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   囊性纤维化 的翻译结果: 查询用时:1.233秒
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囊性纤维化
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  cystic fibrosis
     Overweight and obesity in Δ F508 homozyg-ous cystic fibrosis
     ΔF508纯合子囊性纤维化患者的超重及肥胖
短句来源
     CFTR and cystic fibrosis
     CFTR与囊性纤维化
短句来源
     Objective To detect cystic fibrosis transmembrane conductance regulator(CFTR)gene△F508 mutation in chinese patients with congenital bilateral absence of vas deferens(CBAVD).
     目的研究男性先天性双侧输精管缺如(CBAVD)患者其囊性纤维化跨膜转运调节物(CFTR)基因第10号外显子区域上△F508的突变情况。
短句来源
     PRELIMINARY STUDIES ON CYSTIC FIBROSIS IN CHINA──INVESTIGATION ON SWEAT SODIUM CONCENTRATION IN 282 CHILDREN
     我国囊性纤维化病的初步研究──282名儿童汗液钠离子浓度调查
短句来源
     Detection of Cystic Fibrosis Transmembrane Conductance Regulator Gene △F508 Mutation in Chinese Patients with Congenital Bilateral Absence of Vas Deferens
     CBAVD患者囊性纤维化跨膜转运调节物基因△F508的研究
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  “囊性纤维化”译为未确定词的双语例句
     Detection of fibrosis transmembrane conductance regulator gene⊿F508 mutation in Chinese patients with congenital bilateral absence of vas deferens
     先天性双侧输精管缺如患者囊性纤维化跨膜转运调节物基因⊿F508突变的研究
短句来源
     Does carbon dioxide retention during exercise predict a more rapid decline in FEV1 in cystic ribrosis?
     囊性纤维化患者运动时二氧化碳潴留是否可预测其FEV1值的快速下降
短句来源
     Conclusions Chinese patients with CF show similar clinical manifestations to patients in the European and North American populations, but the CFTR mutation was different.
     结论 中国人囊性纤维化临床表现与白种人表现相似 ,但是CFTR基因突变部位可能与白种人不同。
短句来源
     The sweat of 282 children,normal or with relevant symptoms has been collected by quantatitive pilocarpine iontophoresis method and the sodium concentration estimated.
     采用定量毛果芸香碱电渗汗液收集和检查方法,收集了2月~14岁的282例正常和有类似囊性纤维化病症状儿童的汗液,检查了他们的汗液钠离子浓度。
短句来源
     To investigate whether CFTR mutations have a effect on results of ICSI in obstructive azoospermia patients,ICSI procedure was performed in 3 CFTR mutations carriers and 18 non CFTR mutations carriers respectively. No difference are found in fertilization rate,cleavage rate and pregnancy rate following ICSI for CFTR mutations carriers as compared to non CFTR mutations carriers.
     为探讨囊性纤维化跨膜转运调节物 (CysticFibrosisTransmembraneConductanceRegulator,CFTR)基因突变是否影响先天性梗阻性无精子症患者单精子卵浆内注射 (IntracytoplasmicSpermInjection ,ICSI)治疗的成功率 ,本文对3例先天性梗阻性无精子症CFTR突变基因携带者和 18例CFTR突变基因非携带者进行了ICSI的治疗。
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  相似匹配句对
     Cystic Fibrosis
     纤维化
短句来源
     CFTR and cystic fibrosis
     CFTR与纤维化
短句来源
     Continuous glucose monitoring in adolesce-nts with cystic fibrosis
     青少年纤维化的连续葡萄糖监测
短句来源
     Quality of life of children with cystic fibrosis
     纤维化患儿的生活质量
短句来源
     Hyperglycaemia and insulinopenia in a nenoate with cystic fibrosis
     纤维化新生儿的高血糖和胰岛素缺乏
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  cystic fibrosis
The Mutation Spectrum of the CFTR Gene in Cystic Fibrosis Patients from Bashkortostan
      
Mutations of CFTR were studied in patients with cystic fibrosis (CF) from Bashkortostan.
      
Polymorphisms of the Cytochrome P450 (CYP1A1, CYP2E1) and Microsomal Epoxide Hydrolase (mEPHX) Genes in Cystic Fibrosis and Chro
      
Frequencies of CYP1A1, CYP2E1, and mEPHX polymorphic variants were analyzed in cystic fibrosis, chronic obstructive lung disease, bronchiectatic disease, chronic nonobstructive bronchitis, and recurring bronchitis.
      
Mutations in CYP1A1 and mEPHX were shown to modify the severity of respiratory disorders in cystic fibrosis, the combination of CYP1A1 genotype Val/Val with the "very slow" mEPHX phenotype being most unfavorable (odds ratio OR = 12.30).
      
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  cystic fibrosis of the pancreas
Abnormal paranasal sinuses in patients with cystic fibrosis of the pancreas
      
Fifty-year perspective of "cystic fibrosis of the pancreas"
      
Fifty-year perspective of cystic fibrosis of the pancreas
      
α-Amylase activity in sweat and serum of patients with cystic fibrosis of the pancreas
      
Ultramicro-electrophoresis of protein in sweat from patients with cystic fibrosis of the pancreas and controls
      
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  cystic fibrosis (cf)
Mutations of CFTR were studied in patients with cystic fibrosis (CF) from Bashkortostan.
      
The spectra of mutations and polymorphic loci of the gene of cystic fibrosis transmembrane conductance regulator (CFTR) was studied in 60 cystic fibrosis (CF) families from Bashkortostan.
      
