Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Human Genetics01:28

Human Genetics

610
Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
610
Incomplete Dominance01:43

Incomplete Dominance

22.7K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
22.7K
Behavioral Genetics and Its Designs01:23

Behavioral Genetics and Its Designs

403
Behavior genetics explores how genetic inheritance influences human behavior. It focuses on how genes, passed from parents to offspring, contribute to the development of behavioral traits and tendencies. This branch of genetics seeks to understand the complex interplay between inherited genetic factors and environmental influences in shaping our behaviors.
The primary methodologies used in behavior genetics include family studies, twin studies, and adoption studies, each providing unique...
403
Genetic Lingo01:11

Genetic Lingo

103.1K
Overview
103.1K
Genetic Material01:20

Genetic Material

1.9K
Within the human body, a complex and detailed system of trillions of cells works in unison to sustain life. Each cell houses a nucleus, which contains 46 chromosomes divided into 23 pairs. Chromosomes are highly coiled structures made of the genetic material DNA. These chromosomes are essential carriers of genetic information, with half inherited from the mother through her egg and the other half from the father's sperm, combining to create the unique genetic makeup of an individual.
1.9K
Trihybrid Crosses02:27

Trihybrid Crosses

23.4K
Trihybrid Crosses
Some of Mendel’s crosses examined three pairs of contrasting characteristics. Such a cross is called a trihybrid cross. A trihybrid cross is a combination of three individual monohybrid crosses. For example, plant height (tall vs. short), seed shape (round vs. wrinkled), and seed color (yellow vs. green).
The F1 generation plants of a trihybrid cross are heterozygous for all three traits and produce eight gametes. Upon self-fertilization, these gametes have an equal...
23.4K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Clinico-biological refinement of BCL11B-related disorder and identification of an episignature: A series of 20 unreported individuals.

Genetics in medicine : official journal of the American College of Medical Genetics·2023
Same author

Clinically available testing options resulting in diagnosis in post-exome clinic at one medical center.

Frontiers in genetics·2022
Same author

Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case report.

Clinical case reports·2022
Same author

Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys-Dietz Syndrome.

Pediatric cardiology·2021
Same author

Novel splicing (c.6529-1G>T) and missense (c.1667G>A) mutations causing factor V deficiency.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis·2021
Same author

A rare case of postnatal mosaic trisomy 12 with severe congenital heart disease and literature review.

American journal of medical genetics. Part A·2021

相关实验视频

Updated: Jul 16, 2025

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
09:37

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information

Published on: August 15, 2019

9.8K

遗传学101:什么时候参考

Alyce Belonis1, Sofia Saenz Ayala2

  • 1Division of Human Genetics, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 4006, Cincinnati, OH 45229, USA; Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, OH, USA.

Pediatric clinics of North America
|September 13, 2023
PubMed
概括
此摘要是机器生成的。

遗传学几乎影响所有疾病,而不仅仅是与怀孕或新生儿有关的疾病. 了解遗传影响对于管理一个人的整个生命中的健康和疾病至关重要.

关键词:
家庭史 家庭史 家庭史基因检测是一种基因检测.增长和发展的差异.代谢中的先天性错误医疗史 病史 病史儿科 儿科 儿科

更多相关视频

Infinium Assay for Large-scale SNP Genotyping Applications
13:33

Infinium Assay for Large-scale SNP Genotyping Applications

Published on: November 19, 2013

39.0K
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

33.8K

相关实验视频

Last Updated: Jul 16, 2025

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
09:37

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information

Published on: August 15, 2019

9.8K
Infinium Assay for Large-scale SNP Genotyping Applications
13:33

Infinium Assay for Large-scale SNP Genotyping Applications

Published on: November 19, 2013

39.0K
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

33.8K

科学领域:

  • 遗传学和基因组学 遗传学和基因组学
  • 人类健康和疾病

背景情况:

  • 遗传学传统上与生殖健康,出生缺陷和新生儿查有关.
  • 遗传因素的影响超出了这些传统领域.

研究的目的:

  • 突出基因在整体健康和疾病中的普遍作用.
  • 强调在整个生命周期中考虑遗传倾向的重要性.

主要方法:

  • 关于各种疾病的遗传影响的文献综述.
  • 分析基因构成对健康结果的影响.

主要成果:

  • 遗传因素有助于几乎所有疾病的倾向和进展.
  • 遗传学在个人一生中起着重要作用,从出生到老年.

结论:

  • 遗传学在整个生命周期的健康和疾病中发挥着根本性的作用.
  • 对遗传学的全面理解对于有效的医疗保健和疾病管理至关重要.