Bordetella pertussis

  • 百日咳杆菌
Bordetella pertussisBordetella pertussis
  1. Effects of excitatory amino acids and its specific receptor on bordetella pertussis brain injury of rats

    兴奋性氨基酸和特异性受体对大鼠百日咳杆菌脑损伤的作用

  2. Molecular Cloning , Expressing , Purification and Characterization of Recombinant Pertactin of Bordetella Pertussis

    百日咳杆菌粘着素的分子克隆、表达、纯化及生物学特性研究

  3. Whooping cough is a serious respiratory disease caused by Bordetella pertussis .

    百日咳是一种由百日咳杆菌引起的严重的呼吸系统传染病,百日咳疫苗是预防百日咳最有效和最经济的手段。

  4. Molecular Characterization of Bordetella Pertussis Isolates in China

    中国百日咳鲍特菌分离株的分子流行病学研究

  5. Studies on the removal of endotoxin and purification of protective antigens of Bordetella pertussis

    多价气性坏疽抗毒素百日咳杆菌去内毒素及保护性抗原的纯化

  6. Detection of Specific Antibody against Bordetella Pertussis in 0 ~ 15 Year Old Healthy Children and the Puerpera

    0~15岁健康人群及产妇血清百日咳抗体水平的检测

  7. Toxicity and antigenicity of the outer membrane protein and Its fractions of bordetella pertussis

    百日咳杆菌外膜蛋白及其组分的毒性与免疫原性

  8. Purification and Characterization of Filamentous Hemagglutinin from Bordetella Pertussis Culture

    百日咳杆菌丝状血凝素的纯制及其生物学特性的研究

  9. The application of Chinese hamster ovary ( cho ) cell on Determination of Bordetella pertussis immunogen

    中华仓鼠卵巢细胞在检测百日咳菌免疫原中的应用

  10. Caused by the bacterium Bordetella pertussis , it initially resembles a cold with a short dry cough .

    致病菌为百日咳博尔德氏杆菌,潜伏期一周,类似普通感冒,伴有短促的干咳。

  11. Outer membrane proteins of Bordetella pertussis function as a modulator on promoting degranulation of mastocyte in vitro

    百日咳鲍特菌外膜蛋白体外促肥大细胞脱颗粒的作用

  12. LPS , Bordetella pertussis , Clone : 5111 , Mab anti .

    百日咳杆菌,克隆号:5111,单克隆抗体抗。

  13. Methods An IBI model was induced by injection of bordetella pertussis suspension ( BPS ) via the left internal carotid arteries of the rats .

    方法向大鼠左颈内动脉注射百日咳杆菌悬浮液(0.2ml/kg体重),诱发感染性脑损伤模型。

  14. Pertussis is an acute infectious disease of the respiratory system , which is mainly caused by Bordetella pertussis and found in non-immunised children of developing countries .

    百日咳是主要由百日咳杆菌引起的一种传染性强的急性呼吸系统疾病,主要见于发展中国家未接种相应疫苗的儿童。

  15. Beside group a , egg albumin was injected into the abdominal cavity plus the method to kill Bordetella pertussis , to create asthma model in the rats .

    除a组外,采用腹腔注射卵白蛋白和灭活百日咳杆菌的方法,制成大鼠哮喘模型。

  16. Objective : To explore changes and mechanism of EAAs and its specific N-methyl-D-aspartate receptor ( NMDAR ) on bordetella pertussis brain injury in rats .

    目的:探讨兴奋性氨基酸、N甲基D天冬氨酸受体(NMDAR)在大鼠百日咳杆菌脑损伤中的变化及作用机制。

  17. The rats in group A were sensitized by injection of ovalbumin ( OA ) together with aluminum hydroxide and Bordetella pertussis as adjuvants .

    A组大鼠用卵蛋白(OA)辅以百日咳杆菌菌苗和氢氧化铝为佐剂注射致敏。

  18. Objective To clone the S1 subunit of Bordetella pertussis , induce its mutant S1 for the construction of prokaryotic expression system and identify the expressed fusion protein .

    目的克隆百日咳毒素S1亚单位,获得其突变体(S1/9K-129G,rS1),构建原核表达系统,并鉴定融合蛋白的特异性。

  19. Methods Each Wistar rat was injected with Cavy 's spinal cord homogenate , mycobacteria and IFA , and Bordetella Pertussis bacilli .

    方法应用豚鼠脊髓匀浆加完全弗(氏)佐剂和百日咳杆菌免疫Wistar大鼠。

  20. Methods The structural gene encoding pertussis toxin SI subunit of Bordetella pertussis was amplified by PCR , cloned into vector pCR 2.1 - TOPO , and transformed to E.

    方法采用PCR法从百日咳杆菌染色体中获得S1亚单位的结构基因并克隆到质粒pCR2.1-TOPO中,转化宿主菌DH5α和TOPO10。

  21. Whooping cough or pertussis is an acute respiratory infectious disease caused by the bacterium Bordetella pertussis . It is easily transmissible in humans , especially in infants and children .

    百日咳是由百日咳鲍特氏菌引起的一种急性呼吸道传染病,传染性较强,人群普遍易感,其中尤以婴幼儿多见。

  22. Methods Guineapigs were induced to establish EAE model by injecting guineapig with spinal cord homogenate ( GPSCH ) in complete Freund 's adjuvant ( CFA ) bordetella pertussis vaccine ( BPV ) .

    方法采用注射完全福(氏)佐剂-豚鼠全脊髓匀浆(CFA-GPSCH),并辅以注射百日咳疫苗(BPV),诱导豚鼠EAE模型。

  23. Methods Full length of S1 and Prn genes of three vaccine strains were amplified by PCR . The PCR amplicons were sequenced after being cloned into PGEM-T easy vector and the results were compared with those of Bordetella pertussis strains in GenBank .

    方法分别克隆疫苗株的S1和Prn基因至PGEM-Teasy载体、进行测序,并与GenBank中收录的百日咳杆菌S1和Prn蛋白基因序列进行比较、分析。