查询词典 positive

Results NGF and its mRNA were localized in chondrocytes in the sclera, especially in the binucleate cell. In NGF and its mRNA respectively, the amount of the positive cells in the occluded eyes was significantly higher than that of the control eyes (P.05). In NGF F(subscript DG=20.556, P.001 or in its mRNA F(subscript DG=25.520, P.001, the amount of the positive cells among the occluded groups or the control groups was significantly decreased along with the time.

结果 NGF蛋白及其mRNA均表达於巩膜的软骨细胞中尤其在双核细胞中；两者在各时间段遮盖眼巩膜中阳性细胞数均明显高於对照组(P.05)；免疫组织化学F(下标 DG=20.556 P.01和原位杂交F(下标 DG=25.520 P.01在对照组各组间阳性细胞的表达数目随时间变化明显下降。

One was the pqsA' positive expression plasmid constructed by cloning the pqsA'-lacZ fusion digested from pYHP441 into miniCTX-1, whose sequence was then integrated into wild type PAO-1 chromosome by biparental mating procedure. The other was pqsA-E operon knock-out plasmid whose sequence between pqsD and pqsE operon was inserted by tetracycline cassette by the site specific insertion mutagenesis strategy and the mutant constructed by biparental mating of S17-1 that harbored the plasmid and pqsA' positive expression mutant.

一种是酶切质粒pYHP441获得pqsA'-lacZ片段后，亚克隆入质粒miniCTX-1中，构建成PqsA'的阳性表达质粒，随后将构建的质粒，通过双亲交配过程整合入野生型铜绿假单胞菌株PAO-1染色体组中；另一种是通过点特异插入诱变策略，将四环素基因盒插入启动子pqsD和pqsE之间，构建的阴性质粒转化入大肠杆菌S17-1株后，和上述pqsA'阳性表达突变株进行双亲交配过程。

A numerical algorithm and a numerical experiment are given. 2. The least norm, positive semidefinite and positive definite real solutions of bisymmetric matrix equations (A~TXA, XA — YAD)=(D, 0)are considered by applying the generalized singular value decomposition.

利用广义奇异值分解讨论了矩阵方程(A~T XA，XA-YAE)=(E，0)在对称次反对称矩阵集合中的解、极小范数解和在双对称矩阵集合中的解、极小范数解及正定解； 3。

Results No positive expressions of nm23Hl and NF-kBP65 were found in normalgroup; whereas positive expressions were observed in retinoblastoma, blepharal basal cell carcinoma , blepharal squamous cell carcinoma and meibomian gland carcinoma.

结果：nm23H1和NF-kBP65在正常视网膜及眼睑组织细胞中呈阴性表达，在视网膜母细胞瘤、眼睑基底细胞癌、眼睑鳞状细胞癌及睑板腺癌等眼部肿瘤中呈阳性表达。

Methods 44 asthma patients with wheezing rale heard and bronchial provocation tested positive or bronchodilatation tested positive were treated for 2 to 3 months according to GINA,then the questionnaire of asthma quality of life in adultsand asthma control testwere completed by these patients.

2005年第101次美国胸科学会年会上，有人报告哮喘控制测试不仅与其它现有的、以西方人生活方式和习惯为基础编制的哮喘量表评价方法高度一致，而且要简单易用并更明了有效[1]。

In the lens regeneration of Bufo raddei Strauch, The mRNA of Pax-6 gene expression was positive at 7 day, 30 day during lens regeneration. The gene of Pax-6 was positive during the different time of lens development and regeneration.

晶状体再生的第30天晶状体纤维开始分化，荧光定量的结果显示再生30天比21天Pax6基因的表达量高，表明在此时期Pax-6基因对再生的过程中调控晶状体纤维分化方面起到了关键的调控作用。

