Answer:
respiration
Explanation:
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During T cell maturation, the t cells must pass two tests. first, immature t cells that can recognize MHC molecules are Selection. Second, immature t cells that recognize and bind to molecules normally found in the body are Activation.
Selection is the first test that T cells must pass. During this process, immature T cells that can recognize MHC molecules are selected. MHC molecules are found on the surface of cells and are involved in antigen presentation. When T cells come into contact with MHC molecules, they are able to recognize the molecules and begin the process of selection. During selection, the T cells that recognize MHC molecules are chosen over those that do not. This helps ensure that the cells that are selected are those that can properly respond to antigens.
The second test that T cells must pass is activation. During activation, T cells that recognize and bind to molecules normally found in the body are selected. These molecules are called self-antigens and can include proteins, carbohydrates, and lipids. When T cells come into contact with self-antigens, they are able to recognize the molecules and begin the process of activation. During activation, the T cells that recognize self-antigens are chosen over those that do not. This helps ensure that the cells that are selected are those that will not attack the body’s own cells.
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Answer:
SNPs have shown that only 0.1 % of DNA sequences are different in the human genome between different individuals, thereby all the inherited phenotypic variation observed in our species is associated with only 0.1 % of differences at the genome level
Explanation:
Haplotypes are block-like sequences of DNA that are inherited together due to low recombination rates. Moreover, single-nucleotide polymorphism (SNP) mapping is a very useful methodology used to map the site of SNP mutations (i.e., SNP variants). In this regard, it has been observed that there are approximately 10 million common SNPs in the human genome. These SNPs contribute to the wide range of phenotypic variation observed in human populations for different traits (e.g., eye color, hair, weight, height, etc). Moreover, researchers have determined that SNPs can be clustered into haplotypes, thereby haplotypes can be accurately sampled by as few as approx. 300,000 selected SNPs, which are sufficient to represent all of the genetic variation across different human genomes.
None: Only those mutations that occur in the germ line and result in gametes will have a chance of being passed on to progeny. An alteration in DNA that occurs after conception.
Somatic mutations can occur in any of the body's cells except germ cells (sperm and egg) and are therefore not passed on to children. These alterations can (but not always) cause cancer or other diseases. Mutations in somatic cells are called somatic mutations. Because they do not occur in the cells that give rise to gametes, the mutation is not transmitted to the next generation sexually. Human somatic cells have 46 chromosomes: 22 pairs and 2 sex chromosomes that may or may not form a pair. This is the 2n or diploid condition. Human gametes have 23 chromosomes, each of 23 unique chromosomes, one of which is a sex chromosome. Somatic cells are the cells in the body other than sperm and eggs (called germ cells). In humans, somatic cells are diploid, meaning they contain two sets of chromosomes, one inherited from each parent. Mutations in a somatic cell occur in somatic cells and are transmitted by mitosis, resulting in cancer. However, mutations in a gamete are passed on by meiosis, resulting in mutated offspring. A genetic mutation occurs during DNA replication, and chromosomal mutations occur during meiosis.
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I believe the correct answer will be A
