Francis Harry Compton Crick, who co-discovered the structure of deoxyribonucleic acid (DNA) in 1953 in Cambridge, England, also developed The Central Dogma of Molecular Biology, and further clarified the relationship between nucleotides and protein synthesis. Crick received the Nobel Prize in Physiology or Medicine that he shared with James Watson and Maurice Wilkins in 1962 for their discovery of the molecular structure of DNA. Crick's results on the genetic material found in all living organisms advanced theories of inheritance and spurred further studies into the field of genetics and embryology.
Cold Spring Harbor Laboratory (CSHL) is a non-profit research institution that specializes in cancer, neuroscience, plant biology, quantitative biology, and genomics. The organization is located on the shores of Cold Spring Harbor in Laurel Hollow, New York. The Brooklyn Institute of Arts and Sciences established the CSHL in 1890, to provide scientists with facilities to research Charles Darwin's evolutionary theory. The first mission of CSHL was biological science education. Since 1998, CSHL has housed the Watson School of Biological Sciences, a PhD program dedicated to scientific research. Nobel Laureates who conducted experiments at the CSHL include Barbara McClintock, Alfred Hershey, James Watson, Francis Crick, and Sydney Brenner. Throughout its history, researchers at CSHL have studied embryology, reproductive medicine, and genetics.
Matthew Stanley Meselson conducted DNA and RNA research in the US during the twentieth and twenty-first centuries. He also influenced US policy regarding the use of chemical and biological weapons. Meselson and his colleague Franklin Stahl demonstrated that DNA replication is semi-conservative. Semi-conservative replication means that every newly replicated DNA double helix, which consists of two individual DNA strands wound together, contains one strand that was conserved from a parent double helix and that served as a template for the other strand. Meselson's work enabled researchers to better explain and control cellular development by showing how DNA are copied when a cell divides and interpreted when a cell makes proteins.
Apoptosis, or programmed cell death, is a mechanism in embryonic development that occurs naturally in organisms. Apoptosis is a different process from cell necrosis, which is uncontrolled cell death usually after infection or specific trauma. As cells rapidly proliferate during development, some of them undergo apoptosis, which is necessary for many stages in development, including neural development, reduction in egg cells (oocytes) at birth, as well as the shaping of fingers and vestigial organs in humans and other animals. Sydney Brenner, H. Robert Horvitz, and John E. Sulston received the Nobel Prize in Physiology or Medicine in 2002 for their work on the genetic regulation of organ development and programmed cell death. Research on cell lineages before and after embryonic development may lead to new ways to reduce or promote cell death, which can be important in preventing diseases such as Alzheimer's or cancer.