The expression of Bcl-2mRNA and P53mRNA in hippocampus after 16Hz, 130dB infrasound treatment In 1 day group, Bcl-2mRNA and P53mRNA were expressed lightly in CA1-CA3 areas in hippocampus and dentate gyrus. Blood vessels dilated lightly. In 7d group, Bcl-2mRNA and P53mRNA were more expressed in areas mentioned above. Dilation of capillaries and small vessels was more obvious. Bcl-2mRNA and P53mRNA were strong positive in endothelial cells of vessels. In 14d group, Bcl-2mRNA and P53mRNA expression was obviously increased in pyramidal cells of hippocampus and granular cells of dentate gyrus, showing deep blue staining. a The endothelial cells in some vessels were also strong positive for Bcl-2mRNA and P53mRNA. Dilation of capillaries and small vessels was lessened. In 21d group, Bcl-2mRNA and P53mRNA expression was decreased in pyramidal cells. In 28d group, little change about the expression and distribution of Bcl-2mRNA and P53mRNA was observed. Lots of Bcl-2mRNA and P53mRNA were scattered in cortex of temporal lobe around hippocampus and callosal gyrus area. Dilation of capillaries and small vessels was lessened obviously. The expression of Bcl-2mRNA and P53mRNA in hippocampus after 16Hz, 90dB infrasound treatment.

次声作用后Bcl-2mRNA和P53mRNA在海马的表达，16Hz、130dB次声作用1d组：两者在海马〓区和齿状回轻度表达，海马内血管轻度扩张；7d组：两者表达在上述区域较1d增多，微血管和小血管扩张较显，血管内皮细胞内可见呈强阳性表达的Bcl-2mRNA和P53mRNA；14d组：海马锥体细胞和齿状回颗粒细胞内Bcl-2mRNA和P53mRNA阳性表达明显增多，呈深兰色，在部分血管内皮细胞内两者强阳性表达，微小血管扩张状态较7d减轻；21d组：锥体细胞胞浆内Bcl-2mRNA和P53mRNA表达减弱；28d组：上述表达及分布与21d组相比无明显改变，海马周围颞叶皮层和扣带回区域亦可见大量散在分布的Bcl-2mRNA和P53mRNA表达，血管扩张状态已明显减轻。90dB次声作用1d-7d后，较对照组无明显变化，14d-21d后轻度表达，28d后，Bcl-2mRNA和P53mRNA表达较强。

Immunocytochemistry was used to observe the change of TH-IR positive neurons in substantia nigra and nNOS-IR positive neurons in caudatum, respectively.

同时设立SVHRP治疗组，测定小鼠爬竿和游泳时间以检测其运动协调性。

The most heavy flow ability of barrage swirl is controlled by fastenning device and barrage size, the most heavy discharge is more when barrage aperture is bigger, the influence of barrage position on discharge is not obvious; The pressure of the end of the shaft and fastenning device increases which aroused by barrage, and there is a restraining action to flow waving of the shaft; The barrage aperture is smaller, the increase of pressure is heavier, the influence of position to the increase of pressure is not obvious; The positive pressure of the level section in the hole between fastenning device and barrage increases obviously, the change of press along length reduces, mural press in the hydrosphere separating area of outlet of fastenning device becomes positive pressure, which is propitious to the increase of flow cavitate number in the low pressure area of the outlet of fastenning device; The influence of change of swirl cavum diameter caused by barrage to ventilating state is obvious.

阻塞旋流最大泄流能力由起旋器及阻塞体型共同控制，降低了泄洪洞的泄流量，孔径大的阻塞最大下泄流量较大，阻塞位置对泄流量的影响不明显；阻塞引起竖井及起旋器端头压力增大，对竖井部分的水流波动具有抑制作用；阻塞孔径越小，压力增加越大，位置对压力增大影响不明显；起旋器与阻塞之间水平洞段的止压力明显增加，沿程压力变化减小，起旋器出口的水气分离区壁面压力变为正压力，有利于起旋器出口低压区水流空化数的提高；阻塞引起的旋流空腔直径变化对通气状态产生明显影响。

Results: Based on the study mentioned above, about 323 bp positive band were amplified under the anneal temperature of 65℃ by total volume of 25 25ul PCR reaction. Sequencing results prove the positive band were fragments of Cytb genes from both Cervus elaphus Linnaeus and Cervus nippon Temminck.

结果：在方法学考察的基础上，在25ul PCR反应体系，退火温度为65℃的条件下，能准确扩增出约323bp 大小的阳性DNA条带，经测序验证结果表明，系正品鹿茸原动物的Cytb基因序列片段，而伪品鹿茸未扩增出条带。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。