This is the use of biological processes, organisms, or systems to manufacture products intended to improve the quality of human life.
This is the the theory that describes protein building in this order: DNA to RNA to protein. DNA is transcribed to RNA which is translated to protein. Protein is never back-translated to RNA or DNA; DNA is never directly translated to protein
This theory of inheritance states that genes are located on chromosomes which undergo segregation and independent assortment.
This is a type of heredity where two dominant alleles are both fully expressed in a phenotype
This is a 3 letter sequence of DNA or messenger RNA code that stands for one amino acid in a protein
This is the inability to perceive differences between some or all hues that other people can distinguish, most of the time it is due to a genetic disorder but can have other causes.
This is an autosomal recessive heredity disease that affects the respiratory and digestive systems.
This is a technique used to distinguish between individuals of the same species using only samples of their DNA.
This is a biochemical process used for determining the order of the nucleotide bases, adenine, guanine, cytosine, and thymine, in any DNA molecule. By comparing the DNA sequence of two organisms, scientists can see if the organisms are related or not, as well as how closely they are related.
This is the structure of DNA as first published by James Watson and Francis Crick in 1953
This is caused by trisomy 21 (a nondisjunction), causing highly variable degrees of learning difficulties and physical disabilities
This is the process of separating DNA fragments by size using an electric field and a fluorescent dye.
This is the application of a wide range of sciences to answer questions of interest to a legal system. DNA analysis is one component that may be used to place a suspect at a crime scene.
This is a genetic mutation caused by the insertion or deletion of one or more nucleotides that changes the amino acid sequence from the site of the mutation forward.
The next level of offspring from the parent. For humans, it occurs about once every 30 years
This is showing possible outcomes, genotypes and phenotypes, of offspring from two parents. This is usually shown using a Punnett square.
These are inherited diseases that cause negative, abnormal physical effects in organisms.
This is a trait that is a blend of the dominant and recessive gene; inheritance pattern where the phenotype of a heterozygote is intermediate between those of the two homozygotes; neither allele of the pair is dominant but combine and display a new trait.
This is one of Mendel's principles that govern the process of genetic inheritance. It states that allele pairs separate independently during the formation of gametes (sex cells). This means that traits are passed to offspring independently of one another.
This is the complete set of all chromosomes of a cell of any living organism. They are often displayed in a photograph of chromosomes that have been grouped into matching pairs.
Law Of Dominance
One of Mendel's Laws of Inheritance. This law states an organism has two different alleles for a trait and the allele that is expressed in the phenotype, masking the expression of the other allele,is said to be dominant. The allele whose expression is masked is said to be recessive.
Law Of Segregation
This is Mendel's first law. For each inherited trait, there are at least one pair of alleles. This states that during gamete formation each member of an allelic pair separates from the other member to form the genetic make-up of a gamete (sex cell).
This is a process where a parent cell divides into four sex cells with half the chromosomes.
This scientist is known as the Father of Genetics, because of his work with pea plants.
The process of nuclear division in cells that produces daughter cells that are genetically identical to each other and to the parent cell.
This is a type of Punnett square genetic cross that predicts the result of crossing two different alleles for the same gene.
This is one form of RNA that that serves as a template for protein synthesis. It is transcribed from DNA and then translated at ribosomes to produce a protein.
This is the possibility of one of many different genes on a chromosome; presence of more than two alleles for a genetic trait.
This is a random error/change in the DNA sequence. These may be inherited or occur in cells during the lifetime of the organism
This is the only part of a DNA/RNA nulceotide that changes. It is found along with the 5-carbon sugar and the phosphate group.
This can be a fatal genetic disorder in which metabolic wastes build up in an individual's body.
This is a genetic mutation caused by the replacement of a single base nucleotide with another nucleotide. This term also includes insertions or deletions of a single base pair.
This is a two-part process that ends in the assembly of proteins at the ribosomes within cells. The first part, transcription, begins in the nucleus, when the DNA code is transferred to mRNA. The second part, translation, takes place at the ribosomes, where both mRNA and tRNA work to assemble proteins.
This is a diagram that shows the gene combinations that might result from a genetic cross
This is a form of a gene that is hidden by another, dominant, form of the same gene
This is an artificial genetic sequence from combining two other sequences in a plasmid
This is a situation in which genes are attached to an organism's sex chromosomes; the sex of an organism influences the expression of a gene; traits controlled by genes located on sex chromosomes.
Process by which two cells from different parents unite to produce the first cell of a new organism
Sickle Cell Anemia
This is a genetic disorder where the red blood cells change their shape and can get stuck in capillaries
This is a fatal genetic disorder, inherited in an autosomal recessive pattern, in which harmful quantities of a fatty substance called ganglioside accumulate in the nerve cells in the brain.
This is the second step of production of proteins where mRNA is decoded to produce a specific polypeptide
This is the result of nondisjunction of chromosomes during meiosis. This mutation results in three copies, instead of the normal two. It can happen with sex or autosomal chromosomes.
This is one form of RNA that transports a specific amino acid to a ribosome during protein synthesis.