校正:针对唐氏综合征的非侵入性产前检测 (NIPT) 在产前查计划中的实施和影响:系统性审查和元分析
PloS one
|February 4, 2025
概括
这项研究纠正了先前发表的一篇文章DOI. 校正确保了科学文献的准确引用和引用. 研究人员应在所有未来的引用中使用更新的DOI.
科学领域:
- 科学出版业的科学出版.
- 图书统计学 图书统计学
- 学术传播学术交流
背景情况:
- 准确的引用对于科学完整性至关重要.
- DOI (数字物体标识符) 确保持续链接到学术文章.
- 在DOI中的错误可能会阻碍对研究的访问,并影响引用跟踪.
研究的目的:
- 为错误的物品DOI提供纠正.
- 为科学界确保准确的引用.
- 维护学术交流的完整性.
主要方法:
- 在原始出版物中识别错误的DOI.
- 检查文章的正确DOI.
- 发出正式的纠正通知.
主要成果:
- 原来的DOI被发现是不正确的.
- 正确的DOI已被确定并提供.
- 这一更正正确了文献信息.
结论:
- 准确的DOI对于可靠的科学记录保持至关重要.
- 这种纠正有助于正确引用和访问研究.
- 确保DOI的准确性符合学术出版的标准.
相关概念视频
Oogenesis
63.4K
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...
63.4K
Teratogenicity
2.3K
The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
2.3K
Meiosis I
192.8K
Meiosis is a carefully orchestrated set of cell divisions, the goal of which—in humans—is to produce haploid sperm or eggs, each containing half the number of chromosomes present in somatic cells elsewhere in the body. Meiosis I is the first such division, and involves several key steps, among them: condensation of replicated chromosomes in diploid cells; the pairing of homologous chromosomes and their exchange of information; and finally, the separation of homologous chromosomes by...
192.8K
Genetic Screens
4.9K
Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
4.9K
Karyotyping
56.7K
Overview
56.7K


