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1)  HLA-DQA
HLA-DQA基因
2)  SLA-DQA gene
SLA-DQA基因
1.
Cloning and prokaryotic expression of SLA-DQA gene of inbred miniature Wuzhishan pig;
近交五指山小型猪SLA-DQA基因的克隆及在大肠杆菌的原核表达
2.
The SLA-DQA gene in Sutai pigs was analyzed by PCR-RFLP method,the results showed that the 722 base of ORF in SLA-DQA gene has a A→G mutation,after digested by restriction endonuclease TaqⅠ,there showed two kinds of genotypes,AA and AG.
本研究采用PCR-RFLP方法对苏太猪SLA-DQA基因多态性进行分析,结果表明,苏太猪SLA-DQA基因开放阅读框第722个碱基存在1个A→G突变,从而导致了氨基酸Gly到Arg的转变,并产生了TaqⅠ酶切位点。
3.
The partial intron 1,complete exon 2 and partial intron 2 of SLA-DQA gene was amplified and a uniform fragment of 341bp was obtained in Diannan small-ear pigs(DN) and Bama miniature pigs(BM).
对滇南小耳猪和巴马小型猪的SLA-DQA基因的部分内含子1、完整的外显子2和部分内含子2共341bp片段进行了PCR-RFLP酶切分型,结果表明:2品种经EcoRⅠ酶切后BB基因型频率(0。
3)  DQA gene
DQA基因
1.
The 249 bp fragment of exon 2 of DQA gene is amplified successfully by PCR and cloned into pMD18-T vector,it the recombined carriers into E.
为了探明黑线仓鼠MHC的结构与功能并寻找分子标记,对MHCⅡ类DQA基因的外显子2进行克隆和序列分析。
4)  HLA-DQB_1 gene
HLA-DQB_1基因
1.
HLA-DQB_1 genes involved in the genetic susceptibility of gastric ulcer in Guangdong Hans;
广东地区汉族人HLA-DQB_1基因对胃溃疡患者的遗传易感性研究
5)  HLA-DR gene
HLA-DR基因
1.
HLA-DR genotypes were detected by SSP-PCR in 40 patients with acquired aplastic anemia and 107 normal controls, and the expressions of HLA-DR gene in AA patients and normal controls were compared.
本研究探讨再生障碍性贫血(AA)患儿HLA-DR基因表达情况及其与免疫抑制治疗疗效的关系,评价HLA-DRB1*15基因型检测的临床意义。
2.
Objective:To evaluate relationship between HLA and IgA nephropathy,we study HLA-DR gene susceptibility to IgA nephropathy in Guangxi Zhuang population.
目的:探讨广西籍壮族IgA肾病(IgAN)与HLA-DR基因的相关性,并进行序列分析。
3.
Objective: To evaluate relationship between HLA and IgA nephropathy and it’s clinical presentation,pathology, We study HLA-DR gene susceptibility to IgA nephropathy in Guangxi Zhuang and Han population.
目的:探讨广西地区汉族、壮族IgA肾病(IgAN)与人类白细胞抗原(HLA)-DR基因的相关性,以及其临床表现、病理改变与HLA-DR基因的相关性。
6)  HLA gene
HLA基因
1.
To investigate the correlation between the HLA genes and pathogenesis of aplastic anemia (AA), polymerase chain reaction with specific sequence primers (PCR-SSP) method was used to HLA typing in 82 patients with AA and 400 normal healthy individuals as control.
本研究探讨HLA基因与再生障碍性贫血(aplastic anemia,AA)发病之间的相关性。
2.
The HLA gene types in 30 DMD patients were compared with those of 668 unrelated donors from Umbilical Cord Blood Center of Guangdong Province .
结果表明 :DMD疾病组的HLA基因呈正态遗传 ,DMD患者HLA基因表达与广东健康人群无统计学上显著差异 ;DMD患者中 1/ 4寻找到合适用于移植的干细胞 ,其中在广东脐血库寻找到≥ 5个HLA ABDR基因配合的几率为 5 0 % ,在中国造血干细胞库寻找到 6个HLA ABDR基因配合的几率为 2 6%。
补充资料:HLA
分子式:
CAS号:

性质:一个复杂的抗原群,决定了人类组织的组织配伍性,正如ABO血型抗原决定了输血的配伍性一样。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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