Molecular Characterization of G6PD Deficiency at a North Indian Centre: Implications for Diagnostic Testing Laboratories in Different Regions of India.
作者信息
Singh Namrata, Kapadia Alpeshkumar Bipinbhai, Sharma Prashant, Das Reena, Jain Karuna, Sachdeva Man Updesh Singh, Khadwal Alka Rani, Bal Amanjit, Varma Neelam
机构信息
Department of Hematology, Level 5, Research Block A, Postgraduate Institute of Medical Education and Research, Sector 12, Chandigarh, India.
Adult Clinical Hematology Unit, Department of Internal Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
出版信息
Indian J Hematol Blood Transfus. 2020 Oct;36(4):766-768. doi: 10.1007/s12288-020-01275-y. Epub 2020 Apr 1.
Abstract
摘要
相似文献
1
Molecular Characterization of G6PD Deficiency at a North Indian Centre: Implications for Diagnostic Testing Laboratories in Different Regions of India.印度北部某中心葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症的分子特征：对印度不同地区诊断检测实验室的启示
Indian J Hematol Blood Transfus. 2020 Oct;36(4):766-768. doi: 10.1007/s12288-020-01275-y. Epub 2020 Apr 1.
2
First report of glucose-6-phosphate dehydrogenase (G6PD) variants (Mahidol and Acores) from malaria-endemic regions of northeast India and their functional evaluations in-silico.首次报道来自印度东北部疟疾流行地区的葡萄糖-6-磷酸脱氢酶（G6PD）变异体（Mahidol 和 Acores）及其在体内的功能评估。
Acta Trop. 2020 Feb;202:105252. doi: 10.1016/j.actatropica.2019.105252. Epub 2019 Oct 31.
3
Molecular basis of G6PD deficiency in India.印度葡萄糖-6-磷酸脱氢酶缺乏症的分子基础。
Blood Cells Mol Dis. 2004 Sep-Oct;33(2):141-5. doi: 10.1016/j.bcmd.2004.06.003.
4
Study of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency and Genotype Polymorphism of G6PD B and G6PD (A+/A-) in Patients Treated for Plasmodium vivax Malaria in a Tertiary Care Hospital in North East India.印度东北部一家三级护理医院中接受间日疟原虫疟疾治疗的患者的葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症及G6PD B和G6PD（A+/A-）基因型多态性研究
Cureus. 2020 Nov 12;12(11):e11463. doi: 10.7759/cureus.11463.
5
6
Heterogeneity of G6PD deficiency prevalence in Mozambique: a school-based cross-sectional survey in three different regions.莫桑比克葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症患病率的异质性：在三个不同地区开展的一项基于学校的横断面调查
Malar J. 2017 Jan 19;16(1):36. doi: 10.1186/s12936-016-1674-y.
7
Community expansion and gene geography of sickle cell trait and G6PD deficiency, and natural selection against malaria: experience from tribal land of India.镰状细胞性状和葡萄糖-6-磷酸脱氢酶缺乏症的群体扩张与基因地理学，以及针对疟疾的自然选择：来自印度部落地区的经验
Cardiovasc Hematol Agents Med Chem. 2012 Mar 1;10(1):3-13. doi: 10.2174/187152512799201190.
8
A large, systematic molecular-genetic study of G6PD in Indian populations identifies a new non-synonymous variant and supports recent positive selection.一项针对印度人群 G6PD 的大型、系统的分子遗传学研究鉴定了一种新的非同义变异，并支持了近期的正选择。
Infect Genet Evol. 2010 Dec;10(8):1228-36. doi: 10.1016/j.meegid.2010.08.003. Epub 2010 Aug 14.
9
Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutation.两种不同的印度G6PD变体，即G6PD贾姆讷格尔和G6PD罗希尼，由相同的949 G→A突变引起。
Blood Cells Mol Dis. 2005 Sep-Oct;35(2):193-5. doi: 10.1016/j.bcmd.2005.03.001.
10
G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India.G6PD A-是印度卡纳塔克邦西迪人群中G6PD缺乏症的主要病因。
Ann Hum Biol. 2020 Feb;47(1):55-58. doi: 10.1080/03014460.2019.1699954. Epub 2019 Dec 13.
本文引用的文献
1
Molecular Characterization of G6PD Deficiency: Report of Three Novel G6PD Variants.葡萄糖-6-磷酸脱氢酶缺乏症的分子特征：三种新型葡萄糖-6-磷酸脱氢酶变体的报告
Indian J Hematol Blood Transfus. 2020 Apr;36(2):349-355. doi: 10.1007/s12288-019-01205-7. Epub 2019 Oct 16.
2
G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India.G6PD A-是印度卡纳塔克邦西迪人群中G6PD缺乏症的主要病因。
Ann Hum Biol. 2020 Feb;47(1):55-58. doi: 10.1080/03014460.2019.1699954. Epub 2019 Dec 13.
3
First report of glucose-6-phosphate dehydrogenase (G6PD) variants (Mahidol and Acores) from malaria-endemic regions of northeast India and their functional evaluations in-silico.首次报道来自印度东北部疟疾流行地区的葡萄糖-6-磷酸脱氢酶（G6PD）变异体（Mahidol 和 Acores）及其在体内的功能评估。
Acta Trop. 2020 Feb;202:105252. doi: 10.1016/j.actatropica.2019.105252. Epub 2019 Oct 31.
4
Prevalence and Genetic Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency in Anemic Subjects from Uttar Pradesh, India.印度北方邦贫血患者中葡萄糖-6-磷酸脱氢酶缺乏症的患病率及基因特征
J Pediatr Genet. 2019 Jun;8(2):47-53. doi: 10.1055/s-0039-1677729. Epub 2019 Jan 30.
5
Glucose-6-phosphate dehydrogenase (G6PD) mutations and haemoglobinuria syndrome in the Vietnamese population.越南人群中的葡萄糖-6-磷酸脱氢酶（G6PD）突变与血红蛋白尿综合征。
Malar J. 2009 Jul 10;8:152. doi: 10.1186/1475-2875-8-152.
6
Molecular variants of G6PD deficiency among certain tribal communities of Orissa, India.印度奥里萨邦某些部落社区中葡萄糖-6-磷酸脱氢酶（G6PD）缺乏症的分子变异体
Ann Hum Biol. 2008 May-Jun;35(3):355-61. doi: 10.1080/03014460801961289.
7
A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.印度南部尼尔吉里斯部落群体中葡萄糖-6-磷酸脱氢酶基因的一种新型R198H突变。
J Hum Genet. 2008;53(2):181-184. doi: 10.1007/s10038-007-0225-3. Epub 2007 Nov 28.
8
Molecular basis of G6PD deficiency in India.印度葡萄糖-6-磷酸脱氢酶缺乏症的分子基础。
Blood Cells Mol Dis. 2004 Sep-Oct;33(2):141-5. doi: 10.1016/j.bcmd.2004.06.003.
Zotero 插件