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Genomes participating in rheumatoid arthritis, method of the diagnosis thereof, method of evaluating the onset possibility thereof, diagnostic kit for detecting them and therapeutic method and remedies for rheumatoid arthritis
Genomes participating in rheumatoid arthritis, method of the diagnosis thereof, method of evaluating the onset possibility thereof, diagnostic kit for detecting them and therapeutic method and remedies for rheumatoid arthritis
Mutations in a genome associating in rheumatoid arthritis (RA) are found in human DR3 genomic DNA having the base sequence represented by SEQ ID NO:1. The invention provides a genome having such mutations, transcripts thereof, a method of highly accurately evaluating the RA onset or the RA onset possibility by using the mutations thereof, an evaluation kit therefor, and a therapeutic method and remedies for RA.
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机译:在具有由SEQ ID NO:1表示的碱基序列的人DR3基因组DNA中发现了与类风湿性关节炎(RA)相关的基因组中的突变。本发明提供了具有这种突变的基因组,其转录本,通过使用其突变高度准确地评估RA发作或RA发作可能性的方法,其评估试剂盒以及RA的治疗方法和疗法。
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