HLA-DQA1 3 ' UTR IS AN UNEXPLORED SOURCE OF DISEASE ASSOCIATIONS IN THE HLA COMPLEX

Temurhan Sonay; Oguz Fatma Savran; Dorak Mehmet Tevfik

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HLA-DQA1 3 ' UTR IS AN UNEXPLORED SOURCE OF DISEASE ASSOCIATIONS IN THE HLA COMPLEX

机译：HLA-DQA1 3'UTR是HLA复合体中疾病关联的异常来源

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《Tissue antigens.》 |2015年第5期|共1页
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Temurhan Sonay; Oguz Fatma Savran; Dorak Mehmet Tevfik;
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正文语种 eng
中图分类人体形态学;
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1. HLA-DQA1 3 ' UTR IS AN UNEXPLORED SOURCE OF DISEASE ASSOCIATIONS IN THE HLA COMPLEX [J] . Temurhan Sonay, Oguz Fatma Savran, Dorak Mehmet Tevfik Tissue antigens. . 2015,第5期

机译：HLA-DQA1 3'UTR是HLA复合体中疾病关联的异常来源
2. The inter-regional distribution of HLA class II haplotypes indicates the suitability of the Sardinian population for case-control association studies in complex diseases. [J] . Lampis R, Morelli L, Congia M, Human Molecular Genetics . 2000,第20期

机译：HLA II类单倍型的区域间分布表明撒丁岛人群适合进行复杂疾病的病例对照研究。
3. Association of Major Histocompatibility Complex Class I Chain-Related Gene A and HLA-B Alleles with Behcet's Disease in Turkey. [J] . Mizuki N, Meguro A, Tohnai I, Japanese Journal of Ophthalmology . 2007,第6期

机译：土耳其的主要组织相容性复合体I类链相关基因A和HLA-B等位基因与白塞氏病的关联。
4. Association of HLA-B*5101 and Characteristics of Patients with Behcet's Disease in China using HLA-B51 OligoChip [C] . Sun Yuping, Shen Hong, Liu Jie, International Forum on Progress on Post-Genome Technologies(5'IFPT); 20070910-11; Suzhou(CN) . 2007

机译：HLA-B51 OligoChip与HLA-B * 5101和中国白塞氏病患者特征的关联
5. Defining the mechanism of MHC class II peptide editing by HLA-DM: I. HLA-DM recognizes the flexible conformation of major histocompatibility complex class II. II. Mapping the interaction surface of DR1 with DM by superantigen blocking. III. Determinati [D] . Chou, Chih-Ling. 2003

机译：定义HLA-DM编辑MHC II类肽的机制：I. HLA-DM识别II类主要组织相容性复合物的柔性构象。二。通过超抗原阻断作用绘制DR1与DM的相互作用表面。三，确定性
6. Association of human leukocyte antigen (HLA)-DQ and HLA-DQA1/DQB1 alleles with Vogt–Koyanagi–Harada disease [O] . Bing Liu, Tuo Deng, Linxin Zhu, -1

机译：人类白细胞抗原（HLA）-DQ和HLA-DQA1 / DQB1等位基因与Vogt-Koyanagi-Harada病的关联
7. Association of human leukocyte antigen (HLA)-DQ and HLA-DQA1/DQB1 alleles with Vogt–Koyanagi–Harada disease [O] . Bing Liu, Tuo Deng, Linxin Zhu, 2018

机译：人白细胞抗原（HLA）-DQ和HLA-DQA1 / DQB1与Vogt-Koyanagi-Harada病的缔合

HLA-DQA1 3 ' UTR IS AN UNEXPLORED SOURCE OF DISEASE ASSOCIATIONS IN THE HLA COMPLEX

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