相关实验视频
Updated: Jul 1, 2025

09:53
In Vivo Nanovector Delivery of a Heart-specific MicroRNA-sponge
Published on: June 15, 2018
7.4K
伊朗人群中miRNA-146a基因变异与多发性硬化症的关联
Atefeh Zamani1, Masoumeh Dehghan Manshadi2, Mansoureh Akouchekian3
1Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Medical journal of the Islamic Republic of Iran
|March 4, 2024
概括
miR-146a基因rs2910164多态性与伊朗人的多发性硬化症 (MS) 易感性有关. 在这个人群中,rs2431697的多态性没有与MS相关.
科学领域:
- 遗传学 是一个遗传学.
- 免疫学 免疫学 免疫学
- 神经学 神经学
背景情况:
- 多发性硬化症 (MS) 是中枢神经系统的一种自身免疫性炎症性疾病.
- 微RNA-146a (miR-146a) 是一种调节免疫反应的非编码RNA.
研究的目的:
- 调查伊朗人口中miR-146a基因多态 (rs2910164和rs2431697) 与MS风险之间的关联.
主要方法:
- 通过PCR-RFLP和四级原始ARMS-PCR进行rs2910164和rs2431697多态的基因型定型.
- 与60名多发性硬化患者和100名健康对照进行的病例控制研究.
- 使用千二测试和哈迪-韦恩伯格平衡评估的统计分析.
主要成果:
- miR-146a基因rs2431697的多态性与MS没有关联.
- 在miR-146a基因rs2910164多态和MS之间发现了显著的关联 (P = 0.012).
结论:
- 在伊朗人群中,miR-146a基因rs2910164多态可能导致MS易感性.
- 需要进一步的研究来阐明miR-146a在MS病变发生过程中的作用.
更多相关视频
相关概念视频
MicroRNAs
3.0K
MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
3.0K
Single Nucleotide Polymorphisms-SNPs
15.1K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.1K
Genome-wide Association Studies-GWAS
13.4K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
13.4K
lncRNA - Long Non-coding RNAs
8.6K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
8.6K