Polymorphism of GSTM1 and GSTP1 genes was studied in patients with cystic fibrosis (CF) and chronic bronchopulmonary diseases (CBPD) living in Bashkortostan.
      
Background: Exocrine pancreatic insufficiency is a major clinical manifestation of cystic fibrosis (CF).
      
103 outpatients, aged 11-16 years, suffering from cystic fibrosis (CF), asthma, or hematological/oncological conditions were assessed.
      
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This paper reports the isolation of a strain of Mucoid pseudomonas Aeroginosa (M. P. Aeroginosa) and the observation of its microbiological characteristics such a cultural and biochemical characteristics The drug susceptibility test, toxicity test, mucus inhibition test and serotyping had been done. This organism was isolated from the sputum of a patient who Was suffered from chronic pulmonary infection with cystic fibrosis.In comparision with common pseudomonas Aeroginosa, this strain(M.P.Aeroginosa) produced...

This paper reports the isolation of a strain of Mucoid pseudomonas Aeroginosa (M. P. Aeroginosa) and the observation of its microbiological characteristics such a cultural and biochemical characteristics The drug susceptibility test, toxicity test, mucus inhibition test and serotyping had been done. This organism was isolated from the sputum of a patient who Was suffered from chronic pulmonary infection with cystic fibrosis.In comparision with common pseudomonas Aeroginosa, this strain(M.P.Aeroginosa) produced mucoid colonies that secreted numerous capsular polysaccaride.The other differences were that glucose oxidation test was negative and strong toxicity was present. The result of mucus inhibition test varied according to the strain variance of Staphylococcus Aereus. The scrotyping of this strain Showed that probably it belongcd to a different serum-type other than the 12 sera-types in our country.

本文对分离出一株粘液铜绿假单胞菌进行了较全面的观察,该菌系从一慢性肺部感染囊性纤维化病人痰标本中分离得到。它与一般铜绿假单胞菌比较,除产生大量荚膜多糖呈大露珠状、粘稠的菌落外,葡萄糖氧化试验阴性,有较强的毒力,粘液产生抑制试验的结果可因金黄色葡萄球菌菌株不同而有差异。该菌对国内12个群分型血清均不凝集,可能属另外的血清型。

The ion channel properties of sweat gland epithelial cell membrane from normal individuals and patients with cystic fibrosis (CF) were investigated by patch clamp technique. More than 400 cells were recorded and at least 7 types of channels or channel states were observed. Effects of Forskolin on channels were found to be different between the CF and the normal subjects: The ratio of excitation induced by Forskolin in secretory gland cell membrane normal subjects was much higher than that from the CF. The difference...

The ion channel properties of sweat gland epithelial cell membrane from normal individuals and patients with cystic fibrosis (CF) were investigated by patch clamp technique. More than 400 cells were recorded and at least 7 types of channels or channel states were observed. Effects of Forskolin on channels were found to be different between the CF and the normal subjects: The ratio of excitation induced by Forskolin in secretory gland cell membrane normal subjects was much higher than that from the CF. The difference had statistical significant (p< 0.005). But for the reabsorptive duct cells, there was no significant difference between the normal and the CF (p>0.5). There results indicate that Forskolin could be help in identifying the abnormality of CF defected gene. But gland cells instead of duct cells should be chosen.

本文报道用片膜钳技术研究正常人及囊性纤维化病人(CF)的汗腺上皮细胞膜单个离子通道活动的特性,并比较分析了它们对Forskolin的反应。在400多个膜片上找出了至少七种或七个状态的离子通道的特性。观察到正常人和CF的部分汗腺上皮细胞(包括腺细胞与管细胞)膜离子通道对Forskolin有兴奋反应。发现腺细胞的兴奋反应率在正常人明显高于CF病人,差异非常显著。而管细胞的兴奋反应率,两组问无明显差异。以上结果提示,用Forskolin可协助鉴定CF的缺损,但宜选用腺细胞,不宜选用管细胞。

In according the fetal small intestine macrovillar enzymes (MVE)(including AKP, iso AKP, GGT and etc)being excreted into amniotic fluid, A simple and available method was used for analysis of MVE activities in amniotic fluid, AKP and GGT of amniotic fluid in 35 normal cases were determined, and the normal rangs of AKP and GGT in different time of Pregnancy were set up. The activities of AKP and GGT are respectively 25.8±9.3, 402±58.3(16~26week), 30.7±10.8, 441±70. 2(26~36week), 37.5±11.2, 437±72.3(>36week)....

In according the fetal small intestine macrovillar enzymes (MVE)(including AKP, iso AKP, GGT and etc)being excreted into amniotic fluid, A simple and available method was used for analysis of MVE activities in amniotic fluid, AKP and GGT of amniotic fluid in 35 normal cases were determined, and the normal rangs of AKP and GGT in different time of Pregnancy were set up. The activities of AKP and GGT are respectively 25.8±9.3, 402±58.3(16~26week), 30.7±10.8, 441±70. 2(26~36week), 37.5±11.2, 437±72.3(>36week). This results are very useful for prenatal diagnosis of cystic Fibrosis.

根据胎儿消化道上皮分泌的酶可经肠道排入羊水,利用简便、易行的酶分析法对35例正常妊娠羊水的胎儿肠绒毛上皮细胞酶:AKP、GGT进行测定。(初步确定了不同妊期入羊水AKP、GGT进行测定。初步确定了不同妊期人羊水AKP、GGT活性的正常参考值。AKP、GGT活性分别为:25.8±9.3、402±58.3(16~26周),30.7±10.8、441士70.2(26~36周),37.5±11.2、437士72.3(36周以上)。为进一步开展囊性纤维化病变的产前诊断奠定了基础。

 
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