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Anti-bacterial mechanism of baicalin-tobramycin combination on carbapenem-resistant Pseudomonas aeruginosa 被引量:1
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作者 li-min jin Hui Shen +3 位作者 Xing-Ying Che Ye jin Chun-Mei Yuan Neng-Hua Zhang 《World Journal of Clinical Cases》 SCIE 2023年第17期4026-4034,共9页
BACKGROUND Pseudomonas aeruginosa(P.aeruginosa)is an important cause of nosocomial infections,and contributes to high morbidity and mortality,especially in intensive care units.P.aeruginosa is considered a'critica... BACKGROUND Pseudomonas aeruginosa(P.aeruginosa)is an important cause of nosocomial infections,and contributes to high morbidity and mortality,especially in intensive care units.P.aeruginosa is considered a'critical'category bacterial pathogen by the World Health Organization to encourage an urgent need for research and development of new antibiotics against its infections.AIM To investigate the effectiveness of baicalin combined with tobramycin therapy as a potential treatment method for carbapenem-resistant P.aeruginosa(CRPA)infections.METHODS Polymerase chain reaction(PCR)and RT-PCR were used to detect the expression levels of drug-resistant genes(including VIM,IMP and OprD2)and biofilmrelated genes(including algD,pslA and lasR)in CRPA that confer resistance to tobramycin,baicalin and tobramycin combined with baicalin(0,1/8,1/4,1/2 and 1MIC).RESULTS There was a correlation between biofilm formation and the expression of biofilmrelated genes.In addition,VIM,IMP,OprD2,algD,pslA and lasR that confer biofilm production under different concentrations in CRPA were significantly correlated.The synergistic effect of baicalin combined with tobramycin was a significant down-regulation of VIM,IMP,algD,pslA and lasR.CONCLUSION Baicalin combined with tobramycin therapy can be an effective treatment method for patients with CRPA infection. 展开更多
关键词 BAICALIN Pseudomonas aeruginosa TOBRAMYCIN Carbapenem-resistant Pseudomonas aeruginosa Therapy
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野生型PTEN过表达对体外活化肝星状细胞内钙离子浓度的影响 被引量:1
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作者 郝礼森 宋小杰 +5 位作者 王玉兰 刘玉龄 宋洁 张明婷 靳丽敏 张朋垒 《中国现代医学杂志》 CAS 北大核心 2017年第28期12-15,共4页
目的探讨野生型第10号染色体缺失的磷酸酶张力蛋白同源物基因(PTEN)过表达对体外活化肝星状细胞(HSC)内钙离子浓度的影响。方法体外培养活化大鼠肝星状细胞系(HSC-T6),利用腺病毒载体,将野生型PTEN基因转染活化HSC;Western blot及实时... 目的探讨野生型第10号染色体缺失的磷酸酶张力蛋白同源物基因(PTEN)过表达对体外活化肝星状细胞(HSC)内钙离子浓度的影响。方法体外培养活化大鼠肝星状细胞系(HSC-T6),利用腺病毒载体,将野生型PTEN基因转染活化HSC;Western blot及实时荧光定量聚合酶链反应(q RT-PCR)检测HSC的PTEN蛋白及m RNA表达;采用钙离子荧光探针Rhod-2/AM,于激光扫描共聚焦显微镜下检测HSC内钙离子浓度变化。实验分组:(1)Control组:腺病毒转染时以DMEM代替病毒液;(2)Ad-GFP组:转染表达绿色荧光蛋白(GFP)的对照空病毒Ad-GFP;(3)Ad-PTEN组:转染携带野生型PTEN基因并表达GFP的重组腺病毒Ad-PTEN。结果野生型PTEN在活化大鼠HSC大量表达,3组HSC内钙离子浓度比较,差异有统计学意义(P<0.05),Ad-PTEN组HSC内钙离子浓度(251.60±90.88)低于Control组(1 953.95±132.99)及Ad-GFP组(1 937.57±115.17),而Control组与Ad-GFP组之间HSC内钙离子浓度比较,差异无统计学意义(P>0.05)。结论野生型PTEN过表达可降低体外活化大鼠HSC内钙离子浓度。 展开更多
关键词 肝星状细胞 第10号染色体缺失的磷酸酶张力蛋白同源物基因 细胞内钙离子浓度
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FEA-based structural optimization design of a side cooling collimating mirror at SSRF
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作者 li-min jin Na-Xiu Wang +2 位作者 Wan-Qian Zhu Feng-Gang Bian Zhong-Min Xu 《Nuclear Science and Techniques》 SCIE CAS CSCD 2017年第11期198-203,共6页
Based on finite element analysis of thermal mechanical behavior, structural optimization design was proposed for a side cooling collimating mirror subjected to high heat load for a beamline at SSRF(Shanghai Synchrotro... Based on finite element analysis of thermal mechanical behavior, structural optimization design was proposed for a side cooling collimating mirror subjected to high heat load for a beamline at SSRF(Shanghai Synchrotron Radiation Facility). The temperature distribution,stress concentration effect, maximum equivalent(vonMises) stress, and slope error of the mirror were analyzed.In particular, the cooling water channels of the traditional structural design were optimized, and the modified designs were further optimized. Although the traditional structural and the improved designs could meet requirements for the temperature and thermal stress, the deformation gradients were relatively large for several structural designs, and this led to larger slope error. The further improved structural designs could be of better performance. 展开更多
