1)β-thalassemiaβ-地中海贫血
1.The Development in β-thalassemia for Gene Therapy;β-地中海贫血的基因治疗研究
2.DNA chip construction for β-thalassemia and achondroplasia;β-地中海贫血与先天性软骨发育不全诊断性基因芯片的构建
3.Clinical analysis and inquire into interfere measure of 15 cases She nationality children with β-thalassemia in the east of Fujian Province.;闽东地区畲族小儿β-地中海贫血15例临床分析及干预措施探讨
英文短句/例句
1.Analysis of Paramenters of Red Blood Cell in the Screening of β-Thalassaemia Minor轻型β-地中海贫血的红细胞参数分析
2.FTIR-HATR to Identify β-Thalassemia and Its Mechanism StudyFTIR-HATR诊断β-地中海贫血及其机理研究
3.Significance of red blood cell indicators for screening of beta-thalassaemia patients红细胞参数对β-地中海贫血筛查的意义
4.Prenatal diagnosis of a case at-risk for compound heterozygotes of SEA HPFH deletion and β-thalassemia in a Chinese family.缺失型β-地中海贫血一个家系的产前诊断
5.Survey of molecular epidemiology of β-thalassemia in the population of household registration in Zhuhai cyty广东省珠海市户籍人群中β-地中海贫血的分子流行病学调查
6.Prophylaxis of Transplantation-related Complications after Allogeneic Stem Cell Transplantation in β-thalassemia Major;儿童重型β-地中海贫血异基因造血干细胞移植后并发症的防治
7.The First Part Association Analysis of the ~G-γ Hemoglobin Gene Promoter -158C/T Polymorphism with Hemoglobin E/β-Thalassemia Major血红蛋白E/β-地中海贫血~Gγ-珠蛋白基因-158位点的多态性分析
8.Haploidentical hematopoietic stem cell transplantation for beta-thalassemia major in children单倍体造血干细胞移植治疗儿童重型β-地中海贫血
9.Study on gene distribution and blood routine test parameter variation in β-thalassemia patientsβ-地中海贫血的基因分布及其血常规参数变异分析
10.Analysis on types of gene mutation in 184 patients with β-thalassemia in Baise百色地区184例β-地中海贫血患儿基因突变类型分析
11.Study on hypermethylation of gene HDAC3 in β-thalassemiaHDAC3基因在β-地中海贫血中甲基化状态及其意义研究
12.DNA Chip Construction for Diagnosing β-thalathemia and Achondraplasia;β-地中海贫血与先天性软骨发育不全诊断性基因芯片的构建
13.Beta thalassemia on children: the molecular basis and treatment儿童β地中海贫血的分子基础和治疗
14.Analysis of β-thalassemia Mutation in east area of Sichuan四川东部地区β地中海贫血基因突变分析
15.Genotypes of β Thalassemia in Guangxi广西地区β地中海贫血基因突变类型分析
16.Construction of the gene mutation library of Chinese β-thalassemia;中国人β地中海贫血突变基因库的构建
17.Identification of a Novel Silent β Thalassemia Gene;一种新的静止型β地中海贫血基因的鉴定
18.Diagnosis ofβ-thalassemia by single cell nested polymerase chain reaction单细胞巢式聚合酶链反应诊断β地中海贫血
相关短句/例句
thalassemia[英][,θ?l?'si:mi?][美][,θ?l?'sim??]β-地中海贫血
1.Accurate and rapid prenatal diagnosis of β-thalassemia by a multiplex primer extension and denaturing high performance liquid chromatography technique;引物延伸变性高效液相色谱产前诊断β-地中海贫血
2.Genetic and prenatal gene diagnosis of β-thalassemia. SONG Dan,;β-地中海贫血的基因诊断及产前基因诊断
3.Research of β-thalassemia in Shui People of Guizhou;贵州省三都水族人群β-地中海贫血发病情况调查
3)beta-thalassemiaβ-地中海贫血
1.Objective: To investigate the clinical application value of prenatal gene diagnosis for alpha-thalassemia and beta-thalassemia.目的:研究检测α-地中海贫血及β-地中海贫血在产前基因诊断中的临床应用价值。
2.Beta-thalassemia major is a serious hereditary hemolytic anemia which does great harm to human being.β-地中海贫血是一种对人类健康危害严重的遗传性溶血性贫血病,是因β-珠蛋白基因及其调控序列的点突变或缺失致使β-珠蛋白肽链合成减少或完全停止,这不仅使患者血红蛋白水平降低,而且使原来在数量上与之持平的α-珠蛋白肽链相对过剩,这些相对过剩的游离α-珠蛋白肽链并不能形成稳定的四聚体,它们沉积在红细胞中导致了大量无效红细胞生成和红细胞寿命缩短,引起了严重的溶血性贫血。
4)β-thalassaemiaβ-地中海贫血
1.Noninvasive prenatal diagnosis of β-thalassaemia using size-fractionated cell-free fetal DNA in maternal plasma;利用孕妇外周血浆中小片段游离胎儿DNA进行β-地中海贫血无创性产前诊断
2.β-thalassaemia is one of the autosomal genetic blood diseases characterized by absent or decreased production of normal beta hemoglobin.β-地中海贫血(beta-thalassemia)是一组由于β珠蛋白肽链合成减少或缺乏而引起的以贫血为特征的遗传性血液病,发病率为0。
5)β-thalassemiaβ地中海贫血
1.Study on genic mutation types of β-thalassemia and prenatal diagnosis in Xiamen area;厦门地区β地中海贫血基因突变类型及产前基因诊断研究
2.A pilot study on the detection and clinical significance of PRA in children with β-thalassemia major;重型β地中海贫血患儿群体反应性抗体检测及临床意义
3.Evaluation of hemoglobin agarose electrophoresis and Hb-F alkali denaturation test in diagnosis of β-Thalassemia;全自动血红蛋白电泳与Hb-F碱变性试验在β地中海贫血中的应用及评价
6)Beta-thalassemiaβ地中海贫血
1.Amniotic fluid gene detection in prenatal diagnosis of alpha-and beta-thalassemia;α和β地中海贫血的羊水产前基因诊断
2.Closely linked polymorphic marker: successful application in preimplantation genetic diagnosis for beta-thalassemia;紧密连锁的多态性位点在β地中海贫血植入前遗传学诊断中的应用(英文)
延伸阅读
地中海贫血 一种常染色体显性遗传性疾病,又称海洋性贫血。由于遗传性酶缺陷,血红蛋白A中某个珠蛋白肽链减少或生成受抑制,导致血红蛋白合成障碍而产生贫血。现称珠蛋白生成障碍性贫血。 本病于1925年由T.B.库利等首先描述,虽以地中海区域较多见,但实际遍布世界各民族。中国南方各省,尤其广东、广西也是高发区之一。 临床分为α 和β两大亚型(见珠蛋白生成障碍性贫血)。
