相关实验视频

Updated: Jul 1, 2025

Evaluation of Hepatic Glucose Production in a Polycystic Ovary Syndrome Mouse Model
09:44

Evaluation of Hepatic Glucose Production in a Polycystic Ovary Syndrome Mouse Model

Published on: March 5, 2022

3.0K

IGF2BP2和IGFBP3基因型,哈普类型和遗传模型研究多囊性卵巢综合征

Fatemeh Govahi Kakhki1, Saman Sargazi2,3, Farzaneh Montazerifar1,4

  • 1Department of Nutrition, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.

Journal of clinical laboratory analysis
|March 12, 2024
PubMed
概括

在IGF2BP2和IGFBP3的遗传变异与多囊性卵巢综合征 (PCOS) 的风险增加有关. 特定的rs1470579和rs2854744基因型,以及某些等位基因组合,在研究的人群中显著影响PCOS易感性.

关键词:
在IGF2BP2BP2中使用.在 IGFBP3 中使用.基因多形态的多态化多囊性卵巢综合征是多囊性卵巢综合征.

更多相关视频

A Hyperandrogenic Mouse Model to Study Polycystic Ovary Syndrome08:20

A Hyperandrogenic Mouse Model to Study Polycystic Ovary Syndrome

Published on: October 2, 2018

11.2K
Author Spotlight: Investigating the Mechanisms and Inducing Models of Polycystic Ovary Syndrome04:49

Author Spotlight: Investigating the Mechanisms and Inducing Models of Polycystic Ovary Syndrome

Published on: July 5, 2024

1.0K

相关概念视频

Oogenesis02:07

Oogenesis

In human women, oogenesis produces one mature egg cell or ovum for every precursor cell that enters meiosis. This process differs in two unique ways from the equivalent procedure of spermatogenesis in males. First, meiotic divisions during oogenesis are asymmetric, meaning that a large oocyte (containing most of the cytoplasm) and minor polar body are produced as a result of meiosis I, and again following meiosis II. Since only oocytes will go on to form embryos if fertilized, this unequal...
63.7K
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

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...
13.4K
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

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