Related Experiment Video
Updated: Apr 24, 2026

09:51
Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
Published on: May 25, 2018
35.9K
Lasker∼Koshland to genetics pioneer
1Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
Cell
|September 13, 2014
Summary
Mary-Claire King received the 2014 Lasker∼Koshland Special Achievement Award for her pioneering work in genetics. Her research advanced disease gene identification, human evolution insights, and human rights advocacy.
Area of Science:
- Genetics and Genomics
- Human Evolution
- Biomedical Research
Background:
- Mary-Claire King's groundbreaking research has significantly impacted medical genetics.
- Her work bridges the gap between genetic discoveries and clinical applications.
Discussion:
- King's innovative genetic approaches have been crucial for identifying genes linked to diseases.
- Her contributions extend to understanding human evolutionary history through genetic analysis.
Key Insights:
- Revolutionized disease gene identification using genetic methodologies.
- Provided critical insights into human evolution and population genetics.
- Demonstrated the power of genetics in advancing human rights.
Outlook:
- Her legacy continues to inspire geneticists and researchers worldwide.
- Future research will build upon her foundational work in disease gene discovery and human evolution.
Related Concept Videos
The DNA Helix
19.8K
Deoxyribonucleic acid, or DNA, is the genetic material responsible for passing traits from generation to generation in all organisms and most viruses. DNA is composed of two strands of nucleotides that wind around each other to form a spring-like structure called a double helix. However, the double helix is not perfectly symmetrical. Instead, there are regularly occurring grooves in the structure. The major groove occurs where the sugar-phosphate backbones are relatively far apart. This space...
19.8K
The DNA Helix
128.7K
Overview
128.7K
Genetic Screens
4.6K
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...
4.6K
Incomplete Dominance
18.8K
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.
18.8K
Genetic Lingo
84.1K
Overview
84.1K
Human Genetics
2.0K
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...
The complex relationship between genetics and psychology is observable through common biological components such...
2.0K

