Answer:
ans this question is no 3
Explanation:
Because it sends electrical output signals to the muscles affecting the muscles ability to functions.
I think its the Diurnal Cycle.
Ok, so I wrote these out just to make it a little bit easier for you to understand what I am about to explain.
So for the first one you have two different traits that can be inherited- having freckles or having no freckles, F and f respectively. The dominant trait (or having freckles) is shown by the capital F, and is almost always expressed over the recessive trait, or the lowercase f. So, for example, if you have a genotype of Ff, the trait having freckles will show up instead of not having freckles. The only way that you could have the trait of no freckles show up is if there are two recessive alleles for having no freckles, or ff. In this case, you have two parents who are both heterozygous for the trait of having freckles, so in other words the mother has Ff and the father has Ff. Each parent passes down one allele to the offspring, so since you are breeding Ff and Ff, you should result in having the possible genotypes of FF, Ff, Ff, and ff. This means that there is a 25% chance that the offspring will be homozygous for having freckles, a 50% chance that the offspring will be heterozygous for having freckles and a 25% chance that they would be homozygous for having no freckles, or a 1:2:1 ratio.
Incomplete dominance is a little bit different that just a normal monohybrid cross. Instead of just the dominant gene showing up in a heterozygous genotype, both traits show up. So like the question says, if a homozygous red flower plant was crossed with a homozygous white flower plant, their offspring would not just be white or red, they would be pink because it is a mixture of white and red. So then if you crossed the heterozygous, or Rr plants, the result would be a 25% chance of getting a homozygous RR red plant, a 50% chance of getting a pink Rr plant, and a 25% chance of getting a white rr plant, or another 1:2:1 ratio.
Sorry for the wordy answer, but hopefully this helps you understand this a little better :)
Answer:
1. Liver
2. Liver and Kidneys
3. Mitochondria
4. Lumen of the small intestines
5. Liver
Explanation:
1. Glucose is phosphorylated into glucose-6-phosphate which is the first step of both glycogen synthesis and glycolysis, this process occurs in the liver
2. Glucose 6-phosphate is a product of a process named gluconeogenesis which occurs in the liver it serves as a substrate for glucose-6-phosphatase in the liver.
3. Creatinine kinase is an enzyme that catalyzes the phosphorylation of creatine. In regeneration process of ATP, creatine phosphate transfers a high-energy phosphate to ADP which produces ATP and creatine
4. Initially lipase digestion lipase digestion happens in the small intestine where the bile salts reduce the surface tension of the fat droplets allowing the lipases to attack the triglyceride molecules. These molecules are taken up into the epithelial cells that line the intestinal wall, where they are resynthesized into triglyceride
5. The job of the liver is to produce ketone bodies. If the liver had this enzyme, the ketone bodies it produces would be immediately broken down by the liver before they are released, thereofore, no release of ketone bodies into the bloodstream
Organisms are broken into decomposers. hope that helped