助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   gene 在 心血管系统疾病 分类中 的翻译结果: 查询用时:0.164秒
图标索引 在分类学科中查询
所有学科
心血管系统疾病
生物学
肿瘤学
基础医学
畜牧与动物医学
内分泌腺及全身性疾病
神经病学
外科学
泌尿科学
更多类别查询

图标索引 历史查询
 

gene
相关语句
  基因
    Experimental studies on restenosis after angioplasty and myocardial ischemia by gene therapy of vascular endothelial growth factor
    血管成形术后再狭窄及心肌缺血应用hVEGF基因治疗的实验研究
短句来源
    Relationship between G_s a,Gβ_3 Gene Polymorphism and essential hypertension or response to Erbesartan
    Gsα和Gβ3基因多态性与原发性高血压及厄贝沙坦治疗反映的关系
短句来源
    Prevention of vein graft restenosis with widl-type P53 gene transfection and laser irradiation
    野生型P53基因转染和低能量激光照射防治移植静态再狭窄的实验研究
短句来源
    Cloning,Sequence Analysis,Expression Feature and Biological Function Prediction of a Nove1 Leukemia-associated Gene LRP16
    一个新的白血病相关基因—LRP16的克隆、序列分析、表达特征及其生物学功能推测
短句来源
    Adenovirus-mediated gene transfer of vascular endothelial growth factor B induces angiogenesis in chronic ischemic myocardium
    腺病毒介导血管内皮生长因子B基因转染慢性缺血心肌血管新生的研究
短句来源
更多       
  “gene”译为未确定词的双语例句
    Experimental Studies of the Effects of Caspase-3 Inhibitor and Exogenous Bcl-2 Gene on Cardiomyocytes Apoptosis after Hypoxia/Ischemia
    Caspase-3抑制剂及外源性Bcl-2对缺氧/缺血后心肌细胞凋亡的实验研究
短句来源
    Identification of a Novel β Thalassemia Mutation and Development of a Method for High-throughput Mutation Detection of β-globin Gene
    β地中海贫血的新突变鉴定和高通量突变检测方法研究
短句来源
    Experimental Study of Intracoronary Local Gene Transfer with Protein-coated Metallic Stents Preventing Restenosis after Angioplasty
    冠状动脉内蛋白涂层金属支架局部转基因预防血管成形术后再狭窄的实验研究
短句来源
    Expermental Study of Plasmid-Mediated Intravascular Local Gene Transfer Using Protein-coated Metallic Stent Preventing Restenosis after Angioplasty
    质粒介导下冠状动脉内蛋白涂层金属支架局部转基因预防血管成形术后再狭窄的实验研究
短句来源
    AML1a Gene Expression and Its Significance in Acute Leukemia.
    AML1选择性剪接体在急性白血病中的表达及其意义的研究
短句来源
更多       
查询“gene”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  gene
NEW TECHNOLOGY FOR DRUG DISCOVERY BASED UPON INSERTION OF LIGANDS INTO GENE SEQUENCES BY NUCLEAR RECEPTOR PROTEINS
      
A gene regulatory mechanism has been proposed in which steroid hormones and certain other drugs bind to nuclear receptor proteins followed by transfer to DNA where they are inserted between base pairs.
      
Polymerase chain reaction was used to amplify a 439-bp fragment of a 65,000-kDa (Mr) heat shock protein gene (hsp65) of Mycobacterium.
      
Cloning of an APETALA3 homologous gene (PtAP3) from Populus tomentosa and genetic transformation of its sense and anti-sense con
      
A pair of primers were designed according to published literature on Populus trichocarpa gene (PTD), and PtAP3, an AP3 homologous gene from Populus tomentosa was isolated by PCR using genomic DNA of the male clone of P.
      
更多          


A slow moving hemoglobin with the same mobility as hemoglobin A2 was found in the red cells of a patient with severe anemia by cellulose actate electrophoresis. The structural analysis of this abnormal hemoglobin showed to be hemoglobin E (α2β226Glu-Lys) Taking into consideration of the clinical symptoms and blood cytology findings, the patient carried a double heterozygote of both 'hemoglobin E and Thalassemia gene. The patient's father also contained the same abnormal hemoglobin,being a heterozygote...