关键词 FINITE element analysis (FEA) SYNCHROTRON radiation Heat load Structural optimization
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Genetic variants associated with endometriosis patients:a systematic review
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作者 Bo Hu Xin jin +4 位作者 Guang-Tao Xu Ping Qian Long Xu li-min jin De-Qing Chen 《Precision Medicine Research》 2021年第1期7-20,共14页
Endometriosis is defined as the presence of endometrium-like tissue outside the uterus,80%of which occur in the ovaries.It is characterized by an estrogen-dependent produces periodic and repeated bleeding,and may be a... Endometriosis is defined as the presence of endometrium-like tissue outside the uterus,80%of which occur in the ovaries.It is characterized by an estrogen-dependent produces periodic and repeated bleeding,and may be accompanied by clinical symptoms such as dysmenorrhea,fatigue,dysuria,deep dyspareunia,and infertility.Due to the complex etiology and the yet-unknown pathogenesis of endometriosis,and the treatment effect is not ideal,causing significant physical and mental harm to reproductive-age women;thus,it has become a hot research topic.Endometriosis is still a mysterious disease of unknown origin and pathogenesis.Genetic factors are known to affect the manifestation and progression of endometriosis.A selection of genetic studies revealed genetic mutations and polymorphisms of endometriosis and their effects on the risk of developing this disease.This paper aimed to discuss the genetic variants associated with the risk of endometriosis and provided information to enrich the gene spectrum of endometriosis. 展开更多
关键词 ENDOMETRIOSIS Genetic variants Single nucleotide polymorphism
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Two unrelated patients with rare Crigler-Najjar syndrome type I:two novel mutations and a patient with loss of heterozygosity of UGT1A1 gene 被引量:2
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作者 Yan LI Yu-jin QU +8 位作者 Xue-mei ZHONG Yan-yan CAO li-min jin jin-li BAI Xin MA Yu-wei jin Hong WANG Yan-ling ZHANG Fang SONG 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2014年第5期474-481,共8页
Cdgler-Najjar syndrome type Ⅰ (CN-I) is the most severe type of hereditary unconjugated hyperbilirubinemia. It is caused by homozygous or compound heterozygous mutations of the UDP-glycuronosyltransferase gene (UG... Cdgler-Najjar syndrome type Ⅰ (CN-I) is the most severe type of hereditary unconjugated hyperbilirubinemia. It is caused by homozygous or compound heterozygous mutations of the UDP-glycuronosyltransferase gene (UGT1A1) on chromosome 2q37. Two patients clinically diagnosed with CN-I were examined in this paper. We sequenced five exons and their flanking sequences, specifically the promoter region of UGT1A 1, of the two patients and their parents. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to determine the UGT1A1 gene copy number of one patient. In patient A, two mutations, c.239_245delCTGTGCC (p.Pro80HisfsX6; had not been reported previously) and c.1156G〉T (p.Va1386Phe), were identified. In patient B, we found that this patient had lost heterozygosity of the UGTIA1 gene by inheriting a deletion of one allele, and had a novel mutation c.1253delT (p.Met418ArgfsX5) in the other allele. In summary, we detected three UGTIA 1 mutations in two CN-I patients: c.239_ 245delCTGTGCC (p.Pro80HisfsX6), c.1253delT (p.MeH18ArgfsX5), and c.1156G〉T (p.Va1386Phe). The former two mutations are pathogenic; however, the pathogenic mechanism of c.1156G〉T (p.Va1386Phe) is unknown. 展开更多
关键词 Crigler-Najjar syndrome type (CN-I) HYPERBILIRUBINEMIA UDP-glycuronosyltransferase gene (UGT1A 1) Mutation Loss of heterozygosity
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