Answer:
B) a nonsense mutation; this is because a nonsense mutation results in the change of a regular amino acid codon into a stop codon, which ceases translation. This fits with the problem's description of the protein that causes the symptoms as too short, as translation is the process by which proteins/polypeptides are created. A missense mutation would not be the answer because it still codes for an amino acid, which would not shorten the protein. A duplication of the gene would probably just lengthen the protein or not affect its length at all.
Will be found in the environment in which it was planted in the turnda
Answer:
•Photosynthesis removes carbon dioxide from the atmosphere, and cellular respiration puts it back.
Explanation:
Photosynthesis:
It is the process in which in the presence of sun light and chlorophyll by using carbon dioxide and water plants produce the oxygen and glucose.
Carbon dioxide + water + energy → glucose + oxygen
water is supplied through the roots, carbon dioxide collected through stomata and sun light is capture by chloroplast.
Cellular respiration:
It is the breakdown of glucose molecule in the presence of oxygen to yield large amount of energy. Water and carbon dioxide are also produced as a byproduct.
Glucose + oxygen → carbon dioxide + water + 38ATP
In this way it release the carbon dioxide back into atmosphere.
The disorder is Emphysema.
It is a type of chronic obstructive pulmonary disease that presents as an abnormal and permanent enlargement of air spaces distal to the terminal bronchioles. It frequently occurs in association with obstructive problems and chronic bronchitis.
Answer:
When we talk about the inheritance of traits, or the passage of traits from parents to future generations down the line, we are not just talking about the visual (phenotypical) expression of those traits, but also, their underlying explanation, which is the genotype. A genotype is basically how the genes of the parents combine in such a way that the children inherit a set of traits from the parents, and express them phenotypically, or not.
In the case of blood types, we have four phenotypic groups: A, B and O. Each one of these types is characterized by the underlying set of genes that are responsible for what is expressed. While the O blood type presents a genotype ii, which is recessive, the A and B types will have the following genetic patterns: Ia Ia, or, Ia i (characteristic of the O genetic material) for the A type and: Ib Ib, or Ib i, for the B type. When there is a genetic conjugation from parents genetic material, regarding blood type, we would have these sets of genes combining. In most of the possible combinations genetically speaking, we have the recessive i gene appearing, including in the A and B dominant blood types. This means that when crossed, there will always be a chance of at least one offspring presenting the O blood type, even if one of the parents is dominant A, or B.
In answer: it is the fact that all three types present the recessive allele i, typical of the O blood type, that when pairings of genes happen between parents, the genetic characteristic of the O type may present itself in a dominant fashion, instead of the usual recessive pattern.
