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泰国南部穆斯林的人类白细胞抗原

HLA in southern Thai-Muslims.

作者信息

Chiewsilp P, Mongkolsuk T, Sujirachato K, Junpong S, Rattanasombat K, Uden C

机构信息

Department of Pathology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

出版信息

J Med Assoc Thai. 1997 Sep;80 Suppl 1:S30-7.

PMID:9347643
Abstract

UNLABELLED

One hundred and two Southern Thai-Muslims (STM) from Nakhon Si Thammarat province were studied for HLA class I and II by SSP ARMS-PCR and PCR-SSO, respectively. The allele frequencies, haplotype frequencies, delta value and linkage disequilibrium between alleles were expressed. The most frequent alleles for HLA-A, HLA-B and HLA-C were A24(02,03), A11 (01,02), A02(01,03,05-07,11): B15(01,04-07,12,19,20), B07(02-05), B51(01-05)/B52 (011,012); and Cw07(01-03), Cw04(01,02), Cw08(01-03), respectively. The HLA class II alleles frequently found were DRB11202, DRB115021, DRB10701; DRB30301; DRB5* 0101; DQA10101, DQA10103, DQA10601; DQB10301, DQB10501, DQB10201; and DPB11301, DPB12301 and DPB10501. Two common HLA class I and II haplotypes with significant linkage disequilibrium were A24 (02,03)-Cw08 (01-03)-B15 (01,04-07,12,19,20) -DRB11202 and A33 (01,02)-Cw0302-B5801-DQB10201. The absence of B27 and DRB1 1401, the presence of A2301 and high frequency of A*68 were observed in STM.

CONCLUSION

Certain level of genetically distinction among STM, CT and NET existed. However, the genetic diversity of STM was relatively closer to CT than NET.

摘要

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分别采用序列特异性引物扩增-聚合酶链反应(SSP ARMS-PCR)和聚合酶链反应-序列特异性寡核苷酸探针杂交法(PCR-SSO)对来自那空是贪玛叻府的102名泰国南部穆斯林(STM)进行了HLA I类和II类基因研究。表达了等位基因频率、单倍型频率、δ值以及等位基因之间的连锁不平衡。HLA-A、HLA-B和HLA-C最常见的等位基因分别为A24(02,03)、A11(01,02)、A02(01,03,05 - 07,11);B15(01,04 - 07,12,19,20)、B07(02 - 05)、B51(01 - 05)/B52(011,012);以及Cw07(01 - 03)、Cw04(01,02)、Cw08(01 - 03)。经常发现的HLA II类等位基因有DRB11202、DRB115021、DRB10701;DRB30301;DRB50101;DQA10101、DQA10103、DQA10601;DQB10301、DQB10501、DQB10201;以及DPB11301、DPB12301和DPB10501。两种具有显著连锁不平衡的常见HLA I类和II类单倍型为A24(02,03)-Cw08(01 - 03)-B15(01,04 - 07,12,19,20)-DRB11202和A33(01,02)-Cw0302-B5801-DQB10201。在STM中观察到B27和DRB11401缺失,A2301存在且A68频率较高。

结论

STM、CT和NET之间存在一定程度的遗传差异。然而,STM的遗传多样性与CT相比相对更接近NET。

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