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
   p 73 gene 的翻译结果: 查询用时:0.183秒
图标索引 在分类学科中查询
所有学科
肿瘤学
心血管系统疾病
妇产科学
儿科学
眼科与耳鼻咽喉科
泌尿科学
临床医学
外科学
更多类别查询

图标索引 历史查询
 

p gene     
相关语句
  p73基因
     Effect of 14-3-3σ on Transcriptional Activity of p73 Gene
     14-3-3σ对p73基因转录活性的影响
短句来源
     Study on apoptosis of K562 cell line and expression of p73 gene induced by MTX and IFN-α-2b
     MTX和IFN-α-2b诱导K562细胞凋亡及p73基因表达的研究
短句来源
     Expression of P73 Gene in Human Glioma and Correlation Between Expression of P73 and P53、P21 Gene
     P73基因在人脑胶质瘤中的表达及与P53、P21基因表达的相关性研究
短句来源
     p73 Gene and Leukemia
     p73基因与白血病
短句来源
     p73 Gene and Tumor
     p73基因与肿瘤
短句来源
更多       
  p73基因的
     The Expression and Clinical Implications of MDM2 and p73 Gene in Childhood Acute Leukemia
     儿童急性白血病MDM2基因与p73基因的表达及其临床意义
短句来源
     Expression and Clinical Significance of p63 and p73 Gene in Laryngeal Squamous Cell Carcinoma
     喉鳞状细胞癌中p63,p73基因的表达及临床意义
短句来源
     Results The VEGF, bFGF mRNA and protein expression in A549 cell and H1299 cell were decreased after transferred p73 gene(P<(0.05)).
     结果 转染 p73基因后,A549 细胞、H1299 细胞中 VEGF、bFGF mRNA和蛋白表达水平均下降,较未转染 p73基因的细胞有显著性差异(P<0.05)。
短句来源
     The mutation of p73 gene was analyzed by PCR-single-strand conformation polymorphism (SSCP).
     采用PCR鄄单链构象多态性(SSCP)检测p73基因的突变情况。
短句来源
     MATERIAL AND METHODS: The expression of P73gene in breast cancer tissues was detected by RT-PCR and apoptosis by TUNEL.
     材料与方法 :应用TUNEL、RT-PCR等技术检测乳癌组织P73基因的表达及其与肿瘤细胞凋亡、激素受体的关系。
短句来源
更多       
  p73基因mrna
     Methods The expressions of p73 gene were observed by RT PCR among liver cancer and tissues adjacent to tumor and normal liver tissues;
     方法 采用RT PCR方法检测p73基因mRNA在癌组织、癌旁组织及正常肝组织中的表达差异 ;
短句来源
     Results Level of transcripts of p73 gene in liver cancer was obviously higher than that in adjacent tissued or normal liver tissues ( P <0.05);
     结果 癌组织中p73基因mRNA的转录水平明显高于癌旁组织及正常组织 (P <0 0 5 ) ;
短句来源
     MethodsThe restriction endonuclease enzyme digestion combined with PCR was used to detect p73 gene and methylation in 42 patients with acute lymphoblastic leukemia.
     方法应用RT-PCR技术检测42例ALL患者的p73基因mRNA表达情况,并结合患者的临床资料进行分析,同时采用限制性内切酶酶切结合多聚酶链反应方法(REP法)检测p73基因第一外显子甲基化情况。
短句来源
     Conclusion: The expression of p73 gene may be related to differentiation level of lung cancer but not related to clinical stage.
     结论:p73基因mRNA的表达可能与肺癌分化程度有关,与临床分期无关。
短句来源
  p73蛋白
     Conclusion Probably high expression of P73 gene is one hot spot gene alteration of gastric carcinoma and expression of P73 protein in gastric carcinoma may play an important role in the course of cancerous development.
     结论P73高表达可能是一个胃癌发生的热点基因变化,在胃癌中P73蛋白的表达对胃癌的发生发展可能起着重要作用;
短句来源
     P73 gene expression was not related to sex, smoking, PTNM periods (P>0.05), and it related to postoperative survivals.
     P73蛋白表达与性别、吸烟、PTNM(pathologicaltumornodematasta sis ,PTNM)分期无关 (P >0 .0 5 ) ;
短句来源
     Results: P73 gene expression up regulated and was detected in 82.9%(29/35) of human SCLC tissues while expressed at low level in tissues adjacent to cancer and non cancer lung tissues(P<0.005).
     结果 :P73蛋白表达阳性率在肺癌组织中为 82 .9% (2 9 35 )明显高于相应的癌旁组织4 2 .9% (15 35 )和远癌肺组织 0 (0 35 ) (P <0 .0 0 5 ) ;
短句来源
     2.p73 gene expression of the pancreatic malignant neoplasms was 55.4%(31/56) while the malignant neoplasms’s was 15.4%(2/11).
     3、p73蛋白在有淋巴结转移者和无淋巴结转移者的阳性表达率分别为37.0%(10/27)和71.4%(15/21),两者比较有显著差异(P<0.05)。
短句来源
     Conclusions: Marked up regulation of P73 gene expression is found in human SCLC.
     结论 :P73蛋白在SCLC中的表达显著上调。
短句来源
更多       