A slow moving hemoglobin with the same mobility as hemoglobin A2 was found in the red cells of a patient with severe anemia by cellulose actate electrophoresis. The structural analysis of this abnormal hemoglobin showed to be hemoglobin E (α2β226Glu-Lys) Taking into consideration of the clinical symptoms and blood cytology findings, the patient carried a double heterozygote of both 'hemoglobin E and Thalassemia gene. The patient's father also contained the same abnormal hemoglobin,being a heterozygote of hemoglobin E ( HbE )

对一例严重贫血患者进行检查,醋酸纤维薄膜电泳显示其红细胞内含有一种泳动速度比HbA慢而与HbA_2相同的异常血红蛋白。对它进行一级结构分析证明它是HbE(α_(2)β_(2) 26Glu→Lys)。结合临床症状和血细胞学检查结果,初步认为患者具有血红蛋白Е复合地中海贫血双重杂合子。其父具有与患者相同的异常血红蛋白为HbE杂合子。

15 cases of hemoglobin E ( HbE), including 12 cases of HbE-β-thal-assemia and 3 cases of HbE, were reported. Clinical, laboratorial and genetic studies revealed that HbE could be divided into two groups, HbE and HbE-β-thalassemia, the latter being further divided into two types according to HbE contents. HbE-β-thalassemias with HbE content above 45% showed severe clinical symptoms and laboratory findings, while that with HbE content below 45% not,the latter type being called HbE -β+-thalassemia. Ultrastruc-tural...

15 cases of hemoglobin E ( HbE), including 12 cases of HbE-β-thal-assemia and 3 cases of HbE, were reported. Clinical, laboratorial and genetic studies revealed that HbE could be divided into two groups, HbE and HbE-β-thalassemia, the latter being further divided into two types according to HbE contents. HbE-β-thalassemias with HbE content above 45% showed severe clinical symptoms and laboratory findings, while that with HbE content below 45% not,the latter type being called HbE -β+-thalassemia. Ultrastruc-tural studies showed that erythroblasts in bone marrow were irregular inshape with electronic dense inclusion bodies and suggested intramedullary hemolysis. Investigation of family history revealed that this disease was autosomal codominant in mode of inheritance. Authors suggested that this HbE gene might be brought from Guangdong to Sichuan Province more than 300 years ago.

在四川发现的15例HbE,根据临床表现、实验室检查及血红蛋白分析,将其分为两类,第一类是HbE复合β地中海贫血,第二类是HbE。前者又依HbE含量高于或低于45%,分为一、二型。一型中部分病例为HbE复合β°地中海贫血,二型属HbE复合β~+地中海贫血。在HbE复合β°地中海贫血骨髓中见到电子密度高的包涵体,而成熟红细胞中则无,这是原位溶血的依据。家系调查证实,此病属共显性遗传。该地此病的遗传基因,可能是300年前广东客家人移川时带入的。

A slow moving hemoglobin variant with similar mobility as Hb A2 was fouad in hemolysates of two patients with severe anemia by cellulose acetate electr-ophoresis. Primary structure analysis confirmed that it belonged to Hb E. These two patients and their mother or father carried the same abnormal hemoglobin. According to their clinical symptoms and hematological findings, they were recognized as double heterozygotes of Hb E and β-thalassemia )βE/β+). The thalassemia genes originated also from the either...

A slow moving hemoglobin variant with similar mobility as Hb A2 was fouad in hemolysates of two patients with severe anemia by cellulose acetate electr-ophoresis. Primary structure analysis confirmed that it belonged to Hb E. These two patients and their mother or father carried the same abnormal hemoglobin. According to their clinical symptoms and hematological findings, they were recognized as double heterozygotes of Hb E and β-thalassemia )βE/β+). The thalassemia genes originated also from the either side of their parents. Hb E purified from the hemolysate of case No.1 gave an oxygen equilibrium characteristic nearly identical to Hb A.

两例严重贫血的住院患者,经醋酸纤维薄膜电泳检查,显示其红细胞内含有一种电泳迁移率与HbA_2 相同的异常血红蛋白。经一级结构分析证明为 HbE[β26(B8)Glu→Lys]。结合家系调查、临床表现及血细胞学检查结果,证明第一例的遗传变异来源于母亲,另一例则来自父亲。而且他们的父亲或母亲均有HbA_2 增高,符合轻度β-地中海贫血。因此,确证此两例为见于我省的携有HbE和β-地中海贫血的双重杂合子。从病例1血样纯化的HbE具有与HbA相似的氧平衡特征。

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关gene的内容
在知识搜索中查有关gene的内容
在数字搜索中查有关gene的内容
在概念知识元中查有关gene的内容
在学术趋势中查有关gene的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社