The methods of G6PD is fluorescence spot test.
G6PD检测应用荧光斑点法。
Conclusions The G6PD gene in Yunnan people is heterogeneous.
结论云南省G6PD基因具有明显异质性。
Now a study in Asia shows how the gene for G6PD-deficiency can indeed help.
现在，在亚洲进行的一项研究揭示了这种致病基因确实具有抵御疟疾的功效。
Conclusions a high G6PD frequency is found in Dong ethnic group in Guizhou Congjiang.
结论贵州省从江侗族是G6PD缺乏症的高发区。
In some women, most often black women, the two X chromosome each encode a different G6PD isoenzyme.
在一些妇女，特别是黑人妇女，两条x染色体各自编码一种不同的G6PD同工酶。
Methods: Blood samples from 7488 persons at repreduction-age were examined on G6PD/6PGD hematology.
方法用G6PD/6PGD比值法。 对7488例育龄人群进行了红细胞葡萄糖6-磷酸脱氢酶缺乏症临床检测。
Objective:To elucidate the molecular basis of G6PD deficiency in the Han and Li nationalities in Hainan, China.
目的：阐明海南汉族、黎族人群中葡萄糖-6-磷酸脱氢酶缺乏症的分子基础。
Objective To establish the methods for neonatal screening of glucose 6 phosphate dehydrogenase (G6PD) deficiency.
目的建立适于葡萄糖6磷酸脱氢酶(G6PD)缺乏新生儿筛查的检测方法。
Objective To establish the methods for neonatal screening of glucose-6 phosphate dehydrogenase (G6PD) deficiency.
目的：建立适合葡萄糖6-磷酸脱氢酶（G6PD）缺乏新生儿筛查的检测方法。
No significant difference in isoenzyme patterns of GPI, G6PD, LDH, PO and EST were observed among the seven areas.
结果显示，七个地区马来丝虫感染蚴的GPI、G6PD、LDH、PO、EST这五种酶的同工酶型没有差异。
All these cases had acute hemolytic anemia, jaundice, hemoglobinuria and reduced G6PD activity to different extents.
所有患者都具有急性溶血性贫血，黄疸等临床表现及不同程度的血红蛋白尿、G6PD酶活性降低。
Objective To analyze the types and distribution of glucose-6-phosphate dehydrogenase(G6PD) gene mutations in Yunnan province.
目的分析云南人群中葡萄糖6 磷酸脱氢酶（G6PD）缺乏症患者的基因突变类型及分布特点。
Objective to study the changes of oxygen free radical (OFR) in G6PD deficient neonates with hyperbilirubinemia during phototherapy.
目的探讨G6PD缺陷新生儿光疗时氧自由基变化。
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most frequent genetic enzymopathy, mainly caused by mutations of G6PD gene.
葡萄糖- 6 -磷酸脱氢酶(G6PD)缺乏症是最常见的遗传性酶病，主要由于G6PD基因突变所致。
Objective To investigate dependability of detecting glucose-6-phosphate (G6PD) activity by biochemistry analyzer for examining G6PD deficiency.
目的探讨在全自动生化仪上直接测定葡萄糖六磷酸盐脱氢酶(G6PD)活性对检测G6PD缺乏的可靠性。
MethodsA total of 6 220 preschool children were screened for erythrocyte glucose6Phosphate dehydrogenase deficiency (G6PD) with diagnostic kit.
方法对6 220例学龄前儿童采用改良G6PD荧光斑点试验和测定比值法（手工操作法）进行G6PD缺乏症检测。
Results:The activity of G6PD was increased significantly in malignant lymphoma( P <0.01), G6PD deficiency was increased significantly ( P <0.05).
结果：与正常人相比恶性淋巴瘤G6 PD活性显著增高（P<0 。0 1） ，G6 PD缺乏率显著增高（P。
Objective:To approach the value and applicability of the activity of Glucose-6-phosphate dehydrogenase (G6PD) for the auxiliary diagnosis of thalassemia.
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 evaluate the relationship between the incidence of hyperbilirubinemia and the degree of the G6PD (glucose-6 phosphate dehydrogenate) deficiency.
目的：探讨葡萄糖6磷酸脱氢酶缺乏程度与患儿高胆红素血症发生率的关系。
Objective: To study the rate of the combined tests of thalassemia and G6PD deficiency in detection of before marriage, to direct aristogenesis and good brood.
目的探讨地中海贫血和G6PD缺乏联合检测在婚前检查中的发病率，并指导优生优育。
Objective To explore the hemolytic mechanism of glucose 6 phosphate dehydrogenase (G6PD) deficient erythrocytes in the view of phosphorylation of membrane protein.
目的从红细胞膜蛋白磷酸化改变的角度探讨葡萄糖6磷酸脱氢酶(G6PD)缺乏症溶血的机制。
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.
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。
Objective to research into the morbidity and characteristics of hyperbilirubinemia which develops among the G6PD (glucose-6 phosphate dehydrogenate) deficiency neonates.
目的研究葡萄糖6磷酸脱氢酶(G6PD)缺乏的新生儿高胆红素血症发生率及发病特点。
Objective: the erythrocyte membrane contents of sialic acid was estimated in order to study the Glucose-6-phosphate dehydrogenase (G6PD) deficient erythrocyte hemolysis.
目的：测定葡萄糖- 6 -磷酸脱氢酶(G6PD)缺乏时红细胞膜唾液酸的含量，以进一步了解G6PD缺乏溶血的机理。
Objective: To investigate the credibility of quantitive fluorometric assay for glucose-6-phosphate dehydrogenase (G6PD) activity in dried blood spot specimens on filter paper.
目的探讨荧光测定法测定滤纸片干血斑标本G6PD酶活性的可靠性。
AbstractObjectiveTo research into the morbidity and characteristics of hyperbilirubinemia which develops among the G6PD (glucose6 phosphate dehydrogenate) deficiency neonates.
目的研究葡萄糖6磷酸脱氢酶(G6PD)缺乏的新生儿高胆红素血症发生率及发病特点。
Methods: Using mon-vessel screen method of thalassemia and relative value of G6PD detect thalassemia and G6PD deficiency for man and woman of detection of before marriage in 4268 duplet.
方法应用地中海贫血一管筛查法和G6PD比值法检测4268对婚前男女的地中海贫血和G6PD缺乏。
The results showed that: fungal elicitor treatment improved the activities of glucose-6-phosphate dehydrogenase (G6PD), phenylalanine ammonia-lyase (PAL), phenolics and taxol production .
结果表明：真菌诱导子处理提高了细胞的G6PD、PAL的活性和酚类化合物含量；
Some results from the studies on the deficiency of glucose-6-phosphate dehydrogenase (G6PD) from patients and their family have been obtained by virtue of blood biochemistry and histology.
本文对G6PD缺陷症患者及其家族进行多项血液生化及组织学方面研究。此类患者G6PD 活力低下；
Glucose-6-phosphate dehydrogenase (G6PD) is an estrogen-mediated enzyme, In human breast carcinoma, the level of G6PD activity usually is correlated with the concentartion of estradiol receptors (ER).
磷酸葡萄糖脱氢酶（G6PD）是一个雌激素诱导酶，人乳腺癌较高雌激素受体水平与较高G6PD活性有关。
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