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   complex karyotype 的翻译结果: 查询用时:0.18秒
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complex karyotype
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  复杂核型
     The 2 cases of healthy volunteers showed normal karyotypes, thus, a specific SKY technique was successfully established. In the 8 cases of leukemia patients, SKY identified aberrations including 9q-,t(9;22),t(15;17) and the complex karyotype 47,XY,+9?
     2例健康志愿者均示正常核型,8例白血病患者中,SKY分析分别发现9q-,t(9;22),t(15;17),及复杂核型47,XY,+9?
短句来源
     Complex karyotype was 86.3% in DLBCL. The most frequent structural abnormalities in DLBCL involved ehromosomes 3,6,14 and 1,with had high frequencies of 3q27 (41.2%) and 6q21 ,6q23,6q25 involvement (23.5%).
     DLBCL 中复杂核型占86.3%,染色体结构异常累及最多的是3,6,14,1号染色体,41.2%为3q27异常,43.1%的病例有1号染色体异常。 6q21、6q23和6q25异常占23.5%。
短句来源
     In the follow-up of the 48 cases, 17 cases (11 cases were elderly patients) transformed into acute leukemia, among whom 8 cases were found in high complex karyotype.
     48例患者经追踪观察,17例(11例为老年患者)转化为急性白血病,其中复杂和高度复杂核型异常者8例。
短句来源
     The results showed that aberration at the short arm of chromosome 12 were detected in 16 cases with 12p balanced translocation, in 10 cases with 12p deletion, 6 cases with 12p addition, and in 1 case with inversion 12. By complex karyotype classification, 12p translocation included 6 simple aberrations, 6 complex aberrations, and 4 highly complex aberrations;
     结果表明 :31例中 12p平衡易位 16例 ,12 p缺失10例 ,add( 12 p) 6例 ,inv( 12 ) 1例。 按复杂核型分类法 ,16例 12p易位中简单畸变 6例 ,复杂畸变 6例 ,高度复杂畸变 4例。
短句来源
     3 had negative M-FISH results, of whom one had del(2q)×2 abnormalities, who was RT-PCR-positive for PML/RARα fusion transcript; one had complex karyotype abnormalities, whose RT-PCR was negative for PML/RARα fusion transcript; one had t(9;22) translocation, whose RT-PCR was negative for PML/RARα fusion transcript, but positive for BCR/ABL fusion transcript.
     3例M FISH呈阴性结果 ,其中 1例核型分析揭示del(2 q)× 2异常 ,RT PCR显示PML RARα融合转录本阳性 ,1例有复杂核型异常 ,RT PCR显示PML RARα融合转录本阴性 ,1例有t(9;2 2 )易位 ,RT PCR显示PML RARα融合转录本阴性而BCR ABL融合转录本阳性。
短句来源
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  “complex karyotype”译为未确定词的双语例句
     Results In a case of acute lymphoblastic leukemia L2, the complex karyotype: 46,XY,der(2)t(2;9),der(9)t(9;12;22) was identified by M FISH, which was detected as 46,XY,der(9)t(9;12) by classical cytogenetics;
     结果 对其中 1例常规核型分析显示为 4 6 ,XY,der(9) t(9;12 )的急性淋巴细胞白血病 - L 2型病例 ,M- FISH检出其具有复杂的染色体易位 :4 6 ,XY,der(2 ) t(2 ;9) ,der(9) t(9;12 ;2 2 )。
短句来源
     The most common chromosomal aberrations included high complex karyotype and +8. The detection rate of abnormal karyotype was 29. 4% in refractory anemia (RA) ,66. 6% in refractory cytopenia with multilineage dysplasia (RCMD) , 76% in refractory anemia with erythroblasts(RAEB).
     难治性贫血(RA)异常核型检出率29.4%,难治性血细胞减少伴多系增生异常(RCMD)异常核型检出率66.6%,难治性贫血伴原始细胞增多(RAEB)异常核型检出率76%。
短句来源
     It was observed that RAEB/RAEB-T patients had higher frequencies of extra chromosomal aberrations(50%) and complex karyotype(30%) than did the RA/RAS patients (26.3%,5.3% respectively);
     RA/ RAS组中缺失以 del(2 0 q) (q11)多见 (6 3.2 % ) ,而 RAEB/ RAEB- T组中以 del(2 0 q)(q12 )多见 (70 .0 % ) ;
短句来源
     Six cases with complex karyotype abnormalities were confirmed to be AML1/ETO positive by the successive R-banding and FISH assay, and the involved genes were clearly visualized in FISH image.
     6例复杂易位患者通过显带后连续中期FISH检测不仅确定AML1/ETO融合基因的存在,同时精确定位。
短句来源
     Normal karyotppes werefound in 3 cases (3/35 ), translocation t(15; 17) was found in 31 cases (31/35) and variant transforation in 1cases (1/35). The clinic data of 21 cases were evaluated and 19(19/21 ) achieved a complete remission(CR). 2 cases (one of them detnonsrated a more complex karyotype and the other a variant translocation) did notabtain CR.
     骨髓染色体分析,正常3例(3/35),31例(31/35)有t(15;17),1例(1/35)具有变异易位.可评价的21例中19例(19/21)达到CR,具有复杂枝型和变异易位各1例未能取得缓解。
短句来源
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  相似匹配句对
     The karyotype of R.
     t-测验的结果表明R.
短句来源
     The karyotype of R.
     ciliaris和R.
短句来源
     KARYOTYPE OF SYNAPTONEMAL COMPLEX IN ERI SILKWORM
     蓖麻蚕联会复合体核型分析
短句来源
     Studies on Chromosome Karyotype of Panzerina lanata J.Sojak Complex
     脓疮草复合体的染色体研究
短句来源
     On the Complex of Law
     论法的习惯情结
短句来源
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  complex karyotype
Surface spreads of pachytene spermatocyte nuclei from two cats were used to construct a synaptonemal complex karyotype for the cat.
      
