Explanation:
The goal of timing nitrogen (N) applications to corn is to supply adequate N when the crop needs it, without supplying excess that can potentially be lost. Because N reactions in the soil are closely linked to both temperature and moisture conditions, this goal is often hard to achieve.
<span>Carbohydrates is the correct answer</span>
Answer:
The interference with the transport of pyruvate into mitocondria results in weight gain.
Explanation:
Pyruvate is the end product of glycolysis. After being formed the pyruvate is transported into mitochondria to carry out the second stage of aerobic respiration that is TCA cycle.
Now if the pyruvate is not transported into mitochondria then the pyruvate will accumulate in the cytosol.The accumulation of pyruvate prevent further breakdown of glucose.
As a result the uncatabolized glucose is the converted into glycogen and the glycogen will accumulate in the liver and muscle leading to weight gain.
Your skeletal muscle is found between the bones
Answer:
75%
Explanation:
Hypophosphatemic rickets is a disorder characterized by hypophosphatemia (low level of phosphate in the blood), defective intestinal absorption of calcium, and rickets (impaired mineralization of cartilaginous growth plates) or osteomalacia (impaired mineralization of the osteoid) unresponsive to vitamin D. It can be inherited or acquired.
When it comes to inheritable hypophosphatemic rickets, the disorder is most often inherited in an X-linked dominant manner. This means that the gene is inherited through the X chromosome and that one dominant allele is enough to cause it.
As the mother is heterozygous for the trait, she has one dominant and one recessive allele (XHXh). The father has one X chromosome, which he inherited from his mother, and as he has the condition, the dominant allele will be present on it (XHY).
This means that, if the child is a girl, she will definitely have the disorder. Girls inherit one X chromosome from each of their parents. Even if she inherited the one with the recessive allele from her mother, she would get the one with the dominant allele from her father.
If the child is a boy, he has a 50% chance to inherit the condition. Boys inherit the Y chromosome from their father and the X chromosome from their mother. As the mother is heterozygous, he can either get the chromosome without the dominant allele or the one with it. This means that there is a 50% chance of inheriting the disorder.
If we say that there are equal chances of this couple having female and male children, when we combine these results, we get a 75% chance of them inheriting hypophosphatemic rickets.
