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   p 450 genes 的翻译结果: 查询用时:0.171秒
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p genes
相关语句
  p450基因
     Cloning and expression of P450 genes CYPA14 and CYPA16 from Candida tropicalis 1230
     热带假丝酵母1230细胞色素P450基因CYPA14与CYPA16的克隆和表达
短句来源
     Cloning and mRNA expression levels of cytochrome P450 genes CYP6AE12 and CYP9A18 in the cotton bollworm, Helicoverpa armigera (Hübner)
     棉铃虫P450基因CYP6AE12和CYP9A18的克隆与mRNA表达水平
短句来源
     Two novel P450 genes (CYP9A18 and CYP6AE12) from the insecticide-resistant strain (YS-FP) of Helicoverpa armigera (Hübner) were cloned with RT-PCR and RACE.
     采用RT-PCR和RACE技术克隆到2个新的棉铃虫细胞色素P450基因:CYP6AE12和CYP9A18。
短句来源
     Cytochrome P450 Genes and Their Application in Plant Improvement
     细胞色素P450基因及其在植物改良中的应用
短句来源
     Fluorescent signals were scanned to detect cytochrome P450 genes differentially expressed in patients and normal subjects. (Results) Among 32 cytochrome P450 genes,six genes(CYP4F3,CYP1A1,CYP27A1,CYP1B1,CYP2B6,CYP51) were found to be differentially expressed between the cells of benzene-poisoned patients and normal controls cells,CYP4F3 gene was up-regulated among all patients.
     结果共有6条细胞色素P 450基因呈差异性表达,包括CYP 4F 3、CYP 1A 1、CYP 27A 1、CYP 1B 1、CYP 2B 6、CYP 51,其中CYP 4F 3基因在所有苯中毒工人中均表达上调。
短句来源
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  “p 450 genes”译为未确定词的双语例句
     In addition, the 5' and 3' UTRs were compared between the CYP6N3v1 v3 and other known insect P450s. The multiplicity of translational control of insect P450 genes was discussed.
     另外 ,还比较了CYP6N3v1 v3与其它已知的昆虫P450的 5’ 及 3’ 非翻译区的结构 ,讨论了昆虫P450翻译水平调控的复杂性。
短句来源
     EXPRESSION REGULATION OF CYTOCHROME P450 GENES AND THE MOLECULAR BASIS OF P450 MONOOXYGENASE MEDIATED INSECTICIDE RESISTANCE IN INSECT
     昆虫细胞色素P450基因的表达与调控及P450介导抗性的分子机制
短句来源
     STUDY ON THE DIVERSITY OF CYTOCHROME P450 GENES FROM AEDES ALBOPICTUS
     白纹伊蚊细胞色素P450 CYP6家族基因多样性的研究(英文)
短句来源
     melangoster was found to be associated with the over transcription of P450 Cyp 6g1 Two P450 genes( Cyp315a1, Cyp302a1) in the ecdysteroid synthesis pathway were identified.
     P45 0介导的果蝇对DDT的抗性被证明是Cyp6g1基因超量表达的结果。
短句来源
     Regulation of cytochrome P450 genes by liver-enriched transcription factors
     肝富集的转录因子与细胞色素P450基因的表达调控
短句来源
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  相似匹配句对
     P450 and Cyt.
     P450、Cyt.
短句来源
     Cytokines and Cytochrome P450
     细胞因子与细胞色素P450
短句来源
     The detecting wavelength was 450nm.
     检测波长450nm。
短句来源
     450±1.2?
     女性为 97.64 5 0± 1.2 42 6。
短句来源
     ,such as CYP450 and GST genes.
     如,细胞色素P450家族基因、谷胱甘肽硫转移酶基因等。
短句来源
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  p genes
Transcript profiling of cytochrome P450 genes in HL-60 human leukemic cells: Upregulation of CYP1B1 by all-trans-retinoic acid
      
Direct Assessment of Promoter Activity of Human Cytochrome P450 Genes Using Optimized Transfection in Vitro and in Vivo
      
Most cytochrome P450 genes induced by both abiotic and biotic stresses contained the recognition sites of MYB and MYC, ACGT-core sequence, TGA-box and W-box for WRKY transcription factors in their promoters.
      
Expression of 29 cytochrome P450 genes among them was induced by various treatments.
      
The 7K cDNA collection contains 49 cytochrome P450 genes.
      
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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。

 
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