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GENOMICS OF IN-STENT RESTENOSIS

机译:即时再造的基因组学

摘要

Described herein is the identification of sixteen candidate susceptibility loci linked to in-stent restenosis (ISR). Of these regions, seven contain the genes NOV, ARNTL, TAF4B, PKP4, EPHB l, ST 18 and FLJ21986 (which encodes a hypothetical protein). The remaining eleven susceptibility loci are located in cytobands 2p 16.1, 4q31.21, 7p21.2, Ip31.1, 2p24.1, 2q22.3, 13ql4.3, 15q25.1 and 18q22.3. Provided are methods for identifying a subject having an increased risk of developing restenosis, comprising obtaining a nucleic acid sample from the subject and determining the nucleotide present at the chromosomal positions identified herein as part of a haplotype associated with an increased risk of developing restenosis.
机译:本文描述了与支架内再狭窄(ISR)相关的16个候选易感基因座的鉴定。在这些区域中,有七个包含基因NOV,ARNTL,TAF4B,PKP4,EPHB1,ST 18和FLJ21986(其编码一种假设的蛋白质)。其余的11个易感性基因座位于细胞带2p 16.1、4q31.21、7p21.2,Ip31.1、2p24.1、2q22.3、13ql4.3、15q25.1和18q22.3。提供了用于鉴定具有发生再狭窄的风险增加的受试者的方法,包括从该受试者获得核酸样品并确定存在于本文鉴定的染色体位置上的核苷酸,该核苷酸是与发生再狭窄的风险增加相关的单倍型的一部分。

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