Cytogenetic analysis of the relapsed tumor showed a complex karyotype: 47,XX,i(1)(q10), der(4)t(4;19) (q33~q35;q13.1), + 8,t(15;17)(q24;p11.2~p12),der(19)t (19;20)(q13.1;p11.2),der(22)t(20;22)(q13;q13).
      
Cytogenetic and molecular characterization of a small ring chromosome in the complex karyotype of a girl with Turner syndrome
      
A 2-year-old boy with features suggestive of cri-du-chat syndrome had a complex karyotype: 45,XY,-22,5p-,t(5p;22q).
      
The lymph-node metastasis was near-triploid and showed a complex karyotype.
      
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1,574 metaphases from bone marrow cells of leukemic patients(44) and normal controls(4) were studied with a set of defining criteria for metaphase chromosome quality. The frequencies of prophases, anaphases and terraploidies were 2, 5 and 0.4% respectively. Short time culture could improve metaphase quality in leuke-mias but not that of normal controls. Possible reasons for the poor quality of leukemic metaphases and improvement after short time culture were discussed. Metaphases with trisomy 8 as sole abnormality...

1,574 metaphases from bone marrow cells of leukemic patients(44) and normal controls(4) were studied with a set of defining criteria for metaphase chromosome quality. The frequencies of prophases, anaphases and terraploidies were 2, 5 and 0.4% respectively. Short time culture could improve metaphase quality in leuke-mias but not that of normal controls. Possible reasons for the poor quality of leukemic metaphases and improvement after short time culture were discussed. Metaphases with trisomy 8 as sole abnormality showed better quality than those with other abnormalities and metaphases with a complex karyotype, a worse quality.

用一套简单质量标准对44名白血病人及4名正常对照的1574个分裂细胞进行了染色体质量半定量研究,并测得分裂前期、晚期细胞、四倍体细胞的频率各为2、5及0.4%。短期体外培养显著提高白血病染色体质量,但对正常细胞无明显影响。在急非淋中,核型为47,+8的病人染色体质量为最佳,核型严重异常者为最差。

The fertile F1 hybrid between red deer (Cervus elaphus xanthopygus,2n=68) and sik?deer (C.nippon hortalorum,2n=66) has been reported in captivity as well as in nature.The diploid chromosome number is 67.The G-banding patterns of every chromosome of the sika deer and red deer are identical except for No.1 chromosome.According to the G-banding pattern,No.1 chromosome of sika deer corresponds to,the two acrocentric chromosomes of Ted deer,and therefore may involve a Robertsonian translocation.In order to confirm...

The fertile F1 hybrid between red deer (Cervus elaphus xanthopygus,2n=68) and sik?deer (C.nippon hortalorum,2n=66) has been reported in captivity as well as in nature.The diploid chromosome number is 67.The G-banding patterns of every chromosome of the sika deer and red deer are identical except for No.1 chromosome.According to the G-banding pattern,No.1 chromosome of sika deer corresponds to,the two acrocentric chromosomes of Ted deer,and therefore may involve a Robertsonian translocation.In order to confirm this suggestion,the meiosis of F1 hybrid has been examined by ele-ctromicroscopically.Thirty-one normal autosomal bivalents,an acrocentric/metacentric tri-valent and an XY pair of synaptonemal complex karyotype were observed.The proximal telomeric knobs of the two acrocentric elements were paired and projected in the same direction from the metacentric element.The configuration of the trivalent may be a prerequisite for normal disjunction and balanced gamete formation,therefore,it can be accounted for the high fertility of the F1 hybrid.

作者以界面铺张-硝酸银染色技术,对东北马鹿和东北梅花鹿的F_1可育杂种的精母细胞联会复合体进行亚显微观察及分析。在减数分裂前期,杂种鹿精母细胞中形成31条完整的常染色体联会复合体、一个端着丝粒染色体/中着丝粒染色体的三价体和XY双价体。这进一步证明,两种亲本鹿的染色体具有高度的同源性,其差别仅在于一个罗伯逊易位。三价体的顺式构型可能和杂种鹿的可育性有关。

Electron microscopy of observing rye synaptonemal complex with cellspreading method and analyzing the synaptonemal complex karyotype of the rye cultivar, Victory, was for the first time covered in China. It suggests that there are two chromosomal translocations in the variety. A small fraction of long arm of 1R translocated onto the shorts arm of 6R,and 3 units of the percentage length have translocated from the long armof 4R onto the long arm of 2R, so that the long arm has become the sho-rt arm of 4R....

Electron microscopy of observing rye synaptonemal complex with cellspreading method and analyzing the synaptonemal complex karyotype of the rye cultivar, Victory, was for the first time covered in China. It suggests that there are two chromosomal translocations in the variety. A small fraction of long arm of 1R translocated onto the shorts arm of 6R,and 3 units of the percentage length have translocated from the long armof 4R onto the long arm of 2R, so that the long arm has become the sho-rt arm of 4R. Accordingly, it is believed that the rye cultivar, Victory,is a translocation heterozygote. Perhaps the method is useful in the studies on experimental texonomy of plant.

国内首次以“胜利”黑麦品系为材料,在电镜下观察联会复合作并分析了联会复合体核型。在同染色体核型比较后,认为“胜利”黑麦存在着两个可能的易位:1R长臂的一小段易位到6R短臂;4R长臂向2R长臂易位三单位长度,使4R长臂变成短臂。从而判断“胜利”黑麦为易位杂合体。这个研究方法可以在植物实验分类学研究中得到应用。

 
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