression and switching, key factors of globin gene switching is still unknown till now.
目的探讨葡萄糖-6磷酸脱氢酶（G-6PD）活性对珠蛋白生成障碍性贫血（地贫）的辅助诊断价值及其适用范围。
Objective:To approach the value and applicability of the activity of Glucose-6-phosphate dehydrogenase (G6PD) for the auxiliary diagnosis of thalassemia.
合并地贫血的G6PD缺乏症患儿珠蛋白基因缺陷类型多样，但G6PD缺乏症与地贫不同基因型之间并无明显的相关性。
The globin gene types in G6PD deficiency children are multifarious, but there is no obvious relationship between G6PD deficiency and the different globin gene types.
珍珠蛋白的新肤性可使肌肤维持极佳的保水度，在面膜添家中可使水分不流失外，亦有滋润度，敷后有如丝缎般柔滑亮丽。
Pearl protein can help reserve the nutrients and moisture in the mask, and give you a smooth and silky skin.
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.
目的探讨葡萄糖- 6磷酸脱氢酶(G - 6pd)活性对珠蛋白生成障碍性贫血(地贫)的辅助诊断价值及其适用范围。
Objective To explore the value and applicability of the activity of glucose-6 phosphate dehydrogenase (G-6PD) for the auxiliary diagnosis of thalassemia.
然后通过扩增新鲜扁桃体组织中珠蛋白基因及模拟手套被质粒污染的情况下扩增质粒基因，验证该无DNA操作过程对避免污染的有效性。
Validity oft his "non-DNA" principle was evaluated by amplification of globin gene from fresh tonsil tissues and plasmid gene on condition that gloves were contaminated by plasmid.
同样的精卵结合方式很可能应用于“移植前基因诊断”，给那些患有其他基因疾病的人，包括白血病和珠蛋白生成障碍性贫血患者带来希望。
The same ready acceptance is likely to apply to PGD, which offers hope to sufferers of other genetic disorders, including leukaemia4 and thalas-saemia.
结果富含小分子肽的珠蛋白水解液在水解度为12.6%时，对ACE的抑制率最高； 在显微镜下观察水解液对血红细胞有一定的凝集作用；
Results The globin hydrolysate which fully contained small molecule peptide showed the highest ACE inhibitory activity and some hemagglutinative activity with the degree of hydrolysis of 12.6%.
方法在比较使用联苯胺及其衍生物显现血手印的同时，实验了通过强氧化剂破坏血红素、沉淀珠蛋白，采用激活血痕、蛋白染色的方法，使血手印清晰显出。
Blood fingerprint was developed distinctly by using strong oxidation agent to destroy ferroheme, deposit pearl protein, also blood stain activation and protein decoration method were applied.
方法在比较使用联苯胺及其衍生物显现血手印的同时，实验了通过强氧化剂破坏血红素、沉淀珠蛋白，采用激活血痕、蛋白染色的方法，使血手印清晰显出。
Blood fingerprint was developed distinctly by using strong oxidation agent to destroy ferroheme, deposit pearl protein, also blood stain activation and protein decoration method were applied.
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