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DNA Methylation of KLRC1 and KLRC3 in Autoimmune Thyroiditis:Perspective of Different Water Iodine Exposure
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作者 Yao Chen Jinjin Liu +6 位作者 Mengying Qu Bingxuan Ren Huaiyong Wu Li Zhang Zheng Zhou Lixiang Liu Hongmei Shen 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2024年第9期1044-1055,共12页
Objective This study aimed to identify differentially methylated genes(DMGs) associated with natural killer cells in patients with autoimmune thyroiditis(AIT), focusing on the influence of varying water iodine exposur... Objective This study aimed to identify differentially methylated genes(DMGs) associated with natural killer cells in patients with autoimmune thyroiditis(AIT), focusing on the influence of varying water iodine exposure levels.Methods Participants were divided into categories based on median water iodine(MWI)concentrations: iodine-fortified areas(IFA, MWI < 10 μg/L), iodine-adequate areas(IAA, 40 ≤ MWI ≤ 100μg/L), and iodine-excessive areas(IEA, MWI > 300 μg/L). A total of 176 matched AIT cases and controls were recruited and divided into 89, 40, and 47 pairs for IFA, IAA, and IEA, respectively. DMGs were identified using 850K Bead Chip analysis for 10/10 paired samples. Validation of DNA methylation and m RNA expression levels of the DMGs was conducted using Methyl Target^(TM) and QRT-PCR for 176/176paired samples.Results KLRC1, KLRC3, and SH2D1B were identified as significant DMGs. Validation revealed that KLRC1 was hypomethylated and highly expressed, whereas KLRC3 was hypermethylated and highly expressed in individuals with AIT. Furthermore, KLRC1 was hypomethylated and highly expressed in both IFA and IEA.Conclusion The DNA methylation status of KLRC1 and KLRC3 may play crucial roles in AIT pathogenesis. Additionally, DNA methylation of KLRC1 seems to be influenced by different iodine concentrations in water. 展开更多
关键词 Autoimmune thyroiditis DNA methylation klrc1 klrc3 SH2D1B IODINE
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荧光定量PCR技术验证KLRC1为人类染色体12p12.3-13.2上系统性红斑狼疮相关的候选基因
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作者 任莉莉 李富荣 +2 位作者 刘冬周 齐晖 欧阳志斌 《南方医科大学学报》 CAS CSCD 北大核心 2007年第5期672-674,共3页
目的探讨KLRC1基因是否系统性红斑狼疮(SLE)易感染色体区段12p12.3-13.2上的候选基因,为SLE的分子机制研究提供依据。方法根据前期基因芯片研究结果,确认位于SLE染色体连锁位点上的基因KLRC1,利用TaqMan实时荧光定量PCR方法在SLE活动期... 目的探讨KLRC1基因是否系统性红斑狼疮(SLE)易感染色体区段12p12.3-13.2上的候选基因,为SLE的分子机制研究提供依据。方法根据前期基因芯片研究结果,确认位于SLE染色体连锁位点上的基因KLRC1,利用TaqMan实时荧光定量PCR方法在SLE活动期及静止期患者外周血T、B淋巴细胞亚群检测其表达。结果SLE外周血单核细胞和T淋巴细胞亚群中,KLRC1基因的ΔCt值显著高于正常人(P<0.01),在B淋巴细胞亚群中,KLRC1基因的ΔCt无明显变化。在SLE患者外周血T、B淋巴细胞亚群中KLRC1基因的表达在活动期和静止期不存在显著性差异,SLEDAI积分与基因表达水平间无相关性。结论KLRC1基因可能是12p12-13区段SLE致病的一个候选基因,但是与疾病的活动性无关。 展开更多
关键词 系统性红斑狼疮 候选基因 klrc1 荧光实时定量PCR 染色体
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Corrigendum to“Glycyrrhizic acid,a natural sweetener,through KLRC2/ZAP70/MAPK pathway attenuates spleen deficiency syndrome in rats”[Food Bioscience 71(2025)107032]
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作者 Xiaojing Zhang Tingting Li +1 位作者 Wenxin Xia Xueyan Fu 《Food Bioscience》 2025年第10期1788-1790,共3页
The authors regret that in the published version of this article,we would like to clarify that the target proteins shown in Figs.5C and 7B were derived from the same batch of protein samples.Therefore,when selecting r... The authors regret that in the published version of this article,we would like to clarify that the target proteins shown in Figs.5C and 7B were derived from the same batch of protein samples.Therefore,when selecting representative bands for the same organ,we used the same internal reference bands.We sincerely apologize for not originally including this explanation in the figure captions,and we have now added this information to the caption of Fig.7 to ensure clarity. 展开更多
关键词 ZAP target proteins klrc corrigendum glycyrrhizic acid rat spleen MAPK selecting representative bands
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