G6PD

Research Progress of the Gene Mutations of G6PD Deficiency in Minority Nationalities in Southern China

我国南方少数民族地区葡萄糖-6-磷酸脱氢酶缺乏症及基因突变研究进展

Study on the mutations of G6PD gene in Dong ethnic group in Guizhou Congjiang

贵州省从江县侗族人群葡萄糖-6-磷酸脱氢酶基因突变型的检测

Conclusions The G6PD gene in Yunnan people is heterogeneous .

结论云南省G6PD基因具有明显异质性。

Objective : To study the effect of G6PD deficiency on membrane phospholipid structures .

目的：通过测定葡萄糖－6－磷酸脱氢酶（G6PD）缺乏红细胞膜磷脂的含量及其不对称性的变化，研究G6PD缺乏对红细胞膜结构的影响。

Study on G6PD Gene Mutation of Chinese Minority Nationalities

我国少数民族G6PD缺乏症基因突变的研究

Identification of three common G6PD gene mutations in Yi minority in Yunnan province

云南省彝族三种常见葡萄糖-6-磷酸脱氢酶基因突变型分析

G6PD Mutations Found Among Dai People in Yunnan Province

云南傣族中所见的G6PD突变型

Value of joint detection of hemoglobin electrophoresis and G6PD deficiency

血红蛋白电泳和G6PD联合检测在诊断贫血中的价值

Analysis of 217 cases screened neonatal with G6PD deficiency in Liuzhou

柳州市新生儿筛查检出红细胞G6PD缺陷217例分析

Results G6PD were detected in all samples ;

结果全部病例均检测到葡糖6磷酸脱氢酶（G6PD）重排；

Study of Newborn Umbilical Blood Screening of G6PD Deficiency

新生儿脐血筛查葡萄糖6-磷酸脱氢酶缺乏的研究

A Biochemical and Histological Investigation on G6PD Deficiency in Blood

G6PD缺陷症血液生化及组织学研究

Objective To establish a more effective method for diagnosis of G6PD with three biochemical methods combined with gene detection .

目的联合三种生化法和基因检测对G6PD缺陷症进行诊断，以提高这种儿科临床常见溶血性疾病的确诊率。

Expression of G6PD Gene by Nested RT-PCR in Kunming Mouse Early Embryos

巢式RT-PCR检测昆明小鼠早期胚胎中G6PD基因表达

Analyze the results of hemoglobin eletrophoresis in 56 patients with G6PD deficiency

56例G6PD缺乏症患者血红蛋白电泳结果分析

Level of G6PD in the Sera of 81 Leprosy Patients

81例麻风血清中6&葡萄糖磷酸脱氢酶的测定结果

Conclusion : Guangdong Zhuang and Yao nationality have similar G6PD gene mutation type .

结论：广东壮族、瑶族人群中具有共同的G6PD基因突变型。

G6PD Isozymes in Transferring Soybean DNA into Wheat Seeds by Ion Implantation

离子注入法转大豆DNA小麦发芽种子中G6PD的研究

Observation on the consumption of blood glucose values in vitro and G6PD activity in polycythemia

红细胞增多症体外糖消耗及葡萄糖&6磷酸脱氢酶活性观察

Development of Kunming Mouse Early Embryos in Vitro and Expression of G6PD under Simulated Microgravity

模拟微重力条件下昆明小鼠早期胚胎体外发育及其G6PD基因表达

Of 416 cases , 80 ( 19.23 % ) cases were in the state of G6PD deficiency .

在416例黄疸患儿中，G6PD缺乏的有80例（19·23%）。

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。

Total G6PD and LDH values were assayed cytochemical methods .

并应用定量细胞化学法对LDH和6PD全酶活性进行了测定。

The G6PD genotypes are associated intimately with the clinical manifestation .

G6PD基因突变型改变与其临床表现有着极其密切的关系。

Changes of erythrocyte membrane lipid in hereditary G6PD deficiency

遗传性葡萄糖-6-磷酸脱氢酶缺乏症红细胞膜脂质的改变

The value of the combined tests of thalassemia and G6PD deficiency in detection of before marriage

地中海贫血和G6PD缺乏联合检测在婚前检查中的价值

Study on common mutations of G6PD gene in Miao 、 Shui and Yao ethnic groups

少数民族葡萄糖-6-磷酸脱氢酶基因突变检测

The Study on the Genotypes of G6PD Deficiency from Zhuang People in the Southwestern Guangxi

广西西南部壮族居民G6PD缺乏症的基因型研究

Thalassemias Complicated by G6PD Deficiency Caused MOSF : One Case Report and the Literature Review

海洋性贫血合并G6PD缺乏症1例报告并文献复习

Qualitative determination of G6PD in red blood cells from human population in high malarious area with tetrazolium

四氮唑蓝定性法检测高疟区人群红细胞葡萄糖6-磷酸脱氢酶