1) anaemia+virus
贫血+病毒
2) chicken anemia virus
鸡贫血病毒
1.
Expression,purification and identification of the chicken anemia virus vp2;
鸡贫血+病毒vp2基因的表达、纯化及重组蛋白的鉴定
2.
Cloning, sequencing and comparing of VP2 gene of chicken anemia virus Harbin isolate;
鸡贫血+病毒哈尔滨分离株VP2基因克隆 测序和比较
3.
AIM:To clone the chicken anemia virus-derived Apoptin gene from the chicken s bursa of Fabricius and to do a sequencing analysis on it.
目的:为了寻找肿瘤特异凋亡蛋白,克隆鸡法氏囊组织中鸡贫血+病毒Apoptin蛋白的编码基因并进行序列分析。
3) chicken anaemia virus
鸡贫血病毒
1.
Expression of Chicken Anaemia Virus(CAV) Apoptin Gene in E.coli and Analysis of It′s Immunity;
鸡贫血+病毒细胞凋亡素基因的原核表达及其免疫学活性
2.
VP1 and VP2 genes of chicken anaemia virus were cloned into transfer vector pBacPAK8, then recombinant transfer plasmids pBac vp1 and pBac vp2 were obtained, respectively.
将鸡贫血+病毒 VP1和 VP2基因分别克隆入转移载体 p Bac PAK8中 ,获得重组转移质粒 p Bac-vp1和 p Bac-vp2。
4) CAV
鸡贫血病毒
1.
CHANGESOFIMMUNOPATHOLOGYPOSTvNDVCHALLENGEOFCAVINFECTEDCHICKSIMMUNIZEDWITHNDVACCINE;
鸡贫血+病毒感染新城疫免疫雏鸡vNDV攻击后免疫病理学变化
2.
vp1 and vp2 gene from chicken infectious anemia virus (CIAV) were amplified from pBluemCAV by PCR and cloned into pPIC9K vector, respectively.
结果表明,重组酵母菌株表达出约54ku和24ku的目的蛋白,与针对鸡贫血+病毒的单克隆抗体发生特异性反应。
3.
Chicken anemia virus(CAV)not only induces chicken infectious anemia disease,but also is the main pathogen of chicken immunodeficiency disease.
对于鸡贫血+病毒的许多鸡胚分离物和细胞分离物 ,一次性PCR不能扩增出可见电泳条带 ,而套式PCR都能扩增出特异的DNA片段 ,从而说明 ,套式PCR的敏感性大大高于一次性PCR ,可消除一次性PCR产生的假阴性结
5) Chicken anemia virus(CAV)
鸡贫血病毒(CAV)
6) chicken anemia virus
传染性贫血病毒
1.
To explore current infection statuses of chicken anemia virus(CAV),avian reticuloendotheliosis virus(REV) and avian reovirus(REOV) in white meat-type chicken flocks in China,antibodies to the 3 viruses were tested based on serum samples that collected from meat-type chickens at different ages of 8 companies in 5 provinces during 2003-2004.
为了解鸡传染性贫血+病毒(CAV)、禽网状内皮增生病病毒(REV)和呼肠孤病毒(REOV)在我国白羽肉用型鸡中的感染状态,在2003-2004年,检测了来自5省市8个公司不同年龄鸡群血清样品中3种病毒抗体的存在状况。
参考词条
补充资料:Fanconi贫血
Fanconi贫血
Fanconi anemia,FA
又称“先天性再生障碍性贫血”。一种儿童期的骨髓疾病,常染色体隐性遗传,其临床特点为全血细胞减少,同时伴有多发性先天性畸形,如小头、小眼球、斜视及骨骼畸形。染色体检查可见较多的染色体断裂、部分互相易位、环状或双着丝粒体等畸变。治疗可采用皮质激素与雄激素联合应用,必要时输血治疗。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。