 

查询“p 73 gene”译词为其他词的双语例句

 

查询“p 73 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。
  p gene
The p73 gene codes for various different protein isoforms.
      
No mutations were detected in the p73 gene or in p53, and no loss of heterozygosity of the p53 gene was found.
      
LOH, amplifying DNA by PCR using 5 markers, of 1p36 region (one intragenic to p73 gene) was found in 17% of cases but no significant correlation was observed with p73 overexpression.
      
We investigated LOH in an intragenic microsatellite marker, and those centromerically flanking the p73 gene, at 1p?36, and their correlations with patient age and 10 pathologic parameters in a series of 193 breast carcinomas.
      
Thus, mutations in the p73 gene appear to play little if any role in hereditary or sporadic breast cancer.
      
更多          


A survey of the distribution of ABO,P and Rh blood groups was made among960 primary and middle school students of Tujia Minority in Luota,Xiche andMiaoshi Communes in Longshan county.Slide method was used for the identificationof ABO and P blood groups and direct bromelin method,for Rh blood group.Thedistribution of ABO blood group system in The Minority of Tujia is shown inTable 1.The sequence of the frequencies of phenotypes is A>O>B,AB.As for thegene frequencies,the sequence is O>A>B.In view of...

A survey of the distribution of ABO,P and Rh blood groups was made among960 primary and middle school students of Tujia Minority in Luota,Xiche andMiaoshi Communes in Longshan county.Slide method was used for the identificationof ABO and P blood groups and direct bromelin method,for Rh blood group.Thedistribution of ABO blood group system in The Minority of Tujia is shown inTable 1.The sequence of the frequencies of phenotypes is A>O>B,AB.As for thegene frequencies,the sequence is O>A>B.In view of the frequencies of the pheno-types of P blood group system,P_1 is much more frequent than P_2(Table 2),on thecontrary,the gene frequency P(gene of P_2)is higher than P(gene of P_1)(Table 4).As for the Rh blood group,among 930 investigated individuals,we found only8 phenotypes.The sequence of the frequencies of these phenotypes is CCDee>CcDE>ccDE>CcDee>CCDE>ccDee>CCdE and ccdee(Table 3).The rate of Rh posi-tive is 99.78% and Rh negative,0.22%.The sequence of frequencies of Rh genecomplexes is R' R~e>r>R~o>R~z,while r,r'and r~y are zero(Table 4).Detailedcomparisons are made between our results and those reported by the Shanghai Inst-itute of Biological Products(Table 5 to 8).The probable reason why the frequencyof the phenotype P_1 is much higher than P_2 while the gene frequency is quite thecontrary is discussed in thits paper.

共调查了土家族青年学生960人的 ABO、P 及 Rh 等血型系统,结果表明在 ABO 血型系统中,表现型频率的次序为 A>O>B>AB 型,而基因频率的次序为 O 基因>A 基因>B 基因。P 血型的表现型频率,P_1远高于 P_2,但其基因频率却相反,P_2高于 P_1。在我们调查的930例 Rh 血型中各表现型频率的次序为 CCDee>CcDE>ccDE>CeDee>CCDE>ccDee>CCdE 及 ccdee·Rh阳性占99.78%,Rh 阴性仅占0.22%。基因频率的次序为 R~1>R~2>r>R~0>R~z·r′、r″及置 r~y 为O。我们将调查结果与上海生物制品研究所血型组的调查结果作了较详尽的比较,并指出土家族与各民族间某一血型的表现型分布上的差别以及基因频率的差别的显著性基本上一致,但也有个别不尽相同的情况。此外,本文还讨论了土家族 P 血型 P_1远多于 P_2而 P_1基因频率反较 P_2为小的可能原因。

In order to test the promoter function of two HBV DNA fragments, a soluble cell-free system extracted from Hela celis was used. In the in viiro transcriptional system using the 1.4kb DNA fragment as the templa-te, there were two RNA products whose transcriptional initiation sites were supposed to be at nucleotide 276±5% and 821±5% respectively on the HBV map. The first transcriptional initiation site is identical to the one that is directed by the HBV C gene promoter known before.The rela-tionship between...

