Heredity is the study of transmission of traits and biological information between generations.
Variation is simply differences in genetic sequence.
Genes are the unit of heredity and a segment of DNA carrying information.
Morphological traits are physical characteristics such as height, weight, and eye color.
Physiological traits are functions such as metabolic rate, blood pressure, and body temperature.
Behavioral traits are actions such as aggression, fear, and social interaction.
Genetic variation is variation seen within the genes; uniqueness of the gene in terms of quantity.
Phenotypic variation is a physical manifestation of the genetic variation; appearance, behavior, and biological mechanisms.
Mutations are changes in DNA caused by gene sequence mutated by external factors, such as in the course of time or abrupt moments like exposure to radiation.
Gene Flow is the movement of genes from one population to another.
Sex introduces new genetic combination that leads to genetic shuffling.
Classical Genetics is based on Mendel's first and second laws.
Molecular Genetics is based on the Central Dogma of Molecular.
Evolutionary Genetics is based on the theory of Natural Selection proposed by Darwin.
Thomas Hunt Morgan proved that genes are located on the chromosomes during drosophila in 1918.
R.A. Fisher began the study of quantitative genetics by partitioning phenotypic variance into a genetic and an environmental component in 1926.
William Bateson discovered the linkage between genes and coined the term “genetics” in 1904.
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Archibald Garrod discovered the alkaptonuria, a human disease, has a genetic basis in 1902.
Gregor Mendel published experiments in plant hybridization which lays out the basic theory of genetics in 1866, but it was widely ignored until 1900.
Ernst Haeckel's experiments proved that the genetic material is located in the nucleus in 1871.
Hermann J. Muller discovered the role of genetics in cancer in 1926.
A year after, together with Reginald, Punnet, Bateson discovered the science of genetic linkage and coined the term “epistasis” to describe the interaction between two different traits in 1910.
Walter Sutton hypothesized that the behavior of chromosomes during meiosis led to the discovery that genes are located on chromosomes in 1903.
Carl Correns, Hugo de Vries, and Erich Von Tschermak rediscovered Mendel’s work in 1900.
Wilhelm Johannsen coined “gene” in 1904.
Friedrich Miescher isolated “nucleic acid” from pus cells in 1871.
Muller demonstrated that x-rays induce mutations in 1944.
Kary Mullis invented the process called Polymerase Chain Reaction (PCR) in 1983, a technique that amplifies a segment of the DNA until millions of copies are produced in just a short period of time.
The Human Genome Project was started in 1990 with the goal to sequence and map the genome of man.
Stanley Cohen and Herbert Boyer combined DNA from two different species in vitro, then transformed it into bacterial cells, marking the first DNA cloning in 1977.
Avery, Macleod, and McCarty showed in 1944 that DNA can transform bacteria, demonstrating that DNA is the hereditary material.
Reverse transcriptase, an enzyme found in retroviruses, was discovered in 1970 and used in cloning genes.
The sequence of the entire human genome was announced in 2003.
Ian Wilmut and Keith Campbell successfully cloned Dolly the sheep in 1996, the first mammal to be cloned from an adult cell.
Marshall Nirenberg solved the genetic code in 1966, showing that 3 DNA bases code for one amino acid.
Paul Berg was the first to create a recombinant DNA molecule in 1972.
Frederick Sanger introduced the process of sequencing the genome of a bacteriophage in 1977, a process later done in other organisms as well.
James Watson and Francis Crick determined the structure of the DNA molecule in 1953, which led to the knowledge of how it replicates.