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SUMO1基因多态性与非综合征性唇裂伴或不伴腭裂相关。

SUMO1 polymorphisms are associated with non-syndromic cleft lip with or without cleft palate.

作者信息

Song Tao, Li Guolin, Jing Guangping, Jiao Xiaohui, Shi Jinna, Zhang Bing, Wang Li, Ye Xiangmei, Cao Fenglin

机构信息

Department of Oral Maxillofacial Surgery, School of Stomatology, Harbin Medical University, Harbin, China.

出版信息

Biochem Biophys Res Commun. 2008 Dec 26;377(4):1265-8. doi: 10.1016/j.bbrc.2008.10.138. Epub 2008 Nov 5.

Abstract

Small ubiquitin-like modifier 1 (SUMO1) haploinsufficiency results in cleft lip and palate in animal models. However, no studies have linked SUMO1 to non-syndromic cleft lip with or without cleft palate (NSCLP) in humans. In the present study, we investigated the potential association between SUMO1 single nucleotide polymorphisms (SNPs) and risk for human NSCLP. From 181 patients and 162 healthy controls, we found statistically significant correlations between a 4-SNP SUMO1 haplotype and NSCLP. These data are the first to suggest a role for SUMO1 gene variation in human NSCLP development.

摘要

小泛素样修饰物1(SUMO1)单倍体不足在动物模型中会导致唇腭裂。然而,尚无研究将SUMO1与人类非综合征性唇裂伴或不伴腭裂(NSCLP)联系起来。在本研究中,我们调查了SUMO1单核苷酸多态性(SNP)与人类NSCLP风险之间的潜在关联。在181例患者和162名健康对照中,我们发现一种4-SNP SUMO1单倍型与NSCLP之间存在统计学上的显著相关性。这些数据首次表明SUMO1基因变异在人类NSCLP发生发展中起作用。

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