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- HLA - DQ alleles 等位基因
- Methods: Sera from 74 transplant patients and 35 mouse DQB1 monoclonal antibodies were tested with DQ single antigen beads for their DQ allelic and serological specificities. 方法： 我们采用DQ单抗原磁珠检测法检测了74例移植患者和35例小鼠DQB1单克隆抗体及其DQ等位基因和血清学特异性。
- Studies on the Association between HLA-A, B, Cw, DR, DQ Alleles and Variations in Serum Leptin Levels in Patients with Psoriasis Vulgaris in Northern Chinese Han 北方汉族寻常型银屑病与HLA-A、B、Cw、DR、DQ等位基因及血清瘦素相关性研究
- HLA - DQ allele HLA-DQ等位基因
- Methods HLA DQA1 alleles in ABI patients ( n =81) and healthy controls ( n =99) were detected by PCR SSP techniques. 方法 采用聚合酶链反应 -序列特异性引物技术检测了81例 ABI患者及 99名正常对照的 HL A- DQA1位点的等位基因频率。
- Objective To evaluate the association of HLA?DQ polymorphism with chronic lymphocytic thyroiditis (CLT) in Chinese Han nationality. 目的分析汉族慢性淋巴细胞性甲状腺炎（CLT）与HLA?DQ位点基因多态性的相关性。
- There can be more than two alleles for a gene. 一个基因可能有两个以上的等位基因。
- DQA?1 *0301 was probably the susceptible gene and DQB?1 *0602 the resistant gene for CLT, so both susceptability and resistance for CLT were present in HLA?DQ gene locus. ? HLA?DQA1?0301可能与CLT的易感性相关，而DQB1?0602可能与CLT的抗性相关，在HLA?DQ位点存在有易感及抗性的双重作用，等位基因之间的共同作用可能是影响CLT发生的重要因素之一。
- We can identify DQA1 and DQB1 epitopes by DQ single antigen beads assay of the antibodies, correlating the beads' reaction patterns with either DQA1 or DQB1 alleles. 我们能够通过抗体的DQ单抗原磁珠检测法来判断DQA1和DQB1表位，包括DQA1和DQB1等位基因的磁珠反应模式。
- Note:? - Possible or unidentified alleles. 注:?-可能性较大或未确定的等位基因。
- Methods:Survey 20 special antigen frequency of site of HLA\|DR and DQ in 32 Fujian s patients with VMC by lymphocytotoxicity testing with monoclone antibody of HLA. 方法:用HLA单克隆抗体以微量淋巴细胞毒性试验调查32例福建地区VMC患者HLA-DR和DQ位点共20个特异性抗原频率,并与43例本地区正常人加以对照。
- No, because some alleles are dominant to others. 因为有些等位基因对于别的（隐性基因）是显性的。
- Reveille JD,Schrohenloher R,Acton RT,et al.DNA analysis of HLA，DR and DQ genes in American black with systemic lupus erythematosus.Arthritis Rheum,1989,32:1243，1251. 彭学标，徐文严，岳晓玉，等.;江苏籍汉族系统性红斑狼疮与HLA，DR基因的相关性研究
- Objective To analyze the genetic predisposition to lacunar cerebral infarction (LCI) by genotyping of HLA DQA1 alleles according to trait of multiple genes leading to disease. 目的 针对腔隙性脑梗死多基因致病的特点 ,进行人类白细胞抗原 (HLA) DQA1等位基因分型 ,分析腔隙性脑梗死的遗传易感性。
- Methods By using NIH, 66 special positions of the HLA A, B and C alleles in 39 patients with ABI and 41 case of control group in the north area of china were tested and analysed. 方法 采用微量淋巴细胞毒分型方法 ,对我国北方汉族人群 39例ABI患者和 41例健康对照组的HLA A、B、C各等位基因共计 6 6个位点进行检测分析。
- Heterozygous Having two different alleles at a given locus. 杂合性：在一个基因位点上具有两个不同的等位基因。
- In9/26 cases of gastric cancer, 8/36 cases of colorectalcancer and 6/15 cases of lymgh node metasis, someorall of the tumor cells expressed HLA--DR antigen,but HLA--DQ antigen was expressed only on a fewtumor cells in two cases of the DR tumors. HLA-DR抗原表达率分别为34.;62%25、22
- Donors of HLA 1/6-2/6 mismatch were accepted at registry search. 多份移植脐血HLA匹配为 1 6 - 2 6位点不相合。
- GG 10.52%, and alleles frequencies were C 66.01% and T 33.99%. 等位基因频率:C66.;01%25、T33
- Perhaps PPT is not associated with HLA-DP and HLA-DQ alleles. 产后甲状腺炎与HLA-DP、HLA-DQ位点可能无相关性。