In order to test the promoter function of two HBV DNA fragments, a soluble cell-free system extracted from Hela celis was used. In the in viiro transcriptional system using the 1.4kb DNA fragment as the templa-te, there were two RNA products whose transcriptional initiation sites were supposed to be at nucleotide 276±5% and 821±5% respectively on the HBV map. The first transcriptional initiation site is identical to the one that is directed by the HBV C gene promoter known before.The rela-tionship between the location of the second initiation site and the gene open reading frame suggests that the promoter may direct the synthesis of P gene mRNA.The 0.8kb DNA fragment starts from the core structure gene, not in-cluding the regulating sequence. Deducing from the 708±5% nt-long RNA product, the transcriptional initiation site is 588 + 5% on the HBV DNA map. Associated with this RNA start site, there is an ATG codon at po-sition 677 downstream, suggsting that the ATG codon may be a start site of a new open reading frame.

自adr亚型乙型肝炎病毒DNA重组质粒中获得两个DNA片段,用体外转录方法研究启动子的位点。其中1.4kb片段有两个转录产物,其转录起始点分别位于乙型肝炎病毒DNA序列的276±5%位和821±5%位,第一个转录起始点与已报道的乙型肝炎病毒核心抗原基因上游启动子位置一致,第二个转录起始点在888位P基因的起始密码子上游。0.8kb片段自校心抗原结构基因起始密码子ATG以下的序列开始,不含有已知的调控序列,其708±5%核苷酸长的RNA产物,根据其长度计算共转录起始点位于乙型肝炎病毒DNA序列588±5%位,与此位置相关的下游ATG密码子位于677位。

The autho rs found that rhizomania resistant charac tor was controlled by two pairs of dominant genes by our observing on the resistance of differ rent original materials, their cross progenies and test cross progenies to the disease in the breeding of rhizomania resistance. The gene types and genetic niodel of sugarbeet (Beta vulgaris) rhizomania resistance were infered acco rding to the result. Let us assume that"P" and "R"represent the two pairs domnant genes, so the RRPP for immune...

The autho rs found that rhizomania resistant charac tor was controlled by two pairs of dominant genes by our observing on the resistance of differ rent original materials, their cross progenies and test cross progenies to the disease in the breeding of rhizomania resistance. The gene types and genetic niodel of sugarbeet (Beta vulgaris) rhizomania resistance were infered acco rding to the result. Let us assume that"P" and "R"represent the two pairs domnant genes, so the RRPP for immune type; RrPP, RRPp for disease resistanc e typel RrPp, RRpp, rrPP for disease tolerant type Ⅰ; Rrpp, rrp for disease tolerant typeⅡ and rrpp for sensitive type.The cultivated sugarbeet has lost a pair of the dominant gene in their cultivating process. If the sugarbeet lost the "p", we obtain only the stock of disease tolerant type, but it is not possible get the stocks of disease resistant and immune types in our selecting works.However, we wi1l get the disease resistant or immune type, after the sugarbeet will pick up the lost"P"gene by crossing with their ancestors.

在从事甜菜抗丛根病育种工作中,通过对各类育种材料的抗病性观察,及对其互交和测交后代的调查,发现甜菜的抗丛根病性是由两对显性基因控制的。经过一步分析,提出了甜菜抗丛根病的基因型和遗传模式。假定以“R”和“P”代表这两对显性基因,免疫型为RPRP;抗病型为RPRp、RPrP耐病Ⅰ型为RPrp、RpRp、rPrP;耐病Ⅱ型为Rprp、rPrP;敏感型为rprp。推测:糖用甜菜在驯化过程中,丢失了其中的一对显性基因,假设丢失的“P”,那么,只有耐病Ⅰ型(RpRp)、耐病Ⅱ型(Rprp)和敏感型(rprp)。这样,采用选择的方法,只能选育出耐病型品种,不可能选育出抗病型和免疫型的品种。只有通过与其祖先杂交,将丢失的“P”基因找回来,才能育成抗病型和免疫型品种。

 
<< 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p 73 gene的内容
在知识搜索中查有关p 73 gene的内容
在数字搜索中查有关p 73 gene的内容
在概念知识元中查有关p 73 gene的内容
在学术趋势中查有关p 73 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