Answer:
The CTL has specific receptors that can recognize infected or damaged cells.
Explanation:
The cytotoxic T cells (CTL) is a type of white blood cells that specifically helps in destroying virus-infected cells (also damaged cells and cancer cells).
This type of cells has a special receptor called T-cells receptors (TCR) which ones recognize specific antigens (molecule that stimulate the immune systems because are “strange” to them). Virus inside a cell could bind to a special molecule called class I MHC, this molecule moves the virus to the surface of the cell where it can be recognized by a CD8+ specific antigen-receptor of the CTL.
Answer:
A mutation is a change in a DNA sequence. Mutations can result from DNA copying mistakes made during cell division, exposure to ionizing radiation, exposure to chemicals
called mutagens, or infection by viruses. Germ line mutations occur in the eggs and sperm and can be passed on to offspring, while somatic mutations occur in body cells and are not passed on.
Mutation has been the source of many Hollywood movies, but it's really a simple process of a mistake made in a DNA sequence as it's being copied. Some of that's just the background noise that DNA copying is not perfect, and we should be glad of that or evolution couldn't operate. But mutation can also be induced by things like radiation or carcinogens in a way that can increase the risk of cancers or birth defects. But it's pretty simple; it's basically an induced misspelling of the DNA sequence.
That's a mutation.
When a variant alters a protein that plays a critical role in the body, it can disrupt normal development or cause a health condition. A condition caused by variants in one or more genes is called a genetic disorder. In some cases, gene variants are so severe that they prevent an embryo from surviving until birth.
Sorry me nobody else knew either lollll
Answer: C. Cells in meiosis have unique genetic information
Explanation: Meiosis is the cell division that forms four daughter cells from one parent cell. It includes two successive divisions called as meiosis I and meiosis II. Crossing over during prophase I of meiosis I imparts new gene combinations to the daughter cells of meiosis. Hence, daughter cells formed by the end of meiosis have some new gene combinations, that is, unique genetic information.
